MMS
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A special word
from Jim Humble

I want to wish all of you a very happy, successful and prosperous New Year. This certainly is a very exciting and significant time in world history—2017—the beginning of the third millennium.

Sadly, it is all too easy in today’s world to adapt the attitude of “Look at the world today, have you ever seen such a mess?” This certainly seems to be the case, and there are many “wrongs” that appear to be triumphing. But, I would like to challenge each and every one of you to adapt an attitude of “What can I do today, here and now, to make the world a better place?” By this, I am not suggesting you have to go out and perform some grand acts. To make a difference in the world it does not necessarily require “big things”, but rather little things, (kind acts, lending a helping hand), done on a consistent basis, can go a long ways to make a difference in this world. 

Will you join me this coming year to make a personal commitment to always “help one another” whenever you have the opportunity? This can be applied in many ways, and certainly if you have been helped through the use of MMS, help others who need this amazing master miracle working solution as well—spread the word.  

These past couple of years, you have not heard all that much from me personally, as I have been busy working on my newest book, the MMS Health Recovery Guidebook. But now, as we begin 2017, I have several new things to share with you. So stay tuned as over the next few weeks, as I will be announcing, via this newsletter, some significant news. 

Best wishes to all of you, for a successful New Year,

Jim Humble

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Happy New Year 2017!!!!

A 100% cure for THE #1 killer in the history of the world and very few with the disease know it!
(Estimates have been as high as 50 billion killed by Malaria)

NOTE: How many have died since 1997 when Jim Humble discovered the cure? Low Estimate: 20 million!

 

Malaria is reported to have wiped out half of all people who have ever lived – and continues to be one of the biggest killers today.

disease picture for malaria newsletter

Malaria – 50 billion?
The idea that malaria could have been the cause of death for 50 billion people in human history derives from a statement from journalist Sonia Shah, whose book, “The Fever: How Malaria Has Ruled Humankind for 500,000 Years” explores the history of the disease.

Taking the statement at face-value – and assuming the speculative figures from demographer Carl Haub that over 100 billion people have lived on earth are accurate – this would mean that malaria has killed more than 50 billion people.

The figure is startling – but not completely implausible.

Author of “Parasites: Tales of Humanity’s Most Unwelcome Guests”, Rosemary Drisdelle, crunched the numbers using both Haub’s numbers and Shah’s claim, noting that if most people died between 8000BC and 1650AD, this could account for 5.4 million deaths a year.

 

 

Considering the lack of treatment that would have been available, and the fact that the disease has apparently been with humanity for 500,000 years, it’s not completely implausible.

In 1999, the WHO reported that malaria could have claimed the lives of close to 200 million people in the 19th century alone – and the group’s contemporary death figures say as many as 1.2 million deaths a year are still being attributable to the disease.

Taking this into account, it’s clear that malaria is the world’s biggest killer disease, having claimed billions of human lives.

“Did malaria kill between 53 and 54 billion of the 96 billion who lived before 1900? I’m neither an epidemiologist nor a statistician…We’ll never know for sure, but based on my reading I think it’s possible,” Drisdelle said.

https://businesstech.co.za/news/general/71652/the-biggest-killer-diseases-in-history/

 

Malaria is one of the few parasitic infections considered to be immediately life-threatening, and a patient with the diagnosis of P. falciparum malaria should be considered a medical emergency because the disease can be rapidly fatal

With the exception of tuberculosis, malaria kills more
people than any other communicable disease in the world. Approximately 300–500 million individuals throughout the
world are infected with Plasmodium spp., and 1.5 to 2.7
million people a year, most of whom are children, are being
killed by the disease. More people are dying from malaria
today than 30 years ago. Malaria is endemic in over 90 countries with a population of 2.4 billion people, which is 40% of the world’s population (4). Malaria prevention is difficult, and no drug is universally effective. Vaccine development studies are ongoing, but malarial vaccines are not yet in general use.

There has also been a definite increase in the number of
cases of P. falciparum malaria reported, which may be related to increased resistance to chloroquine.

http://www.hardydiagnostics.com/wp-content/uploads/2016/05/Malaria.pdf

 

Malaria may have killed half of all the people that ever lived. And more people are now infected than at any point in history. There are up to half a billion cases every year, and about 2 million deaths - half of those are children in sub-Saharan Africa.


"It's worse than it was 50 years ago," says malaria expert Robert Desowitz of the University of North Carolina, Chapel Hill.

So, why doesn’t the world know there is a 100% cure for THE #1 killer in the history of the world?

 

How could this be? Why doesn’t the world know? If this is true, then wouldn’t “they” tell us?

To REALLY understand the answers to the above most frequently asked questions we hear about Jim Humble’s cure for malaria, we have to ask the following questions;

1. How could this 100% “cure” for malaria be kept from the world?
2. Why would this information not be made public?
3. Who is in control of getting this information to the world?
4. What would happen if this information was made public?
5. When will this information be allowed to be spoken of on the world’s mainstream media?


1. How could this 100% “cure” for malaria be kept from the world?

This is a question that the majority of the world knows the answer and just don’t want to accept that it could be true! The answer being; the people that are in control of getting this information out don’t want it out! This leads me to the following question.


2. Why would this information not be made public?

If the people not wanting this information out are ALSO in control of the majority of the news medias around the world, the world’s health agencies, medical schools, and pay to have laws passed to only allow “them” to make such announcements, then it won’t be made public period!
If the “approvals” of a new drug or therapy are controlled by these same people then there would be no approval or research done either about a cure for Malaria. The same people that control the media are the same people that fund medical research projects, write the curriculum for medical schools and are heavily invested in pharmaceuticals as well, i.e have a complete monopoly of the worldwide medical industry with no competition. Health agencies worldwide are “supported” by pharmaceuticals, in fact, the CDC in Atlanta has over 20 drug patents says, Senator Robert Kennedy Jr. How can an agency make money off pharmaceuticals? Isn’t that a conflict of interest? So, is anyone surprised that a cure for Malaria would not be published worldwide do to all the money to be made in “treatment and research” than a cure!

White House and CDC hold patent on Ebola and its treatment


With the recent panic over a global Ebola pandemic, our friends at Natural News discovered that the US federal government actually took out a patent on the Ebola virus in 2010. The patent application is in the name of, ‘The Government of The United States Of America As Represented By The Secretary, Department Of Health & Human Services, Center For Disease Control.’
‘The invention provides the isolated human Ebola (hEbola) viruses denoted as Bundibugyo (EboBun) deposited with the Centers for Disease Control and Prevention ("CDC"; Atlanta, Georgia, United States of America) on November 26, 2007 and accorded an accession number 200706291,’ the patent description reads, ‘The present invention is based upon the isolation and identification of a new human Ebola virus species, EboBun. EboBun was isolated from the patients suffering from hemorrhagic fever in a recent outbreak in Uganda.’
Natural News goes on to explain that the patent not only grants DHHS and the CDC exclusive ownership of the Ebola strain it extracted from a Ugandan victim, it also claims ownership over all other similar Ebola variations. Showing what the CDC’s true agenda might be, the patent also claims exclusive ownership of most, if not all, Ebola treatments, tests, experiments, vaccines and drugs.
The report concludes, ‘This patent may help explain why Ebola victims are being transported to the United States and put under the medical authority of the CDC. These patients are carrying valuable intellectual property assets in the form of Ebola variants, and the Centers for Disease Control clearly desires to expand its patent portfolio by harvesting, studying and potentially patenting new strains or variants.’


http://www.whiteoutpress.com/articles/2014/q3/cdc-ebola-patent-could-earn-billions-pandemic/


http://www.naturalnews.com/046290_
Ebola_patent_vaccines_profit_motive.html

The reason is obvious why this information is not made public and even ridiculed!

It reminds me of the saying; All truth passes through three stages. First, it is ridiculed. Second, it is violently opposed. Third, it is accepted as being self-evident. The discovery of truth is prevented more effectively, not by the false appearance things present and which mislead into error, not directly by weakness of the reasoning powers, but by pre-conceived opinion, by prejudice. Arthur Schopenhauer.

3. Who is in control of getting this information to the world?

 

The mainstream media i.e (television, radio, newspapers and magazines), the world’s governments, world health organizations, the United Nations and other organizations that are concerned with the “health” of the world, as a whole.


NOTE: Controlling the media of the world is a VERY powerful position to propagate an agenda!

Who owns these medias and what are “their” goals?
Look at what people have said about the power of the press and who owns it!

• “Not every item of news should be published. Rather must those who control news policies endeavor to make every item of news serve a certain purpose:”
- Joseph Paul Goebbels, Nazi Propaganda Minister -

 

“We are grateful to the Washington Post, the New York Times, 

Time Magazine, and other great publications whose directors have attended our meetings and respected their promises of discretion for almost forty years. It would have been impossible for us to develop our plan for the world if we had  been subject to the bright lights of publicity during these years. But, the world is now more sophisticated and prepared to march towards a world government. The super-national sovereignty of an intellectual elite and world bankers is surely preferable to the national auto-determination practiced in past centuries.”
- Brother David Rockefeller -
C.F.R. and Trilateral Commission Founder

• "It is not enough for journalists to see themselves as mere messengers without understanding the hidden agendas of the message and myths that surround it."

- John Pilger -


• "We [the Zionists] have it all under such control that no one -- no one or no-body can [reach] people unless it is done through our media control. (Who has had control of the mass media in the 20th century? -- Chairman of ABC pp Leonard Goldenson, President of CBS -- James H. Rosenfield, Chairman of RCS -- David Sarnoff, Chief Executive of NBC -- Fred Silverman, President of PBS -- Lawrence Grossman, Chairman of Time -- Arthur Heiskell, Editor of U.S. News & World Report -- Marvin Stone, Chief Executive of Dow Jones -- Warren H. Phillips, Editor of Newsweek -- Lester Bernstein, President of TV Guide -- Walter Annenberg, President of New York Times -- Sulzberger family, TV program producer -- Norman Lear -- these and more all are Jews!!) We have it sewed up!!"
- Harold Wallace Rosenthal from the Harold Wallace Rosenthal Interview 1976 -


• “In March, 1915, the J.P. Morgan interests, the steel, shipbuilding, and powder interest, and their subsidiary organizations, got together 12 men high up in the newspaper world and employed them to select the most influential newspapers in the United States and sufficient number of them to control generally the policy of the daily press....They found it was only necessary to purchase the control of 25 of the greatest papers.' " 'The world can therefore seize the opportunity [Persian Gulf crisis] to fulfill the long--held promise of a New World Order where diverse nations are drawn together in common cause to achieve the universal aspirations of mankind.”
-- George Herbert Walker Bush"


"Spin" - One of the most important films of the last 25 years
[00:57:26]


- Artist Brian Springer spent a year scouring the airwaves with a satellite dish grabbing back channel news feeds not intended for public consumption. The result of his research is SPIN, one of the most insightful films ever made about the mechanics of how television is used as a tool of social control to distort and limit the American public's perception of reality. -
- by Brian Springer, 1992 -
(Posted here: Thursday, November 29, 2007)


Who Owns the U.S. Media?

 


- The control of the opinion-molding media is nearly monolithic. All of the controlled media — television, radio, newspapers, magazines, books, motion pictures speak with a single voice, each reinforcing the other. Despite the appearance of variety, there is no real dissent, no alternative source of facts or ideas accessible to the great mass of people which might allow them to form opinions at odds with those of the media masters. -
- by Serbian Defense League, Exposing Zionism and Anti-Goyism -
(Posted here: Saturday, December 01, 2007)


Just One Example Of Who 'They' Are In Media


- The next time someone challenges you for using the phrase "they control the media" you can give them a very specific, accurate answer.
It is "they" who control the influential and popular websites, news and media. Also interesting in the list are websites and cable news channels well known for practicing outright censorship are here, too.
And they OWN myspace.com, too. -
- from Ted Twietmeyer, Aug 01, 2007 -
(Posted here: Wednesday, August 01, 2007)


Who Rules the Corporate Media?

OPERATION MOCKINGBIRD, CIA, State Media Since 1940s


- by Alex Constantine for Portland Independent Media Center, March 26, 2004 -
(Posted here: March 31, 2004)


The Invisible Hand of the Media


- With local television stations all reporting the same news simultaneously, one claiming the title "news leader", another billing itself as the one with "total news", it is apparently becoming more difficult for the public to distinguish one from the other--or from common entertainment, according to former CIA agent, Philip Agee. -
- Author Unknown, Sep 18, 1997 -
(Posted here: May 13, 2005)

 

4. What would happen if this information was made public?

The world would know how to cure Malaria 100% of the time and many, many people would be alive. This would lead to many other dis-eases cured, see: https://www.youtube.com/user/MMStestimonials
http://www.mmstestimonials.is.

The families in charge of the world’s money and power would lose a lot of $$$$$ control and power!


5. When will this information be allowed to be spoken of on the world’s mainstream media?

ANSWER: NEVER, as long as the same people stay in control. We have to break that control by getting the TRUTH out- that there is a 100% cure for Malaria -cheap and simple!


So, I hope everyone understand why the information about the world’s greatest health discovery, in regard to malaria, is not universally known. Here is an example of how a 100% successful clinical study of MMS use for malaria was completely squashed. Look at this video proving that MMS cures Malaria 100% of the time done by the Uganda Red Cross and an organization named Water Resource Center.

Here is the clinical study(with blood tests before and after), conducted by Water Resource Center with cooperation with the Uganda Red Cross, THEN BOTH DENIED IT HAPPENED!

Why would they deny it happened? I think we all know why!!

https://www.youtube.com/watch?v=FrwZN1cPfX8

 

Excerpts from Video:
This version of the video includes an introduction by Jim Humble, and followed with comments by Leo Koehof, the person who trained the Red Cross staff on the proper treatment protocol and is seen numerous times in the video. Koehof also produced his own video that he released before this one came to light (http://www.youtube.com/watch?v=8lzPpZ...).

5:25 -- Klaas Proesmans talks about how he came across several interesting technologies in the field of water, health and energy, including sodium chlorite.

6:07 -- Klaas Proesmans: "It has been said and written that the use of sodium chlorite cleans the body within one hour to four hours of the malaria parasite. That was too good to be true not to go further and do an investigation..."

7:19 -- The waving flag of the "Uganda Red Cross Society" clearly shown at the field test site.

9:55 -- Leo Koehof speaking at the clinic to Proesmans and staff that he just received test results back from the local jail where prisoners were treated for malaria and cured within 24 hours.

10:43 -- Klaas Proesmans: "In total we identified 154 malaria positive patients, together with the local health {authorities} or the doctors. All of them were treated. All of them were, between 24 hours and 48 hours, malaria negative... without any side effects!"

11:07 -- Hannington Segirinya, Former Uganda Red Cross Youth Council President: "I'm so much impressed by this water. It's so unbelievable. From, a layman's view, you may think it's impossible. But, I... It's very possible. I've seen people healed. Looks like there are results from yesterday and seeing the results of today after taking the water. It's super impressive."

12:35 -- Vincent Okonera, URCS (Uganda Red Cross) Senior Branch Manager, Iganga: "I'm excited because of the instant results that are happening among all the people that we have so far tested. It is incredible... unbelievable to see that some were tested of malaria positive yesterday... turns up to be negative today, and feels quite extremely better and more happier and healthier. So, to me this is a very good partnership... and I feel that... if there is opportunity to increase this to this communities, it will be so much of great impact and beneficial to us... to the health of these good people. "

13:30 -- Klaas Proesmans closing statement: "We closed the operation to report back to the Secretary General here in Uganda Red Cross Society. And, to report back to the Water Resource Center about the results of this field test. Now, all in all... a 100% cured people... less than 5 days... all within 24 hours to 48 hours! That asks for further investigation."


Testimony from Bishop Samula, Uganda


HIV/AIDS AND MALARIA DEFEATED.

MMS (Miracle mineral solution ) UPDATE IN UGANDA.
I greet everybody in the name of our Lord and congratulate you upon
ending the year. Happy new year 2017. Also pray hard this year he more successful for the Genesis ll Church as we make the world a better place free from diseases.

Today I will be sharing with you my experience about MMS. Mainly
telling you my experience with the Genesis II Church Sacramental
protocols particularly handling Malaria and HIV/AIDS here in Uganda
(East Africa).

Having born in a natural medicine background, my grandfather helped people with traditional medicinal plants in our locality. So i picked interest in the the health sector and helping people live a health life. With that i acquired knowledge and learned almost all the herbs he used because I stayed with him helping to prepare the herbs and administering them to the sick people who came for them at the clinic room at home.

After my grandfather it was me to run the clinic, so i had to improve
the medicine mostly putting much research on the medicine. Thanks to the internet where i fast met MMS and the Genesis ll Church. In 2013 I came across MMS on the internet as a cure for many diseases which were a threat to mankind.

Sincerely couldn't believe that MMS can cure all the diseases as
claimed on the internet. It was time for me to make some research on
MMS, almost read anything I came across about MMS.

Surprisingly I found a video on YouTube about MMS clinical trial in
Uganda about malaria. After the video I was really convinced to try it
on my self, as evey thing in the video showed how MMS cured malaria successfully. Contacted the Genesis ll Church which helped me with all the nessesary information including books of Jim humble and I also applied for the online video course which I completed successfully in few weeks.

I tried MMS on my self which I got from a friend Leo, for my allergic
congentional breath which I suffered for years. It had persisted on
several treatments but never came back after few days of using MMS and up to now.

After all that it was the start of the journey as I introduced it
among the products in the clinic. Since then I don't hope to ever
regret why I came across MMS. It has made the dream of helping people come true.

For now I will show you the status of MMS mainly handling Malaria here in Uganda as its still the main killer and leading cause of poverty among among the population plus HIV/AIDS which has caused great suffering to the people. For the above diseases even the available mode of medicine is not accessible to the people due to poverty induced by diseases.

As per now at the clinic and my team we have experienced a bigger
picture how MMS can handle these diseases with great success. For
people who am working with most of them are my former patients who MMS frops saved their lives.

We have successfully handled malaria by using the standard maralia
protocol of the Genesis ll Church. I hope with time MMS will replace
all the available options malaria and save lives.

When i started on the HIV/AIDS it was not easy to tell someone that i
had a cure for the diaease until they started seeing the very sick on
their death beds recover very fast and looking health. So far we have
helped hundreds regain their health in our small capacities.
With this I call upon every one who can help MMS reach more people to support our missions in any form. This will help restore health and thus saving lives.


God bless you and happy new year.
Rev. Samula Albert Araali
From Uganda Africa.

If you'd like to help us get Bishop Samula in Uganda, the supplies he needs please make a donation at https://g2voice.is/donate

I hope everyone can see that the cure for Malaria is being suppressed on purpose for the control and profits of the few while the majority of the world suffers from not only Malaria but MANY other easily cured dis-eases of the body. Tune in Sunday, January 1st, 2017 on www.G2voice.is at 10 A.M. EST New years day!
Hope to see many there.

Let’s change the world together!
Archbishop Mark S. Grenon



References:

• The 8 families that own the FED: http://www.globalresearch.ca/the-federal-reserve-cartel-the-eight-families/25080
• G2Voice Broadcast episode #001: https://www.youtube.com/edito=U&video_id=VEc9FZVg408
http://beforeitsnews.com/alternative/2016/12/look-whos-really-behind-the-mainstream-media-3454762.html
• We really runs the world: https://www.youtube.com/watch?v=bKwO1onXAaIh

http://www.illuminati-news.com/media.htm
• 5 MOST POWERFUL Families That SECRETLY Rule The World | Top 5 Countdown: https://www.youtube.com/watch?v=aqsT5OUOh-I
• Complete List of BANKS Owned or Controlled by the Rothschild Family: http://humansarefree.com/2013/11/complete-list-of-banks-ownedcontrolled.html

• The 8 families that own the FED: http://www.globalresearch.ca/the-federal-reserve-cartel-the-eight-families/25080
• Suppressed Time line: http://www.illuminati-news.com/2007/1007.html
• Who controls the media? http://www.illuminati-news.com/media.htm
http://www.naturalnews.com/046290_
Ebola_patent_vaccines_profit_motive.html

http://www.ecowatch.com/cdc-corruption-robert-kennedy-jr-2096438139.html
http://www.nature.com/news/2002/021003/full/news021001-6.html

 

 

 

 

MMS Saves Lives.

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https://businesstech.co.za/news/general/71652/the-biggest-killer-diseases-in-history/

 
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What are your prescription and over the counter “drugs” doing to your body? 
G2Voice Broadcast #14

Sunday, Dec. 18th 10 AM EST
www.g2voice.is 

 

To me, prescription and over-the-counter “drugs” are the #1 killer and cause of “dis-ease” of the body in the world. Those are the real drugs.  They are VERY toxic to the body and the sooner people we are helping get off their “meds”, the quicker they detox and the faster their body's HEAL! I saw my very healthy dad have a stroke from an “experimental” drug which left him as shell of a man until he died a few years later.  He trusted the doctors and that was his downfall which led to his lack of “quality of life” before he died! We have been taught since very young from schools, news and even in the scripts from movies that doctors and the medical careers are honorable jobs and should be treated with respect. I have stopped believing that, as I have seen with my own eyes, people taking “meds” and following the advice of their doctors as their health deteriorates to even death.  We are always told that we need to ask a doctor when we have any health issues. If not, then we are penalized, ridiculed and even fined by paying Medical insurance that we don't want or even need!

 

Note: Health care reform is not “insurance reform”, that is what the government is talking about. If it is health care reform, you'd see medical colleges changing their curriculum from a toxic drug-based Allopathic method to plant based or natural therapies which will NEVER happen do to the lack of profits! Until the “medical industry” known as the FDA, AMA, CDC, NIH, DOJ and EPA are either eliminated or reorganized by “honest” individuals which are not representing ANY corporation because of lack funding, then and ONLY then, we would see “healthcare” reform! But, I always promote “selfcare” as the VERY best way to maintain or restore health.

 

Here are two excellent documentaries that show the dangers of pharmaceutical drugs and the corruption of the FDA! Please educate yourself. It is your health that is at stake!

 

 

 

Death by Medicine, Gary Null: https://www.youtube.com/watch?v=RwCUDCQMLwY

War on Health - Gary Null's documentary exposing the FDA :
https://www.youtube.com/watch?v=h0CQrL5nzwo

 

 

Arnold Seymour Relman, the former editor-in-chief of the New England Medical Journal, and professor of medicine at Harvard University, once stated: “The medical profession is being bought by the pharmaceutical industry, not only in terms of practice of medicine, but also in terms of teaching and research. The academic institutions of this country are allowing themselves to be the paid agents of the pharmaceutical industry. I think it’s disgraceful.” http://www.medicine.news/2016-09-23-doctor-tells-all-claims-prescription-drugs-are-killing-us.html

 

Dr. Peter Gotzsche, co-founder of the Cochrane Collaboration (the world’s most foremost body in assessing medical evidence), hopes to make clear this very problem. He is currently working to inform the world about the dangers associated with several pharmaceutical grade drugs. Based on his research, he estimates that 100,000 people in the United States alone die each year from the side-effects of correctly used prescription drugs, noting that “it’s remarkable that nobody raises an eyebrow when we kill so many of our own citizens with drugs.” He published a paper last year in the Lancet arguing that our use of antidepressants is causing more harm than good, and taking into consideration the recent leaks regarding antidepressant drugs, it seems he is correct.

http://www.collective-evolution.com/2016/02/17/meet-the-doctor-who-says-prescription-drugs-are-killing-us-and-hes-not-the-only-one/

 

Salesperson for Merck: https://www.youtube.com/watch?v=LUduiwgHMQs

 

Dangerous Drugs:
You taking any of these?

 

Note: Vioxx from Merck – 60,000 deaths!

Botox just had a 680 million suit filed in California.

 

Every day, Americans are injured by side effects of dangerous drugs. For many, their only recourse is to file lawsuits against the companies that sell the products.

The pharmaceutical industry makes sky-high profits that allow them to move quickly from one faulty drug to the next. From 2004 to 2008, Pfizer, one major pharmaceutical company, took in $245 billion. During that same time period, another company, Eli Lilly, made $36 billion from just one of its drugs (Zyprexa).

Between 2004 and 2010, major drug companies paid out $7 billion in fines, penalties and lawsuits — just a drop in the bucket when compared with soaring profits. No one seems to care that every day, Americans are injured or killed by dangerous prescription drugs.

Since 2000, the Food and Drug Administration (FDA) has approved an average of 24 drugs a year, including many that pose health risks and serious long-term side effects.

Drug companies help this happen when they conduct flawed or dishonest clinical trials by:

Failing to report negative results to the FDA.

Studying side effects for a short period of time.

Studying a tiny group of people.

 

The FDA responds to adverse reactions to drugs in a variety of ways, such as meetings, reports, reviews, demands for more trials, letters to doctors, added warnings to labels, and requirements that patients enroll in special programs for drugs. FDA action, however, can take years — something patients may not have.

Consumers who have been injured by a prescription drug often take action of their own by filing lawsuits against drug companies. These lawsuits can cover exorbitant medical costs, as well as pain and suffering. The most important role of the lawsuits is that they speak the drug companies’ language — money — and can teach them a lesson.

Among the dangerous drugs out there are:

Type 2 diabetes drugs Avandia and Actos.

Antidepressants Paxil, Prozac, Effexor, Zoloft and Lexapro.

Mood stabilizer Depakote.

Birth control pills Yaz and Yasmin.

Acne medication Accutane.

Blood thinners Pradaxa and Xarelto

Osteoporosis treatment Fosamax.

GranuFlo and NaturaLyte, which are used in dialysis.

Hair loss pill Propecia.

These drugs come with side effects that range from birth defects and liver damage to suicidal behavior, blood clots, bladder cancer, Crohn’s disease, heart attacks, strokes, uncontrollable bleeding and heart failure.

 

Diabetes Drugs

 

Actos

Actos (pioglitazone) received FDA approval in 1999, and was celebrated as the next great type 2 diabetes drug. It has been prescribed to 10 million people around the world. Actos’ bright future began to grow dim in 2007, however, when the FDA added a black-box warning to the label, warning patients of the risk of heart failure.

In 2011, the FDA added another warning to the Actos label — for bladder cancer. The label change came after Takeda Pharmaceuticals, which manufactures Actos, released study results showing that long-term use of Actos increases the risk of bladder cancer by 40 percent. France and Germany banned Actos in 2011. The FDA is waiting until final results from that study are released in 2013 to take any further action on Actos.

While the FDA sits on its hands, a new study published in the British Medical Journal shows long-term use of Actos increases the risk of bladder cancer by 83 percent. Thousands of patients have filed lawsuits after going through multiple surgeries, radiation and chemotherapy — all thanks to the would-be miracle drug Actos.

 

Are you suffering from injuries related to a prescription drug or medical device?

 

Avandia

Avandia, another type 2 diabetes drug, also launched in 1999, but was later implicated in heart attacks. The FDA estimates that Avandia caused 83,000 heart attacks from 1999 to 2007, the year in which the FDA added a black-box warning to the drug. In September 2010, the FDA significantly restricted use of Avandia, allowing access only to a select group of doctors and patients.

GlaxoSmithKline has settled at least 35,000 Avandia lawsuits, paying out $3 billion in late 2011 to settle cases involving several of its drugs as well as a government investigation. The two-year investigation by the U.S. Senate Finance Committee revealed that the drug company knew of the heart risks associated with Avandia for a long time and tried to hide concerns about the drug.

 

Antidepressants

Paxil

In 1992, SmithKline Beecham — which would later become GlaxoSmithKline — launched Paxil (Paroxetine), which is a  selective serotonin reuptake inhibitor (SSRI). Like other antidepressants, Paxil carries a black-box warning that it can increase suicidality in children, adolescents and young adults.

FDA reported in 2006 that 11 suicide attempts had occurred in patients given Paxil in trials. Based on the allegation that GlaxoSmithKline misled consumers about Paxil’s safety — including increasing suicidal behavior — a $64 million class-action suit was settled in 2007.

One FDA study shows that pregnant women who take Paxil during the first trimester have double the risk of having a baby with a heart defect, compared to other women. GlaxoSmithKline has spent almost $1 billion to settle birth-defect litigation.

Pro zac

Pro zac (fluoxetine) is an antidepressant made by Eli Lilly that hit the market in 1987. Pro zac is an SSRI that is used for depression, obsessive compulsive disorder (OCD), bulimia nervosa and panic disorder.

This medicine that has been prescribed to over 50 million people worldwide may cause serotonin syndrome and increases the risk of suicidal thinking and violent behavior.

In 1989, Pro zac made the news as one man, Joseph Wesbecker, wounded 12 people and killed eight, before killing himself. Just weeks before the shooting, Wesbecker had started taking Pro zac. The victims’ families sued Eli Lilly and lost. In 2011, a 16-year-old boy received a three-year sentence after stabbing one of his friends. His doctor attributed his actions to a Pro zac-induced mood disorder.

More than 150 lawsuits have been filed faulting Eli Lilly for not properly testing Pro zac to show that it may make users aggressive and suicidal. Eli Lilly is also facing lawsuits over birth defects that resulted from a woman’s use of Pro zac during pregnancy.

In 2006, the FDA added labeling to all SSRIs warning of the increased risk of pulmonary hypertension in the newborn (PPHN), which can be fatal.

 

Effexor

Approved in 1993, Effexor (venlafaxine) is manufactured by Wyeth — which was later purchased by Pfizer — to treat depression, generalized anxiety disorder, social anxiety disorder and panic disorder. In 2005, sales of Effexor totaled $3.5 billion.

In 2003, Wyeth warned health care professionals that in children ages 6 to 17 Effexor was not shown to be effective or safe, causing hostility and suicidal events. The U.K. General Practice Research Database was used in 2007 to compare antidepressants Celexa (citalopram), Prozac (fluoxetine), dothiepin and Effexor. The study showed that Effexor carries the highest risk of suicidality.

Effexor and all antidepressants carry the FDA’s black-box warning about the risk of suicide during the early stages of treatment, especially in kids. Effexor use during pregnancy can cause serious birth defects, and many parents have sued Pfizer after their baby has suffered.

 

Zoloft

Zoloft (sertraline) is an antidepressant created by Pfizer and approved by the FDA in 1999. By 2011, nearly 100 million people had taken Zoloft. Mainly used to treat major depressive disorder, Zoloft is part of the SSRI drug class. SSRIs come with a risk of suicidality and violent behavior, especially in children and adolescents.

Using Zoloft while pregnant can lead to birth defects, including persistent pulmonary hypertension in infants (PPHN), which can be fatal. In May 2012, more than 60 Lexapro (escitalopram) were filed on behalf of babies born with birth defects.

 

Lexapro

Approved by the FDA in 2002 to treat depression and anxiety, Lexapro (escitalopram) is a popular SSRI but is associated with birth defects. The drug, made by Forest Laboratories, had sales topping $355 million in 2011.

Dozens of lawsuits have been filed after women took Lexapro and gave birth to children with birth defects. Birth defects resulting from Lexapro include persistent pulmonary hypertension of the newborn (PPHN), limb defects, spina bifida, cranial defects and neural tube defects.

 

Depakote

Depakote (divalproex sodium) is an anticonvulsant and is used to treat mood disorders, seizures and migraines. It was approved for its first indications by the FDA in 1983. The drug later was illegally marketed for unapproved uses, such as for youths with bipolar or seniors with dementia. As a result, Abbott Laboratories, the drug’s manufacturer, was required to pay $700 million in criminal penalties.

Many women have filed lawsuits against Abbott Laboratories, after Depakote led to birth defects such as developmental delays, spina bifida, cleft palate and bodily malformations. A 2006 study showed that 20 percent of women taking the medication while pregnant gave birth to children with birth defects, and as a result the FDA gave the medication a black-box warning concerning potential birth defects.

 

Hormone Drugs

 

Testosterone

There are a number of testosterone replacement drugs currently on the market. The most popular and most prescribed drug in the U.S. is AngroGel (testosterone gel) manufactured by Abbott Laboratories’ subsidiary, AbbVie.

The National Institutes of Health (NIH) funded one of the most recent studies published in PLOS ONE. The study was based on the records of 55,000 men who were prescribed testosterone in the U.S. Researchers found the risk of heart attacks doubled for men who had used testosterone during the first three months. There have been other studies that also show an increased cardiovascular risk.

Based on these findings, watchdog group, Public Citizen, petitioned the FDA to add a black box warning to all testosterone drugs. Dr. Sidney Wolf wrote in an article published in BMJ on February 27, 2014 that 1 in 167 men over aged 65 will have a heart attack because of testosterone drugs. For men under 65 with preexisting heart conditions, that risk jumps to 1 in 100.

Men who suffered heart attacks and strokes are already filing lawsuits against testosterone replacement drug makers.

 

 

Birth Control Pills

 

Yaz and Yasmin

Released in the United States in 2006, Yaz (drospirenone/ethinyl estradiol) is a birth control pill manufactured by Bayer. Yaz is a sister drug to Yasmin, which was approved in 2001. Both medications contain drospirenone/ethinyl estradiol, so they carry the same risk.

From 2008 to 2009, Yaz was the top-selling birth control pill in the United States. In April 2012, Yaz continued in popularity as the fourth best-selling oral contraceptive. Yet several studies show that Yaz puts women at an increased risk for blood clots. Blood clots can contribute to deep vein thrombosis (DVTs), pulmonary embolism (PE), stroke or heart attack.

On April 10, 2012, the FDA required Yaz to include a warning that drospirenone-containing pills increase the risk of blood clots by threefold. Also, a former FDA commissioner, David Kessler, filed an affidavit, claiming that Bayer withheld early reports of blood clots from the FDA in 2004.

A multidistrict litigation (MDL) has been set up in Illinois to handle the 10,000-plus lawsuits over Yaz and Yasmin side effects.

 

Acne Medication

 

Accutane

Approved by the FDA in May 1982, Accutane (isotretinoin) is an oral medication from Roche that was once available for treating acne. Prescribed to more than 13 million patients, many users experienced cured acne after four to five months of treatment.

Serious side effects from Accutane include inflammatory bowel disease, ulcerative colitis, Crohn’s disease, suicidal thoughts, birth defects, liver damage and gastrointestinal disorders. The Adverse Event Reporting System (AERS), a computer database of post-marketing adverse side effects, includes around 23,000 Accutane reports from 1982-2002, covering everything from alopecia (hair loss) and depression, to headache, dry skin and induced abortion.

As of 2002, 172 babies had been born with a congenital defect or anomaly after the mother had taken Accutane. Through 2002, there was a cumulative total of 173 suicides in association with Accutane.

The FDA met with Roche, the manufacturer of Accutane, in 2000 to set up a program to ensure that no woman took Accutane during pregnancy and that no pregnancies would occur while a woman was taking Accutane. The SMART (System to Manage Accutane Related Teratogenicity) program was designed to minimize the risk of birth defects by requiring a qualification sticker on prescriptions, consent forms, an information guide, a patient video, a guide for those who prescribe drugs and pharmacists and carton instructions.

Warnings concerning severe stomach pain, diarrhea and rectal bleeding were hidden in 3,000 words of possible side effects, and in 2005 Kamie Kendall won $10.5 million in damages after having her colon and rectum removed.

Andrew McCarrell won $25 million after having his colon removed in 2007. In 2009, Roche Pharmaceuticals responded to multiple personal injury lawsuits by removing Accutane from the market. But the legal settlements didn’t end there. In 2012, Gillian Gaghan was awarded $2 million for injuries related to inflammatory bowel disease after using Accutane for six months.

 

Cholesterol Drugs

Crestor

Crestor (rosuvastatin), made by AstraZeneca, was approved in August 2003. It is known to lower bad cholesterol up to 52 percent. Global sales reached $6.6 billion in 2011.

Crestor belongs to a class of drugs known as statins. Crestor can cause rhabdomyolysis (muscle tissue damage), kidney (renal) failure and chronic or abnormal bleeding.

The FDA has written letters to AstraZeneca demanding it stop running commercials that exaggerate the drug’s benefits and downplay its dangers. In 2005, the FDA added a warning to the drug that all patients who use high doses of Crestor — 40 mg a day — are at an increased the risk of developing life-threatening muscle damage.

Sydney Wolfe from the Public Citizens Health Research Group — a nonprofit advocacy organization that represents consumer interests in Congress —  said that in two years Crestor was linked to 117 cases of rhabdomyolysis and 41 cases of kidney failure, 11 of which resulted in death.

 

Blood Thinners

 

Pradaxa

 

Millions of Americans take blood thinners to reduce the risk of stroke caused by atrial fibrillation (irregular heartbeat). For decades, patients had limited options for blood thinners with most taking warfarin, a medication that requires diet changes and regular blood tests. All of that changed in October 2010, when the FDA approved Boehringer Ingelheim’s Pradaxa (dabigatran), a blood thinner that does not require the same maintenance as warfarin. Within two years, more than 3.7 million U.S. patients had filled Pradaxa prescriptions.

All blood thinners make patients more susceptible to bleeding accidents, however, with Pradaxa there is no antidote to stop bleeding, which can lead to disabling or fatal injuries. Hundreds of bleeding accidents associated with Pradaxa have been reported, and 542 deaths were reported in 2011.

Studies of Pradaxa also show an increased risk of heart attack and heart disease compared with warfarin. Nearly 200 people have filed Pradaxa lawsuits, most of which are consolidated in a multidistrict litigation (MDL) in Illinois.

 

Xarelto

 

One of the newest blood thinners is Xarelto (rivaroxaban), approved by the FDA in July 2011. Xarelto is approved for use after knee and hip replacement surgery to reduce the risk of blood clots. In November 2011, the drug’s indications were expanded to include atrial fibrillation (AF).

There is no bleeding antidote for Xarelto, which means users of the drug can experience dangerous, uncontrollable bleeding events. Additionally, since the drug was fast-tracked, unknown side effects may also be putting patients at risk.

 

Osteoporosis Treatment

 

Fosamax

The FDA approved Fosamax (alendronate sodium), made by Merck, in 1995 to treat osteoporosis in postmenopausal women. It is estimated that millions worldwide have used the drug for osteoporosis and other indications, including Paget’s disease.

Some people taking Fosamax have suffered from injuries such as ONJ, or jaw death, joint and muscle pain, atrial fibrillation, and inflammation and ulcers of the esophagus. Nearly 1,000 people have filed lawsuits against Merck after experiencing severe side effects.

 

Pain Medication

 

Vioxx

Initially approved for acute pain such as rheumatoid arthritis in adults or menstrual related symptoms, Vioxx (rofecoxib) was available from 1999 to 2004. Vioxx is a part of a class of drugs called non-steroidal anti-inflammatory drugs, or NSAIDs, and functions like ibuprofen. Merck manufactured the drug which reached sales of $2.5 billion in 2003.

Multiple studies revealed that this drug meant to assist patients was actually increasing the risk of heart attack. September 2004 Merck voluntarily withdrew the drug from the market. Over 60,000 people have filed claims against Merck after Vioxx use led to heart attacks, strokes and other injuries.

The company set up a $4.85 billion dollar fund to assist in resolving consumer claims. Additionally, Merck pleaded guilty to charges based on illegal marketing and agreed to pay fines of $950 million.

 

Gastrointestinal Drugs

 

Reglan

Reglan (metoclopramide) was approved by the FDA in 1980 and is used to treat migraines, heart burn, acid reflux, nausea, vomiting and gastroparesis, a digestive condition. In 2011, around 1 million people filled prescriptions of Reglan. That same year the Institute for Safe Medication Practices released a report that 1,180 cases of Tardive Dyskinesia resulted from Reglan use.

Tardive Dyskinesia (TD) occurs as a side effect of certain medications and is a neurological disorder causing uncontrollable rapid movements of the face and the body. Severe cases can inhibit talking, walking and eating. Because of this, over 5,000 people have filed lawsuits against manufacturers of metoclopramide.

 

Dialysis Treatment

 

GranuFlo and NaturaLyte

 

Many people with acute or chronic kidney failure receive dialysis treatment with GranuFlo and NaturaLyte. Fresenius Medical Care (FMC), the world’s leading provider of kidney dialysis services and products, manufactures these two products. They were approved in 2003 to assist in dialysis treatment. The products are now used by around half of dialysis patients.

Because dialysis machines were not properly calibrated, patients have suffered from excessive amounts of acid in the blood, which can lead to organ damage, heart arrhythmia, heart attack, coma and death. In 2012, these two products briefly were recalled to clarify dosing instructions. FMC now faces mounting lawsuits, after more than 900 patients suffered cardiac arrest after using their products.

 

Hair Loss Pill

 

Propecia and Proscar

 

Men struggling with male-pattern baldness or enlarged prostate may take Propecia or Proscar, which both include finasteride and are manufactured by Merck. The FDA approved Proscar in 1992 and Propecia in 1997.

The FDA’s adverse event database received hundreds of reports of erec tile dysfunction associated with use of finasteride. Even after discontinuing use of the drug, patients may experience side effects. In April 2011, the FDA required updates to the drug label informing users that libido disorders, ejaculation disorders and orgasm disorders can occur during and after use of finasteride. The label also includes a warning concerning increased risk of high-grade prostate cancer.

The reckless behavior of the drug companies shows no signs of changing. Negative clinical trials are never reported or overlooked, and the FDA buys in. Doctors write millions of prescriptions that may be damaging the health of innocent patients. Only by holding companies accountable in court for threatening their very lives, can patients help prevent others from suffering from the same faulty drugs.

 

Read what the drug companies have written about their own drugs!

 

http://mmsnews.is/343-read-what-the-drug-companies-have-written-about-their-own-drugs-02-20-2016

 

Many of us have seen these titles below in medical news around the world about how deadly prescription drugs are in the human body.

 

“How Pharmaceuticals Came to be the 4th Leading Cause Of Death In America” -
http://www.collective-evolution.com

 

“Prescription Painkillers Now the Leading Cause of Accidental Deaths” –

http://io9.gizmodo.com/5919434/prescription-painkillers

 

“Death from Prescription Drugs: The New Epidemic Sweeping Across America” – http://articles.mercola.com

 

“Prescriptions Drugs Now the Leading Cause of Death By Overdose” - http://naturalsociety.com

 

Before the advent of “Big Pharma” early in the 20th century, these statistics just did not exist but now we have to deal with so many needless deaths from toxins that are entering the body through prescribed medications. One thing people can do is to make a more informed decision in what they allow to be put in their bodies. Every pharmaceutical company that has an “approved” drug on the world market has to disclose a list of information good and bad about each drug it produces in publication called, “package insert”. Being “approved” doesn’t mean it is safe or non-toxic in your body as you will see from their own publications!

 

What is in the Package Insert?

 

The package insert is a very detailed publication and filled with information provided by the drug manufacturer and approved by the US Food and Drug Administration (FDA). Each country or region has its own agency that regulates drugs and provides the information that consumers receive with their prescriptions. In India, it is the Central Drugs Standard Control Organization (CDSCO), which is commonly referred to as the Drugs Controller General (DCG). In Europe, it is the European Medicines Agency (EMA), where the package insert is known as the patient information leaflet (PIL).

 

Package inserts (also known as Prescribing Information or drug labels) are available for all prescription medications approved by the FDA. Similar information is available for nonprescription medicines and for some herbal medicines and dietary supplements as well.

 

The package insert can usually be found online on the drug manufacturer's web site and also available in a reference book called the Physicians' Desk Reference (PDR).

 

The information in a package insert is in technical language. It is usually very long and can be difficult to understand. It is a good idea to look through it, because it lists important information about the drug. The package insert follows a standard format for every drug. After some identifying information such as the drug's brand name, generic name, and initial year of FDA approval, the following sections appear:

 

1. Highlights of Prescribing Information

2. Indications and Usage

3. Dosage and Administration

4. Dosage Forms and Strengths

Note: Pay special attention to these bolded sections.

5. Contraindications

6. Warnings and Precautions

7. Adverse Reactions

8. Drug Interactions

9. Use in Specific Populations

10. Over dosage

11. Description

12. Clinical Pharmacology

13. Nonclinical Toxicology

14. Clinical Studies

15. References

16. How Supplied/Storage and Handling

17. Patient Counseling Information

See more at: http://www.thewellproject.org/hiv-information

 

A woman here in Colombia whom we are giving “sacramental guidance” has been telling me about the symptoms she has been having the past few years from certain drugs.   She is taking a drug called, “atenolol”. Below, is a list of the “Adverse Reactions” in the package insert from the Drug company.

 

See: NDC Code(s): 16571-430-11, 16571-431-11, 16571-441-11 

 

Packager: Pack Pharmaceuticals LLC

Category: HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule: None 

Adverse Reactions:

NOTE: I bolded the symptoms this woman has been having from the package insert “adverse reactions” section found below. 

“Adverse Reactions”

CARDIOVASCULAR

• Bradycardia

• Cold Extremities

• Postural Hypotension

• Leg Pain

 

CENTRAL NERVOUS SYSTEM

NEUROMUSCULAR

• Dizziness

• Vertigo

• Lightheadedness

• Tiredness

• Fatigue

• Lethargy

• Drowsiness

• Depression

• Dreaming

 GASTROINTESTINAL

• Diarrhea

• Nausea

 RESPIRATORY (see WARNINGS)

• Wheeziness

• Dyspnea

• Bradycardia

• Hypotension

• Bronchospasm

• Heart Failure

• Heart Block

• BBB + Major

• Axis Deviation

• Supraventricular Tachycardia

• Atrial Fibrillation

• Atrial Flutter

• Ventricular Tachycardia

• Cardiac Reinfarction

• Total Cardiac Arrests

• Nonfatal Cardiac Arrests

• Deaths

• Cardiogenic Shock

• Development of Ventricular

• Septal Defect

• Development of Mitral Regurgitation

• Renal Failure

• Pulmonary Emboli

• Hypotension/Bradycardia (Low Blood Pressure)

• Cardiogenic Shock

• Reinfarction

• Cardiac Arrest

• Heart Block (> first degree)

• Cardiac Failure

• Arrhythmias

• Bronchospasm

• Hematologic: Agranulocytosis.

 

Allergic: Fever, combined with aching and sore throat, laryngospasm, and respiratory distress.

 

Central Nervous System: Reversible mental depression progressing to catatonia; an acute reversible syndrome characterized by disorientation of time and place; short-term memory loss; emotional lability with slightly clouded sensorium; and, decreased performance on neuropsychometrics.

 

Gastrointestinal: Mesenteric arterial thrombosis, ischemic colitis.

 

Other: Erythematous rash.

 

The woman we are guiding with our health sacraments decided to stop taking this medication which she had been taking for years. Her doctor had never shown her this information or told her it existed! It is not a good business practice to show how dangerous and toxic the product you are trying to sell to a patient is before they begin to take it, right? I’m being facetious in case you didn’t notice. They, (the drug company), doesn’t want you to know this information, because you probably would not take the drug.

 

Many of the symptoms that the drug itself was causing her are disappearing after a week! Also, she has begun with the Starting Procedure and working her way up to Protocol 2000 while she is with us for a month. This will detox any residual amount of this drug that has accumulated in the body over the years as well as pathogens to “restore her to health”.

 

Below are the top 25 Prescribed drugs in the U.S. See if what you are being prescribed to take is on the list. If so, read the information in the package insert. I included a link. YOU decide if the doctor that prescribe it for you made the right choice for you!

 

I will walk you thru the high points of how the drug companies “package” inserts read:

 

Below is a link to the package insert from the Drug company that produced the “drug” to the top 25th most popular drugs in the U.S. CHECK IT OUT FOR YOURSELF!!  I have made it easy for you to do that.  Just click on the link of the drug you are taking and read what the drug companies say themselves about the drug they produce. You decide if you should be taking anyone of these drugs. It is not the doctor’s responsibility to check out this drug, but yours! You are the one ingesting it not the doctor. You have to dig to get to the sections: 

• Contraindications

• Warnings and Precautions

• Adverse Reactions

• Drug Interactions

The Most Popular Drugs in the United States - Primary Use

NOTE: Let's go thru on of these popular meds and see for ourelves what it says. Do this with your drug and see if it resinates with you?

1. Coumadin (Warfarin sodium) - http://medlibrary.org/lib/rx/meds/coumadin-3/

 

COUMADIN can cause fetal harm when administered to a pregnant woman. While COUMADIN is contraindicated during pregnancy, the potential benefits of using COUMADIN may outweigh the risks for pregnant women with mechanical heart valves at high risk of thromboembolism

 

CONTRAINDICATIONS

 

COUMADIN is contraindicated in:

 

     Pregnancy 

COUMADIN is contraindicated in women who are pregnant except in pregnant women with mechanical heart valves, who are at high risk of thromboembolism [see Warnings and Precautions (5.5) and Use in Specific Populations (8.1)]. COUMADIN can cause fetal harm when administered to a pregnant woman. COUMADIN exposure during pregnancy causes a recognized pattern of major congenital malformations (warfarin embryopathy and fetotoxicity), fatal fetal hemorrhage, and an increased risk of spontaneous abortion and fetal mortality. If COUMADIN is used during pregnancy or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard to a fetus [see Use in Specific Populations (8.1)].

COUMADIN is contraindicated in patients with:

•  Hemorrhagic tendencies or blood dyscrasias 

• Recent or contemplated surgery of the central nervous system or eye, or traumatic surgery resulting in large open surfaces [see Warnings and Precautions (5.6)

•  Bleeding tendencies associated with:

• Active ulceration or overt bleeding of the gastrointestinal, genitourinary, or respiratory tract

• Central nervous system hemorrhage

• Cerebral aneurysms, dissecting aorta

• Pericarditis and pericardial effusions

• Bacterial endocarditis

•  Threatened abortion, eclampsia, and preeclampsia 

•  Unsupervised patients with conditions associated with potential high level of non-compliance 

•  Spinal puncture and other diagnostic or therapeutic procedures with potential for uncontrollable bleeding 

•  Hypersensitivity to warfarin or to any other components of this product (e.g., anaphylaxis) [see Adverse Reactions (6)] 

•  Major regional or lumbar block anesthesia 

•  Malignant hypertension 

 

5 WARNINGS AND PRECAUTIONS

5.1 Hemorrhage

COUMADIN can cause major or fatal bleeding. Bleeding is more likely to occur within the first month. Risk factors for bleeding include high intensity of anticoagulation (INR >4.0), age greater than or equal to 65, history of highly variable INRs, history of gastrointestinal bleeding, hypertension, cerebrovascular disease, anemia, malignancy, trauma, renal impairment, certain genetic factors [see Clinical Pharmacology (12.5)] , certain concomitant drugs [see Drug Interactions (7)] , and long duration of warfarin therapy.

 

Perform regular monitoring of INR in all treated patients. Those at high risk of bleeding may benefit from more frequent INR monitoring, careful dose adjustment to desired INR, and a shortest duration of therapy appropriate for the clinical condition. However, maintenance of INR in the therapeutic range does not eliminate the risk of bleeding.

 

Drugs, dietary changes, and other factors affect INR levels achieved with COUMADIN therapy. Perform more frequent INR monitoring when starting or stopping other drugs, including botanicals, or when changing dosages of other drugs [see Drug Interactions (7)].

Instruct patients about prevention measures to minimize risk of bleeding and to report signs and symptoms of bleeding [see Patient Counseling Information (17)].

 

5.2 Tissue Necrosis

 

Necrosis and/or gangrene of skin and other tissues is an uncommon but serious risk (<0.1%). Necrosis may be associated with local thrombosis and usually appears within a few days of the start of COUMADIN therapy. In severe cases of necrosis, treatment through debridement or amputation of the affected tissue, limb, breast, or penis has been reported.

Careful clinical evaluation is required to determine whether necrosis is caused by an underlying disease. Although various treatments have been attempted, no treatment for necrosis has been considered uniformly effective. Discontinue COUMADIN therapy if necrosis occurs. Consider alternative drugs if continued anticoagulation therapy is necessary.

 

5.3 Systemic Atheroemboli and Cholesterol Microemboli

 

Anticoagulation therapy with COUMADIN may enhance the release of atheromatous plaque emboli. Systemic atheroemboli and cholesterol microemboli can present with a variety of signs and symptoms depending on the site of embolization. The most commonly involved visceral organs are the kidneys followed by the pancreas, spleen, and liver. Some cases have progressed to necrosis or death. A distinct syndrome resulting from microemboli to the feet is known as “purple toes syndrome.” Discontinue COUMADIN therapy if such phenomena are observed. Consider alternative drugs if continued anticoagulation therapy is necessary.

 

5.4 Limb Ischemia, Necrosis, and Gangrene in Patients with HIT and HITTS

 

Do not use COUMADIN as initial therapy in patients with heparin-induced thrombocytopenia (HIT) and with heparin-induced thrombocytopenia with thrombosis syndrome (HITTS). Cases of limb ischemia, necrosis, and gangrene have occurred in patients with HIT and HITTS when heparin treatment was discontinued and warfarin therapy was started or continued. In some patients, sequelae have included amputation of the involved area and/or death. Treatment with COUMADIN may be considered after the platelet count has normalized.

 

5.5 Use in Pregnant Women with Mechanical Heart Valves 

 

COUMADIN can cause fetal harm when administered to a pregnant woman. While COUMADIN is contraindicated during pregnancy, the potential benefits of using COUMADIN may outweigh the risks for pregnant women with mechanical heart valves at high risk of thromboembolism. In those individual situations, the decision to initiate or continue COUMADIN should be reviewed with the patient, taking into consideration the specific risks and benefits pertaining to the individual patient’s medical situation, as well as the most current medical guidelines. COUMADIN exposure during pregnancy causes a recognized pattern of major congenital malformations (warfarin embryopathy and fetotoxicity), fatal fetal hemorrhage, and an increased risk of spontaneous abortion and fetal mortality. If this drug is used during pregnancy, or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard to a fetus [see Use in Specific Populations (8.1)].

5.6 Other Clinical Settings with Increased Risks

 

In the following clinical settings, the risks of COUMADIN therapy may be increased:

•  Moderate to severe hepatic impairment 

•  Infectious diseases or disturbances of intestinal flora (e.g., sprue, antibiotic therapy) 

•  Use of an indwelling catheter 

•  Severe to moderate hypertension 

•  Deficiency in protein C-mediated anticoagulant response: COUMADIN reduces the synthesis of the naturally occurring anticoagulants, protein C and protein S. Hereditary or acquired deficiencies of protein C or its cofactor, protein S, have been associated with tissue necrosis following warfarin administration. Concomitant anticoagulation therapy with heparin for 5 to 7 days during initiation of therapy with COUMADIN may minimize the incidence of tissue necrosis in these patients. 

•  Eye surgery: In cataract surgery, COUMADIN use was associated with a significant increase in minor complications of sharp needle and local anesthesia block but not associated with potentially sight-threatening operative hemorrhagic complications. As COUMADIN cessation or reduction may lead to serious thromboembolic complications, the decision to discontinue COUMADIN before a relatively less invasive and complex eye surgery, such as lens surgery, should be based upon the risks of anticoagulant therapy weighed against the benefits. 

• Polycythemia vera 

• Vasculitis 

Diabetes mellitus 

 

5.7 Endogenous Factors Affecting INR

 

The following factors may be responsible for increased INR response: diarrhea, hepatic disorders, poor nutritional state, steatorrhea, or vitamin K deficiency.

The following factors may be responsible for decreased INR response: increased vitamin K intake or hereditary warfarin resistance.

 

6 ADVERSE REACTIONS

The following serious adverse reactions to COUMADIN are discussed in greater detail in other sections of the labeling:

•  Hemorrhage [see Boxed Warning, Warnings and Precautions (5.1), and Overdosage (10)

•  Necrosis of skin and other tissues [see Warnings and Precautions (5.2)

•  Systemic atheroemboli and cholesterol microemboli [see Warnings and Precautions (5.3)

Other adverse reactions to COUMADIN include:

•  Immune system disorders: hypersensitivity/allergic reactions (including urticaria and anaphylactic reactions) 

•  Vascular disorders: vasculitis 

•  Hepatobiliary disorders: hepatitis, elevated liver enzymes. Cholestatic hepatitis has been associated with concomitant administration of COUMADIN and ticlopidine. 

•  Gastrointestinal disorders: nausea, vomiting, diarrhea, taste perversion, abdominal pain, flatulence, bloating 

•  Skin disorders: rash, dermatitis (including bullous eruptions), pruritus, alopecia 

•  Respiratory disorders: tracheal or tracheobronchial calcification 

•  General disorders: chills 

 

7 DRUG INTERACTIONS

Drugs may interact with COUMADIN through pharmacodynamic or pharmacokinetic mechanisms. Pharmacodynamic mechanisms for drug interactions with COUMADIN are synergism (impaired hemostasis, reduced clotting factor synthesis), competitive antagonism (vitamin K), and alteration of the physiologic control loop for vitamin K metabolism (hereditary resistance). Pharmacokinetic mechanisms for drug interactions with COUMADIN are mainly enzyme induction, enzyme inhibition, and reduced plasma protein binding. It is important to note that some drugs may interact by more than one mechanism.

More frequent INR monitoring should be performed when starting or stopping other drugs, including botanicals, or when changing dosages of other drugs, including drugs intended for short-term use (e.g., antibiotics, antifungals, corticosteroids) [see Boxed Warning].

Consult the labeling of all concurrently used drugs to obtain further information about interactions with COUMADIN or adverse reactions pertaining to bleeding.

 

7.1 CYP450 Interactions

 

CYP450 isozymes involved in the metabolism of warfarin include CYP2C9, 2C19, 2C8, 2C18, 1A2, and 3A4. The more potent warfarin S -enantiomer is metabolized by CYP2C9 while the R -enantiomer is metabolized by CYP1A2 and 3A4.

•  Inhibitors of CYP2C9, 1A2, and/or 3A4 have the potential to increase the effect (increase INR) of warfarin by increasing the exposure of warfarin. 

•  Inducers of CYP2C9, 1A2, and/or 3A4 have the potential to decrease the effect (decrease INR) of warfarin by decreasing the exposure of warfarin. 

Examples of inhibitors and inducers of CYP2C9, 1A2, and 3A4 are below in Table 2; however, this list should not be considered all-inclusive. Consult the labeling of all concurrently used drugs to obtain further information about CYP450 interaction potential. The CYP450 inhibition and induction potential should be considered when starting, stopping, or changing dose of concomitant medications. Closely monitor INR if a concomitant drug is a CYP2C9, 1A2, and/or 3A4 inhibitor or inducer.

 

Table 2: Examples of CYP450 Interactions with Warfarin 

 

Enzyme Inhibitors Inducers
CYP2C9 amiodarone, capecitabine, cotrimoxazole, etravirine, fluconazole, fluvastatin, fluvoxamine, metronidazole, miconazole, oxandrolone, sulfinpyrazone, tigecycline, voriconazole, zafirlukast aprepitant, bosentan, carbamazepine, phenobarbital, rifampin
CYP1A2 acyclovir, allopurinol, caffeine, cimetidine, ciprofloxacin, disulfiram, enoxacin, famotidine, fluvoxamine, methoxsalen, mexiletine, norfloxacin, oral contraceptives, phenylpropanolamine, propafenone, propranolol, terbinafine, thiabendazole, ticlopidine, verapamil, zileuton montelukast, moricizine, omeprazole, phenobarbital, phenytoin, cigarette smoking
CYP3A4 alprazolam, amiodarone, amlodipine, amprenavir, aprepitant, atorvastatin, atazanavir, bicalutamide, cilostazol, cimetidine, ciprofloxacin, clarithromycin, conivaptan, cyclosporine, darunavir/ritonavir, diltiazem, erythromycin, fluconazole, fluoxetine, fluvoxamine, fosamprenavir, imatinib, indinavir, isoniazid, itraconazole, ketoconazole, lopinavir/ritonavir, nefazodone, nelfinavir, nilotinib, oral contraceptives, posaconazole, ranitidine, ranolazine, ritonavir, saquinavir, telithromycin, tipranavir, voriconazole, zileuton armodafinil, amprenavir, aprepitant, bosentan, carbamazepine, efavirenz, etravirine, modafinil, nafcillin, phenytoin, pioglitazone, prednisone, rifampin, rufinamide

 

7.2 Drugs that Increase Bleeding Risk

 

Examples of drugs known to increase the risk of bleeding are presented in Table 3. Because bleeding risk is increased when these drugs are used concomitantly with warfarin, closely monitor patients receiving any such drug with warfarin.

 

Table 3: Drugs that Can Increase the Risk of Bleeding 

Drug Class Specific Drugs
Anticoagulants argatroban, dabigatran, bivalirudin, desirudin, heparin, lepirudin
Antiplatelet Agents aspirin, cilostazol, clopidogrel, dipyridamole, prasugrel, ticlopidine
Nonsteroidal Anti-Inflammatory Agents celecoxib, diclofenac, diflunisal, fenoprofen, ibuprofen, indomethacin, ketoprofen, ketorolac, mefenamic acid, naproxen, oxaprozin, piroxicam, sulindac
Serotonin Reuptake Inhibitors citalopram, desvenlafaxine, duloxetine, escitalopram, fluoxetine, fluvoxamine, milnacipran, paroxetine, sertraline, venlafaxine, vilazodone

7.3 Antibiotics and Antifungals

 

There have been reports of changes in INR in patients taking warfarin and antibiotics or antifungals, but clinical pharmacokinetic studies have not shown consistent effects of these agents on plasma concentrations of warfarin.

Closely monitor INR when starting or stopping any antibiotic or antifungal in patients taking warfarin.

 

7.4 Botanical (Herbal) Products and Foods

 

More frequent INR monitoring should be performed when starting or stopping botanicals.

Few adequate, well-controlled studies evaluating the potential for metabolic and/or pharmacologic interactions between botanicals and COUMADIN exist. Due to a lack of manufacturing standardization with botanical medicinal preparations, the amount of active ingredients may vary. This could further confound the ability to assess potential interactions and effects on anticoagulation.

Some botanicals may cause bleeding events when taken alone (e.g., garlic and Ginkgo biloba) and may have anticoagulant, antiplatelet, and/or fibrinolytic properties. These effects would be expected to be additive to the anticoagulant effects of COUMADIN. Conversely, some botanicals may decrease the effects of COUMADIN (e.g., co-enzyme Q10 , St. John’s wort, ginseng). Some botanicals and foods can interact with COUMADIN through CYP450 interactions (e.g., echinacea, grapefruit juice, ginkgo, goldenseal, St. John’s wort).

The amount of vitamin K in food may affect therapy with COUMADIN. Advise patients taking COUMADIN to eat a normal, balanced diet maintaining a consistent amount of vitamin K. Patients taking COUMADIN should avoid drastic changes in dietary habits, such as eating large amounts of green leafy vegetables.

 

NOTE: (NaturalNews) Aluminum Lake food coloring, used to heavily coat liquid medicines for children, contains dangerous amounts of aluminum and harmful synthetic petrochemicals. These "petrochemicals" are carcinogens containing petroleum, antifreeze and ammonia, which cause a long list of adverse reactions. Aluminum poisoning can lead to short and long term central nervous system (CNS) damage, such as memory impairments, autism, epilepsy, mental retardation, and dementia.

 

COUMADIN tablets for oral use also contain:

All strengths: Lactose, starch, and magnesium stearate
1 mg: D&C Red No. 6 Barium Lake
2 mg: FD&C Blue No. 2 Aluminum Lake andFD&C Red No. 40 Aluminum Lake
2-1/2 mg: D&C Yellow No. 10 Aluminum Lake andFD&C Blue No. 1 Aluminum Lake
3 mg: FD&C Yellow No. 6 Aluminum Lake, FD&C Blue No. 2 Aluminum Lake, and FD&C Red No. 40 Aluminum Lake
4 mg: FD&C Blue No. 1 Aluminum Lake
5 mg: FD&C Yellow No. 6 Aluminum Lake
6 mg: FD&C Yellow No. 6 Aluminum Lake andFD&C Blue No. 1 Aluminum Lake
7-1/2 mg: D&C Yellow No. 10 Aluminum Lake andFD&C Yellow No. 6 Aluminum Lake
10 mg: Dye-free

 

 

• Blue #1: Research shows it causes kidney tumors in mice.

• Blue #2: Research shows even higher incidence of tumors, specifically gliomas in male rates (a type of tumor that starts in the brain or spine).

• Red #2: Toxic to rodents, even at modest levels, and causes tumors of the bladder.

• Red #3: FDA recognized it in 1990 as a cause of thyroid cancer in animals. It was banned in cosmetics, but still allowed in food and medicine.

• Red #40: Most popular dye of all. Debilitates the immune-system in mice. Allergic reactions common.

• Green #3: Causes bladder and testes tumors.

• Yellow #5: Affects behavior and induces severe hypersensitivity reactions.

• Yellow #6: Causes adrenal tumors in animals.

 

Learn more: http://www.naturalnews.com/034813_
childrens_medicines_aluminum_pills.html#ixzz4SlI1oXmw

 

 

Table 8: WARIS II – Distribution of Events According to Treatment Group 

Event Aspirin (N=1206) Warfarin (N=1216) Aspirin plus Warfarin (N=1208) Rate Ratio (95% CI) p -value  
a Major bleeding episodes were defined as nonfatal cerebral hemorrhage or bleeding necessitating surgical intervention or blood transfusion.b The rate ratio is for aspirin plus warfarin as compared with aspirin.c The rate ratio is for warfarin as compared with aspirin.d Minor bleeding episodes were defined as non-cerebral hemorrhage not necessitating surgical intervention or blood transfusion.e Includes death, nonfatal reinfarction, and thromboembolic cerebral stroke.CI=confidence intervalND=not determined
  No. of Events  
Major Bleedinga 8 33 28 3.35b (ND) 4.00c (ND) NDND  
Minor Bleedingd 39 103 133 3.21b (ND)2.55c (ND) NDND  
Composite Endpointse 241 203 181 0.81 (0.69-0.95)b 0.71 (0.60-0.83)c  0.030.001  
Reinfarction 117 90 69 0.56 (0.41-0.78)b 0.74 (0.55-0.98)c  <0.0010.03  
Thromboembolic Stroke 32 17 17 0.52 (0.28-0.98)b 0.52 (0.28-0.97)c  0.030.03  
Death 92 96 95 0.82  

 

There were approximately four times as many major bleeding episodes in the two groups receiving warfarin than in the group receiving aspirin alone. Major bleeding episodes were not more frequent among patients receiving aspirin plus warfarin than among those receiving warfarin alone, but the incidence of minor bleeding episodes was higher in the combined therapy group.

 

Some foods and beverages can interact with COUMADIN and affect your treatment and dose

•  Eat a normal, balanced diet. Talk to your healthcare provider before you make any diet changes. Do not eat large amounts of leafy, green vegetables. Leafy, green vegetables contain vitamin K. Certain vegetable oils also contain large amounts of vitamin K. Too much vitamin K can lower the effect of COUMADIN. 

•  Always tell all of your healthcare providers that you take COUMADIN. 

•  Wear or carry information that you take COUMADIN.

 

Warfarin was first used as a rat poison or rodenticide because it was considered to be too potent to be safely used in humans, but after a blood test was developed to measure and adjust its blood-thinning effects, warfarin has become the most widely used oral anticoagulant in the United States.Aug 20, 2013

Is Warfarin Rat Poison AskDrLouise.com

askdrlouise.com/blog/is-warfarin-really-rat-poison/

 

NOTE: How can this unnatural substance be good for you?

Check the rest if you or your family is taking any of these meds. WARN THEM!!!

 

2. Hydrocodone/acetaminophen (Vicodin) ForPain :  http://medlibrary.org/lib/rx/meds/vicodin-hp-2/

 

3. Simvastatin (Zocor) — High cholesterol: http://medlibrary.org/lib/rx/meds/zocor-2/

 

3. Lisinopril — High blood pressure: http://medlibrary.org/lib/rx/meds/lisinopril-66/

 

4. Levothyroxine sodium (Synthroid) – Hypothyroid: http://medlibrary.org/lib/rx/meds/lisinopril-66/

 

5. Amlodipine besylate (Norvasc) - High blood pressure: http://medlibrary.org/lib/rx/meds/norvasc-5/

 

6. Omeprazole (Prilosec) - Acid reflux http://medlibrary.org/lib/rx/meds/prilosec-1/

 

7. Azithromycin (Zithromax) – Antibiotic: http://medlibrary.org/lib/rx/meds/zithromax-2/

 

8. Amoxicillin – Antibiotic:  http://medlibrary.org/lib/rx/meds/amoxicillin-64/

 

9. Metformin HCL (Glucophage) – Diabetes: http://medlibrary.org/lib/rx/meds/glucophage-2/

 

10. Hydrochlorothiazide - High blood pressure: http://medlibrary.org/lib/rx/meds/hydrochlorothiazide

 

11. Alprazolam (Xanax) – Anxiety: http://medlibrary.org/lib/rx/meds/xanax-xr/

 

12. Lipitor (atorvastatin) - High cholesterol: http://medlibrary.org/lib/rx/meds/lipitor-7/

 

13. Furosemide  - High blood pressure: http://medlibrary.org/lib/rx/meds/furosemide-52/

 

14. Metoprolol tartrate (Lopressor) - High blood pressure: http://medlibrary.org/lib/rx/meds/lopressor/

 

15. Zolpidem tartrate (Ambien) – Insomnia: http://medlibrary.org/lib/rx/meds/ambien-5/

 

16. Atenolol - High blood pressure: http://medlibrary.org/lib/rx/meds/atenolol-39/

 

17. Sertraline HCL (Zoloft) – Depression  http://medlibrary.org/lib/rx/meds/atenolol-39/

 

18. Metoprolol succinate (Toprol) - Blood pressure: http://medlibrary.org/lib/rx/meds/toprol-xl-3/

 

19. Citalopram (Celexa) – Depression: http://medlibrary.org/lib/rx/meds/celexa-3/

 

20. Oxycodone/acetaminophen – Pain: http://medlibrary.org/lib/rx/meds/oxycodone-and-acetaminophen-8/

 

22. Ibuprofen – Pain: http://medlibrary.org/lib/rx/meds/ibuprofen-41/

 

23. Plavix (clopidogrel) - Heart disease: http://medlibrary.org/lib/rx/meds/plavix-9/

 

24. Gabapentin (Neurontin) – Seizures: http://medlibrary.org/lib/rx/meds/neurontin-3/

 

25. Singulair (montelukast) – Allergies: http://medlibrary.org/lib/rx/meds/montelukast-sodium-8/

 

 

NOTE: You will notice that there are different package inserts from different drug companies producing the same drug so check out the company package insert of the drug you are taking and compare to the other companies to see if they agree.

I have written this newsletter so people that are considering taking a certain drug can make an “informed” decision. You will notice that the drug companies tell you to ask your doctor if a certain drug is “good” for you. That would be like asking a used car salesman if this car is good for me. 99% of the time he will say, yes of course it is because he wants to sell you the car. He makes money off the car! I believe that the person being asked or told to take a certain drug, should do his or her “due diligence” and see what the drug companies say about the drug they are producing. They are telling the world what drugs they are making and what results they are seeing from the people taking them. You need to listen to what they are putting in print! Now, if you decide that a certain drug being prescribed for you is “not good” for your health then you should have every right to deny taking it!  

The Genesis II Church of Health and Healing has sacraments that can protect our “temple” the body, from 99% of the things that can hurt it, i.e. toxins and pathogens. Each one of us personally needs to take responsibility for what enters our temples. I hope everyone will research what has been written to warn us all of the dangers of many pharmaceutical products whether they are in the form of pills, vaccines, intravenously or any other manner of entering the body!

Watch our G2Voice on our YouTube channel: G2Voice Here is the first broadcast: https://www.youtube.com/watch?v=VEc9FZVg408

 

 

If anyone needs help with a health issue, please feel free to contact me directly at: This email address is being protected from spambots. You need JavaScript enabled to view it.

Spainsh: This email address is being protected from spambots. You need JavaScript enabled to view it.

 

Let's change the world together,

Archbishop Mark S. Grenon

 

References: 

 Death by Medicine, Gary Null: https://www.youtube.com/watch?v=RwCUDCQMLwY

 

https://www.drugwatch.com/dangerous-drugs.php

 

http://www.collective-evolution.com/2014/10/14/the-most-dangerous-heavily-promoted-prescription-drugs-possible-natural-alternatives/

 

http://www.life-sources.com/pages/The-12-most-Dangerous-Prescription-Drugs....html

 

Salesperson for Merck: https://www.youtube.com/watch?v=LUduiwgHMQs

 

http://www.naturalnews.com/034813_
childrens_medicines_aluminum_pills.html#ixzz4SkBFczjR

 

Is Warfarin Rat Poison AskDrLouise.com

 

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Vaccines: Are they destroying the body’s ability to fight disease and causing new diseases?

 

 

We have been told our whole life by doctors, school systems, the FDA, CDC, NIH and the main stream media that vaccines are “safe and effective” without researching it ourselves. The problem is they are not, in fact, they are so toxic that everyone who receives a vaccine has a toxic response. Maybe it is just at the site of the injection, i.e. inflammation and pain, or something much more destructive like brain damage or even death! The whole concept of vaccines is based on the “hypothesis” that by injecting a small amount of a known dis-ease into the human body, the body’s immune system will create an immunity to said dis-ease. WRONG! This idea of “vaccine induced” herd immunity has never been proven or even worked! There is a “natural herd immunity” that exists and this is basically when someone, for instance, gets the measles, chicken pox or mumps they, 95% of the time, never get that dis-ease again in their lives, hence: immunity for these diseases! No one disputes that the body can naturally create an “acquired immunity” from dis-ease. The human body is VERY smart! The problem is this falsehood of vaccine induced herd immunity is unscientific and what is being taught in medical universities, allowed by the FDA and promoted by the main stream media, i.e. “fake news” as being completely true!

 

I highly recommend watching the following videos before receiving ANY vaccine. There are many more below in the reference section:

 

A honest and brave Doctor’s testimony: The Brilliance of Dr. Suzanne Humphries on The Dangers of Vaccines: https://www.youtube.com/watch?v=McfXd_Xuojs

 

The Idea that Vaccines Make Us Healthy Is an Illusion

https://www.youtube.com/watch?v=50pU7VLw728

 

Vaccines are causing many diseases by killing the immune system.

 

Vaccines: The True weapons of mass destruction: https://www.youtube.com/watch?v=9WoMps4Pmpo

Dementia in the 40’s why? : http://www.organicandhealthy.org/2016/11/dementia-now-striking-people-in-their.html

Herd Immunity: https://www.youtube.com/watch?v=TFWBelim1Hw

 

Children suffer vaccine side effects: https://www.youtube.com/watch?v=s7Sxq6wYbA8

 

Vaccinated vs. Unvaccinated children:

 

http://healthimpactnews.com/2016/study-unvaccinated-children-healthier-than-vaccinated-kids-doctors-agree/

 

https://vactruth.com/2014/02/26/unvaccinated-children-healthier/

 

http://healthimpactnews.com/2014/studies-outside-the-u-s-show-unvaccinated-children-healthier-than-vaccinated-children/

 

Note: ALL of the major medical schools teach the “Allopathic” method of medicine and are owned by the same people that own the pharmaceuticals and the banks that fund them.

“Allopathic medicine is based on the “germ theory”, that microbes and viruses, cause disease. Medical science bases the use of vaccines on the theory that the body forms antibodies to “fight” natural viruses. They believe that these antibodies live on after the virus is contained, thereby creating immunity.

 

First, we must consider the facts known to evaluate medicine’s viral theory. Science has proved that viruses are not alive, that they are predominantly protein but that they contain organic DNA. Science has proven that virus increases only in the presence of live cells, and that they cause certain cells, and/or parts of cells to dissolve. What is believed and taken as fact but not proved, is that viruses are non -discriminatingly destructive “things” that self-replicate. That is like saying that laundry soap, because it is found in homes inhabited by humans, self-replicates. Those assumptions and conclusions are shallow and ludicrous. Medical science operates from fear, and it attacks the body. All medical procedures for treating disease are written by pharmaceutical-related individuals and groups. That is a severe conflict of interest. Self-produced health or medication-dependent profit, which do you think that they want?

 

A rational and logical conclusion would be that virus are solvents (cleansers) manufactured by individual cells to dissolve degenerative tissue (disease) caused by accumulated waste and industrial toxins, including medicines. Virus contain DNA because cells have used substances within themselves to synthesize virus; DNA is a part of that. When the cleansing and healing processes cease, cells stop producing large amounts of virus.

 

Normally, healthier bodies symbiotically utilize bacteria and parasites to cleanse themselves of cellular degenerative tissue and organic waste. They are the bodies preferred janitors. Bacteria and parasites consume the degenerative tissue and organic waste and reduce it to a tiny fraction of the original mass eaten. They can consume 100 times their weight and reduce it to 1-percent excretion. When eating a healthy raw diet, our bodies easily secrete and/or excrete the 1-percent excretions from bacteria and parasites.

 

However, when bodies become too toxic with industrial toxins, including medicines, the bacteria and parasites are poisoned to death. Under such toxic conditions, the only cleansing method that the body can utilize is virus. So, cells synthesize viruses. I reiterate, viruses are solvents that dissolve degenerative tissue and organic waste. They are beneficial in preventing disease; they do not cause disease. The symptoms that accompany viral, bacterial or parasitical detoxifications are a necessary process but can be mitigated with the consumption of plenty of raw eggs and raw dairy fats.

 

The key is: We should trust, nurture and understand the body and Nature, not fear them.

 

Inoculating people to prevent viral infections is ridiculous and dangerous. After many years of experimentation, Louis Pasteur realized that the idea of vaccination was doomed. He confessed on his deathbed to his assistants that a poor (toxic) environment within the body creates disease. Microbes do not cause disease.

 

Regarding the immediate trauma that vaccines cause in many people, the eminent scientist and physician, Dr. William F. Koch, M.D., Ph.D. said:

 

The injection of any serum, vaccine or even penicillin has shown a very marked increase in the incidence of polio - at least 400%. Statistics are so conclusive no one can deny it.

 

The long- term effects of vaccines are just as harmful. Vaccines are 
made of disease, mercury, aluminum, formaldehyde and other poisonous chemicals. Pharmaceutical houses manufacture diseases in animal tissue. The diseases are sterilized to make vaccines. Sterilization alters the RNA, DNA, structure and actions of diseases and viruses. When a sterilized disease or virus enters the body, the body tries to analyze it and create antibodies to regulate the disease or virus. The body cannot find the logical reason for the unnatural disease or virus. Nor can it find the key to the time that the bacteria or virus will be active. Therefore, the body creates mutant antibodies, bold emphasis mine, that do not go dormant for up to decades.

 

These mutant antibodies remain active long after the disease or virus becomes inactive. The mutant antibodies eat sub-particles from the inside of amino acids (proteins) in the blood that renders proteins unstable. The amount of proteins damaged and lost to mutant antibodies depends on the number of vaccines. Because amino acids are the primary building blocks of cells, the consequence is cellular malnutrition. In all animals, the malnutrition causes gradual genetic mutations, resulting in weaknesses, diseases, malfunctions and deformities.

 

The life span of mutant antibodies varies, from at least 1 year (penicillin) up to 50 years (polio). Each vaccine multiples the number of mutant antibodies, which increases cellular malnutrition and results in greater weaknesses, diseases, malfunctions and deformities.

Reference: from pages 132-137; We Want To Live: The Primal Diet by Aarjonus Vonderplanitz: http://www.wewant2live.com/

 

You’ll notice Andreas Moritz agrees with the fact that toxicity is the major cause of dis-ease of the body:

Illness is a Toxicity Crisis:
https://www.youtube.com/watch?v=sXanVbgGliQ 

 

Have vaccines ever eradicated a dis-ease? The answer is no. We’ve been taught that small pox and polio were eradicated by vaccines when the facts show differently. Isolation and sanitation were responsible. Edward Jenner was one the first person to take cow pox from cattle and make a vaccine. The name came from the Latin word for cow “vacca” hence; the word vaccine. In England when the vaccines were stopped after many people protested because of the horrible side -affects, the dis-ease simply faded away. Were the vaccines causing the cow small pox to proliferate in the human body?

 

Look how the history of vaccines went on after Jenner’s initial testings: 

 

“It's been only 70 years since World War II, and the mad scientists from companies like I.G. Farben, BASF, Hoechst, Dow and Bayer, who created the gas chambers and tested dangerous vaccines on innocent Jews, didn't just go away. In fact, they went to work for U.S. corporations and pharmaceutical companies that run the vaccine industry today. At least a dozen of these cold blooded killers were hired fresh out of prison, just 4 to 7 years after the Nuremberg trials found them guilty of mass murder and enslavement. (http://frank.mtsu.edu/~baustin/trials3.html)

 

In fact, at the close of WWII, the IG Farben building in Frankfort was protected from allied bombings by the highest levels of military command. Why? IG Farben was the FDA/CDC type of "pharmaceutical arm" of Hitler's 4th Reich, and the Rockefellers had a financial interest in maintaining and controlling this pharmaceutical empire, which would soon be catapulted on U.S. soil. Research reveals that Hitler also invested heavily in Merck and other pharmaceutical companies. Nazi convicted mass murderers became executives for major U.S. chemical and pharmaceutical companies. Fritz ter Meer, found guilty of slavery and mass murder at Auschwitz, served only seven years in prison and became Chairman of the Board at Bayer in 1956. Still trust U.S. vaccines? Carl Krauch, Executive Member of IG Farben and Head of Military Economics for Hitler, found guilty of slavery and mass murder, served just 6 years in prison, then became Chairman of the Board for BASF in 1952. Still want to get those flu shots? How about that HPV shot for your daughter or son?

 

This is the same vaccine industry today which protected and employed Nazi war criminals. The very industry that produced the Nazi gas chambers was purchased by Bayer. So, exactly whom are you trusting with your children's health and welfare? Currently, the U.S. Government and the CDC rely solely on the manufacturers of vaccines to report problems, injuries and deaths. This atrocity is like letting murderers be their own judges in court! Where are the checks and balances this country was founded upon? Vaccines have economic and political agendas now, and the FDA does absolutely no testing of their own before making decisions to release vaccines to the masses.

 

Want more research before you or your child get injected with a new concocted disease for which there is no cure? Listen to stunning admissions by vaccine industry experts, including Dr. Maurice Hilleman (formerly w/Merck), who admitted to the deadly nature of the most trusted vaccines. (http://www.naturalnews.com/033584_Dr_Maurice_Hilleman_SV40.html)

 

Today's vaccines not only contain live versions of the diseases you DO NOT WANT, but also contain GMOs, hormones from infected cows, pigs, chickens and monkeys, untested virus combinations (like H1N1), aluminum, mercury,  emulsifiers, and crossbred bacteria from animals, mosquitoes, and diseased humans:

http://www.naturalnews.com/035431_
vaccine_ingredients_side_effects_MSG.html#ixzz4TNiwiuAP

 

 

NOTE: The FDA requires a “package insert” to be created by the pharmaceutical company that produces every FDA “approved” drug on the market. The pharmaceutical is allowed to do the clinical studies also without the FDA’s oversight. Any side- affects are listed most of the time, but some are not as in the case of the MMR. The first MMR package insert by Merck mentioned the adverse- effect of the MMR vaccine causing “autism” and the second edition does not. Who allowed that?

 

Original MMR Package Insert Has Autism As An Adverse Effect

 

The drug company that makes the M.M.R. vaccine (Merck) publishes an extensive list of warnings, contraindications, and adverse reactions associated with this triple shot. It may be found in the vaccine package insert given to doctors administering MMR, and inside the Physician's Desk Reference (PDR)(8,9). However, this information is never given to patients or parents. The insert is quoted immediately below.

 

An Excerpt from the Original M.M.R. Drug Insert

 

The following afflictions affecting nearly every body system -- blood, lymphatic, digestive, cardiovascular, immune, nervous, respiratory, and sensory -- have been reported following receipt of the MMR shot: encephalitis, encephalopathy, neurological disorders, seizure disorders, convulsions, learning disabilities, subacute sclerosing panencephalitis (SSPE) demyelination of the nerve sheaths, Guillain-Barré syndrome (paralysis), muscle incoordination, deafness, panniculitis, vasculitis, optic neuritis (including partial or total blindness) retinitis, otitis media, bronchial spasms, fever, headache, joint pain, arthritis (acute and chronic) transverse myelitis, thrombocytopenia (blood clotting disorders and spontaneous bleeding) anaphylaxis (severe allergic reactions) lymphadenopathy, leukocytosis, pneumonitis, Stevens-Johnson syndrome, erythema multiforme, urticaria, pancreatitis, parotitis, inflammatory bowel disease, Crohn's disease, ulcerative colitis, meningitis, diabetes, autism, immune system disorders, and death

 

 

The M.M.R. vaccine manufacturer has begun censoring autism from the package insert for its second version of the M.M.R. vaccine ("M.M.R. 2"). Most of the above indications continue to be cited, except for the admission of an autism link, which has been selectively removed. The vaccine manufacturer previously admitted to causing autism, but only in private communications with doctors. Their statements to the public and the media were the complete opposite.

Parents in the British medical system are often ignored when they report problems with vaccines, because the doctors act as the gatekeepers. Parents cannot directly report bad reactions to regulators. They must instead go through their doctor, who may refuse, in order to protect himself. Keep in mind that doctors in Britain get monetary bonuses for administering vaccines, which could be considered a conflict of interest.

Reference: https://currenthealthscenario.blogspot.com.co/2015/09/original-mmr-package-insert-has-autism.html

 

 

Package inserts confirming diseases such as autism etc: 

Package Insert From FDA: Diphtheria Toxoids and Pertussis Vaccine Tripedia®

 

Page 11

 

Adverse events reported during post-approval use of Tripedia vaccine include idiopathic thrombocytopenic purpura, SIDS, anaphylactic reaction, cellulitis, autism, convulsion/grand mal convulsion, encephalopathy, hypotonia, neuropathy, somnolence and apnea. Events were included in this list because of the seriousness or frequency of reporting.’ 

http://www.fda.gov/downloads/Biologics
BloodVaccines/Vaccines/ApprovedProducts/ucm101580.pdf

 

 

Toxic vaccine ingredients and their adverse effects:

 

Bovine cow serum: Extracted from cow skin. When injected causes connective tissue disorders, arthritis and lupus; also, shortness of breath, low blood pressure, chest pain and skin reactions.

 

Sorbitol: Synthetic sweetener which metabolizes very slowly and aggravates IBS and gastrointestinal issues.

 

Gelatin: Derived from the collagen inside animals' skin and bones. Injecting gelatin poses the risk of infection from synthetic growth hormones and BSE infectivity (mad cow disease).

 

Sodium chloride: Raises blood pressure and inhibits muscle contraction and growth.

 

Egg protein: Vaccines are prepared in eggs (certainly not organic). May contain growth hormones, antibiotics, and salmonella bacteria.

 

Thimerosal: A neurotoxic mercury which causes autism: There are 25 mcg in one average flu vaccine, and the EPA safety limit is 5 micrograms, so children who are vaccinated simultaneously with multiple* vaccines receive over 10 times the safety limit of mercury in one day.

 

Human albumin: The protein portion of blood from pooled human venous plasma; when injected causes fever, chills, hives, rash, headache, nausea, breathing difficulty, and rapid heart rate. Injecting "pooled blood" can result in a loss of body cell mass and cause immunodeficiency virus infection, or contain SV40, AIDS, cancer or Hepatitis B from drug addicts.

 

Formaldehyde: Highly carcinogenic fluid used to embalm corpses. Ranked one of the most hazardous compounds to human health; can cause liver damage, gastrointestinal issues, reproductive deformation, respiratory distress and cancer. Plus, formaldehyde has been known to fail to deactivate the virus the vaccine is intended to cure, thus enabling a live virus to enter your blood and infect your system.

 

Phenoxyethanol: A glycol ether/chemical; highly toxic to the nervous system, kidneys, and liver. The FDA warns "can cause shut down of the central nervous system (CNS), vomiting and contact dermatitis" in cosmetics; imagine when injected into your blood.

 

Aluminum phosphate: Greatly increases toxicity of mercury, so caution about minimum mercury tolerance is therefore severely underestimated. CDC scientists and all doctors are well aware of this.

 

MSG (monosodium glutamate): When injected becomes a neurotoxin, causing CNS disorders and brain damage in children.

 

 

References:

 

The Brilliance of Dr. Suzanne Humphries on The Dangers of Vaccines: https://www.youtube.com/watch?v=McfXd_Xuojs

 

Dr. Humphries, author of Dissolving Illusions: Disease, Vaccines, and the Forgotten History, talk about the forgotten history of vaccinations:
https://www.youtube.com/watch?v=2vu9YJ4VHow&spfreload=5

 

List Of Toxic Materials 

(Including BSE?) In Vaccines: http://rense.com/general32/thru.htm

 

Vaccine Nation: https://www.youtube.com/watch?v=j8nrdybZZzA

 

Vaccines Cause Children More Adverse Reactions Than Any Other Drugs http://articles.mercola.com/sites/articles/archive/2014/04/26/vaccines-adverse-reaction.aspx

 

Vaccine Nation: https://www.youtube.com/watch?v=jUMZ-O-OsG0

 

Herd Immunity: https://www.youtube.com/watch?v=TFWBelim1Hw

 

Vaccines: The True weapons of mass destruction: https://www.youtube.com/watch?v=9WoMps4Pmpo

 

Children suffer vaccine side effects: https://www.youtube.com/watch?v=s7Sxq6wYbA8

 

Adverse reaction and Death after MMR Vaccine: https://www.youtube.com/watch?v=lNz_1wJOcaU

 

Uncensored: MMR fraud exposed by people behind Vaxxed: From Cover-Up to Catastrophe:  https://www.youtube.com/watch?v=5jxujaa0wDE

 

HERE'S THE PROOF. THE MMR MEASLES VACCINE INSERT SAYS IT CAUSES MEASLES AND DEATH: https://www.youtube.com/watch?v=eYn8SgeH0Ik

 

CDC Whistle Blower admits MMR Vaccine causes Autism: https://www.youtube.com/watch?v=q62DcaNs_0M

 

Mysterious Death: Body of Doctor Who Linked Vaccines To Autism Found Floating in River: http://www.infowars.com/mysterious-death-body-of-doctor-who-linked-vaccines-to-autism-found-floating-in-river/

 

Dr. Andrew Wakefield tells his side of the story in the MMR Vaccine causes Autism debate: https://www.youtube.com/watch?v=Ra0QtTUuFIc

 

VAXXED: From Cover Up to Catastrophe: https://www.youtube.com/watch?v=neNn97UUM88&index=2&list=
PLty48IsvT4v_oCjU8ZVZzx9zXQYK7fe2l

 

Vaccine-Nation: Poisoning the population one shot at a time by Andreas Moritz: http://www.ener-chi.com/books/vaccine-nation/

 

Illness is a Toxicity Crisis: https://www.youtube.com/watch?v=sXanVbgGliQ 

 

The Idea that Vaccines Make Us Healthy Is an Illusion: https://www.youtube.com/watch?v=50pU7VLw728 

 

Vaccine- nation interview: https://www.youtube.com/watch?v=vqUnyrP4i-0

 

Timeline chronology of the development of Medical industry, vaccines, banks and government in the U.S. etc.: http://www.illuminati-news.com/2007/1007.html

 

Revealed; The Men Who Own and Run the U S Government: https://www.youtube.com/watch?v=bKwO1onXAaI&list=RDbKwO1onXAaI#t=198

 

A vaccine- injured body can be repaired by detoxing slowly and recover depending on the severity of permanent damage as seen from partial recovery to complete recovery of Autism, diabetes, Parkinson, cancer, Alzheimer, allergies, arthritis, ALS, MS and many other chronic diseases by the Genesis II Church Sacraments! Please tune in this Sunday, the 25th Christmas day at www.g2voice.is at 10AM Eastern Standard Time. We hope to see you there!

 

Let’s change the world together!

Archbishop Mark S. Grenon

 

 

 

 

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Vaccines: Are they destroying the body’s ability to fight disease and causing new diseases?     We have been told our whole life by doctors, school systems, the FDA, CDC, NIH and the main stream media that vaccines are “safe and effective” without researching it ourselves. The problem is they are not, in fact, they are so toxic that everyone who receives a vaccine has a toxic response. Maybe it is just at the site of the injection, i.e. inflammation and pain, or something much more destructive like brain damage or even death! The whole concept of vaccines is based on the “hypothesis” that by injecting a small amount of a known dis-ease into the human body, the body’s immune system will create an immunity to said dis-ease. WRONG! This idea of “vaccine induced” herd immunity has never been proven or even worked! There is a “natural herd immunity” that exists and this is basically when someone, for instance, gets the measles, chicken pox or mumps they, 95% of the time, never get that dis-ease again in their lives, hence: immunity for these diseases! No one disputes that the body can naturally create an “acquired immunity” from dis-ease. The human body is VERY smart! The problem is this falsehood of vaccine induced herd immunity is unscientific and what is being taught in medical universities, allowed by the FDA and promoted by the main stream media, i.e. “fake news” as being completely true! I highly recommend watching the following videos before receiving ANY vaccine. There are many more below in the reference section:   A honest and brave Doctor’s testimony: The Brilliance of Dr. Suzanne Humphries on The Dangers of Vaccines: https://www.youtube.com/watch?v=McfXd_Xuojs The Idea that Vaccines Make Us Healthy Is an Illusion:https://www.youtube.com/watch?v=50pU7VLw728 Vaccines are causing many diseases by killing the immune system.   • Vaccines: The True weapons of mass destruction: https://www.youtube.com/watch?v=9WoMps4Pmpo   • Dementia in the 40’s why? : http://www.organicandhealthy.org/2016/11/dementia-now-striking-people-in-their.html • Herd Immunity: https://www.youtube.com/watch?v=TFWBelim1Hw   • Children suffer vaccine side effects: https://www.youtube.com/watch?v=s7Sxq6wYbA8   Vaccinated vs. Unvaccinated children:   • http://healthimpactnews.com/2016/study-unvaccinated-children-healthier-than-vaccinated-kids-doctors-agree/   • https://vactruth.com/2014/02/26/unvaccinated-children-healthier/   • http://healthimpactnews.com/2014/studies-outside-the-u-s-show-unvaccinated-children-healthier-than-vaccinated-children/   Note: ALL of the major  medical schools teach the “Allopathic” method of medicine and are owned by the same people that own the pharmaceuticals and the banks that fund them. “Allopathic medicine is based on the “germ theory”, that microbes and viruses, cause disease. Medical science bases the use of vaccines on the theory that the body forms antibodies to “fight” natural viruses. They believe that these antibodies live on after the virus is contained, thereby creating immunity. First, we must consider the facts known to evaluate medicine’s viral theory. Science has proved that viruses are not alive, that they are predominantly protein but that they contain organic DNA. Science has proven that virus increases only in the presence of live cells, and that they cause certain cells, and/or parts of cells to dissolve. What is believed and taken as fact but not proved, is that viruses are non -discriminatingly destructive “things” that self-replicate. That is like saying that laundry soap, because it is found in homes inhabited by humans, self-replicates. Those assumptions and conclusions are shallow and ludicrous. Medical science operates from fear, and it attacks the body. All medical procedures for treating disease are written by pharmaceutical-related individuals and groups. That is a severe conflict of interest. Self-produced health or medication-dependent profit, which do you think that they want? A rational and logical conclusion would be that virus are solvents (cleansers) manufactured by individual cells to dissolve degenerative tissue (disease) caused by accumulated waste and industrial toxins, including medicines. Virus contain DNA because cells have used substances within themselves to synthesize virus; DNA is a part of that. When the cleansing and healing processes cease, cells stop producing large amounts of virus. Normally, healthier bodies symbiotically utilize bacteria and parasites to cleanse themselves of cellular degenerative tissue and organic waste. They are the bodies preferred janitors. Bacteria and parasites consume the degenerative tissue and organic waste and reduce it to a tiny fraction of the original mass eaten. They can consume 100 times their weight and reduce it to 1-percent excretion. When eating a healthy raw diet, our bodies easily secrete and/or excrete the 1-percent excretions from bacteria and parasites. However, when bodies become too toxic with industrial toxins, including medicines, the bacteria and parasites are poisoned to death. Under such toxic conditions, the only cleansing method that the body can utilize is virus. So, cells synthesize viruses. I reiterate, viruses are solvents that dissolve degenerative tissue and organic waste. They are beneficial in preventing disease; they do not cause disease. The symptoms that accompany viral, bacterial or parasitical detoxifications are a necessary process but can be mitigated with the consumption of plenty of raw eggs and raw dairy fats. The key is: We should trust, nurture and understand the body and Nature, not fear them. Inoculating people to prevent viral infections is ridiculous and dangerous. After many years of experimentation, Louis Pasteur realized that the idea of vaccination was doomed. He confessed on his deathbed to his assistants that a poor (toxic) environment within the body creates disease. Microbes do not cause disease. Regarding the immediate trauma that vaccines cause in many people, the eminent scientist and physician, Dr. William F. Koch, M.D., Ph.D. said: The injection of any serum, vaccine or even penicillin has shown a very marked increase in the incidence of polio - at least 400%. Statistics are so conclusive no one can deny it. The long- term effects of vaccines are just as harmful. Vaccines are made of disease, mercury, aluminum, formaldehyde and other poisonous chemicals. Pharmaceutical houses manufacture diseases in animal tissue. The diseases are sterilized to make vaccines. Sterilization alters the RNA, DNA, structure and actions of diseases and viruses. When a sterilized disease or virus enters the body, the body tries to analyze it and create antibodies to regulate the disease or virus. The body cannot find the logical reason for the unnatural disease or virus. Nor can it find the key to the time that the bacteria or virus will be active. Therefore, the body creates mutant antibodies, bold emphasis mine, that do not go dormant for up to decades. These mutant antibodies remain active long after the disease or virus becomes inactive. The mutant antibodies eat sub-particles from the inside of amino acids (proteins) in the blood that renders proteins unstable. The amount of proteins damaged and lost to mutant antibodies depends on the number of vaccines. Because amino acids are the primary building blocks of cells, the consequence is cellular malnutrition. In all animals, the malnutrition causes gradual genetic mutations, resulting in weaknesses, diseases, malfunctions and deformities. The life span of mutant antibodies varies, from at least 1 year (penicillin) up to 50 years (polio). Each vaccine multiples the number of mutant antibodies, which increases cellular malnutrition and results in greater weaknesses, diseases, malfunctions and deformities. Reference: from pages 132-137; We Want To Live: The Primal Diet by Aarjonus Vonderplanitz: http://www.wewant2live.com/   You’ll notice Andreas Moritz agrees with the fact that toxicity is the major cause of dis-ease of the body: • Illness is a Toxicity Crisis: https://www.youtube.com/watch?v=sXanVbgGliQ    Have vaccines ever eradicated a dis-ease? The answer is no. We’ve been taught that small pox and polio were eradicated by vaccines when the facts show differently. Isolation and sanitation were responsible. Edward Jenner was one the first person to take cow pox from cattle and make a vaccine. The name came from the Latin word for cow “vacca” hence; the word vaccine. In England when the vaccines were stopped after many people protested because of the horrible side -affects, the dis-ease simply faded away. Were the vaccines causing the cow small pox to proliferate in the human body? Look how the history of vaccines went on after Jenner’s initial testings:  “It's been only 70 years since World War II, and the mad scientists from companies like I.G. Farben, BASF, Hoechst, Dow and Bayer, who created the gas chambers and tested dangerous vaccines on innocent Jews, didn't just go away. In fact, they went to work for U.S. corporations and pharmaceutical companies that run the vaccine industry today. At least a dozen of these cold blooded killers were hired fresh out of prison, just 4 to 7 years after the Nuremberg trials found them guilty of mass murder and enslavement. (http://frank.mtsu.edu/~baustin/trials3.html)   In fact, at the close of WWII, the IG Farben building in Frankfort was protected from allied bombings by the highest levels of military command. Why? IG Farben was the FDA/CDC type of "pharmaceutical arm" of Hitler's 4th Reich, and the Rockefellers had a financial interest in maintaining and controlling this pharmaceutical empire, which would soon be catapulted on U.S. soil. Research reveals that Hitler also invested heavily in Merck and other pharmaceutical companies. Nazi convicted mass murderers became executives for major U.S. chemical and pharmaceutical companies. Fritz ter Meer, found guilty of slavery and mass murder at Auschwitz, served only seven years in prison and became Chairman of the Board at Bayer in 1956. Still trust U.S. vaccines? Carl Krauch, Executive Member of IG Farben and Head of Military Economics for Hitler, found guilty of slavery and mass murder, served just 6 years in prison, then became Chairman of the Board for BASF in 1952. Still want to get those flu shots? How about that HPV shot for your daughter or son?   This is the same vaccine industry today which protected and employed Nazi war criminals. The very industry that produced the Nazi gas chambers was purchased by Bayer. So, exactly whom are you trusting with your children's health and welfare? Currently, the U.S. Government and the CDC rely solely on the manufacturers of vaccines to report problems, injuries and deaths. This atrocity is like letting murderers be their own judges in court! Where are the checks and balances this country was founded upon? Vaccines have economic and political agendas now, and the FDA does absolutely no testing of their own before making decisions to release vaccines to the masses.   Want more research before you or your child get injected with a new concocted disease for which there is no cure? Listen to stunning admissions by vaccine industry experts, including Dr. Maurice Hilleman (formerly w/Merck), who admitted to the deadly nature of the most trusted vaccines. (http://www.naturalnews.com/033584_Dr_Maurice_Hilleman_SV40.html)   Today's vaccines not only contain live versions of the diseases you DO NOT WANT, but also contain GMOs, hormones from infected cows, pigs, chickens and monkeys, untested virus combinations (like H1N1), aluminum, mercury,  emulsifiers, and crossbred bacteria from animals, mosquitoes, and diseased humans: http://www.naturalnews.com/035431_vaccine_ingredients_side_effects_MSG.html#ixzz4TNiwiuAP   NOTE: The FDA requires a “package insert” to be created by the pharmaceutical company that produces every FDA “approved” drug on the market. The pharmaceutical is allowed to do the clinical studies also without the FDA’s oversight. Any side- affects are listed most of the time, but some are not as in the case of the MMR. The first MMR package insert by Merck mentioned the adverse- effect of the MMR vaccine causing “autism” and the second edition does not. Who allowed that?   Original MMR Package Insert Has Autism As An Adverse Effect  The drug company that makes the M.M.R. vaccine (Merck) publishes an extensive list of warnings, contraindications, and adverse reactions associated with this triple shot. It may be found in the vaccine package insert given to doctors administering MMR, and inside the Physician's Desk Reference (PDR)(8,9). However, this information is never given to patients or parents. The insert is quoted immediately below. An Excerpt from the Original M.M.R. Drug Insert The following afflictions affecting nearly every body system -- blood, lymphatic, digestive, cardiovascular, immune, nervous, respiratory, and sensory -- have been reported following receipt of the MMR shot: encephalitis, encephalopathy, neurological disorders, seizure disorders, convulsions, learning disabilities, subacute sclerosing panencephalitis (SSPE) demyelination of the nerve sheaths, Guillain-Barré syndrome (paralysis), muscle incoordination, deafness, panniculitis, vasculitis, optic neuritis (including partial or total blindness) retinitis, otitis media, bronchial spasms, fever, headache, joint pain, arthritis (acute and chronic) transverse myelitis, thrombocytopenia (blood clotting disorders and spontaneous bleeding) anaphylaxis (severe allergic reactions) lymphadenopathy, leukocytosis, pneumonitis, Stevens-Johnson syndrome, erythema multiforme, urticaria, pancreatitis, parotitis, inflammatory bowel disease, Crohn's disease, ulcerative colitis, meningitis, diabetes, autism, immune system disorders, and death   The M.M.R. vaccine manufacturer has begun censoring autism from the package insert for its second version of the M.M.R. vaccine ("M.M.R. 2"). Most of the above indications continue to be cited, except for the admission of an autism link, which has been selectively removed. The vaccine manufacturer previously admitted to causing autism, but only in private communications with doctors. Their statements to the public and the media were the complete opposite. Parents in the British medical system are often ignored when they report problems with vaccines, because the doctors act as the gatekeepers. Parents cannot directly report bad reactions to regulators. They must instead go through their doctor, who may refuse, in order to protect himself. Keep in mind that doctors in Britain get monetary bonuses for administering vaccines, which could be considered a conflict of interest. Reference: https://currenthealthscenario.blogspot.com.co/2015/09/original-mmr-package-insert-has-autism.html   Package inserts confirming diseases such as autism etc:  • Package Insert From FDA: Diphtheria Toxoids and Pertussis Vaccine Tripedia® Page 11 ‘Adverse events reported during post-approval use of Tripedia vaccine include idiopathic thrombocytopenic purpura, SIDS, anaphylactic reaction, cellulitis, autism, convulsion/grand mal convulsion, encephalopathy, hypotonia, neuropathy, somnolence and apnea. Events were included in this list because of the seriousness or frequency of reporting.’  http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/ucm101580.pdf       Toxic vaccine ingredients and their adverse effects:   • Bovine cow serum: Extracted from cow skin. When injected causes connective tissue disorders, arthritis and lupus; also, shortness of breath, low blood pressure, chest pain and skin reactions.   • Sorbitol: Synthetic sweetener which metabolizes very slowly and aggravates IBS and gastrointestinal issues.   • Gelatin: Derived from the collagen inside animals' skin and bones. Injecting gelatin poses the risk of infection from synthetic growth hormones and BSE infectivity (mad cow disease).   • Sodium chloride: Raises blood pressure and inhibits muscle contraction and growth.   • Egg protein: Vaccines are prepared in eggs (certainly not organic). May contain growth hormones, antibiotics, and salmonella bacteria.   • Thimerosal: A neurotoxic mercury which causes autism: There are 25 mcg in one average flu vaccine, and the EPA safety limit is 5 micrograms, so children who are vaccinated simultaneously with multiple* vaccines receive over 10 times the safety limit of mercury in one day.   • Human albumin: The protein portion of blood from pooled human venous plasma; when injected causes fever, chills, hives, rash, headache, nausea, breathing difficulty, and rapid heart rate. Injecting "pooled blood" can result in a loss of body cell mass and cause immunodeficiency virus infection, or contain SV40, AIDS, cancer or Hepatitis B from drug addicts.   • Formaldehyde: Highly carcinogenic fluid used to embalm corpses. Ranked one of the most hazardous compounds to human health; can cause liver damage, gastrointestinal issues, reproductive deformation, respiratory distress and cancer. Plus, formaldehyde has been known to fail to deactivate the virus the vaccine is intended to cure, thus enabling a live virus to enter your blood and infect your system.   • Phenoxyethanol: A glycol ether/chemical; highly toxic to the nervous system, kidneys, and liver. The FDA warns "can cause shut down of the central nervous system (CNS), vomiting and contact dermatitis" in cosmetics; imagine when injected into your blood.   • Aluminum phosphate: Greatly increases toxicity of mercury, so caution about minimum mercury tolerance is therefore severely underestimated. CDC scientists and all doctors are well aware of this.   • MSG (monosodium glutamate): When injected becomes a neurotoxin, causing CNS disorders and brain damage in children.       References:   • The Brilliance of Dr. Suzanne Humphries on The Dangers of Vaccines: https://www.youtube.com/watch?v=McfXd_Xuojs • Dr. Humphries, author of Dissolving Illusions: Disease, Vaccines, and the Forgotten History, talk about the forgotten history of vaccinations: https://www.youtube.com/watch?v=2vu9YJ4VHow&spfreload=5 • List Of Toxic Materials  (Including BSE?) In Vaccines: http://rense.com/general32/thru.htm • Vaccine Nation: https://www.youtube.com/watch?v=j8nrdybZZzA • Vaccines Cause Children More Adverse Reactions Than Any Other Drugs http://articles.mercola.com/sites/articles/archive/2014/04/26/vaccines-adverse-reaction.aspx • Vaccine Nation: https://www.youtube.com/watch?v=jUMZ-O-OsG0 • Herd Immunity: https://www.youtube.com/watch?v=TFWBelim1Hw • Vaccines: The True weapons of mass destruction: https://www.youtube.com/watch?v=9WoMps4Pmpo • Children suffer vaccine side effects: https://www.youtube.com/watch?v=s7Sxq6wYbA8 • Adverse reaction and Death after MMR Vaccine: https://www.youtube.com/watch?v=lNz_1wJOcaU • Uncensored: MMR fraud exposed by people behind Vaxxed: From Cover-Up to Catastrophe:  https://www.youtube.com/watch?v=5jxujaa0wDE • HERE'S THE PROOF. THE MMR MEASLES VACCINE INSERT SAYS IT CAUSES MEASLES AND DEATH: https://www.youtube.com/watch?v=eYn8SgeH0Ik • CDC Whistle Blower admits MMR Vaccine causes Autism: https://www.youtube.com/watch?v=q62DcaNs_0M • Mysterious Death: Body of Doctor Who Linked Vaccines To Autism Found Floating in River: http://www.infowars.com/mysterious-death-body-of-doctor-who-linked-vaccines-to-autism-found-floating-in-river/ • Dr. Andrew Wakefield tells his side of the story in the MMR Vaccine causes Autism debate: https://www.youtube.com/watch?v=Ra0QtTUuFIc • VAXXED: From Cover Up to Catastrophe: https://www.youtube.com/watch?v=neNn97UUM88&index=2&list=PLty48IsvT4v_oCjU8ZVZzx9zXQYK7fe2l • Vaccine-Nation: Poisoning the population one shot at a time by Andreas Moritz: http://www.ener-chi.com/books/vaccine-nation/ • Illness is a Toxicity Crisis: https://www.youtube.com/watch?v=sXanVbgGliQ  • The Idea that Vaccines Make Us Healthy Is an Illusion: https://www.youtube.com/watch?v=50pU7VLw728  • Vaccine- nation interview: https://www.youtube.com/watch?v=vqUnyrP4i-0 • Timeline chronology of the development of Medical industry, vaccines, banks and government in the U.S. etc.: http://www.illuminati-news.com/2007/1007.html • Revealed; The Men Who Own and Run the U S Government: https://www.youtube.com/watch?v=bKwO1onXAaI&list=RDbKwO1onXAaI#t=198 A vaccine- injured body can be repaired by detoxing slowly and recover depending on the severity of permanent damage as seen from partial recovery to complete recovery of Autism, diabetes, Parkinson, cancer, Alzheimer, allergies, arthritis, ALS, MS and many other chronic diseases by the Genesis II Church Sacraments! Please tune in this Sunday, the 25th Christmas day at www.g2voice.is at 10AM Eastern Standard Time. We hope to see you there! Let’s change the world together! Archbishop Mark S. Grenon                  

 
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How To Cure An HIV Positive Diagnosis With The G2 Sacraments

G2Voice Broadcast #13 
Sunday Oct. 11th
10 AM EST

www.G2Voice.is

 

Before I explain what I personally believe about how HIV/AIDS has been introduced into this world, I want everyone to understand what the mainstream scientific community and the U.S. Govt. says what HIV is and how the HORRIBLE dis-ease began.

I've been researching thoroughly and reading in depth why we have this dis-ease in our world today since the early 80's. When I was a young Pastor in Massachusetts I was introduced to this dis-ease while ministering to two young men that had contracted GRID, Gay Related Immune Deficiency Syndrome, before it was called HIV. The reason it was called GRID was because homosexuals were the first ones to contract this HORRIBLE dis-ease! You will see later why I believe this group of people were one of the first two groups- the other being hepatitis patients, to be diagnosed with GRIDS which later became known as HIV.

I want everyone to first listen and read a few testimonies from people that were “restored to health” from an HIV positive diagnosis. The good news before the bad news that the scientific, medical and government is telling the world about HIV.


Video Testimonies:

1. Jim talks about his experience in Africa on Project Camelot: https://www.youtube.com/watch?v=qItAYhG-w_g

2. Zed: https://www.youtube.com/watch?v=aR3Ii68Z5SA

3. English subtitled: https://www.youtube.com/watch?v=e20CD7QD2X4

4. Ron: Starts at 5:50: https://www.youtube.com/watch?v=RKdsCQzSiTI&t=44s


Written Testimonies:

1. HIV: Undetectable!!!!!!!!!
Hi everyone!!!!

I'm here to share some great news: after my wife tested NEGATIVE for HPV (already mentioned that story here a while ago), it was my turn:

Took the PCR (RNA) test for HIV and guess what???

Results came UNDETECTABLE!!!! I'm so damn happy!!!

CD4 is still a little low, but the doctors said the Viral Load is THE most important thing and now that NO virus was detected in my blood, he's
more than positive CD4 counts will raise.

Also, it's important to note that I couldn't wait the three months as recommended by Jim after finishing the Protocol because my doctor requested my to take the test.

IMPORTANT: I've been on Protocol 4000 (MMS2) for exactly 105 days (29 days for maintenance)....
And besides the Protocol, Faith and Hope played real important elements, as I prayed a lot with each MMS capsule I took.

Maybe in three months I'll take the elisa test, and God help me that will test negative too!!!

For those who wanted a testimonial, here you have it. I'll try to copy the test results here (sorry for the language, it's in portuguese):

VÍRUS DA IMUNODEFICIÊNCIA HUMANA-1 (HIV-1), QUANTIFICAÇÃO DO RNA
Método: Reação em cadeia da polimerase (PCR) em tempo real

Material: RNA extraído do plasma

RESULTADO VALOR DE REFERÊNCIA

INDETECTÁVEL INDETECTÁVEL

Limite de detecção: 20 cópias/mL (34 UI/mL).

NOTA(1): Um resultado "indetectável" indica que a viremia está ausente
ou se encontra abaixo do limite de detecção do teste.

NOTA(2): Este teste não deve ser utilizado para o diagnóstico de
infecção por HIV-1, exceto em situações clínicas bastante
particulares.

Peace, Love and Health to everyone!
Chris, from Brazil


2. God bless you
My name is Almaze i come from Ethiopia , i am HIV postive and i have 1 son but he is ok from this sickness thanks God .

and i hearing from this Mms before 3 years from one friend of my sister she is also the same like me but thanks God she is complitly ok now and i know if i can found this Mms i will be also ok but i dont know where can i found can you please help me to found this MMS please please by God name i ask you to tell me where i can found or i can buy . From the first day up to now i am looking for , for this but it is not easy to found here in Ethiopia .
Dear Jim Hampel Thanks so much and God bless you where ever you are 


For more written testimonies, see link below:
https://www.dropbox.com/s/vyhzxt00g9kjjwn/More%20testimonies.pdf?dl=0 


NOTE: The following is the official Govt., scientific, and medical explanation of HIV, how to treat it and where this dis-ease originated.

I will then give you an explanation of what I personally believe about how HIV originated and WHY.

 
What is HIV? 

The human immunodeficiency virus (HIV) is a lentivirus (a subgroup of retrovirus) that causes HIV infection and over time acquired immunodeficiency syndrome (AIDS). AIDS is a condition in humans in which progressive failure of the immune system allows life-threatening opportunistic infections and cancers to thrive. Without treatment, average survival time after infection with HIV is estimated to be 9 to 11 years, depending on the HIV subtype. Infection with HIV occurs by the transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk. Within these bodily fluids, HIV is present as both free virus particles and virus within infected immune cells.

HIV infects vital cells in the human immune system such as helper T cells (specifically CD4+ T cells), macrophages, and dendritic cells. HIV infection leads to low levels of CD4+ T cells through a number of mechanisms, including pyroptosis of abortively infected T cells, apoptosis of uninfected bystander cells, direct viral killing of infected cells, and killing of infected CD4+ T cells by CD8 cytotoxic lymphocytes that recognize infected cells. When CD4+ T cell numbers decline below a critical level, cell-mediated immunity is lost, and the body becomes progressively more susceptible to opportunistic infections.

- https://en.wikipedia.org/wiki/HIV

HIV stands for human immunodeficiency virus. If left untreated, HIV can lead to the disease AIDS (acquired immunodeficiency syndrome).

Unlike some other viruses, the human body can’t get rid of HIV completely. So once you have HIV, you have it for life.

HIV attacks the body’s immune system, specifically the CD4 cells (T cells), which help the immune system fight off infections. If left untreated, HIV reduces the number of CD4 cells (T cells) in the body, making the person more likely to get infections or infection-related cancers. Over time, HIV can destroy so many of these cells that the body can’t fight off infections and disease. These opportunistic infections or cancers take advantage of a very weak immune system and signal that the person has AIDS, the last state of HIV infection.

No effective cure for HIV currently exists, but with proper treatment and medical care, HIV can be controlled. The medicine used to treat HIV is called antiretroviral therapy or ART. If taken the right way, every day, this medicine can dramatically prolong the lives of many people with HIV, keep them healthy, and greatly lower their chance of transmitting the virus to others. Today, a person who is diagnosed with HIV, treated before the disease is far advanced, and stays on treatment can live a nearly as long as someone who does not have HIV.

The only way to know for sure if you have HIV is to get tested. Testing is relatively simple. You can ask your health care provider for an HIV test. Many medical clinics, substance abuse programs, community health centers, and hospitals offer them too. You can also buy a home testing kit at a pharmacy or online.

- https://www.aids.gov/hiv-aids-basics/hiv-aids-101/what-is-hiv-aids/


What is AIDS?

AIDS stands for acquired immunodeficiency syndrome. AIDS is the final stage of HIV infection, and not everyone who has HIV advances to this stage.

AIDS is the stage of infection that occurs when your immune system is badly damaged and you become vulnerable to opportunistic infections. When the number of your CD4 cells falls below 200 cells per cubic millimeter of blood (200 cells/mm3), you are considered to have progressed to AIDS. (The CD4 count of an uninfected adult/adolescent who is generally in good health ranges from 500 cells/mm3 to 1,600 cells/mm3.) You can also be diagnosed with AIDS if you develop one or more opportunistic infections, regardless of your CD4 count.

Without treatment, people who are diagnosed with AIDS typically survive about 3 years. Once someone has a dangerous opportunistic illness, life expectancy without treatment falls to about 1 year. People with AIDS need medical treatment to prevent death.

- https://www.aids.gov/hiv-aids-basics/hiv-aids-101/what-is-hiv-aids/

 
What is a Retrovirus?

Any of a group of RNA viruses which insert a DNA copy of their genome into the host cell in order to replicate, e.g. HIV. 1970s: modern Latin, from the initial letters of reverse transcriptase + virus.

Retrovirus: A virus that is composed not of DNA but of RNA. Retroviruses have an enzyme, called reverse transcriptase, that gives them the unique property of transcribing their RNA into DNA after entering a cell. The retroviral DNA can then integrate into the chromosomal DNA of the host cell, to be expressed there. HIV is a retrovirus.

- http://www.medicinenet.com/script/main/art.asp?articlekey=5344


What is CD4 count? 

In molecular biology, CD4 (cluster of differentiation 4) is a glycoprotein found on the surface of immune cells such as T helper cells, monocytes, macrophages, and dendritic cells. It was discovered in the late 1970s and was originally known as leu-3 and T4 (after the OKT4 monoclonal antibody that reacted with it) before being named CD4 in 1984. In humans, the CD4 protein is encoded by the CD4 gene.

CD4+ T helper cells are white blood cells that are an essential part of the human immune system. They are often referred to as CD4 cells, T-helper cells or T4 cells. They are called helper cells because one of their main roles is to send signals to other types of immune cells, including CD8 killer cells, which then destroy the infectious particle. If CD4 cells become depleted, for example in untreated HIV infection, or following immune suppression prior to a transplant, the body is left vulnerable to a wide range of infections that it would otherwise have been able to fight.

- https://en.wikipedia.org/wiki/CD4


What is viral load?

Viral load, also known as viral burden, viral titre or viral titer, is a numerical expression of the quantity of virus in a given volume. It is often expressed as viral particles, or infectious particles per mL depending on the type of assay. A higher viral burden, titre, or viral load often correlates with the severity of an active viral infection. The quantity of virus / mL can be calculated by estimating the live amount of virus in an involved body fluid. For example, it can be given in RNA copies per millilitre of blood plasma. Tracking viral load is used to monitor therapy during chronic viral infections, and in immunocompromised patients such as those recovering from bone marrow or solid organ transplantation. Currently, routine testing is available for HIV-1, cytomegalovirus, hepatitis B virus, and hepatitis C virus.

Viral load monitoring for HIV is of particular interest in the treatment of people with HIV, as this is continually discussed in the context of management of HIV/AIDS.

- https://en.wikipedia.org/wiki/Viral_load


Very good information here: 

FALSE POSITIVE VIRAL LOADS
What Are We Measuring? By Matt Irwin:

http://www.sidasante.com/themes/tests/pcr/false_positive_viral_loads.htm

 
Where Did HIV Come From?

NOTE: The Governments official story:

Scientists identified a type of chimpanzee in Central Africa as the source of HIV infection in humans. They believe that the chimpanzee version of the immunodeficiency virus (called simian immunodeficiency virus, or SIV) most likely was transmitted to humans and mutated into HIV when humans hunted these chimpanzees for meat and came in contact with their infected blood. Studies show that HIV may have jumped from apes to humans as far back as the late 1800s. Over decades, the virus slowly spread across Africa and later into other parts of the world. We know that the virus has existed in the United States since at least the mid- to late 1970s.

- https://www.aids.gov/hiv-aids-basics/hiv-aids-101/what-is-hiv-aids/

Now, let me tell you what I believe that HIV/AIDS is, where it came from and why. First, let me say that I haven't been able to find anywhere where Dr. Gallo said that he created Aids to depopulate the world. If anyone can find him saying that then please send me where it is found. I DO believe that Dr. Gallo and the company that he worked for; Litton, was contracted to work with the Bio-Weapons lab at Ft. Detrick, Maryland to create a “virus” or a means to destroy the T-4 cells of the body which in turn destroys the immune system which ends in the death of the host, being monkeys.

This was talked about by the WHO in 1972 and was implemented by the WHO in the Small Pox program in the 70's in Africa. Not only did it infect the Africans but 15,000 Haitians were part of that program that were living in Uganda and were infected and sent back to Haiti.

In the U.S., the Hep. B vaccine was contaminated with this T-4 cell destroyer and given to homosexual men and Hep B patients in New York, San Francisco and Los Angeles between 1978 – 1980 where this horrible evil dis-ease was first diagnosed. Coincidence?

That is why the world saw this as a homosexual lifestyle disease, which it is not! In April 1984, Dr. Robert Gallo filed a United States patent application for his invention, the scientific evidence is complete and compelling, the AIDS Virus is a designer bi-product of the U.S. Special Virus Program. Read more: https://adonis49.wordpress.com/2015/02/17/i-have-a-patent-for-creating-hivaids-virus-dr-robert-gallo/

The Special Virus program was a federal virus development program that persisted in the United States from 1962 until 1978.
The U.S. Special Virus was then added as ‘compliment’ to vaccine inoculations in Africa and Manhattan.

Shortly thereafter, the world was overwhelmed with mass infections of a human retrovirus that differed from any known human disease, it was highly contagious and more importantly, it could kill.

I believe these evil people that invented and distributed it into the population of the world want to kill the population of the world by 7 Billion as seen at the Georgia Guidestones. It was also talked about by Henry Kissinger, Bill Gates, Ted Turner and many other people and world organizations such as the WHO and the United Nations! While people are dying “they” will make trillions thru treatments and drugs that not only don't work but accelerate the dis-ease to end in a slow horrible death as they saw in the poor monkeys and animals they tortured!

I also believe that people are told they are HIV positive and are not. For example, there are many false positives. Pregnant women can be positive, if you had a tetanus shot you could be positive. How many more false positives are there. Many say there is no “virus” at all and it is the destruction of the immune system by whatever Gallo invented. I believe something was “invented” by Gallo and then it was put into vaccines to infect mankind. Are they looking for autoimmune deficiencies? I've read that the HIV test looks for 47+ autoimmune deficiencies and if one shows up then you are HIV Positive and then pushed to get the AZT anti -retrovirus drugs that begin to destroy your immune system and bring down your CD4 count to make you think you are infected with HIV and doomed to be on “their” drugs for a lifetime! If that is all made up, how many people worldwide are unnecessarily suffering? It gets worse and worse as you see what has been done. HIV TESTS are useless. Here is an article I think everyone should read before being tested for HIV:

HIV tests are antibody tests, they do not test for the presence of viruses. Contrary to what people are told about antibodies, antibodies are not always specific. For example, let's say you want to produce a monoclonal antibody for disease research. First you would take a blood sample and separate the serum. You then take an antigen test target and place it in the serum sample so antibodies attach to this antigen target. Though these antibodies are not all specific. They are a mixture of high affinity (specific) and low affinity (non-specific) antibodies. Of course, these antibodies cannot be used to make monoclonals. So, the antigen test target is placed in a weak solution of sodium sulfate solution to strip off the less specific antibodies. The target is then placed in a slightly stronger solution to remove the slightly more specific antibodies. This process is repeated until only high affinity antibodies, with an extremely high level of specificity are left. These are then used to make monoclonals. The reason this is so important is because this same principle is used in HIV antibody testing. Though in this case the antibodies are not differentiated. So, low affinity antibodies reacting on HIV test targets yield false positives. This is the primary reason HIV antibody tests are known to have over 65 known causes for false positives! Examples in these cases would be false positives due to pregnancy, flu vaccines, typhoid vaccines, polio vaccines, malaria vaccines, gamma globulin, BLV antibodies from cow's milk or beef, and viral hepatitis. Autoimmune disorders, especially lupus, are also known to yield false positives. The risk of false positives increases with autoimmune conditions because the immune system shifts from producing predominately high affinity antibodies to predominately low affinity antibodies. The higher level of low affinity antibodies increases the risk of false positives on antibody tests. To further compound the problem the primary test for HIV is the ELISA, which is supposed to be confirmed by the Western blot. Though Western blot is less accurate than ELISA. The only reason it is done this way is because ELISA is less expensive than Western blot. But to use a less accurate test as a confirmation is just totally ludicrous!

Another problem with antibody tests is they do not prove the presence of a virus for another reason. Let’s say for an example that I had the flu from a influenza virus 2 weeks ago. So, I am now over the flu. If I get tested for influenza antibodies am I going to test positive or negative? I am going to test positive of course, because my immune system has successfully fought off the virus, yielding anti-influenza antibodies in the process. So, I would be influenza antibody positive, but virus negative. The same applies to HIV testing. If you are exposed to the HIV virus but your immune system is strong enough to fight it off you will have the antibodies temporarily, yielding a false positive HIV test, but you are still virus negative. It was proven a long time ago that the HIV virus cannot infect healthy immune systems.

Then there is the question of what really causes AIDS. HIV was stated as the cause by Robert Gallo after he got busted for scientific fraud. He tried to reclaim his credibility by claiming before a world -wide AIDS symposium that he had found the cause of AIDS, which he claimed was HIV. The problems with this claim? Well, first of all he made it up! And secondly, he was wrong! He had absolutely no solid research to back his claim. But the world was scared and had no answers. So, when Gallo lied again the media did not stop to question the fact that there was no evidence of the claim. So, they ran with the claim and it has been a part of AIDS history since. As far as Gallo being wrong, you need to understand what AIDS is to understand why he was wrong. AIDS is not a disease, it is a syndrome, acquired immune deficiency syndrome. A syndrome is not a disease, it is a group of symptoms. So, if you develop certain symptoms you are given an AIDS diagnosis. Well under the original definition of AIDS, which was only opportunistic infections, HIV could not cause AIDS! So, the government was really in a pickle. Here one of their top scientists had lied and was busted for scientific fraud making the US international fools. Now one of the government’s top researchers, Robert Gallo, had lied again, which was highly embarrassing to the government if they could not cover the lie before it was widely publicized. So, they came up with a solution, they changed the definition of AIDS to fit the HIV virus, so they could honestly claim that HIV could cause AIDS. Since HIV could not cause any disease in man, that ruled out using any opportunistic infections. So, they went with the only thing the HIV virus could do, which was to drop the CD4 count. So, the definition of AIDS was changed to include a drop in CD4 cells below 200. Thus, a second international embarrassment by Gallo’s lies was averted!

Now for the rest of the story. Gallo had to lie because he had more than his credibility at stake. Gallo also held the patent rights to the HIV tests. So as long as people could be fooled in to believing that HIV caused AIDS he would continue to make a fortune off of royalties to his HIV tests!

So, under the new definition HIV can cause AIDS, but not under the original definition. The only things that are known to cause AIDS under the original definition are the virus Human Herpes Virus Type 6 variant A (HHV6-A) and the drug AZT (zidovudine), which destroys the bone marrow leading to a drop of stem cells. This in turn leads to a drop of all immune cells, including CD4 cells. The drop in CD4 cells leads to an AIDS diagnosis as does the opportunistic infections created by AZT collapsing the immune system. But that is a whole other story, along with how AIDS came about, etc.

 - http://www.curezone.org/forums/am.asp?i=1545495


NOTE: AIDS, Auto Immune Deficiency Syndrome, is a syndrome not a disease! A syndrome refers to a group of symptoms, while a disease refers to an established condition. Are the symptoms of AIDS caused by the treatments from an HIV positive test like AZT? So, is the scam to get people to take a test that many will be positive because it identifies non- specific antibodies, other antibodies or cellular debris that most human bodies have and then get them on the AZT which will destroy the T-4 cells? Does a toxic body have low CD4 counts? Are many toxic today from prescription or illegal drugs? Or maybe vaccines? Toxic foods? Water?


Where did HIV/AIDS originate?

Cross species transmission successfully was done early 1970's. In 1972 the WHO mentioned that it is possible to create a virus that would destroy the T-cells in the body. “An attempt should be made to ascertain whether viruses can in fact exert selective effects on the immune function… by effecting T-cell as opposed to B-cell function.” Also, mention in this WHO bulletin, “ The Possibility should be looked into that the immune response tot eh virus may itself be impaired if the effective viruses damage more or less selectively the cells responding to the viral antigens.” -Bulletin of the WHO 1972

Here are some more important facts you will learn by following the references below:

• The “visna” sheep virus and bovine viruses were combined to adapt to humans by way of a retrovirus, RNA to DNA and change itself or attach itself to the human DNA. The “visna” virus was a sheep “wasting” virus that destroys the T-4 cells in the body which will completely destroy the body's immune system and rare types of cancer and pneumonias among humans will be prevalent.

• Before HIV destruction, Kaposi's sarcoma was never seen in healthy young men. Also, downplayed to the public is a new microbe (Mycoplasma penetrans), also of unknown origin, that was introduced into homosexuals, along with HIV and the new herpes virus. Thus, not one but three new infectious agents were inexplicably transferred into the gay population at the start of the epidemic (HIV, the herpes KS virus, and M.penetrans). 

• In 1982, May 11th Front page London Times ask the question, was there an association between the WHO small pox vaccine in Africa and the Aids epidemic? A researcher did a study for the WHO and walks into the London Times and throws his investigation on the desk of Pierce Wright and it was published. That article never made it to US newspapers or MSM. WHY? There was a quote from Dr. Robert Gallo, about the article saying, “that is an interesting hypothesis.” Many parts of the world covered this May 11th Article but not in the U.S. Why?  

• Dr. Gallo was the discoverer of the HIV virus and patented it in 1982! If you made something that destroyed the body's natural defenses would you tell anyone? 

• Why would the HIV virus be intentionally added to vaccines? Was it on purpose or accidentally? 

• Could the U.S. Govt. ever do such a thing? In the U.S., the 1930's Tuskegee, Mississippi project where black men were infected with Syphilis and not treated. They infected their wives and their unborn children while penicillin was available that could have cured it! Read the book “Bad Blood” by James Jones

The Higher form of killing by Robert Harris from 1959 -70's over 300 unknown biological experiments conducted by the US covertly on its citizens. It is not only possible but has happened many times! 

• Everyone who is HIV is unique because it takes on their DNA which is different in all people like a personal code or ID.

• 1978 -80's Hep B vaccine given to Homosexuals and Hep B patients in New York, L.A. and San Francisco where it first broke out! 

• Brazil bought a lot of whole blood in the 70's from Africa so that is why it was in Brazil early.

• 15,000 Haitians were inoculated in Uganda during the WHO Small Pox Vaccine Campaign and went back to Haiti to infect their families where the Haitians AIDS outbreak began in Haiti!

• Is HIV a virus or “something” that destroys the immune system. 

• Jacob Seagal, East German biologist says it was made at Fort Detrick in biological warfare project. Situations like this have been investigated with a lot less evidence and why isn't it being investigated? WHY? $$$$$$$$ and Power!

• In 1974 veterinarians actually created an AIDS-like disease when newborn chimps were removed from their mothers and weaned exclusively on virus-infected milk from cows infected with "bovine C-type virus." Within a year, the chimps died of leukemia and pneumocystis pneumonia (the "gay pneumonia" of AIDS). 

• AZT is a toxin that destroys the cells and immune system so it will keep every patient HIV positive by destroying the immune system further and keeping the CD4 count low which will eventually kill the host i.e. animal or person.

• That is the title of Chapter 9 of Dr. Peter Duesberg’s ground-breaking book, Inventing the AIDS Virus. By the time you have read the chapter, you will have become darkly suspicious of the medical research establishment of this country if you weren’t already.

What Dr. Duesberg does in those 60 or so pages is nothing less than monumental: 

• He provides a history of the introduction of AZT as a failed chemotherapeutic drug (it was too toxic to be of any use against cancer) and its re-introduction as a so-called "cure" for AIDS through political means.

• He shows that the trials for AZT were a mockery of good science and medicine, that the single efficacy and safety margin study has been refuted in multiple studies, and that the human trials (Phase II) were hopelessly flawed and carried out by doctors and researchers beholden to the AZT manufacturer, Burroughs Welcome. 

• He shows precisely why AZT cannot possibly be a cure for AIDS, and, presenting information that he uses later in Chapter 11, shows why AZT is a likely cause of AIDS.

Here are some good articles to read about AZT 

• AZT: A Medicine from Hell by Anthony Brink - http://www.virusmyth.com/aids/hiv/abazt.htm 

• THE TRUTH ON AZT:
http://www.virusmyth.com/aids/hiv/vvazt.htm 

• With Therapies Like These, Who Needs Disease?: http://www.healthy-again.net/azt.htm


References:

• History of HIV/AIDS by Dr. Leonard Horovitz : https://www.youtube.com/watch?v=HgiMqgjS-zM 

• HIV Patent: https://adonis49.wordpress.com/2015/02/17/i-have-a-patent-for-creating-hivaids-virus-dr-robert-gallo/ He also holds the patent on the HIV tests! 

• Film: House of Numbers: https://www.youtube.com/watch?v=BwgmzbnckII  

• Strecker Memorandum: https://www.youtube.com/watch?v=fevYSHQoeD4 

• The Man-Made Origin of AIDS:Are Human and Viral Experiments Responsible For Unleashing The HIV Holocaust?? http://www.rense.com/general45/cant.htm 

• Positively False - Birth of a Heresy - HIV AIDS https://www.youtube.com/watch?v=Q-iccGpFto8  

• Excellent site on the controversy: http://www.virusmyth.com/aids/ 

• Georgia Guidestones: http://www.rense.com/general16/georgiaguidestones.htm 

• Henry Kissinger: https://www.facts-are-facts.com/article/americas-development-plan-for-the-world 

• Bill Gates depopulation agenda using vaccines: http://yournewswire.com/bill-gates-admits-vaccines-are-best-way-to-depopulate/ 

• Ted Turner depopulation ideas: https://www.youtube.com/watch?v=jjIMoaUBHB0 

• Ted Turner’s UN Foundation has Given $1 Billion to UN Projects
Major focus of foundation is population control, condoms, abortion and sterilizations
http://www.lifesitenews.com/ldn/2006/oct/06101109.html 

• The HIV=AIDS Fraud - G Edward Griffin ON HIV AIDS Big Pharma Fraud https://www.youtube.com/watch?v=v63NQg-eFjo 

• The Massive Fraud Behind HIV Tests: http://www.whale.to/b/rappoport1.html 

• Dogs HIV False Positive: https://www.youtube.com/watch?v=ZGJgzAO16Jc 

• Confusion among Doctors? https://www.youtube.com/watch?v=26fyHAIqB40 

• HIV tests are antibody tests: http://www.curezone.org/forums/am.asp?i=1545495

Whatever has been the cause of people dying with the so-called HIV Positive diagnosis or AIDS or a destroyed immune system, if you've listened and read the testimonies above you see that these people have restored their health! We will talk more above HIV and AIDS this weekend and show everyone how to cure themselves from an HIV Positive diagnosis.

Tune in LIVE at: www.G2voice.is
at 10 AM EST
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I hope that many who have been diagnosed with being HIV Positive will understand that they don't have to be afraid any longer!

Let's change the world together!
Archbishop Mark S. Grenon

MMS Saves Lives.

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Jim Humble and Tiger

This breakthrough can save your life, or the life of a loved one. In 1996, while on a gold mining expedition in South America, I discovered that chlorine dioxide quickly cured malaria. Since that time, it has proven to restore partial or full health to hundreds of thousands of people suffering from a wide range of disease, including cancer, diabetes, hepatitis A, B, C, Lyme disease, MRSA, multiple sclerosis, Parkinson’s, Alzheimer’s, HIV/AIDS, malaria, autism, infections of all kinds, arthritis, high cholesterol, acid reflux, kidney or liver diseases, aches and pains, allergies, urinary tract infections, digestive problems, high blood pressure, obesity, parasites, tumors and cysts, depression, sinus problems, eye disease, ear infections, dengue fever, skin problems, dental issues, problems with prostate (high PSA), erectile dysfunction and the list goes on. This is by far not a comprehensive list. I know it sounds too good to be true, but according to feedback I have received over the last 18 years, I think it’s safe to say MMS is able to overcome most diseases known to mankind.

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Go back up MMS Health Recovery Guidebook (2016)

Introducing the MMS Health Recovery Guidebook, including my new Health Recovery Plan (HRP), available for download. Discover the latest up-to-date information on my MMS technology, significant completely new data, and improvements that myself and others have determined through on-going use of MMS around the globe.

Over 50 updated tried and proven protocols are outlined, including some key tips and secrets for all those who wish to recover their health from most illness and disease and/or learn about prevention and longevity!

The health recovery procedures given in this book are the result of 20 years of teaching people how to use MMS. Scores of people worldwide have used and applied the principles outlined in my first books, or taught in seminars. As a result, over the years I have received a great deal of feedback, much of which has contributed to this book and to the development of my new Health Recovery Plan.

Unfortunately there is much misinformation floating around regarding MMS, and this too, has compelled me to write this book. I have written this guidebook to help you learn the fundamentals of the Master Mineral Solution (MMS) in a clear and concise manner. This book is chock full of a number of protocols that when followed properly, help restore people’s health. Our Key Protocols go together with a number of Supporting Protocols to make up the Health Recovery Plan. In this book you’ll learn about the overall sequence or strategy for this plan.

If you have a serious health issue of one kind or another from which you need to recover—this book is for you. Likewise, if your health seems to be “OK” but you would like to nevertheless achieve optimum health, this book is also for you. Whatever category you fit in—a basic ongoing routine with MMS can help you (and/or your loved ones and pets/animals) get healthy, keep you healthy, and help you maintain a good quality of life! The key is to use MMS properly—this book will show you how.

 

 
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Go back up The Master Mineral Solution of the 3rd Millennium (2011)

This is my second book on MMS. It includes more past history about the continuing story of MMS. You’ll learn about the basics of MMS, including the chemistry of it and how and why it works. Also included are instructions for several ways how you can make your own MMS.

The Master Mineral Solution of the Third Millennium is essential to those who want to learn the chemical and technical foundation of how MMS works. A chemical explanation for laymen and scientists alike is included. Learn about oxidizers, and how oxidation destroys pathogens. This is a must have reference book for those who want to delve deeper into understanding how MMS works. This book includes some of the basic original MMS protocols, however, if you are in need of health recovery today, I suggest you order my latest book, the MMS Health Recovery Guidebook for the updated protocols and information on overcoming most diseases of mankind.

If you are interested in the story of MMS there are three chapters in this book telling the continuing story of MMS in this world. Should you want the full story you will need to also buy my first book, The Miracle Mineral Solution of the 21st Century. It is estimated that 20,000,000 people had used MMS by the year 2008. Hundreds of thousands of lives have been saved and the suffering of thousands has been overcome.

 

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Go back up Secrets of Enlightenment (2012)

This book gives simple answers to most of the questions people ask, such as: Where did I come from? Why am I here? Why don’t I remember my existence before this life? What is my purpose in life? Etc.

This book has been 60 years in the writing and compilation (this lifetime). It is unique and quite different than most books about enlightenment.  I believe that you learn about spirituality and life by living life and taking part in the game of life, not by being tucked away in a cloistered setting. You may not believe in past lives, but in case you do, I believe I have received much of the information about life given in this book from past lives. This book gives simple answers to most of the questions people ask, such as: Where did I come from? Why am I here? Why don’t I remember my existence before this life? What is my purpose in life? Etc.

Secrets of Enlightenment points out that life is a game and that you should play it to the hilt. In these pages you’ll discover secrets, or what I call an understanding of life, that is not found in any other book on Earth and if that is not so, I will be happy to refund your money at any time.

 

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A Genesis II Church broadcast discussing various health-related topics every week. Liveshow every Sunday at 10AM EST. [Timezone Converter]

With Your Hosts

• Archbishop Mark Grenon
• Bishop Joseph Grenon

www.G2Voice.is
G2Voice on YouTube
G2Voice on Spreaker

Educational Products

 

MMS Training Video Course
(NEW): English ($199)
(NEW): Spanish ($199)

Old MMS Video Course ($199)
Italian
Portuguese
Hebrew
Arabic

Archbishop Jim Humble

jim humble-100• Website: www.jimhumble.is
Watch Jim on YouTube
Jim on Facebook

• Contact Jim at:
This email address is being protected from spambots. You need JavaScript enabled to view it.

Important links

jim humble staff-100Genesis II Church:
genesis2church.is
Forum / MMS support:
g2cforum.org
MMS Truthful Wiki
mmswiki.is

MMS training

jim humble tiger-100Be sure to study the MMS Protocols.

For MMS forum discussion check www.g2cforum.org

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