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MMS
Newsletter
 

 

G2voice #062: Alzheimers: A toxicity issue.
Nov.19th,2017
www.g2voice.is

 

NOTE: Same protocol for all neurological syndromes, disorders, diseases and conditions – Remember we show you testimonies and how to cure yourself!

Former FDA Commissioner Dr Herbert Ley: “The thing that bugs me is that people think the FDA is protecting them. It isn’t. What the FDA is doing and what the public thinks it’s doing are as different as night and day.”

I. Alzheimer’s Disease: It’s a toxicity problem
G2voice Broadcast #19
Sunday, Nov. 19th
at 10 AM EST
www.g2voice.is

 

This week we will be discussing Alzheimer’s Disease which is another form of Dementia. It is a horrible dis-ease that not only affects the person with it but the whole family! As the title says, I believe toxicity is the reason for such a devastated dis-ease that is NOW affecting 1 in 9 people over 65 and costing Americans 236 billion or making the medical industry 236 billion! The same medical industry states that Alzheimer’s Disease is incurable.

Official government stance in regard to Alzheimer’s Disease:

Alzheimer’s disease is an irreversible, progressive brain disorder (emphasis mine)that slowly destroys memory and thinking skills, and eventually the ability to carry out the simplest tasks. In most people with Alzheimer’s, symptoms first appear in their mid-60s. Estimates vary, but experts suggest that more than 5 million Americans may have Alzheimer’s. https://www.nia.nih.gov/
alzheimers/publication/alzheimers-disease-fact-sheet

“While there remains no cure for the condition (emphasis mine), everyone who develops it will sadly still have the disease when they die. It is therefore essential that people have access to the right support and services to help them live well with dementia and that research into better care, treatments and eventually a cure remain high on the agenda.”

Haroon Siddique
Nov. 14, 2016
https://www.theguardian.com/society/2016/nov/14/dementia-and-alzheimers-leading-cause-of-death-england-and-wales

 

“Alzheimer’s is not a normal part of aging. Just ask any family member who has cared for a loved one with Alzheimer’s and they will tell you how different the disease is from normal aging. Alzheimer’s can strike people as young as their forties; there are some half a million individuals in the United States with early-onset dementia. Recent research has pinpointed disruptions in specific memory networks in Alzheimer’s patients, such as those involving the posteromedial cortex and medial temporal lobe, that appear distinct from normal aging.

The larger point is that while Alzheimer’s is still incurable (emphasis mine)it’s not untreatable. There are four FDA-approved medications available for treating Alzheimer symptoms and many others in clinical trials. Strategies to enhance general brain and mental wellbeing can also help people with Alzheimer’s. That’s why early detection is so important”.
P. Murali Doraiswamy is the head of biological psychiatry at Duke University and is a Senior Fellow at Duke’s Center for the Study of Aging.

Source: https://www.scientificamerican.com
/article/can-alzheimers-be-cured/

Don’t believe it! “They” have told us that about Cancers we’ve seen cured, Autism, MRSA, Herpes, Diabetes etc. They NEED people to believe that to keep them coming back for “treatments” where they make ALL “their” money! Let me start out by having each one of you hear from people that did the Genesis II Church Protocols to cure the dis-ease of Alzheimer’s Dis-ease, a form of Dementia!

 

Testimonies::

 

Alzheimer's gone

I am familiar with Alzheimer's, so when I had symptoms occur, they were familiar to me. I noticed I was not coping socially, and starting to have total gaps in my memory (and thus withdrawing). Because I had heard of mms being used to cure dementia I decided I had nothing to loose. I followed the protocl 1 for one month, slowly building up to the full dose of 3 drops every hour for 8 hours, and staying with the regime, for the full period, (it is important to note that if the dose is causing you to feel unwell, cut back on the doses per day and keep it low for 2 days then start to increase to the level you can tolerate, but do not stop all together). By the end of the treatment I noticed a remarkable change in my cognition, and as time goes on my condition continues to improve. I feel like a new person, I am social again, happy, and look forward to each new day.

Sam

1. An elderly guy (in his 80-90's), who claimed he was the last survivor of the chemical company (since closed), that use to operate in New Plymouth, and made Agent Orange, and many other toxic sprays. After 50 odd years working there, he said that he was so full of toxins that he couldn't remember things that he had done the day before, along with other health effects relating to a build up of toxins in the body. Someone told him about MMS, which he tried. He phoned me on the second day all excited, saying that he remembered all he had done the day before. He claimed to be 100% better within about a week on MMS. He is now an advocate for MMS, telling everyone who is willing to listen.

2. Alzheimers: I have seen many problems solved with MMS. My favorite was when my mother was diognosed with Alzheimers and was given a pill, which after taking the first one at 10 PM, paralized her body but allowed her to talk and she was scared. I listened to her cry when it happened. She did not even know what she was taking. After she told me which bottle, I googled the pills which turned out to be Alzheimers meds and not effective. So my mother when asked, if she wanted to keep taking them, she said no. I gave her 6 drops of the MMS and fifteen minutes later she was fast asleep. In the morning I gave her 6 more drops and an hour later 6 more. By 9:30 AM we had a normal conversation about how she met my father some 65 years before, her clarity of thought had returned. After 1 week of protocol 1000 she felt so good she stopped taking the MMS and after a month her symptoms returned. 1 week on protocol 1000 again she felt great and stopped taking the MMS I tried to get to keep taking it but after a week she felt she had enough sure enough it came back a month later and then we would start again. However the clarity of thought provided my mother was undeniable. 3 years later most of my siblings had forgotten about her alzheimers diognosis.
Keith Pace

PS- Jim Humble you're my Hero.

3. Helped Dementia: My father had a very serious back operation and was under anesthesia for approximately 5 hours. In post-op he was confused. As his stay in the hospital progressed he regressed. He was experiencing significant dementia. The doctors claimed that the surgery just brought forth and underlying problem that was already there. My dad, being 78 at the time was very healthy, ran a ranch, prior to surgery.One day I got I remembered the MMS1 and decided to give it a try on my dad. By this time he was in assisted care. I did Clare's combination on him and by the time I left that day he was much clearer. I came back the next day and did the same with even greater improvement. By the third day, after the doses, he was back to himself and able to go home. If not for the MMS I don't think he would of ever been able to leave assisted living. He was getting worse and worse, not knowing where he was or who we were. I was so excited!!! The MMS really works!!

Thanks you for your commitment to help others!

Dianne G

4. In 1990, I developed ALS, a 100% fatal disease with no cure or treatment. In 1995, four different MD’s told me I had six months to live, I PROVED THEM WRONG. I am an ALS survivor of 21 years from the date of my first symptom; my doctor told me that 90% of people with ALS die within 1-5 years. He also told me that there was NO CURE and they had NO CLUE as to the cause of ALS. Now, that was either a lie or he was a bone head. I now know that a NEURO-toxin, such as Mercury, will cause damage to your NEURO-system, resulting in PARALYSIS. Now, what is ALS? Nothing more than damage to your NEURO-system, resulting in PARALYSIS. Now, don’t tell me that the MD’s don’t know that. Eric

 

NOTE: The following information is the current Medical industry belief about Alzheimer's and treatments. I want everyone to hear what they say and see what the cause really is for Alzheimer’s as well as, many other neurological dis-eases which we at the Genesis II Church of Health and Healing have seen cured!

 

Alzheimer's disease is officially listed as the sixth-leading cause of death in the United States. It is the fifth-leading cause of death for people age 65 and older. As the population of the United States ages, Alzheimer's is becoming a more common cause of death. Although deaths from other major causes have decreased significantly in the last decade, deaths from Alzheimer's disease have increased significantly — 71 percent. In 2013, over 84,000 Americans died from Alzheimer's according to official death certificates; however, in 2016, an estimated 700,000 people with Alzheimer's will die, and the disease likely will contribute to many of those deaths. 1 in 9 over age 65! This is an Epidemic!
Alzheimer's is the only disease among the top 10 causes of death in America that cannot be prevented, cured or even slowed. SEE: https://www.alz.org/facts/

Alzheimer's disease is one of the costliest chronic diseases to society. The growing Alzheimer's crisis is helping to bankrupt Medicare.

• In 2016, total payments for health care, long-term care and hospice are estimated to be $236 billion for people with Alzheimer's and other dementias, with just under half of the costs borne by Medicare.
• Medicare and Medicaid are expected to cover $160 billion, or 68 percent, of the total health care and long-term care payments for people with Alzheimer's disease and other dementias.
• Nearly one in every five Medicare dollars is spent on people with Alzheimer's and other dementias. In 2050, it will be one in every three dollars.


Unless something is done, in 2050, Alzheimer's is projected to cost more than $1 trillion (in 2016 dollars). Costs to Medicare will increase 360 percent. This dramatic rise includes a nearly five-fold increase in government spending under Medicare and Medicaid and a nearly five-fold increase in out-of pocket spending. https://www.alz.org/facts/

Alzheimer’s disease and dementia are often used interchangeably as many people believe that one means the other. In fact, the distinction between the two diseases often causes confusion on the behalf of patients, families and caregivers. Discover how the two diagnoses, while related, are remarkably different.

Alzheimer’s and dementia are still a mystery in many ways. This is why the two similar diseases are often mixed up in every day conversation and understanding. According to the National Institute on Aging (NIA), Dementia is a brain disorder that affects communication and performance of daily activities and Alzheimer’s disease is a form of dementia that specifically affects parts of the brain that control thought, memory and language.
Read on to discover more particulars on how the two diseases vary and why there’s still a lot of scientific research needed—as well as public awareness—around these world-wide epidemics.

What is dementia?


Dementia is an umbrella term for a set of symptoms including impaired thinking and memory. It is a term that is often associated with the cognitive decline of aging. However, issues other than Alzheimer’s can cause dementia. Other common causes of dementia are Huntington’s Disease, Parkinson’s Disease and Creutzfeldt-Jakob disease.

What is Alzheimer’s Disease?

According to the Center for Disease Control, Alzheimer’s disease is a common cause of dementia causing as many as 50 to 70% of all dementia cases. In fact, Alzheimer’s is a very specific form of dementia. Symptoms of Alzheimer’s include impaired thought, impaired speech, and confusion. Doctors use a variety of screenings to determine the cause of dementia including blood tests, mental status evaluations and brain scans.

How Are They Different?

When a person is diagnosed with dementia, they are being diagnosed with a set of symptoms. This is similar to someone who has a sore throat. Their throat is sore but it is not known what is causing that particular symptom. It could be allergies, strep throat, or a common cold. Similarly, when someone has dementia they are experiencing symptoms without being told what is causing those symptoms.
Another major difference between the two is that Alzheimer’s is not a reversible disease. It is degenerative and incurable at this time. Some forms of dementia, such as a drug interaction or a vitamin deficiency, are actually reversible or temporary.
Once a cause of dementia is found appropriate treatment and counseling can begin. Until a proper diagnosis is made, the best approach to any dementia is engagement, communication and loving care.
http://www.alzheimers.net/difference-between-alzheimers-and-dementia/

 

What is Alzheimer's disease?

Alzheimer's disease is a progressive, neurodegenerative disease that occurs when nerve cells in the brain die and often results in the following:
• impaired memory, thinking, and behavior
• confusion
• restlessness
• personality and behavior changes
• impaired judgment
• impaired communication
• inability to follow directions
• language deterioration
• impaired thought processes that involve visual and spatial awareness
• emotional apathy
With Alzheimer's disease, motor function is often preserved.


When Alzheimer's was first identified by German physician, Alois Alzheimer, in 1906, it was considered a rare disorder. Today Alzheimer's disease is recognized as the most common cause of dementia (a disorder in which mental functions deteriorate and break down). An estimated 5.3 million Americans have Alzheimer's disease. According to the Alzheimer's Association, this number includes 5.1 million people over the age of 65, as well as 200,000 to 500,000 people younger than 65 who have early-onset Alzheimer's and other types of dementias.

1

 

 

How is Alzheimer's different from other forms of dementia?

Alzheimer's disease is distinguished from other forms of dementia by characteristic changes in the brain that are visible only upon microscopic examination during autopsy. Brains affected by Alzheimer's disease often show presence of the following:
• fiber tangles within nerve cells (neurofibrillary tangles)
• clusters of degenerating nerve endings (neuritic plaques)
http://uhealthsystem.com/health-library/neuro/disorder/alzheim

 

Dementia and Alzheimer's leading cause of death in England and Wales

2


Scan of a person with Alzheimer’s disease. The ONS said 11.6% of deaths in England and Wales in 2015 were attributable to Alzheimer’s or dementia. Photograph: Alamy Stock Photo

Like all types of dementia, Alzheimer's is caused by brain cell death. It is a neurodegenerative disease, which means there is progressive brain cell death that happens over a course of time. The total brain size shrinks with Alzheimer's - the tissue has progressively fewer nerve cells and connections.Apr 29, 2016

http://www.medicalnewstoday.com/articles/159442.php

 

Alzheimer's disease, a severe form of neurodegenerative brain disorder that now claims over half a million American lives each year, making it the third leading cause of death in the US, right behind heart disease and cancer.
Processed foods have most of their vital nutrients eliminated and replaced with refined sugars and synthetic chemicals, most of which have never been tested for human safety due to a federal regulatory loophole.
It is this deadly combination that appears to be at the heart of the dementia problem, as Alzheimer's is intricately linked to insulin resistance.

A study published in the New England Journal of Medicine in August 2013 demonstrates that even mild elevation of blood sugar — fasting levels over 100 mg/dl — is associated with an elevated risk for dementia.

The connection between sugar and Alzheimer's was first revealed in 2005, when the disease was tentatively dubbed "type 3 diabetes." At that time researchers discovered that your brain produces insulin necessary for the survival of your brain cells.
A toxic protein called ADDL removes insulin receptors from nerve cells in your brain, thereby rendering those neurons insulin resistant, and as ADDLs accumulate, your memory begins to deteriorate. Diabetics also have a doubled risk of developing Alzheimer's disease.

http://articles.mercola.com/sites/articles/archive/2015/11/12/prions-alzheimers-lyme-disease.aspx

 

What toxins are causing Alzheimer’s Dis-ease?

 

“We now show that some of the highest levels of aluminium ever measured in human brain tissue are found in individuals who have died with a diagnosis of familial Alzheimer’s disease.
The levels of aluminium in brain tissue from individuals with familial Alzheimer’s disease are similar to those recorded in individuals who died of an aluminium-induced encephalopathy while undergoing renal dialysis.”
“Toxic metals such as aluminum do not belong in prophylactic medications administered to children, teenagers, or adults. Vaccines are normally recommended for healthy people, so safety (and efficacy) standards must be impeccable. Parents, especially, should not be compelled to permit their loved ones to receive multiple injections of toxic metals that could increase their risk of neurodevelopmental and autoimmune ailments. Safe alternatives to current disease prevention technologies are urgently needed.”


“. . .infinitely more reactive and induce intense inflammation in a number of tissues. Of special concern is the effect of these nanoparticles on the brain and spinal cord, as a growing list of neurodegenerative diseases, including Alzheimer’s dementia, Parkinson’s disease, and Lou Gehrig’s disease (ALS) are strongly related to exposure to environmental aluminum.”
http://naturalsociety.com/neurologist-warns-exploding-cognitive-disorders-chemtrail-toxins/

 

Truth or politically correct? Official Canadian public stand on Aluminum: https://www.ccohs.ca/oshanswers/diseases/alzheime.html

Scientists Prove Link Between Aluminum and Early Onset Alzheimer’s Disease
http://www.greenmedinfo.com/blog/scientists-prove-link-between-aluminum-and-early-onset-alzheimer-s-disease

 

Another way toxins are getting into the brain:
The concerned neurosurgeon is only commenting on one known toxin, too. There are others, like barium and strontium, and a practically endless cocktail of carcinogenic constituents that can possibly cull the global population. Also speaking out against chemtrails is Dr. Edward Group, who explains how chemicals sprayed from chemtrails can “turn on” certain issues such as shingles within your body (under certain circumstances).
Aluminum exposure from chemtrails is helping to lead to aluminum-induced cognitive disorders among the population, as doctor Blaylock, suggests. Aluminum can even affect unborn babies, not just the elderly, since it crosses into the placenta via the blood.
Another toxin being found in chemtrails is Strontium-90. It isn’t any better. Neither is Barium.
The impact of these compounds upon human health is unmistakable.
So why is this happening?
http://naturalsociety.com/neurologist-warns-exploding-cognitive-disorders-chemtrail-toxins/

 


Aluminum:
Aluminum is present in many things around us. It’s in food, air, water, and soil and is said to be harmless when swallowed because it doesn’t absorb into the body when consumed. Aluminum is put into vaccines as an adjuvant to help them “work better” or to “enhance” them. So what is the concern about injecting aluminum into the blood stream?

According to the FDA:

“Aluminum may reach toxic levels with prolonged parenteral administration [this means injected into the body] if kidney function is impaired . . . Research indicates that patients with impaired kidney function, including premature neonates [babies], who received parenteral levels of aluminum at greater than 4 to 5 micrograms per kilogram of body weight per day, accumulate aluminum at levels associated with central nervous system and bone toxicity [for a tiny newborn, this toxic dose would be 10 to 20 micrograms, and for an adult it would be about 350 micrograms]. Tissue loading may occur at even lower rates of administration.” [Department of Health and Human Services, Food and Drug Administration, Document NDA 19-626/S-019, Federal Food, Drug and Cosmetic Act for Dextrose Injections.]

And also:

“Aluminum content in parenteral drug products could result in a toxic accumulation of aluminum in individuals receiving TPN therapy. Research indicates that neonates [newborns] and patient populations with impaired kidney function may be at high risk of exposure to unsafe amounts of aluminum. Studies show that aluminum may accumulate in the bone, urine, and plasma of infants receiving TPN. Many drug products used in parenteral therapy [injections] may contain levels of aluminum sufficiently high to cause clinical manifestations [symptoms] . . . parenteral aluminum bypasses the protective mechanism of the GI tract and aluminum circulates and is deposited in human tissues. Aluminum toxicity is difficult to identify in infants because few reliable techniques are available to evaluate bone metabolism in . . . infants . . . Although aluminum toxicity is not commonly detected clinically, it can be serious in selected patient populations, such as neonates [newborns], and may be more common than is recognized.” [Department of Health and Human Services, Food and Drug Administration, Document 02N-0496, Aluminum in Large and Small Volume Parenterals Used in Total Parenteral Nutrition. Available online at: http://www.fda.gov/ohrms/dockets/98fr/oc0367.pdf]

So basically from those documents we learn that if a premature baby receives more than 10 mcg of aluminum in an IV, it can accumulate in their bones and brain, and can be toxic.
The FDA maximum requirements for aluminum received in an IV is 25 mcg per day. The suggested aluminum per kg of weight to give to a person is up to 5mcg. (so a 5 pounds baby should get no more than 11mcg of aluminum.) Anything that has more than 25 mcg of aluminum is *supposed* to have a label that says:

WARNING: This product contains aluminum that may be toxic. Aluminum may reach toxic levels with prolonged parenteral administration if kidney function is impaired. Premature neonates are particularly at risk because their kidneys are immature, and they require large amounts of calcium and phosphate solutions, which contain aluminum.
Research indicates that patients with impaired kidney function, including premature neonates, who receive parenteral levels of aluminum at greater than 4 to 5 [micro]g/kg/day accumulate aluminum at levels associated with central nervous system and bone toxicity. Tissue loading may occur at even lower rates of administration. [http://www.accessdata.fda.gov/scripts/
cdrh/cfdocs/cfcfr/CFRSearch.cfm?fr=201.323
]

— Vaccines, for some reason, are not required to have this label and also are not required to follow the maximum dosage of 25 mcg.
So doing some math — the following are examples of weight with their corresponding maximum levels of aluminum, per the FDA:

8 pound, healthy baby: 18.16 mcg of aluminum
15 pound, healthy baby: 34.05 mcg of aluminum
30 pound, healthy toddler: 68.1 mcg of aluminum
50 pound, healthy child: 113 mcg of aluminum
150 pound adult: 340.5 mcg of aluminum
350 pound adult: 794.5 mcg of aluminum
So how much aluminum is in the vaccines that are routinely given to children?
• Hib (PedVaxHib brand only) – 225 mcg per shot
• Hepatitis B – 250 mcg
• DTaP – depending on the manufacturer, ranges from 170 to 625 mcg
• Pneumococcus – 125 mcg
• Hepatitis A – 250 mcg
• HPV – 225 mcg
• Pentacel (DTaP, HIB and Polio combo vaccine) – 330 mcg
• Pediarix (DTaP, Hep B and Polio combo vaccine) – 850 mcg
At birth, most children are given the hepatitis B vaccination. The amount of aluminum in the Hepatitis B vaccine alone is almost 14 TIMES THE AMOUNT OF ALUMINUM THAT IS FDA-APPROVED.
At well-child check-ups, it’s common for 2 month, 4 month, 6 month etc., appointments to include up to 8 vaccinations that add up to more than 1,000 mcg of aluminum. Look at the chart above and notice that that amount isn’t even safe for a 350 pound adult. And many children get up to 8 vaccinations a visit several times a year!
According to the FDA and the AAP (American Academy of Pediatrics), what happens if a child receives more than the maximum required dose of aluminum?
• Aluminum builds up in the bones and brain and can be toxic.
• Aluminum can cause neurological harm.
• Aluminum overdose can be fatal in patients with weak kidney’s or kidney disorders or in premature babies. (How many children are tested to see if their kidney’s are functioning properly before they are vaccinated? Could this also be why the Hepatitis B shot, given to infants at birth, has been linked to SIDS? Neonatal Deaths After Hep B vaccination.)
[Aluminum Toxicity in Infants and Children, Committee on Nutrition,American Academy of Pediatrics, Pediatrics Volume 97, Number 3 March, 1996, pp. 413-416]

Other toxins causing Neurological dis-eases:Found in Flu shots?
Thimerosal
Thimerosal is a compound made up of approximately 50% mercury. Mercury is the second most poisonous element known to man (next to uranium and its derivatives.) When someone says, “MERCURY!” we immediately think of the news stories about the child at school who broke a thermometer in biology class and the HAZ-MAT team was called in and all the students were in peril. Did you know they make that big of a deal (meaning bringing in the HAZ-MAT crew) for less mercury than what is contained in 1 vaccine [http://www.epa.gov/mercury/spills/index.htm]? Thimerosal is used as a preservative in vaccines to help prevent bacteria growth in multi-use vaccines. It is also used in the creation process of a vaccine, and then through a purification process it is “removed” and only “trace” amounts are left. First, I urge you to read this article: Is There Thimerosal in the Flu Vaccine?


Next, let’s discuss what “trace amounts” means. (If you notice in the document above next to many of the “Thimerosal”‘s, there is an asterisk next to it. The asterisk notates that ” *Where “thimerosal” is marked with an asterisk (*) it indicates that the product should be considered equivalent to thimerosal-free products.”)
Before we move on, a little story — I was at the grocery store a little while ago looking at a large bag of “Stevia” — the new fad in no-calorie sweeteners. I was reading the back of the bag and I came to a little spot at the bottom that said “Each serving contains less than 2 calories which the FDA considers dietetically zero.” What?! That doesn’t even make sense! If something is said to be “calorie-free”, it should be calorie-free, right?? If something has calories in it, it has calories in it. You cannot place some carrots on the counter and tell me there are no carrots on the counter. A serving size of Stevia is 1tsp, so let’s assume that 1 tsp contains 1.9 calories. Remember, we have to assume because we DON’T ACTUALLY KNOW. It’s the FDA that says the calories in Stevia don’t exist, but just for the mere fact that there is this disclaimer on the bag lets us know that there are, in fact, carrots on the counter… er, I mean calories in the bag. But going back, we’re going to say there are 1.9 calories per serving. Using Stevia is “cup for cup.” In other words, you use the same amount of Stevia as you would regular sugar. So, I’m going to make some fantabulous “low-calorie” chocolate chip cookies with my “no-calorie” Stevia. I’m on a strict diet, so all I need to add up to find out how many calories are in my batch of cookies are all of my ingredients EXCEPT sugar, right? But wait… I’m adding 2 cups of Stevia into my batch of cookies. There are 48 teaspoons in a cup, which means I’m adding 96 teaspoons of Stevia — which also would equate to 182.4 EXTRA calories. There’s no argument that it has greatly reduced the number of calories in my batch of cookies versus using conventional sugar, but the fact remains: NO-CALORIE IS NOT NO-CALORIE.


So the fact that those vaccines containing thimerosal with an asterisk beside it virtually says the same thing and is extremely misleading. They should be “considered equivalent to thimerosal-free products” gives the illusion that there is no thimerosal in vaccines, or at least not enough to have to worry about. But remember, if I eat 8 batches of my cookies that are supposed to be low calorie because of my “calorie-free” Stevia, I’m actually consuming 1,459.2 calories that the FDA says aren’t really there. This can be applied to vaccines as well. Many “well-child” check-ups include up to 8 vaccines in one sitting.

So how much does “trace” mean? According to the CDC, it says less than or equal to 0.3mcg per dose. Sailhome.org does a nice job of putting this into perspective:
• 2 ppb mercury is the mandated limit in drinking water
• 200 ppb mercury in liquid waste renders it a toxic hazard
• 25,000 ppb is found in infant flu shots
• 50,000 ppb is found in regular flu shots — recommended for children, pregnant women, the elderly…
Also the math on how many ppb in a “thimerosal free” vaccine:
0.3 mcg / 0.5mL =
0.3 mcg / .0005L =
…3,000 mcg / 5L =
600 mcg / L
1 mg/KG = 1 PPM (formal definition of PPM)
1 L = 1 KG (density of water or saline solution)
1 mcg/L = 1 PPB (because 1 KG and 1 L of water are equivalent)
THEREFORE:
600 mcg / L =
600 ppb Thimerosal in the “thimerosal-free” vaccine
Flu vaccine has “only” 25 mcg Thimerosal. The shot is 0.5mL. Let’s do some math:
25 mcg / 0.5mL =
25 mcg / .0005L =
250,000 mcg / 5L =
50,000 mcg / L
1 mcg / L = 1 ppb, therefore
The shot has 50,000 ppb of Thimerosal
Remember that 2 ppb mercury is the mandated limit in drinking water and normally 200 ppb would label something a toxic hazard.
After we find all of this information out, we have to ask ourselves: Why is mercury dangerous??
A Research Video from the University of Calgary

***Notice that mercury doesn’t only stunt neurological growth, it actually reverses it, or destroys it.


Yeast Extract/MSG
Yeast extract is a common name used for various forms of processed yeast. Many people have yeast allergies, and vaccines can induce an anaphylactic response after being vaccinated due to the yeast.
Aside from that, ALL yeast extract contains MSG. Many people have either an allergy or a sensitivity to MSG (I am one of them). MSG has been known to cause:
• Migraine headaches
• Sleeping disorders
• Irritable Bowel Syndrome
• Asthma
• Diabetes
Alzheimer’s disease
• Lou Gehrig’s disease
• Attention Deficit Disorder
• Seizure
• Stroke
• Anaphylactic reaction

 

Neurological Disorders

Neurological disorders are diseases of the brain, spine and the nerves that connect them. There are more than 600 diseases of the nervous system, such as brain tumors, epilepsy, Parkinson's disease and stroke as well as less familiar ones such as frontotemporal dementia.


NOTE: Chlorine Dioxide is approved for ALS in Spain:

Neurological Conditions

  •  ALS
  •  Alzheimer's Disease
  •  Arteriovenous Malformation
  •  Brain Aneurysm
  •  Brain Tumors
  •  Dural Arteriovenous Fistulae
  •  Epilepsy
  •  Headache
  •  Autism
  •  Memory Disorders
  •  Multiple Sclerosis
  •  Parkinson's Disease
  •  Peripheral Neuropathy
  •  Post-Herpetic Neuralgia
  •  Spinal Cord Tumor 
  •  Stroke 
  •  AND MANY MORE! WHY?

https://www.ucsfhealth.org/conditions/neurological_disorders/

Alzheimer's among children? Same toxins?

A rare disease known as Niemann-Pick disease type C (NPC), which afflicts one in 150,000 children and teenagers, is largely unheard of but leaves patients and families in a state of desperation. If diagnosed, a child will experience quick and progressive mental and physicala deterioration over the course of several years — similar to Alzheimer’s disease, hence its nickname of “childhood Alzheimer’s.” Like Alzheimer’s, Niemann-Pick disease type C has no cure and typically leads to death.
Niemann-Pick disease type C isn’t related to Alzheimer’s, however — not even early-onset Alzheimer’s, which tends to strike people in their 40’s and 50’s. NPC is a lipid storage disease, a type of inherited metabolic disorders in which an excess of cholesterol gathers in the body’s cells and tissues. This accumulation of lipids gradually leads to permanent damage in the cells and tissues of the brain, peripheral nervous system, liver, and bone marrow. In cases of NPC, patients will often experience seizures, dementia, coordination and movement problems, as well as difficulty speaking, eating, and swallowing.
http://www.medicaldaily.com/childhood-alzheimers-niemann-pick-disease-372960
• Interesting: Marijuana Compound Removes Alzheimer’s Plaque From Brain Cells, Study Finds http://www.popsci.com/marijuana-compound-removes-alzheimers
• Might Alzheimer’s Disease Be “Foodborne”? http://www.realfarmacy.com/alzheimers-foodborne/
• Alzheimer’s Disease: What If There Was A Cure? http://coconutketones.com/

If any reading this newsletter would like to contact me about help with Alzheimer's ,Dementia or any other dis-ease for that matter, feel free to contact me at: This email address is being protected from spambots. You need JavaScript enabled to view it. or This email address is being protected from spambots. You need JavaScript enabled to view it. (Spanish)
G2sacraments.org is now shipping world wide. Trying to keep the cost low you can get a g2kit for 40 dollars shipped from the USA to anywhere in the world where shipping is allowed! 
To get our sacrament please click here

thank you!

 

 

Please listen in to our G2Voice Broadcast this Sunday, Nov/ 19th

at 10 AM EST where we will discuss further discuss the topic: Alzheimer's Dis-ease, A Toxicity Issue: www.g2voice.is

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

MMS Saves Lives.

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Shipping G2Sacraments World Wide!


Hello everyone, thank you so much for signing up for our newsletter! We had a great increase in subscribers since the last newsletter went out and we want to welcome you all!  As you know our mission has been to get our sacraments to anyone and everyone around the world! It has been about 2 and a half years since we started making and providing our sacraments! We initially started in the USA, then reached out to our neighbors in Canada and Mexico. Now we are proud to announce we are starting to ship one special package worldwide! Click the image to order sacraments worldwide!
 


Our problem has always been the cost of shipping. We hate to charge anyone. so much to simply receive our sacraments, so we found the cheapest option out there to ship 1-G2kit (4 ounce bottle of HCl and MMS) so anyone worldwide can order from us! Not all of our products will be available worldwide but the G2kit has always been the most important and needed. We try to keep the cost as low as possible, so the total cost for 1-G2kit worldwide will be 40 dollars period. It is 20 dollars for the kit and the cheapest option to ship 1 package is 20 dollars from USA to anywhere in the world. At this moment we do not know how the customs in every country will process our shipment, but we believe it should make it through just about anywhere.  The package is our church sacrament so it should be receivable to just about anyone.


Thank you for your continued support! Please share this with your friends, family, and anyone worldwide to start receiving the Sacraments of the Genesis II Church of Health and Healing!

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Good Health!
Bishop Jordan Grenon

MMS Saves Lives.

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G2Voice Broadcast #60 -What are your prescription and over the counter “drugs” doing to our body?

 

 


Sunday, Nov. 5, 2017 at 10 AM EST


Sunday is daylight savings end so now we are on EST

 

NOTE: Check out the medicine you take daily below and look into:
• Contraindications
• Warnings and Precautions
• Adverse Reactions
• Drug Interactions
The Most Popular Drugs in the United States - Primary Use


NOTE: Let's go through one of these popular medicines and see for ourselves what it says. Do this with your drug and see if it resonates with you?
EXAMPLE


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

The #1 Killer in the world is toxicity! The reason I say that is, if you look at the statistics you will see that Doctors and their pharmaceutical/medical prescribed protocols is added together in 2016, are the #1 killer of mankind. Why? They both are making the human body more toxic hence; death by doctors and pharmaceuticals! “Iatrogenics” means death by doctors and the protocols they have been taught to prescribe are the causes for death.
To me, “Iatrogenics”, death by doctor, vaccines, prescriptions and over-the-counter “drugs” are the #1 killer and cause of “dis-ease” of the body in the world. All these drugs are TOXINS! 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 medicine to plant based or natural therapies which will NEVER happen due to the lack of profits! Until the “medical industry”, known as the FDA, AMA, CDC, NIH, DOJ and EPA cooperates, 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 resonates 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:

IN 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 who 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 all of us about the dangers of many pharmaceutical products whether they are in the form of pills, vaccines, intravenously or any other manner of entering the body!

Conclusion: Next week: G2Voice Broadcast #61: What is “Gastritis” and how to CURE it!

Sunday is daylight savings end so now we are on EST


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

https://g2sacraments.org/ 
Order our sacraments from our secure website!
Your support helps us keep going! Also by giving our sacraments to others you can save a life of a loved one!

 


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.
Spanish: 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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MMS
Newsletter

G2Voice #61 Why so many cases of “Gastritis” around the world and how to CURE it!


Sunday, Nov. 12th, 10 AM EST at:
www.g2voice.is

 

 

 

Weekly testimonies:
I would like to testify that "one must first have faith that God can heal them," then God
will work out the part that is too difficult for us. But we must first make a decision to
move forward. I was in the hospital and was told, I had osteomelitus (bone infection) in
my big toe. After administration of "MMS," my numbers (labs) improved and my
wound closed. I also treated topically and watched the skin and color improve
tremendously. I would highly recommend giving this product a try! The doctor came in
and asked curiously "what was going on" He then stated "your number sare looking
good." I was told on March 16, 2017 that there was no bone infection.
Thank you
"MMS,"team.

Hi Mark,

I am only new to MMS but have had the following conditions alleviated since starting the protocol a few weeks ago.
I have been under par for the past three years after spending time in India and returning to Australia with a number of "antibiotic" resistant infections that have caused ongoing problems including severe depression and insomnia. I can see from my personal experience with taking MMS that these problems have almost disappeared after four weeks. It makes sense to me that MMS, because of its ability to kill pathogens within water etc., can as easily cure the physical body as it is said to be 90% water. I had not expected it to work so well on mental conditions, so I am very pleased with the results, and was more than interested to find the research above, that links pathogens, bacteria, viruses and parasites so clearly to mental problems. If MMS works across the board on these types of mental stresses which a large percentage of humanity now suffer, without the use of drugs etc., then it is indeed a Miracle in itself.

Sleep patterns
Depression
Narrow angled Glaucoma pressure improved and the need for possible lens replacement on hold.
Aching lower legs improved
Fungus under toe nail gone.
I feel as though I am returning to my "true self" .... that calm loving being within.
Thank you for your continued work on this product and Healing protocols in general.
Regards, Lyndall

Why so many cases of Gastritis around the world? Do we know? I think we have a good idea by looking at the facts and how the stomach works. Is it a bacteria, noxious processed foods, medications including vaccines or a combination of all? I believe it is a combination of all the above that are suppressing, aggravating and even stopping the stomach’s NATURAL processes which in turn affects the whole digestion process. By adversely affecting the NATURAL digestive system of the body ALL the systems of the body are affected and the “homeostasis” or balance we ALL need is lost.
Toxins are either compromising or destroying our body’s systems which in turn affects the following 12 systems of the body:

1. Digestive System - Organs include oral cavity, esophagus, stomach, liver, gallbladder, pancreas, small and large intestine, and rectum.
Functions: break down food and deliver the products to the blood for dispersal to the body cells
2. Circulatory System - Consists of blood, heart, arteries, capillaries, and veins. Pumps blood to and from the heart to supply oxygen to the body.
3. Endocrine System - collection of glands that secrete hormones into the blood which regulate growth, development, and homeostasis.
Organs: hypothalamus, pituitary gland, thyroid, adrenal glands.
4. Lymphatic system - a secondary circulatory system that helps the body fight pathogens and maintain its fluid balance
parts: lymph nodes, tonsils, thymus, spleen
5. Muscular System - organ system that creates movement (muscles, tendons). Also regulates body temperature and protects the body.
6. Nervous System - the body's speedy, electrochemical communication system, consisting of all the nerve cells of the peripheral and central nervous systems
Parts: Brain, Nerves, Spinal Cord
7. Reproductive System - organ system which functions in creating offspring (penis and testes in males, ovaries, uterus, and vagina in females)
8. Respiratory System - Responsible for breathing.
Parts: Lungs, pharynx, larynx, trachea, bronchi, lungs and diaphragm
9. Skeletal System - the hard structure (bones and cartilages) that provides a frame for the body of an animal
10. Urinary System - consisting of the kidneys, ureters, bladder, and urethra, removes wastes from the blood and helps to maintain water and electrolyte balance
11. Integumentary System - organ system that includes hair, skin, and nails and protects the body from pathogens and maintains homeostasis
12. Immune System – made up of portions of many different systems that fight disease
(digestive, lymphatic, nervous, respiratory, circulatory, urinary, integumentary and endocrine systems all work together in synchronicity)
http://mmsnews.is/387-detoxing-every-aspect-of-your-life

 

The good news is: if we stop the toxins from entering the body in various ways then we can enjoy a body where everything works correctly i.e. homeostasis – balance – REAL health and protects us from dis-ease.

As always, I try to show from a few sources what is the consensus among so-called experts of what is Gastritis and how it is caused. As I said above, I believe it is a combination of bacteria , toxic foods, medications and bad diet that are suppressing, aggravating and even stopping the stomach’s NATURAL processes which in turn affects the whole digestion process.

Again, whatever the cause of Gastritis we have VIDEO and Written testimonies of CURES from Gastritis and other stomach problems. Restored health from stomach dis-eases is probably the #1 testimony we hear from people that have done the G2 Sacraments!

Here are articles I found that basically give you an idea of what is Gastritis and how it is caused BUT the treatments I wouldn’t follow except the one that talks about fasting. NOTE: VIDEO and WRITTEN testimonies of Gastritis being CURED from G2 Sacraments are after these articles.

 

What is Gastritis?


Gastritis is a condition primarily characterized by an inflammation of the stomach lining. This happens whenever the protective layer of the stomach is weakened or gets damaged. There is a barrier that protects the stomach from acids that digest the food that you eat. When this barrier is weakened, digestive juices will then cause damage to the stomach lining. It is considered as a troublesome condition that leads to different complications if not treated immediately. One of the resulting effects of gastritis is ulcers, and one condition that could aggravate gastritis is constipation, and therefore must be avoided. This includes avoiding all the things that also lead to constipation.
The inflammatory lesions can be classified in two namely, acute erosive gastritis or chronic atrophic gastritis. With the former often caused by regular use of certain drugs or medications, and the latter is often found to mostly occur in patients who are suffering from a severe case of iron deficiency anemia.


What Causes Gastritis?

• Alcoholism. Excessive alcohol intake could greatly irritate the stomach lining and eventually erode it. The stomach lining then becomes vulnerable to the juices that digest food. Hence, this excessive intake of alcohol could lead to gastritis.
• Use of aspirin, ibuprofen, and other pain relievers. These nonsteroidal anti-inflammatory drugs (NSAIDS) are also among the causes of gastritis. Using these drugs diminishes a particular substance in the body that helps in preserving the lining in the stomach that protects it from digestive juices. When this substance is reduced, the stomach lining also becomes weakened and vulnerable. You may take these pain relievers occasionally, but not all the time so as to avoid gastritis.
• Stress. It has been shown that stress due to various injuries, surgery, or even burns could lead to acute gastritis.
• Infections caused by bacteria. One bacterium that usually affects the stomach is Helicobacter pylori. In fact, people who are infected with such bacteria tend to suffer from chronic gastritis. 50% of the entire world population is said to be infected with the pylori bacterium, (emphasis mine) and infection is passed on from person to person. However, not all of those who get infected with the pylori bacterium suffer from complications. Medical experts say that the vulnerability of one person to the bacteria may be brought about by improper lifestyle like habitual smoking.
• Bile reflux. Bile is a fluid coming from the liver that helps the body in digesting fats. This is stored in the gallbladder. When bile is released, it then travels to the small intestine, passing through some thin tubes. The pyloric valve keeps the bile from getting in the stomach, however, whenever the valve is not able to work properly, bile will enter the stomach and could lead to chronic gastritis.
• Autoimmune disorder. This happens when your own immune system attacks the cells in the stomach lining, causing it to weaken. This is considered as a rare condition but is most likely to occur in people who also have other autoimmune disorders like Type 1 diabetes and Hashimoto’s disease.
• Other illnesses. There are certain studies that show that gastritis is also an effect of other diseases like parasitic infection, Crohn’s disease, as well as AIDS/HIV.

Diagnosis, Signs and Symptoms of Gastritis

Gastritis has various symptoms, which include the following:
• Nausea
• Vomiting
• Loss of appetite
• Dizziness
• Headache
• Pain and a feeling of discomfort.
Chronic gastritis may have the following symptoms:
• Fullness in the abdomen especially after meals
• Heartburn
• Loss of weight
• Occasional hemorrhage from the stomach
• Anemia
Remedies, Treatment and Cure for Gastritis
• Fasting. One of the most effective ways in treating gastritis is fasting.
• When fasting, the stomach is able to rest and the toxic condition gets to subside. Elimination is also hastened when undergoing a fast. It would usually require two to three days to recover but it is highly different with chronic gastritis.
• Fasting may need to be done for seven days or more. Short fasts could be repeated after an interval of 1 or 2 months.
• While on a fast, fruit juices may be taken.
http://naturalhealthmagazine.net/remedies-and-cures-a-z/e-to-f/gastritis/


Helicobacter Pylori
Author: Frank W. Jackson, M.D.

1

This unusual name identifies a specific bacteria that can cause infection of the stomach. This infection can contribute to the development of diseases, such as dyspepsia (heartburn, bloating and nausea), gastritis (inflammation of the stomach), and ulcers in the stomach and duodenum. It will be useful to know some things about the upper digestive tract to understand how and where Helicobacter pylori infection can occur.
When food is swallowed, it passes through the esophagus (the tube that connects the throat to the stomach). It then enters the larger upper part of the stomach. A strong acid that helps to break down the food is secreted in the stomach. The narrower, lower part of the stomach is called the antrum. The antrum contracts frequently and vigorously, grinding up the food and squirting it into the small intestine. The duodenum is the first part of the small intestine, just beyond the stomach. The stomach, including the antrum, is covered by a layer of mucous that protects it from the strong stomach acid.
It is known that alcohol, aspirin, and arthritis drugs such as ibuprofen can disrupt the protective mucous layer. This allows the strong stomach acid to injure underlying stomach cells. In some people, corticosteroids, smoking, and stress appear to contribute in some way. Until the mid 1980s, it was felt that one or more of these factors working together led to the development of gastritis and ulcers. Since that time, evidence has been mounting that Helicobacter pylori (H. pylori) has a major role in causing these diseases.


The Infection

2

H. pylori is a fragile bacteria that has found an ideal home in the protective mucous layer of the stomach. These bacteria have long threads protruding from them that attach to the underlying stomach cells. The mucous layer that protects the stomach cells from acid also protects H. pylori. These bacteria do not actually invade the stomach cells as certain other bacteria can. The infection, however, is very real and it does cause the body to react. Infection-fighting white blood cells move into the area, and the body even develops H. pylori antibodies in the blood.
H. pylori infection probably occurs when an individual swallows the bacteria in food, fluid, or perhaps from contaminated utensils. The infection is likely one of the most common worldwide. The rate of infection increases with age, so it occurs more often in older people. It also occurs frequently in young people in the developing countries of the world, since the infection tends to be more common where sanitation is poor or living quarters are cramped. In many cases it does not produce symptoms. In other words, the infection can occur without the person knowing it. The infection remains localized to the gastric area, and probably persists unless specific treatment is given.


How is H. pylori Infection Diagnosed?

There are currently four ways to diagnose H. pylori infection. During endoscopy (a visual exam of the stomach through a thin, lighted, flexible tube), the physician can remove small bits of tissue through the tube. The tissue is then tested for the bacteria. A breath test is also available. In this test, a substance called urea is given by mouth. A strong enzyme in the bacteria breaks down the urea into carbon dioxide, which is then exhaled and can be measured. And finally, there is a blood test that measures the protein antibodies against these bacteria that are present in the blood. This antibody can mean the infection is present, or that it was present in the past and is now cleared. In other words, a person can have a positive blood test but no infection. Finally, there is a stool test that measures a protein that is shed by the bacteria.

 

Gastritis and Dyspepsia

3

The symptoms are discomfort, bloating, nausea and perhaps vomiting. The person may also have symptoms that suggest ulcers — burning or pain in the upper abdomen, usually occurring about an hour or so after meals or even during the night. The symptoms are often relieved temporarily by antacids, milk, or medications that reduce stomach acidity. Yet, the physician does not find an ulcer when the patient is tested by x-ray or endoscopy. When H. pylori is found in the stomach, it is tempting to believe that it is the cause of the symptoms, although this connection is not yet clear cut. The physician will usually prescribe antibiotic therapy to see if clearing the infection relieves symptoms.

Ulcers

Stomach Ulcers: With stomach ulcers, H. pylori infection is found in 60 to 80 percent of the cases. Again, it is still uncertain how the infection acts to cause the ulcer. It probably weakens the protective mucous layer of the stomach. This allows acid to seep in and injure the underlying stomach cells. However, there is still a great deal of research to be done to unravel this relationship. For example, only aout 20% of patients infeced
with H. pylori will develop ulcers.

Duodenal ulcers: In times past, physicians were taught “no acid, no ulcer.” The medical profession felt the single most important factor causing duodenal ulcers to form was strong stomach acid. Research has now shown that over 80% of all patients who develop duodenal ulcers have H. pylori infection in the stomach as well. Medical studies are under way to determine the relationship between the two and how an infection in the stomach can be related to a duodenal ulcer. Acid is still important; patients without acid in the stomach never get duodenal ulcers. However, physicians now accept the fact that the infection is directly related to the development of duodenal ulcers. It is now rather easy to clear duodenal ulcers with the strong acid-reducing medicines available. But, the ulcers will usually recur unless the H. pylori infection is also cleared from the stomach.

 

Stomach Cancer and Lymphoma

These two types of cancer are now known to be related to H. pylori bacteria. This does not mean that all people with H. pylori infection will develop cancer; in fact, very few do. However, it is likely that if the infection is present for a long time, perhaps from childhood, these cancers may then develop. This is another reason why it is important to treat H. pylori infection.

H. pylori is a very common infection of the stomach. It may be the most common infection in the world. It is now clear that the infection is directly related to the development of stomach and duodenal ulcers, and it is likely that it may be related to cancers involving the stomach. There are several diagnostic tests available, and effective treatment can prevent the recurrence of ulcers and perhaps the development of cancer.
Frank W. Jackson, M.D.
https://www.gicare.com/diseases/helicobacter-pylori/


Gastritis
Gale Encyclopedia of Alternative Medicine
COPYRIGHT 2005 The Gale Group, Inc.

Allopathic treatment i.e. Standard Medical Protocol
H. pylori gastritis
The discovery of H. pylori's role in the development of gastritis and ulcers has led to improved treatment of chronic gastritis. Since the infection can be treated with antibiotics, the bacterium can be completely eliminated up to 90% of the time. The treatment, however, may be uncomfortable for patients and relies heavily on patient compliance. No single antibiotic has been found that would eliminate H. pylori on its own, so various combinations of antibiotics have been prescribed to treat the infection.

TRIPLE THERAPY. As of early 1998, triple therapy was the preferred treatment for patients with H. pylori gastritis. This treatment regimen usually involves a two-week course of three drugs. An antibiotic such as amoxicillin or tetracycline, and another antibiotic such as clarithromycin or metronidazole are used in combination with bismuth subsalicylate, a substance that helps protect the lining of the stomach from acid. However, this treatment often fails due to poor patient compliance and quadruple therapy is required.

DUAL THERAPY. Dual therapy involves the use of an antibiotic and a proton pump inhibitor. Proton pump inhibitors help reduce stomach acid by halting the mechanism that pumps acid into the stomach. Dual therapy has not been proven to be as effective as triple therapy, but may be ordered for some patients who can more comfortably handle the use of fewer drugs.

OTHER TREATMENTS. Scientists have experimented with quadruple therapy, which adds an antisecretory drug, or one that suppresses gastric secretion, to the standard triple therapy. One study showed this therapy to be effective with only a week's course of treatment in more than 90% of patients. The goal is to develop the most effective therapy combination that can work in one week of treatment or less.

Treatment of erosive gastritis
Patients with erosive gastritis may be given treatments similar to those for H. pylori, especially since some studies have demonstrated a link between H. pylori and NSAIDs in causing ulcers. The patient will most likely be advised to avoid NSAIDs.

Other forms of gastritis
Specific treatment will depend on the cause and type of gastritis. These may include prednisone or antibiotics. Critically ill patients at high risk for bleeding may be treated with preventive drugs to reduce the risk of acute stress gastritis. Sometimes surgery is recommended, but is weighed against the possibility of surgical complications or death. Once heavy bleeding occurs in acute stress gastritis, mortality is as high as 60%.
http://www.encyclopedia.com/medicine/diseases-and-conditions/pathology/gastritis

 

The Genesis II Church has the protocols to “restore health” form Gastritis. In fact, stomach problems are the first to go usually because that is the first place the protocols go, the stomach. Because there is direct contact then pathogens are dealt with quickly. If you are suffering form “gastritis” please listen and read the following testimonies.

Video Testimonies – Gastritis and Stomach Problems:
Chronic Sinus infections and Gastritis: https://www.youtube.com/watch?v=RPF29Yc8dyU
Spanish with English Subtitles Stomach and Peritoneal cancer cured with MMS, Testimony - Mega.cl TV Channel: https://www.youtube.com/watch?v=_l5bizEG7gs
Breast Cancer, Gassy Stomach - MMS Testimony: https://www.youtube.com/watch?v=NX4jvji8JEU
English and Spanish Gastritis, Reflux Testimony - MMS Testimonials: https://www.youtube.com/watch?v=q3jbGGXcsH
Spanish with English Subtitles MMS Testimony - Gastritis, Gall bladder, High Blood Pressure:
https://www.youtube.com/watch?v=eEu4bBJRJyA
Spanish MMS testimonio gastritis, inflamación: https://www.youtube.com/watch?v=rjeKX_V3aKc
Spanish Stomach Cancer: https://www.youtube.com/watch?v=5ERFl3rWTk0
Spanish Testimonio de MMS - Gastritis y Migrañas: https://www.youtube.com/watch?v=ZePuN2dOTqU&t=42s
Spanish Testimonio de MMS - Gastritis y salud en general :
https://www.youtube.com/watch?v=pANf82eCk8M&t=9s

 

Written Testimonies:

 

• Stomach issues gone!

I had digestive problems for approximately 5 years. I had diarrhoea within one hour after eating. Sometimes it hit within 3 minutes of ingesting food. It didn't matter if it was toast with coffee, or a full turkey dinner. It caused some very embarrassing moments for me, to say the least. I started taking 6 MMS drops three or four times per day. Within three days, I had no more diarrhoea! I felt the positive effects the very first day! I believe I probably had parasites. I did see what I believe was a parasite in my stool. I still take MMS and MMS2 regularly, just as a precaution. As long as I'm feeling well, I'm going to keep on doing what I'm doing. I only take 3 drops now and I do mix with DMSO. I'm happy to say, I have no side effects! Only positive effects!
Paul
United States

Testimony Mario Guido, Migraine, gastritis and allergies.
After multiple years suffering from colds and allergies because I have a history of asthma since childhood, because all those cold morning, for years had to sleep with a lot of clothes and even two pairs of socks to not catch a cold, but I still wake up every morning sneezing , looked like a human machine gun sneezing, these allergies originated give me a lot of headaches or migraine, that I suffer from 13 or 15 years, where I was first given a pill for a headache from there as never leave, always carried with me from time to time had to go to a gastroenterologist because I had constant stomach problems, doctors told me I had gastritis and others because of so many pills for migraines, they told me I almost died with migraine as there's no cure allergies and even speak, and had to take care of the stomach as it could have a future of ulcers, apart joined my many visits to the ENT or pulmonologist, never knew where to go because every time I leave a bad flu I complicated breathing with bronchial spasms.
In December of 2011 before the holidays, my gastritis had been increased by several weeks, I could not take even a bowl of soup, only took jellies frost because the horrors stomach hurt if she ate something softer or slight, resigned to spending Festivities in bed, my father who lives in Chile told me the MMS, and sent me extra to Peru, I did not pay attention, not ever going to take, because I had many doubts, besides I had scheduled a doctor's appointment in a few days (here in Peru make you wait weeks or months for a medical appointment, weeks to take a test, testing weeks, weeks for the results and waiting until we can die, for we have social insurance) In short an afternoon where I could not take the head or stomach pain and gastritis pills did not effect me, and could not take pills for migraine because it would kill my stomach, haha, I remembered I had the MMS for a corner of the house, I followed my father and take the 1000 protocol.
1st day: 6 drops per hour, as indicated by the old school of the MMS, and my irregularity I did 4 times a day, I felt a slight dizziness but nothing annoying, the end of the day I noticed that the stomach pain barely felt it That day I had lunch frozen apples and crackers.
2nd day: 6 drops per hour, 3 or 4 times a day, it really was not constant, but in turn I realized that I did not feel discomfort in the stomach, and here note that something great was happening, I started researching more about the MMS, for the 3rd day, take it to the letter, every hour for 8 hours a day. At this point I decided to leave the frozen apples and crackers to lunch, and the whole world fear me encourage eating soup again, and I realized I felt that I had absolutely not a single upset stomach . I felt healthy stomach, and the next day he ate everything normally.
Remember to tell them about my migraines?, I am the person who always carried migraine pills you take every other day, for the splitting headache since I started with the MMS, after a week I noticed that in my desk pads were still should have taken during the week, note that migraine I had come from to begin with MMS, better even allergies morning barely had them.
I will not deny that today x MMS changed my life, and several relatives and even friends, and tell you they are.!!
Goodbye pills, high budgets for my flu, migraine, gastritis, allergies, from there I understood why I call Jim Humble Miracle Mineral initially and I agree with you.
I want to say something else, I loosened the stomach at 6 days or so, but I felt sick, that's where lower doses and started taking the bottle maintenance that I always carry with me, 1 or 2 drops of activated MMS hours 8 times a day, with great apple prepared at home and a sip every hour .. problem solved!
Atte. Mario Guido.
http://mmstestimonials.is/all-mms-testimonials?start=260

 

Stomach Ulcers
A few months ago I had to go into hospital because I was very fatigued and could hardly walk anywhere without being out of breath. I knew something was wrong but not sure what the problem was.Also my pulse was getting rapid.I was experiencing palpitations and the pulse was around 98 after sleeping.I started to take your medicine a few weeks before but I did not feel that much better .
I had diarrhea felt sick so I knew it was doing some good but i I did not feel the benefit Anyway I became very faint at work and they sent me to the A/E .They found out I was severely anaemic with a blood count of 5.4.I received 3 bags of blood over 2 days and I felt great.Later they gave me a gastroscopy .(This is when you have a small camera down your throat and it looks into your stomach.
Very unpleasant !)They told me I had a large Hiatus Hernia and ulcers that had healed up.I am convinced that the medicine had done this but I still needed to replenish my bood as I was probably bleeding inside without knowing it for some time.May I add I must have got the Hiatus hernia through a head on collision from a car that came over my side of the road.At the time I felt something tear but the doctors did not appear to be particularly interested.Even when I had this recent problem they would not commit themselves it could have been caused by this accident I had a few years ago.The last time I had a check up my bood count was 12 which is very good.I hope you will find this experience a help and I have actual proof that I had ulcers and they healed.
Sheila
France

Acid Reflux Gone!
I was having a terrible time getting food down and at times very embarrassing if I was in a restaurant. The acid would build up in my stomach and not allow the food to pass into it. The doctor prescribed Prilosec (the purple pill), but the side effects were more then I wanted to deal with (Everything from headaches to trouble breathing).

I started taking Probiotics and after a few days they started working and worked great, but if I ran out or forgot to take them for a couple of days the Acid Reflux started to come back. I started to take MMS (looking for help with gout – but that is another story) and found my Acid Reflux was gone. I stopped taking probiotics after the protocol 1000 and a small maintenance dose of 6 drops a day. Now even when I stop the MMS the acid reflux does not come back.

Some side effects from taking protocol 1000 – after about the second or third day I woke up with no pain. I am 61 years old and very active play sports etc. have muscle and joint pain daily (you know when it takes a min after you stand up to get moving) Have had liver and kidneys checked, and am in great shape. The side effects for Prilosec can kill you MMS has all good ones.

Gerry Gayner
United States

After seeing and reading testimonies of Gastritis CURED you can see that whatever the cause of Gastritis doesn't really matter when using an oxidizer such as Chlorine Dioxide. It is a BROAD SPECTRUM antimicrobial agent that kills pathogens in the pH range of 2.5-10.5 pH. BROAD SPECTRUM means: broad-ˈspectrum adjective [only before noun] broad-spectrum chemicals or medicines are effective against a wide range of pests, diseases etc. So, whether this dis-ease called "Gastritis" is caused by a bacteria, virus, parasite,fungus, or most kinds of toxins, Chlorine Dioxide eliminates their effect on the stomach and therefore the symptoms of the dis-ease disappear hence; CURED!
Here are some more information about Chlorine Dioxide:

• How CD works: https://www.youtube.com/watch?v=yaBURpoIWSo
• BioFilms Killed by CD: https://www.youtube.com/watch?v=VM_mteWQrPg
Chlorine Dioxide for Pathogen Control: https://www.youtube.com/watch?v=Ixk4mVJNotg

This Sunday we will talk more about; why are so many suffering form Gastritis and the G2 Sacrament we recomend to use to CURE this stomach dis-ease that so many suffer from worldwide. Listen in to the G2Voice Braodcast LIVE Sunday, March 26th at 10 AM CST: www.g2voice.is
You can listen to previous G2 Broadcasts on our YouTube channel-G2Voice: Last week - https://www.youtube.com/watch?v=mNlMi0_RXIk
Our FIRST G2 Voice Broadcast: "The discovery of MMS and the History of the G2 Church" with Jim Humble: https://www.youtube.com/edit?o=U&video_id=VEc9FZVg408

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

 

References:
Helicobacter pylori and Cancer: https://www.cancer.gov/about-cancer/causes-prevention/risk/infectious-agents/h-pylori-fact-sheet
Parkinson’s Disease May Be Traced to Gut Bacteria: http://time.com/4587498/parkinsons-disease-gut-bacteria/
Why Inhibiting Acid Production With Prilosec and Prevacid Could Make Ulcers Worse : http://articles.mercola.com/sites/articles/archive/2002/02/06/acid-production.aspx
Cause of Gastritis: http://www.medicinenet.com/gastritis/article.htm
Can Inflammation in Your Gut Be the Root of Your Depression? http://articles.mercola.com/sites/articles/archive/2011/10/06/can-inflammation-in-this-organ-be-at-the-root-of-your-depression.aspx 

exciting news! The https://g2sacraments.org/  Will soon start shipping world wide! Be sure to watch out for the upcoming newsletter and order our sacraments from our secure website!
Your support helps us keep going! Also by giving our sacraments to others you can save a life of a loved one!

 

NOTE: If any one needs Sacramental Guidance with “gastritis” or any dis-ease of the body, please contact us at: This email address is being protected from spambots. You need JavaScript enabled to view it.

 

TUNE IN

 

G2Voice #61 Why so many cases of “Gastritis” around the world and how to CURE it!
Sunday, Nov. 12th, 10 AM EST at:
www.g2voice.is

Let's change the world together!

ArchBishop Mark Grenon

MMS Saves Lives.

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G2Voice Broadcast #59: The PSA HOAX and how many men are suffering needlessly!

 

Sunday Oct. 29th 10 AM EST
www.g2voice.is

 

Testimonies of the week

 

Glaucoma

Here is my testimony of how MMS helped one health problem I had … In 2013, at a regular 2 yearly eye check-up, I was diagnosed with the onset of glaucoma and given a referral to an ophthalmologist. I decided to check out if MMS had a protocol for eye problems/diseases and found one on the website that mentioned glaucoma so delayed making an appointment with the specialist and followed the protocol, taking MMS for eight weeks followed by the eye drops. I am a Christian and believe in the power of prayer so this was part of the treatment with MMS; then while in the waiting room at the ophthalmologist’s I felt an overwhelming peace through my whole being and not at all anxious (I’m not sure if you want or are able/allowed to include this, but I believe in the healing power of God by whatever means He chooses). After several extensive tests on the day of my appointment, the ophthalmologist met with me and showed me the results. He admitted he could not understand the very significant difference between the tests at the optometrist and those just completed but I was well above the indicator line used and there were no signs of glaucoma (the tests from the optometrist showed I was below this indicator line and thus the concern).
I thank the Lord for MMS, for Jim Humble, Mark Grenon and the Genesis II Church who make healing and health possible to so many people worldwide.
Kind regards
Leigh Scarlet
Australia

 

Hey there!
My name is Vero and I live in Mexico.
The first time I heard about MMS was with the release of Quantum Leap. Since then I began researching and started making and taking mms, then giving it to my kids, then recommending it to my friends, and they started giving it to their kids. We even have a WhatsApp group and help each other with information about health.
Thank you Mark and Joe for all your work and Jim oh my God! God bless that man and everybody who is helping humanity wake-up and make this positive change possible in the world.
So, in our group of moms we've had really great results dealing with stomach, ear, throat, infections in our kids. Allergy symptoms, food poisoning, rashes, stuffy nose, cuts, etc. We are so happy for MMS and I use it and recommend it to every person who is willing to listen, everybody who takes it gets better.
People here in Mexico are still a bit afraid and listen to the doctors but I pray to God for them, that they will soon realize the damage the "medicines" do to their bodies.
I have been listening to the broadcasts and they have helped me a lot to learn more about how the body works, so thanks for that. And about the vaccines, I have 4 kids, the first 2 I vaccinated and the youngest two I did not. I can see a great difference in how they react. The first two had allergies, they got sick once a month when babies and they still have trouble controlling themselves and concentrating. I have to confess I have not given them the whole 1000 protocol, but I know that when I get the chance to really finish it their problems will be gone for good since I have seen things disappear with one dose. So, I will be doing that.
The youngest two have very strong immune systems and can fight of any cold or infection if they get one, but it's very rare and when they do they usually get high fever for one or two nights and the next day wake up much better. They have no trouble with stuffy nose, or allergies, or croup, or anything like that which was a big problem with the oldest two until MMS. Doctors and medicines only made things worse for them so I started to search for alternatives, and thank God, I found the ultimate and best one MMS.
My husband had allergies his whole life, problem solved. I was totally toxic and had lots of problems with intestinal issues and now I feel great.
Thank you, thank you, thank you, I can't thank you enough, you guys have been an inspiration and now I want to take the course and help more people because I have found lots of happiness in helping other people heal, I think it's the perfect way to start if we want to heal the planet and make the world a better place. Sooooooo, how much does the course in Mexican pesos cost? and in what bank do I make the deposit?
Thanks again and will keep in touch.
God bless! Vero

 

Prostate Cancer
Hi
My name is Gerald McClellan and am 72 years old of Monroe, NC. I was diagnosed with prostate cancer in Nov 2011 and my doctor said that my prostate had a PSA reading of 5.89 and was over 80% infected with cancer and he suggested that I have it removed or I would not live more than 5 years. Well believing in my doctor I agreed to have it removed and they did remove it in Jan of 2012. I had been scheduled to have a PSA reading done every 3 months to see if my cancer was gone and it wasn't so they scheduled me for 37 treatments of radiation, which was completed in July of 2012. From that point on my PSA readings, which were low but not gone, were doubling every 3 months until I learned about MMS in Jan. 2014. My son ordered it and I started on Jim Humble's protocol 1000+ and when I had my April PSA reading my cancer had reversed for the first time in two years and now is gone. My reading has already been pretty low but not the 0.00 reading I should have had being I don't have a prostate. Well I have documented reading which prove that the MMS did in fact reverse my cancer and got rid of it. I also was using Vitamin B17 between my April reading and June reading to find out if it also worked and it did and my cancer keep going down. So between my June reading and Oct reading I was just taking the MMS2, pill form, and found out that the hyprocloric acid thickened my blood, even though I was on cumiden because of having AFib. And I suffered with a mini-stroke that affected my right eye making me cross eyed to over 18 degrees off center. I could see out of the eye OK but not both at the same time. I went to an eye doctor and had some medical test done. My eye doctor said that I might possibly have to have an operation on the eye but wanted me to wait and see if it got better on its own. If no changes were seen by 6 months then the operation would have to be scheduled. Well I knew that my MMS worked for my cancer so I thought that it might work as well for my stroke also. I made up an activated 10 drop solution and put it with distilled water in a sprey bottle and made up a 70/30% solution of DMSO and spreyed it on my hole right side of my head and around my eyes two to three times a day. I told my eye doctor what I did and I notice improvement after the 3 days and my eye site returned to normal within 10 days. My eye doctor couldn't believe of my rapid recovery and wanted to know what actually it was that I did so I told her about MMS and how I used it to recover. I had her make notes of my use of MMS and had her put them in my medical record and gave her a CD with all of the information about MMS. I also had my urologist put my taking MMS in my medical records he has. Neither doctor would admit that this use of MMS would really work. But the records of recovery speak for themselves.


Signed Gerald D. McClellan
North Carolina
United States

 

Six Years and still no Prostate Cancer!
Sept. 2012 I sat waiting for my husband, Ronnie, to come out of the doctor’s private examining room where he was getting a prostate cancer biopsy. When he came out he was shaking, in a lot of pain. “I couldn't go through with it, I’ll have to go to the hospital”, he said. “The tests show I definitely do have prostate cancer. The Gleason test showed from one to ten, I am a seven, which means the cancer is ready to get aggressive.” After the biopsy, done in the hospital, it agreed with the doctor’s verdict; there was no doubt, Ronnie had a very serious cancer problem. This is his story; I won't go into how that made me feel. We had already suffered through the loss of son, both our Mothers, and a daughter,who had died from breast cancer, all within the span of three years. During which time I had spent fourteen days in the hospital with massive blood clouts on both lungs, and later a frozen shoulder, which led to surgery. During the same period our Indiana home was broken into, taking a lot of valuable tools, and other valuable items. We were still fighting depression. Now there was to be a new problem, Ronnie had to make a decision. Since Ronnie insisted on no chemo, the doctor gave us three choices: surgery, radiation, or a six month hormone therapy shot. We settled for the shot which was supposed to keep the cancer from spreading for six months. It could only be taken two more times, at which time the body would become immune to it. Without any other treatment he may have at least five years of life after that. We grieved for a couple weeks and then started planning to go back to Florida for the winter. First we attended our yearly religious festival, “The Feast of Tabernacles” and requested the prayers of the many brethren there. Prayers were also offered up to God in our own Home Bible study group. When we got to Florida our friends there begin praying for us, too. Needless to say we also did a lot of praying. Ronnie continued struggling with vomiting, frequent painful urination, and discomfort. Added to his other problems he started having severe hot flashes, from the shot, that was a constant irritation. In the meantime we started searching the internet for alternate solutions. Nothing seemed reliable until daughter, Tammy, introduced the web site of Jim Humble to us. We had studied several others but this one really got our attention. We felt like God was answering so many of our prayers. We sent for the book and the minerals Jim introduced. Ronnie mixed the inexpensive liquid combinations himself, and drank it as instructed every day. Gradually he begin to feel better. The symptoms left. We all rejoiced. Before we left Florida, five months later for Indiana, he went for a last check up there in Feb. 2013. The doctor seemed surprised that his prostate was so small, and questioned as to whether Ronnie had ever had prostate cancer. But the records from the first doctor were there! When Ronnie told him he had been taking a mineral called Miracle Mineral Solution that enhanced the immune system, the doctor commented, “Oh? That will never work”. Can you believe that? When the results of his blood test came back his P.S.A. test had dropped from 7.6 to 1.2, and is still about 3.5. He had one more test by the same office that had given him the six month shot. The doctor was so impressed with the result of the P.S.A. test that he asked to see the book, and made the comment, “I'll have to look into that!” He scheduled Ronnie for another appointment in three months, and didn't even examine him. I think he just wanted to see for himself if it was really going to last. But we know Ronnie is cancer free! Some may want more information on this mineral, if so, you need to go to the website “WWW.Jim Humble - MMS. You can get a news letter from them every month by e-mail. He is doing amazing things in Africa where he is freed to work. This mixture of minerals strengthens the immune system so strongly that it will kill many germ related diseases, not just cancer. There is a long list of diseases that it will get rid of if done right. The only thing I can think of that it won't heal is something like broken bones, damaged nerves, dementia, weakness, etc. If you or someone you know that is debilitated with a serious disease spread the word, you may save a life. Also request newsletters from Jim. He was God's answer to Cancer for us. It will give you an idea what this man is doing for people. Visit "List of Studies" on our web site "foust.info" for over 100 bible studies.
Oh, and by the way, Ronnie was really surprised when the pain, he had suffered in his fingers for months, also disappeared. Thank you Jim for your dedication for serving suffering peoples all over the world.
Rhoda and Ron Foust
Williamsburg ,Indiana

 

Prostate issues

 

To World Citizens... I first started using MMS approx 6 years ago,had acute pain in my prostate area,pain dissolved within a few days,and within a week or so all symtoms completely gone,in other words "HEALED". Also use MMS to bathe in,an amazing tonic to rejuvenate a tired body....use MMS for overall health including teeth ,gums,basically your whole physical body. Stay with the recommended dose,easy n safe to use .
James
New Zealand
VIDEO TESTIMONY:

• Prostate Cancer cured with MMS (English Subtitles) - MMS Testimony
https://www.youtube.com/watch?v=b7UCvSOb8rg
• Diabetes, Prostate lumps, AIDS - MMS Testimonials
https://www.youtube.com/watch?v=2unUwnWkP4M
This week we will be covering how the PSA test many men are “encouraged” to have done frequently and especially after the age of 50. This test is “at best” 4 % accurate! Listen to the man that designed the test.

 

LISTEN TO THE GUY THAT DEVELOPED THE PSA TEST BEFORE YOU SUFFER NEEDLESSLY!

The New York Times ran an Op-ed by Richard J. Ablin, the man who invented the prostate-specific-antigen (PSA) test which is widely used to detect signs of early-stage prostate cancer. Ablin, who is now a research professor of immunobiology and pathology at the University of Arizona College of Medicine and the president of the Robert Benjamin Ablin Foundation for Cancer Research, reveals that “in approving the procedure, the Food and Drug Administration relied heavily on a study that showed testing could detect 3.8 percent of prostate cancers, which was a better rate than the standard method, a digital rectal exam.
“Still, 3.8 percent is a small number,” he observes. “Nevertheless, especially in the early days of screening, men with a reading over four nanograms per milliliter were sent for painful prostate biopsies. If the biopsy showed any signs of cancer, the patient was almost always pushed into surgery, intensive radiation or other damaging treatments.”
Prostate cancer is a tricky disease because the cancer grows so slowly. A great many men who are diagnosed with prostate cancer will die of something else—long before the symptoms of the cancer catch up with them. As Ablin points out, because PSA testing is pervasive, “American men have a 16 percent lifetime chance of receiving a diagnosis of prostate cancer, but only a 3 percent chance of dying from it.”
Last year, The New England Journal of Medicine published results from the two largest studies of the screening procedure, one in Europe and one in the United States. The results from the American study that over a period of 7 to 10 years, screening did not reduce the death rate in men 55 and over. The European study showed a small decline in death rates, but also found that 48 men would need to be treated to save one life. “That’s 47 men who, in all likelihood, can no longer function sexually or stay out of the bathroom for long,” Albin adds, referring to the fact that treatments can lead to long-term incontinence and/or impotence.

NOTE: Completely opposite of What the “doctor says below about a “Robot Surgeon”. Don’t fall for that. You’re NOT going to die from Prostate Cancer. Get in touch with us and we can help you with our protocols. You can contact us at: This email address is being protected from spambots. You need JavaScript enabled to view it. for guidance.
Source: The Doctor Who Invented PSA Test Calls It “A Profit-Driven Public Health Disaster”
http://www.healthbeatblog.com/2010/03/the-doctor-who-invented-psa-test-calls-it-a-profitdriven-public-health-disaster-why-this-is-good-new/

In 1970, Richard J. Ablin discovered the PSA. In a 2010 N.Y. Times Op-Ed piece titled, "The Great Prostate Mistake," Mr. Ablin sets the record straight.
"As I've been trying to make clear for many years now, PSA testing can't detect prostate cancer and, more important, it can't distinguish between the two types of prostate cancer - the one that will kill you and the one that won't."
Ablin explains that a PSA test merely measures how much PSA or prostate specific antigen is in your blood. Although elevated levels of PSA can be detected, that alone does not necessarily indicate prostate cancer.
Why? Because common over-the-counter medications like Ibuprofen, benign prostate enlargement (an inevitable part of aging) and infections also elevate PSA levels. Men with high PSA readings can be cancer free, while those with low readings can actually have cancer!
Ablin exclaims, "I never dreamed that my discovery four decades ago would lead to such a profit-driven public health disaster. The medical community must confront reality and stop the inappropriate use of PSA screening. Doing so would save billions of dollars and rescue millions of men from unnecessary, debilitating treatments." (Emphasis added)
The respected British medical journal, Lancet, reported on 13 February 1993 early screening often leads to unnecessary treatment and "33% of autopsies show prostate cancer but only 1% die from it."
Dr. Tim O'Shea, a maverick Doctor of Chiropractic, holistic health lecturer, author and founder of the doctorwithin.com website states: "This means that the immune system can hold many problems in check, as long as it is not compromised by powerful [and/or toxic] procedures."
Source: Beware: PSA prostate cancer screening test is a dangerous hoax, warns discoverer of prostate specific antigen: http://www.naturalnews.com/041796_
PSA_testing_prostate_cancer_medical_hoax.html

This being a hoax and look what men have to go through needlessly! This is horrible to think men have to go through all this and it ISN’T necessary! I know people that have had their prostate taken out and the PSA went up! How’s that for evidence that the PSA isn’t prostate specific!


NOTE: I included a Dr. Samadi’s information about his “robot surgery” techniques and what he says to expect after surgery!
Sex after prostate surgery is very possible and enjoyable for most men.
Dr. Samadi’s robotic prostate surgery, SMART Surgery, was explicitly designed to spare the tiny nerve bundles surrounding the prostate in order to preserve sexual potency.

Men who undergo Dr. Samadi’s robotic prostate surgery have a reasonable chance of regaining complete erectile function for sex after prostate surgery.

Newly Diagnosed?
When first diagnosed with prostate cancer, it’s common for men to wonder what the future will hold. Certainly, a prostate cancer cure is top priority, but then what? David B. Samadi, MD, understands that men want to know:

Will I have sex after prostate cancer?
How will sex after prostate cancer be different?
For many men, prostate cancer treatment choice determines these answers.

If you elect to have robotic prostate surgery your chances of enjoying sex after prostate surgery are very high. However, it is absolutely critical to choose a robotic surgeon with a high case volume and extensive prostate surgery experience. The robot does not perform the surgery and technology is no guarantee of success.

Dr. Samadi is considered one of the best NY robotic surgeons because of his high surgical volume, successful track record, and background in open and laparoscopic prostate surgery.

Sex After Prostate Surgery – What to Expect

Knowing what to expect is a large part of optimizing your sexual recovery from prostate surgery. Dr. Samadi works very closely with men and their partners before and after surgery to help them understand what’s likely to occur.

Impotence and erectile dysfunction (ED) after prostate surgery:

Expect some ED, but know that for most men it is temporary. During recovery, medications like Viagra and Cialis will help.

Orgasm after prostate surgery:
You can expect to enjoy sex after prostate surgery. Many men are surprised to find that they even experience pleasurable orgasm without an erection. Keep in mind that your sexual pleasure does not depend on penetration.

Ejaculation will cease:
Without a prostate gland or seminal vesicles you will no longer experience ejaculation. Even though your orgasm may feel different, it will still be pleasurable.

Leaking urine during sex:
This is possible, but does not happen to all men. It’s harmless and temporary.

Performance anxiety:
Don’t underestimate the emotional roller coaster of prostate cancer surgery and recovery. It’s normal to worry about sex after prostate cancer. Being open and honest with your partner will help.

Keep in mind that your overall health, age, and present ED status are all factors in your recovery to sex after prostate surgery.

Less commonly, the prostate cancer tumor may bulge to one or both sides of the prostate gland, making nerve-sparing surgery extremely difficult or impossible. Dr. Samadi will help you understand your exact prostate cancer status and the position and size of your tumor. In some cases, a nerve graft can be performed to regenerate the penile nerves for sex after prostate surgery.

 

Post-Robotic Surgery

Congratulations on your robotic prostate surgery! The key to enjoying sex after prostate surgery is to start when you’re ready. Dr. Samadi and his knowledgeable team are available to support you and your partner as you work to resume sexual activity.

Sex After Prostate Surgery – Getting Started
Masturbate:
This helps you learn how your body will respond to stimulation after surgery and builds your sexual confidence.

Kegel exercises:
Try out pelvic floors exercises to improve orgasm and urinary control.

Involve your partner:
Work with your partner through physical and emotional intimacy; sex will follow.

ED medications:
Don’t hesitate to try oral medication for erectile dysfunction. They’ll actually speed your recovery through penile rehabilitation and you may only need them for a short time.

Have sex:
Practice makes perfect; the sooner you try, the sooner you’ll get back to enjoying sex after prostate surgery.

Erectile Dysfunction (ED) After Prostate Surgery
For the few men who experience ED after prostate surgery that lasts more than two years, Dr. Samadi provides expert counsel and referral for alternative ED treatments.

Penile injection therapy for sex after prostate surgery:
If oral medications are not effective, penile injection therapy can be used to help the nerves regenerate or recover sufficiently. In a recent study it was shown that it is very valuable to use injection therapy to aid erections soon after surgery to increase the chances of the return of normal function.

Penile implants for sex after prostate surgery:

In some cases, no erectile function will return after prostate surgery. In such cases, you may want to explore the option of a penile implant for a permanent ED solution. A penile implant is an excellent option and is associated with a very high rate of patient and partner satisfaction.

Spouse/Partner

If your husband or partner is undergoing robotic surgery for prostate cancer treatment, or is in the midst of recovery, it can be difficult to know the right things to say or do. Your patience and understanding are the most valuable support you can provide. Find ways to rebuild physical intimacy with your partner, but don’t be discouraged or offended if it takes time for him to feel comfortable being intimate again.

Prostate cancer can be an emotional journey for the entire family. Trust that you and your partner will soon enjoy healthy, happy sex after prostate surgery.

PSA screening disaster

The standard PSA (prostate specific antigen) test was approved by the FDA in 1994, and each year millions of men are screened via a blood test for the PSA antigen, which is manufactured exclusively by the prostate gland.

NOTE: That is a lie!

For many men, this is when the serious life-threatening trouble begins. Early, aggressive allopathic prostate cancer treatment can and does cause permanent damage, including impotence, heart attacks, incontinence and even death from a disease that is, ironically, statistically unlikely to kill them.

 


How to help us with our goal of, “a world without dis-ease”

For information about membership or video course
contact us at: This email address is being protected from spambots. You need JavaScript enabled to view it. or
This email address is being protected from spambots. You need JavaScript enabled to view it.

 

• Becoming a member of the Genesis II Church of Health and Healing

• Ordering Sacrament Products to detox and heal your body (to support us you can get them by contacting us at: This email address is being protected from spambots. You need JavaScript enabled to view it.

• Becoming a Health Minister by doing the online course and train others Contact Jordan at:This email address is being protected from spambots. You need JavaScript enabled to view it.

• Donating to help us continue our worldwide mission by contacting This email address is being protected from spambots. You need JavaScript enabled to view it.

• Donating with Bitcoin www.g2voice.is

 

• Like, share, follow, subscribe on our YouTube sites, Facebook pages and Spreaker Radio site.

• By sending family and friends this newsletter and asking them to sign up for our free newsletters at: http://mmsnews.is/signup

• Sending family and friends our first G2Voice episode to watch, if any of them are suffering with one or more of the dis-eases covered on the G2Voice.

Note: A good introduction to MMS is the MMS Documentary, www.quantumleap.is


(Subtitled in 10 languages)
If anyone needs Sacramental Guidance for ANY disease please contact me at:This email address is being protected from spambots. You need JavaScript enabled to view it. or for Spanish Joseph at: This email address is being protected from spambots. You need JavaScript enabled to view it.

Since we started the G2Voice Broadcast, we have had 4 merchant accounts shut down. The merchant account is used to receive donations for Sacramental products, membership and G2 Church online course. Only explanation for shutting us down has been that we are a high risk! What risk? An online course? Church membership? Sacramental Products? We are looking into other merchant accounts but seems like we will keep having this problem. What everyone needs to do is contact us personally at: This email address is being protected from spambots. You need JavaScript enabled to view it.

You can also support us by ordering our sacraments from https://g2sacraments.org/ We now ship  throughout USA, Canada, and Mexico.

Please like, subscribe and share all the G2Voice Broadcasts with all your family and friends!
Tune in Sunday at: www.g2voice.is 10AM CST
Let's change the world together!
Archbishop Mark S. Grenon
--
Let's change the world together!
Archbishop Mark S. Grenon
Proverbs 3:5&6

 

 

MMS Saves Lives.

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Petition to Stay Daniel Smith's Sentence and End Malaria Death (Change.org)

Thank you.

www.StandByDaniel.com

Who is Daniel Smith?


Had good results with MMSMany do!
Please consider sharing your story and inspire others:

Write Testimonial

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Jim Humble Interviews:
Jim Humble Talks to Freedom Central About MMS (YouTube)

Recent Responses to MMS Critics:
Jim Humble Responds to Rita O'Reilly RTE Current Affairs TV in Dublin Ireland

Guides - Tutorials - Howtos:
How to make MMS: Sodium Chlorite 22.4% (YouTube)


Red Cross MMS Malaria cure cover-up scandal:

LEAKED: Proof Red Cross cured 154 Malaria cases with MMS: This video got leaked 1st of July 2013 and makes it impossible for the Red Cross to keep claiming that their Sodium chlorite 22.4% (MMS) study never took place, as was their response to the 2nd of may video.
youtube.com/watch?v=FrwZN1cPfX8

Red Cross cures 154 Malaria cases in Uganda with MMS:
This video was released 2nd of May 2013.
youtube.com/watch?v=5jY2yab0uLc

Read about the Red Cross MMS Malaria scandal on the MMS Wiki:
http://mmswiki.is/index.php/Red_Cross
http://mmswiki.is/index.php/Red_Cross_Malaria_Cover-up_-_Media_Coverage 
http://mmswiki.is/index.php/Red_Cross_Video_Transcript


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.

Jim Humble's Books

 

mms health recovery guidebook w99

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.

 

 
Download Full Ebook for Only $22.50
 

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.

 

Download Full Ebook for Only $19.99
 

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.

 

Download Full Ebook for Only $18.99