Nine months ago I got a respiratory illness after an international airline flight.  Since then, I have seen 3 doctors, one of them a specialist, had 5 courses of different anitbiotics, and a 6th course prescribed.  My blood work looked fine, with only minor increases in neutrophils, though PCR test showed mycoplasma pneumonia exposure.  Two weeks ago, when I began my experiment with MMS, I had brain fog, was too weak to do more than stand up for 10 minutes, and was essentially confined to bed or chair most of the time.  After 10 days of MMS at a maximum dosage of 25 drops per day(divided doses), and with antioxidants in between doses, I am once again on my feet, cooking and gardening. 

In addition to oral use,  I also made my own sinus irrigation solution of acidified MMS, d-Mannose, distilled water  and enough sodium bicarbonate to adjust the pH to 6.2.  When I used it the first time, my sinuses cleared immediately and the relief was near miraculous.   I note that a patent on a similar solution was granted and that the commercial product is called Snoot.  I also found several journal papers indicating an immune modulating effect for stabilized sodium chlorite.  In light of this evidence, how can FDA prosecute anyone for selling a useful and safe product?

I wish to mention that I had sinus surgery two years ago that did not help my recurrent infections.  My doctor did a CAT scan of sinuses and chest, so the diagnosis was confirmed.  The next course of action would have been an antibiotic a day…Something I did not want to take for sure.  Just think of the danger of c.dificile!  A relative died of that, and I am aware of the risks.

In these times of increasing numbers of antibiotic-resistant bacteria, cryptic organisms like mycoplasmas and clamydophila  pneumonia, MMS becomes a life saving tool, because there are few sucessful protocols available to mainstream physicians and patients thus suffer years of suffering and economic loss.  Surely, if one is entitled to life and liberty, that includes the pursuit of health.  FDA has a long record of advocating for commercial interests at the cost of  consumer health.  This needs to end. Let FDA turn its attention to dangerous drugs which kill hundreds of thousand yearly, and leave citizens alone to make their own health choices.

These following E mails are from a 65 year old gentleman  that was sent home to get his arrairs in order as he did not have much time left. I started him on MMS #1 & # 2 as well as other protocols, On his own he went to a natrualpath for some additional protocols that included mistletoe, Vit. C IV and another for a while. He did not ;mis the MMS with the Vit C but waited several hrs before going back on MMS. These reports are after 7 months. On my protocols he has lost 50 lbs, now walks 5 km per day, exercises at a gym 3 days for up to 2 hrs. Goes to work three days a week and claims life is great. 

PS: My Naturopath had me retest my blood using a German procedure ‘Circulating Tumor Cells’ (laser scanning-microfluorimetry of the epithelial cell antigen); I ship the blood there. The results read ‘over a period of 6 months we can see stable cell numbers at a low cell level’. GOOD NEWS.

I was bitten by a Horse fly age 9 years old. Noone knew anything about Lyme back then. I was left un tested for any spirochete infection. But the infection slowly began to affect my body and my brain from then on, still noone put two and two together. When i was 22 I was diagnosed with Multiple Scelerosis. I have subsequently discovered that M.S is connected to Lyme disease in fact M.S is a spirochete infection not just an autoimmune disease.
 As Dr Lyda Mattman says ‘Multiple scelerosis should be renamed Multiple Spirochetes’.  That is enough for me to know I was infected by the Horse fly.

M.S is chronic untreated  Lyme according to many Doctors out there.

I have been taking MMS for 15 months and wow! I am almost rid of the Lyme disease and co-infections. I say almost because these infections can go dormant for 10,20,50 years if you do not kill it all in the body system.

I am physically stronger, no need for walking aids anymore, my cognetive thinking is now second to none, i have no brain fog, my eyesight is above 20/20 vision, my corodination is brilliant, I can now hold a coversation, I do not have splayed feet anymore (something I have had since the bite age 9) My I.Q has improved by 60% (Lyme and co-infections affect the I.Q.

I am basically a normal healthy human all thanks to MMS and you Jim.

I have been spared a life of ever increasing disability and pain.

My children have congenital Lyme and co-infections and they too have been taking MMS for 15 months (their own choice as they are Gilleck competent)

They are fabulously well and also have cleared their bodies of Lyme and co-infections again they will carry on taking MMS for a while longer as i said because these infections can Lie dormant for a long time and we all want to be sure it is gone for good!

Both have been eyetested and their vision is above 20/20 their eyesight has improved greatly.

My eldest who was a snuffly baby (connected to a spirochete infection) no longer has sinus problems, the eyes are no longer affected (used to have constant eye irratation also connected to a Lyme, co-infection)

Our hair, nails, teeth are brilliant and fabulous with an infection all of these are affected.

We were on a limited time with my children it would only of been a couple of more years (by the time they reached age 18)  that they too would of been diagnosed with an autoimmune disease or become disabled, MMS has saved their lives too!

All of this because of a bite from a horse fly which are carriers of Lyme and other co-infections.

MMS is the saviour as well as Jim of course I am eternally grateful.

I will keep everyone updated about our further progress.

If anyone is concerned about long term use of MMS well if I had of taken antibiotics i would have to take those for up to 10 years causing damage and costing £800 per person per month, as far as i am concerened MMS causes no damage long term, no side affects and is better for the body and costs pence per dose it really is the better option to heal from chronic Lyme.

The “only” thing that helps me with over 50 yrs of Lyme Disease,not to mention all the other uses.

(English translation from Google Translate below)

Ik ben een man van 62 en  had maanden lang last van brandend maagzuur
in de slokdarm
Zuurremmers hielpen wel maar als ik ze niet meer
innam kwam het zuur onmiddelijk terug
Ik kon niet meer liggend slapen
Na een paar keer mms ingenomen te hebben
was de pijn weg en kon ik weer
gewoon slapen
Ook had ik chronisch verkoudheid
Die is ook geheel verdwenen  en dat na 8 maanden
van problemen
IK ben heel blij dat ik zo ben opgeknapt
Eerlijk gezegd heb ik de mms maar zo af en toe genomen
en niet volgens een protocol
Maar toch hielp het
groeten
Henk Damstra

 I am a 62-year-old man who suffered from heartburn for months
in the esophagus
Acid inhibitors helped but if I do not
the acid came back immediately
I could not sleep anymore
After having taken mms a few times
the pain was gone and I could again
just sleep
I also had chronic colds
It also completely disappeared and that after 8 months
of problems
I am very happy that I have been so refurbished
Frankly, I only occasionally took the mms
and not according to a protocol
But still it helped
regards
Henk Damstra

I have a friend who had severe ulcerative colitis for 28 years. It is bacterria living in the last 10 inches of the rectom. Could not hold down a job as he needed a toilet very handy and that came very often at a moments notice. It is incurable the Medical way.

After altering his life style and nutrition along with MMS his doctor pronounced he no longer had the diasease. It was his last checkup before they were ready to remove part of his bowel and go on a bag and his doctor did not beleive it no longer was there!

He has told me if anyone needs verification over the phone he is quite happy to talk to them. He did not do an enama useing MMS but i beleive he should have as it would be very easy to get to the bacteria.

A glimmer of hope

Over the past six months I have been working with a group of terminally ill people. I was asked to provide some help when a drug, currently in Phase II clinical trials, provided not only a stop of the progression of this disease, but some people were actually regaining function that they had previously lost as a result of the disease.

The drug is NP001. It is made from a chemical that many may be familiar with, sodium chlorite.

The problem with a drug trial is that they exclude people from the trial. Efforts were made to broaden the acceptance criteria, some progress was made, but still many were left out of the trial. While the main reason was that they lived in an area that was outside the trial locations, another reason was the progression of the disease in their bodies.

NP001 is administered via IV injection. I explained that there is more than one way to get chlorite into the body and that while it is not as efficient as IV injection, drinking a solution of chlorite will result in some chlorite getting into the blood stream.

A group of these people suffering from this disease decided to run an experiment on themselves. Efforts have been made to get the medical community involved and these have not been totally successful, so far. They have provided support in the form of check ups and blood work designed to monitor for any adverse effects of participating in the experiment, but ethics and legal ramifications prevent them from getting too involved with this.

A research neurologist was kind enough to explain to me that anecdotal evidence over a period of days to weeks is usually thought of as being the result of the placebo effect. However, anecdotal evidence that continues to show positive results with the same people over a period of months to years is much harder to dismiss as placebo. Testing done that supports the positive effect also helps. I was also informed that when the results are spectacular the general bias is to question the original diagnosis.

This experiment is coming up on six months now. The positive benefits seem to be holding on, so I think there is now a glimmer of hope.

Keep in mind that the group involved in this experiment is small. There are about 35 people that are openly vocal about it, and about that number again that are quietly participating. Also, not everyone is showing improvement.

Not knowing a lot about this disease I asked the group this question.

Chlorite is a free radical oxidizer. It does nothing to rebuild the body. What are you going to do to rebuild your bodies after the progression of this disease is slowed down or stopped?

The answer I received was…………. Well, the question was not answered.

I asked again.

This time I was informed that nothing had ever been successful in stopping the progression of this disease, so this question had never come up.

During this holiday time it is very exciting to see this glimmer of hope permeate the group, and to see some of their focus change to how to rebuild the body.

The changes are not drastic, but incremental. No one has jumped out of a wheel chair and started running down the street. However, to someone who has lost function in their hands or arms or legs, suddenly having some function restored and seeing this restored function continue over time is remarkable.

On May 2 1939 Lou Gehrig benched himself after playing 2130 consecutive baseball games with the NY Yankees. His health had deteriorated to the point where he was no longer able to play well. Addressing the crowd before a July 4 1939 game, Lou Gehrig told people that he was the “Luckiest Man on the Face of the Earth.” Two years later on June 2 1941 Lou Gehrig died of amyotrophic lateral sclerosis.

ALS is the illness that the people involved with this experiment are suffering from.

This glimmer of hope started with the drug trial that lead to the oral experiment. The purpose of the experiment is to help people live long enough to be able to use the drug. There appears to be a willingness of the FDA to speed things along, but the process will most likely take a few years and people who are diagnosed with ALS have an average expected life span of three years. I don’t think the FDA can speed things along that fast.

In loose side to side comparisons it appears that the drug is far more effective. The oral solution helps and seems to be able to halt or radically slow down the progression of ALS, but the results from the drug trial seem to be better.

Six months is not a year, but it is more than a day or a week. Making assumptions on the outcome of a clinical trial in the middle of the trial is not the best thing to do. Extrapolating from the observations of a small group of people is also not the best thing to do. Still, I think there is a glimmer of hope.

Chlorite is not a cure for ALS, but it does seem to provide something that people suffering from ALS have in very limited supply – additional time.

If you know of someone that is has ALS, I invite you to cautiously share this glimmer of hope and have them watch the progress of the NP001 trial.

Tom

all my staff now r very healthy…. every minor sickness r heal within days…..

all for that cancer case also living well… concentrate on career only….