Category: Sleep Disorder

Multiple recoveries

Categories: ,
April 29, 2020

Margaret’s most recent ‘Big Wow’ is SPEAKING in her sleep!! I woke to hear the last four words! It has been since 2012 she has spoke four words in a row that was understandable. Many recoveries received and a few big ones to go. Midnight, our American Bulldog I’ve been writing in about, can also add new whiskers to his recovery list. Some are just over a half inch! This has made a big difference in his balance and movements. I must close with telling you guys, Dr Group gave his support for our number 1 sacrament and referenced the research he did with Jim all those years ago. Hopefully you can find with picture that shows time stamp.  Godspeed Michelle Gugel  


Candida - happy I got rid of that stinking annoying brain fog !

Kenneth Walter
May 3, 2017

While attenpting to rid myself of this curse called Candida, which affects so many people and those not yet aware or diagnosed, I started out using the cds, at first just one drop into 4oz of water, and I took 2 doses prior to bed and had to go sleep.

The funny thing, as an older man, I had to usually pee 5-6 times at night which doesn’t allow for enuf rest for my adrenals. When I had finally gotten up, I had only peed two times, which was good and unexpected and by the end of that week I had dosed myself about a dozen times and had gotten up to 7 drops per dose, and no longer need to pee at night and get a full nights rest ! My libido has also improved !! another unexpected surprise.

During all this time, I had been reading about different formulations to fix this curse from the quacks to naturopathic doctors and more and have come to realize, mine is systemic and not gonna be easy to kill off.

Earlier, prior to starting this course of mms, I had success with taking turpentine with sugar, it killed off the biofilm on my brain in about 3 seconds ! I only took 1tsp of turpentine with 1tsp of sugar and it took only a few moments to start, and then the biofilm was gone. I was happy about the biofilm, but disappointed that it didn’t kill off MY candia altogether, so I had to be happy I got rid of that stinking annoying brain fog !

I have on order, some mms2 which is more potent than mms1. I’m praying that does the job to finally kill off this curse. I just won’t know how well I’ll tolerate the mms2 til I take it, but I’m feeling good about it just the same.


Whooping cough - It does work

Sei Leapai
November 16, 2014

My brother had whooping cough. He had been to a GP twice and taken several doses of antibiotics with no success. He had lost weight, his skin was a sickly pale, he could hardly sleep, as sleep brought on the horrible fitting cough. It was awful to watch, and he was like this for weeks, with no relief. Not until our friend recommended MMS. Within an hour of taking MMS, color was returning to his face. I think within a few hours, he had stopped coughing and his appetite had returned. And then that night he told my mum he wanted to cough and his phlegm clogged the sink when he tried! All of the built up mucus was coming up and out!!! It does work. Its worth a try. What have you got to lose?


From Sleepless Nights to Meaningful Speech

Yurliana Montero and Jonatha Quijada
January 1, 2014

The following testimonial is excerpted from page 418 of Healing the Symptoms Known as Autism, 2nd Edition by Kerri Rivera, published in 2014.

The book outlines a protocol in which chlorine dioxide is a key component. More recent editions have since been released with updated information.

A link to the full book in PDF format is provided at the bottom of this page.


My baby girl Yuliangel Nazareth Quijada Montero was diagnosed with autism when she was one and a-half years old.

From that moment she was given a treatment to allow her to sleep and to control her tantrums: “Risperdal” which had absolutely no effect. I gave her up to three pills before bed and even then nothing happened. I was just damaging her brain. She didn’t sleep night or day. I was worried because she screamed all the time and she hit herself.

The 2nd of April 2011 I attended the conference of Fundación Venciendo el Autismo, where I heard for the first time that Autism had a cure. Kerri explained in a very simple way how I could cure my girl. Even though I didn’t have all the economic resources necessary for her treatment, the Foundation helped me with a part of the treatment, MMS and multivitamins.

From there I started noticing changes. With a lot of sacrifice and effort my girl was on a strict casein, soy and gluten free diet.

When I started giving her the MMS I would give her 72/2 on weekends and then I noticed that there was a lot of mucus in her stool. From there she started talking, she slept the entire night and took naps in the afternoon. She pays attention. She knows how to count and all the colors with only three years of age.

For me MMS is a miracle. Since I started giving it to her she is a very healthy little girl, with no colds or any of the diseases she used to have. She is now considered to be very high functioning (14 pts. on the ATEC scale). With MMS, vitamins, and the diet my child is getting out of the Autism spectrum.

She does not go to therapy because of my finances, but my sister Yenitze Montero interacts a lot with my girl, and her grandparents Raiza and Julian help me a lot with the diet. My nephews Jesus and Luis are also helping me with the home therapy, and of course her dad and me fill her with love and care.

My daughter is healthy. She has meaningful speech, she recognizes herself, she sleeps well with no pills and we are all very happy with the results.

God Bless the entire team at Fundación Venciendo el Autismo, especially Kerri Rivera for bringing MMS to my country, it is absolutely miraculous. Blessings.

Yurliana Montero and Jonatha Quijada


Testimony for the treatment of lung cancer

Bozidar Tezak
September 17, 2013

I have my own testimony for the treatment of lung cancer. I have my own medical diagnosis ‘Inter DiaCor’. Having problems with sweating, dry cough, fatigue, nervousness, severe pain in the middle of the back, hard to sleep and pain when lying on the left side. I decided to do a complete analysis of the organism. I found a great contamination of bacteria and viruses in each lung, but really on the left. Also was weak and small alveolar gas exchange. Urgent I started using MMS protocol 1000. Kontrol analysis I have worked for 15 days and the result was 50% less microorganism, still I spent MMS. I’ve done the analysis for 30 days and the result was 100% clean lungs. I continued to drink MMS for 20 days due to parasites in the cerebral cortex, the brain, and by the end I was able to repair all the problems in 52 days. Initially, the viral load was 86.1%, and finally 4.6%. I have all the images of such evidence for other people or seminars. Health resort I have other patients with bone cancer, severe toxemia, depression and the like. The success was great for 30 days. This is truly amazing!


Child with bad infestation of worms

Catherine S
January 1, 2013

We discovered one night while camping, after terrible agitation that our 3 year old granddaughter had worms. Looking back we realised that she’d had them for weeks with night times being the worst, she was having very disrupted sleep. She was grumpy, she was always tired, all these were so unlike her. She’s always such a happy child normally. We mixed up one drop of mms and one drop of citric acid put that one drop on the area from front to back and in less than a minute she relaxed a feel asleep. We check a few moments later and all the worms were dead and all the eggs as well. She has slept like a baby since and cheered up to her normal self. Amazing!!!!!! Tha is One drop One time and worms DEAD. Much better and much saferthan worming tablets.


Malaria-related symptoms improve with CDS use

January 12, 2012

I have a friend who contracted malaria in West Africa when she was 18 and is now 35. Since then she has had a litany of ailments come on that everyone suspects are related to the after effects of malaria, the worst of which is a rare sleep disorder called cataplexy that is a debilitating condition akin to narcolepsy. Since beginning low dosages of MMS and more recently CDS she has noticed a marked improvement in feeling that has suddenly returned to her hand and a decrease in back pain. Can anyone comment on the prognosis for someone on a CDS regimen who “survived” malaria years ago but is still battling side effects?

My thought being that if the brain was damaged by malaria fever and this damage is causing her post-malaria side-effects, then MMS/CDS is unlikely to help since it cannot replace brain cells. However, the CDS should eliminate dormant malaria virus in the liver which is tremendous, so the regime is worth continuing especially since it’s helping alleviate other symptoms. Maybe Jim or others who have experience working with people using MMS/CDS for malaria and have seen this movie before could share their experiences here, many thanks.


NP001 shows slowed progression in ALS patients over six months

December 30, 2011

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


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