Most Recent Testimonials

The following testimonial is excerpted from page 386 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.

Hi, had to share this moment today. Just wish daddy wouldn’t have missed it!

Well, we were seeing daddy off for work this evening, when Vail decided that he wanted to go run around in the grass. I told him we needed to put on socks and shoes and then we could play outside.

He walked straight to the door. We walked in, I pointed at his socks and shoes, and FOR THE FIRST TIME EVER (always knew he could, just too stubborn to do it unless he really wants to!), he promptly walked over, picked up his socks and shoes, and turned and handed them to me!!! (all the while doing it with an attitude!!! lol)

This is just from mom to therapists.

CD and Kerri have been life changing for our entire family. We now can give Vail choices, usually of two items. For example, I showed him two pairs of pants and asked which he wanted to wear, and he grabbed one pair and started to put them on even though he was still in his pajamas.

I showed him two shirts, and he picked a shirt. Same thing with his shoes and socks. He is able to choose now on his own.

I look forward every day to him doing something differently or completely new, and he almost always does now. This was not possible before CD.

THANK YOU KERRI!!! WE LOVE YOU FOR SHARING AND FIGHTING THE FIGHT!!!

LOVE,

—The parents of Vail

Transcript:

Most people who are embarking on the MMS journey are doing so on the advice of friends, family, and associates as supported by available information.

That’s well and good, but there remains a strong desire to hear it from someone we’re trained to trust, a medical doctor.

But finding an informed one who not only knows about MMS but has begun to use it in its practice is today a rare discovery indeed.

But find one we did in Dr. John Humiston, who practices medicine in Tijuana, Mexico.

It’s used to disinfect in a very strong way. Now, of course, what I’ve read, and this is always great because I’ve read people talk about, oh, it’s used for this. I can’t remember what it was, but to disinfect something that’s very toxic, very high amount, and just knocks everything out of it.

Well, yes, at those high doses. So we’re using scare tactics here. Oh, this couldn’t possibly work because it’s used for all these industrial uses. Well, that’s not a balanced view either.

I’ve never heard of a negative use from using anything that was close to a recommended dose. And I don’t think there can be.

One of the things that people have done is to use the words chlorine and chlorine dioxide synonymously. And so that, I mean, as though they are the same thing, even though one is a constituent of the other.

Yeah, and one’s a very reactive compound. The other can react, but, you know, chlorine, they’re very different. I mean, they’re so different.

Once you add dioxide to something, it’s very different. It’s like, it would be like saying sodium chloride salt is the same as chlorine, which is, you know, extremely, you know, off.

They’re related chemically, but one, you’ve got the single element. The other, you’ve got a combination, sodium and chloride, the ion, and very, very different.

I mean, we’re made of chloride. The ocean’s made of chloride. If you turn that all into chlorine, well, you would not be alive. And so that’s not correct.

I think people will do that, but I think that’s one of those initial obstacles that somebody tries to throw up. But it really doesn’t have much, you know, power to it.

And the very fact that it’s got all the industrial applications means it’s not unknown in the world. And it’s used for similar applications.

Now we’re simply converting it to a biological way. Why is it safe biologically?

Because most stuff that’s used industrially is not going to be something you want to put in your body.

It’s safe because it’s an oxidizer and because you handle oxidation, otherwise you could not live on oxygen. That’s number one.

And then you look at the breakdown products. What does it break down into? Very simple, natural compounds that aren’t a problem.

So that’s the other part.

We use a lot of IV ozone here at the clinic. Ozone is a stronger oxidizer than chlorine dioxide. It doesn’t last as long in the body, but it is. And it’s a very unstable toxic gas. That’s what it is.

I mean, if you put that little jet of ozone gas at the rubber glove, in about 10 seconds you’ve got a hole in that glove. It just spontaneously destroys the latex.

And then we put it in your blood.

Hello.

You’re fine because this is where you handle oxygen. This is the blood-carrying serum of your body, the blood.

I mean, the oxygen-carrying liquid of your blood is the organ that carries the oxygen. And so you’ve got antioxidant protection.

You can handle that amount of… it’s given in a controlled way. You can handle that amount of oxidation.

But the viruses can’t, and they never will be able to.

Learn more of what Dr. Humiston and others have to say about MMS.

And meet Jim Humble, the man who developed and then wrote the book on this protocol, in this 90-minute documentary.

When you understand how chlorine dioxide works as a powerful disinfectant, you’ll appreciate the potential of its intelligent and safe application to the often neglected but life-sustaining waters of our bodies.

Shipping late January 2008, Understanding MMS, Conversations with Jim Humble, now in post-production, is offered at discount pricing for advance orders at phylos.com.

Transcript:

My name is Maggie.

My son Gunnar was diagnosed with autism last January. He was four years old. He was born in 2008. Normal pregnancy.

He was born when he had the shakes. And his eyes were darting everywhere. And they were a little bit concerned by the medical staff. They did some testing. And of course they gave him the Hep B vaccine without my consent. Or my husband’s consent, without even telling us.

We brought him home when he was three days old. We got a phone call from the hospital saying he had hypothyroidism. Congenital hypothyroidism. And we needed to start him immediately on Synthroid, on synthetic thyroid medication.

So he was breastfed. But we did have to crush a pill into some formula to give him once a day.

So he was developing normally. We were happy. We wanted him. We willed him to be a boy. He was our beautiful boy.

He was… I’m going to cry… three years old. And I noticed that he wasn’t asking a lot of questions. He wasn’t asking why. He didn’t seem very interested in the world around him. He started to stare off out the window. Hard to get his attention.

I went to his endocrinologist. My husband and I voiced our concerns. And they blew us off. They said, oh, the medication fluctuation, dosage fluctuations cause side effects of fatigue.

Time went on and other caregivers, in-laws, parents, noticed that he was looking out of the corner of his eye a lot. Very picky about foods. Started having some sensory issues.

I took him to the endocrinologist again. And I said, I want an evaluation. And she said, oh, he’s fine. You know, boys are hard to potty train. I said, but he was potty training. And now he’s wetting himself and doesn’t even notice that he soiled himself. This something is not right.

And she had got a page and left the room. And there was a resident in there. And I said, I want an evaluation. So she pulled up a milestones chart and said, is he doing this? I said, he was. He’s not anymore. Is he doing this? No, he never did that. Is he doing this? No, he never did that.

And she went down the list and then she said, Gunnar, can you stand on one foot? And he didn’t even turn. She said, Gunnar, Gunnar, Gunnar. And he didn’t even notice. And she said, I agree with you. He needs an evaluation.

So, it took six months to get the evaluation. They’re so, so very far backed up. It was, and that apparently after talking to other parents, that was pretty quick in comparison. But I kept calling and pushing and pushing to get the evaluation.

So, finally had it in January. He was four years old. And then they didn’t give us a diagnosis that day. They said that they would send it to us in the mail when they concurred with each other.

So, they told us he had autism. So, they wanted us to come back in February for some more in-depth testing.

So, that testing, we had changed diet. We had switched to gluten, dairy, soy-free diet almost immediately after his diagnosis. And we almost immediately saw good things. And his digestive issues were getting better.

And he was waking up in the middle of the night screaming in the fetal position and couldn’t tell us what was wrong. If I touched him, he’d scream, ow! Music was on quietly and he’d cover his ears and turn it down. And he just was uncomfortable in his own skin. He didn’t want to be held. He didn’t want to be rocked. He didn’t want to be sang to. He wasn’t interested in books.

His speech was, want juice, want juice. He wasn’t speaking in sentences.

So, we had him tested and his speech and language was at a 23-month-old level. He was four years old. His gross and fine motor skills are around 26-27 months.

And so, I just went into hyper-research mode. I read everything I could get my hands on. I was up all night, all my free time. I was consumed with, I’m bound to determine to heal my child.

You know, I went into the whole acceptance thing at first because I felt like I was maybe doing a disservice to him. I wanted to change anything about him. I just wanted to get him healthy.

So, I stumbled upon the CD (MMS) protocol and I started watching and started taking notes. And this makes sense to me.

Had some food allergy panels ran, did a comprehensive stool analysis. Actually, both my kids, my neurotypical daughter and my son, and they both tested highly intolerant to gluten, dairy, and soy, among some other things. They both have leaky gut. My son has bacterial dysbiosis, which is leaky gut caused by bacterial overgrowth. And my daughter’s was yeast. She had overgrowth of Candida.

So, the whole family went on the diet. I have hypothyroidism. I had a giant goiter. Within ten days, my goiter was gone.

I decided that this was going to work for us. I just knew it. I just knew in my gut that this was right. I ordered the book. The book came in. And my son was obsessed with the book. My son, who never was interested in books. And our living room is full of books. And his bedroom is full of books. And sister’s bedroom is full of books. And he never wanted to sit down and read a book.

And this came in the mail. And he was obsessed. This book is it. This book is it. Which was the longest sentence he had really said at that point. And my husband and I looked at each other and our eyes filled with tears. And we were like, yeah buddy, this is it. And we just knew.

We just knew in our gut that this was the answer for us. And so, I started with my son.

I did the protocol complete for four months for myself. I saw a lot of improvements in my own health concerns. I had adrenal fatigue and all sorts of things going on. I feel great now.

My son had immediate improvements. He started sleeping through the night. Seven weeks in, he no longer needed his thyroid medication he had been on since he was three days old. Still doesn’t need it to this day.

Started sleeping through the night. Digesting food normally. Eating normally. The sensory issues disappeared. You know, he is affectionate. He is happy. He is healthy.

Sorry. It is just incredible. It is incredible.

Everybody notices how great he is doing. He is just reading books. He is going to mainstream preschool. He is getting ready to go to kindergarten next year.

His ATEC when we started June 23rd last year was an 80 and it is currently at a 5. And there are things that I believe the ATEC doesn’t show. Improvements such as he is asking why questions. He wants an explanation. He wants to play games. He initiates conversation. He jokes.

He is sneaky like a five-year-old should be when he wants something and he bargains. And if I ask him a question, if he doesn’t know it, he says, I don’t know. And then he gives his best explanation. He is healthy. I mean, he is doing incredibly, incredibly well.

I have talked to so many parents that have tried every intervention under the sun and spent beaucoup dollars. And they are not seeing a tenth of the improvement that we have seen in our son. And he is just a little walking miracle and nobody can limit his potential.

He has got a full childhood now. He has got a full life ahead of him. And I am really excited to see what he does with his life. He is really intelligent. He has got a photographic memory. He can memorize things very quickly.

The scripting has slowed. A lot of his speech for a while seemed a little robotic. And now we are getting more and more natural speech. And it is just incredible.

I love helping other parents. This community of parents is just amazing. They are a family. Everybody cheers each other on. Everybody wants each other’s child to improve. Nobody is selling anything. Nobody is trying to make money. Everybody is just trying to heal their children. And we are doing it. And we are all doing it.

It is just absolutely incredible. It is incredible to be a part of. And I am just honored. Very honored to be a part of it.

Summary

A woman describes how her husband experienced symptoms consistent with a heart attack one night. Instead of going to the hospital, she first used herbal remedies (cayenne and lobelia), which she says helped stabilize him, and then followed a 21-day protocol using MMS and DMSO. She reports that during this period he had some difficult reactions but gradually improved, with increased energy, weight loss, and the disappearance of a long-term cough. She believes the protocol cleared his arteries and avoided the need for medical procedures such as surgery.

Testimonial:

Well, I’m here with Lini, and she has a testimony she’s going to share with us.

Lini, take it.

Okay, so my hubby in January of this year had, we call it, we call it a heart event, because we never took him to the hospital or anything else.

He came up at 11 o’clock at night, and he just touched me. I was asleep, and he touched me, and I just, for whatever reason, maybe mother, whatever, I just woke up. He had crawled up. It started like at nine o’clock.

He had all the signs of a heart attack. He was totally grey. He had all the pain in his left side, and he felt nauseous. He said, “I think that there’s something really going on.”

I just looked at him and I said, “Sit right here,” and I just ran downstairs and I got cayenne and lobelia. I’m an herbalist, and so I knew those two things were going to dilate the blood vessels and relax him and everything else, and get the circulation going.

Well, it just opens up, gets the blood vessels going. It stops the heart attack, like in its tracks. So that was my first thing.

Then I said, once that just took like a minute, maybe max of five, you never know when you’re in that situation, but I saw the color come back into his face and everything. Then he was feeling better, but it was still happening.

So I said, “We have two choices. I can do Jim Humble’s 21 day protocol for the heart attack, or we can take you to the hospital.”

And he’s like, “No system for me. Let’s do the protocol,” which is MMS and DMSO.

So we did that. It’s intense. It’s like tablespoons of DMSO and six drops of MMS.

He went through that 21 day protocol, and it wasn’t so easy because he did have some detox reactions. For two of those days he was on the couch, and one of the days he was throwing up, but we refused to stop because we couldn’t. He was feeling better.

That was the really cool thing, and then he just continued. I think it just cleaned up his arteries. I mean, it just cleaned him out.

He had so much energy after that. The really cool thing is he was hacking like crazy every single morning for years and years. So whatever was in his lungs just went away, literally went away in those 21 days.

So he was no longer hacking. He had way more energy. He felt good. He lost some weight.

Yeah, it was scary. It’s scary when you take your own health into your own hands, but I tell you, that’s what you have to do. You have to be responsible for your own health.

He probably would have had stents, open heart surgery, and complications of all those things, and then he would be dealing with the complications.

The following testimonial is excerpted from pages 404-405 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.

We are a family that lives in a country where living is not easy at all. The maternal death rates and child deaths are very high, and there is hardly any chance of getting access to special medical treatments and therapies.

Our son started to show signs of autism since he was 2 years 8 months old. He had begun speaking, but at that moment he stopped talking. He started to show no expression with his eyes, to roll around trees, to scream and to tantrum, and to not allow contact with anyone. Little by little he started to be very hyperactive and to have serious sleeping problems. He didn’t want to wake up and he could not go to sleep at night.

The start of my son’s autism went along with colds, severe coughing, and infectious diarrhea. Our son’s teacher had always had excellent reports about our son’s behavior, but since this severe cold with synovitis in his hip, the transformation began.

Since then, the awful diagnosis and the absence of guidance led us to an abyss. Our son presented total absence of self, almost no language, hyperactivity, and many sicknesses. Six months went by in which he met with a real parade of doctors and therapists that gave us bad treatments, bad diagnoses, and almost no information. Our life became a living hell. We went into a state of denial in which we didn’t want to see anything on the Internet regarding autism.

In that time our son had been diagnosed with severe sinusitis, complications with his adenoids, and limitations that he developed because of his hearing capacity.

By the end of the year 2007, I alone broke the pact I had made with my husband and started to search the Internet, and found Yeroline Ruiz’s page where she commented about the biomedical protocol through which she had gained her son back in months. Little by little I tried to convince my husband, who at the beginning was completely reluctant to the possibility, but by December 2007 we made our first order of supplements and chelators (magnetic clay from the United States).

The supplements took forever to get to us, and when they arrived we gave them to our son without any clue or guidance and hardly any diet. The results were horrible. He got worse and worse, and this lasted about 8 months. During this time the therapists gave us a terrible prediction about our son’s future. Our family problems were also getting worse, and the only guide we had was Yeroline and the Curando el Autismo foundation. Thank God we didn’t give up and we passed the hard times.

We eliminated some of the food that is forbidden in the protocol, and we started to use enzymes. Our son started to improve. His health got a lot better, and we stopped visiting traditional doctors, and I decided to take care of his treatment. The process was not easy because there aren’t even the basics for the protocol in my country. From the flour to the milk, everything is really hard to get. Obviously a DAN! doctor or supplements are unthinkable.

However, even if his health had improved, the autism symptoms were still present. The speech therapy did not help and sometimes even made it worse. With a lot of effort we brought Rosa Dominguez (Tomatis Therapist), and we began applying this technique to our son. The economic effort was very big, but the results were worth it. He was more in control of his body. The clearest sign of this was the control of his sphincter that happened almost magically. His language also improved, even if he still didn’t use it socially, but little by little we verified that our son had no sign of retardation compared to other kids his age.

Even with the improvement, the tantrums, frustration, and limitations of his language remained. We decided then to make a new effort and traveled to Panama to the Stem Cells Institute to make a stem cell transplant.

Our debt was huge, and despite the effort our baby showed two contrary signs: a positive one, that was that our boy was completely connected to his environment (he is never outside of the world anymore), and a negative one: he became aggressive. He had never shown aggression, auto-aggression, or violent behavior, but from the moment the anesthesia was applied these began.

Our child started hitting himself when things didn’t go his way, and he bit other people out of frustration. We remained on our path with despair because we could not see the light. We tried hyperbarics for 70 days in a row, equinotherapy, and others.

In 2011 we came across Puerto Rico’s CEA conference, and we found Kerri’s topic and the SCIA topics very interesting. We decided to do the SCIA tests, and we confirmed that our boy also had a virus and an inflammation, even though his immune system didn’t seem very affected. Because of our country’s limitations we couldn’t complete the SCIA tests, but then we had a lead on how to start a new journey. All we needed was a doctor that could apply the SCIA protocol.

But then there was a miraculous day in which we saw Kerri’s talk, and hope grew inside us. We contacted her immediately, and she answered immediately too, with good will and all the indications as to how to give him MMS and how to apply the protocol.

After two weeks we started seeing a change in our son. Eye contact was way better. He speaks fluid sentences and gives structure to his words.

We are now three weeks into the protocol. We can see almost no aggressions and tantrums. We teach him letters and he recognizes them, reads and writes his name (he does it with some difficulty). His receptive language is 100% active. He is very loving, especially with me (his mom). He hugs me and kisses me and tells me he loves me.

We know we still have a lot to go, but I’m certain that we will make it. My son has now borderline autism. His connection with the world is total. We are still thinking about doing all the SCIA tests, but just to find out our child is cured.

The light and hope that Kerri and the MMS have given us does not compare to anything. Thank God! Kerri is a blessing in our lives!