Most Recent Testimonials

The following testimonial is excerpted from page 399 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.

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My son is getting tiny bit more normal every day!!! I could kiss you!!!!!

The following testimonial is excerpted from page 403 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.

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Juan Eduardo is 9 years old and he was diagnosed with Autism at age 2.

It has been a long road in which we have tried everything. Seven years after trying and failing, in April of this wonderful 2011 we started in the right way. MMS came to our lives.

Juan Eduardo was a self-centered boy and with a lot of fixations to objects. His improvement in school has been slow, but in 5 months he has improved what he improved in 5 years.

MMS in our lives has been wonderful. Despite the hyperactivity and lack of sleep at the beginning of the protocol, the life of Juan Eduardo and our lives have changed drastically in a very positive way.

He will start regular school at the beginning of next year. He is a happy boy. He sleeps all night. He talks a lot more, even if there is a long way to go. His quality of life is so much better.

He shares with whoever is around him. A lot of times he surprises us with his qualities. He has adapted to the MMS in a great way.

We took the panel viral test and the results were amazing. There was no virus.

When I saw the great positive effects the MMS has made, I started to do protocol 1000 for maintenance with 100% success.

Last year I suffered from several episodes of flu in which I had to take antibiotics, but this year I feel excellent. Thank God and Kerri and MMS I haven’t been ill.

I thank God and Kerri for putting you in our lives. I’m sure he has given back everything you selflessly have done for everybody. The smiles and looks in our children’s eyes are priceless.

Thank you Kerri and Jim Humble. A big hug.

Background:

Endothelial herpes can significantly impair vision, often necessitating corneal transplant surgery. This case illustrates the effective use of Chlorine Dioxide Solution (CDS) in treating such a condition.

Patient Presentation:

A patient with endothelial herpes presented with visual acuity of 20/400. Following evaluation, the decision was made to apply CDS in the anterior chamber, accompanied by an air bubble to enhance the dispersion and efficacy of the treatment.

Intervention:

CDS was administered intraoperatively, utilizing a technique that involved positioning an air bubble within the anterior chamber. This method aimed to maximize the antiseptic effect of CDS while also leveraging its electromolecular charge properties.

Outcome:

Post-treatment assessment revealed a remarkable reversal of the condition, achieving visual acuity of 20/20. The patient did not require corneal transplant surgery, and there were no adverse effects noted throughout the treatment process.

Discussion:

This case highlights the promising role of CDS in ophthalmology as a novel therapeutic option for endothelial herpes. The combination of its antiseptic properties and innovative electromolecular charge enhancement presents a significant advancement in treatment modalities for ocular conditions.

Conclusion:

The application of CDS in this case led to excellent visual recovery without complications, suggesting its potential as an effective alternative to surgical intervention in similar cases. Further studies are warranted to establish its efficacy and safety profile across a broader patient population.

The following testimonial is excerpted from page 406 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.

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Since I was a baby I was a very sick child.

I remember I had many gastrointestinal problems, I made my mom’s life miserable with all the diarrhea and vomiting. I couldn’t gain weight and I had no appetite.

All this accompanied me for many years. The diarrhea became chronic constipation, fluid retention and dry skin.

All of this without knowing I had a serious problem, until I gave birth to my first child.

The constipation was a nightmare. My baby got ill. When I fed him breast milk he would get a rash, and then he had convulsions for about 20 seconds.

When I fed him again the same would happen but now the convulsions lasted for nearly a day. The doctors didn’t know what was going on either.

In one of my researches I ran into a page that talked about Autism and Candida being one of the main causes. This is when I find out that my son had chronic candidiasis and that he got it from me when I breast fed him.

I tested my child and myself and we both had Candida, and I have had it since I was a baby.

One day I heard about the existence of a woman named Kerri Rivera who is devoted to helping children with Autism and I contacted her and she gave me all the help to treat my child. I will be forever grateful.

She talked to me about the MMS and how to give it to my son. I also started taking it and in a matter of days I had a white layer in my tongue, it was the Candida getting out.

I have gained my energy back. The headache I had in the mornings is gone. I feel vivid and almost all the Candida is gone.

I’ve been with MMS for a month and I’ve never felt so satisfied with a treatment.

This simple and yet powerful remedy has given my health and family back and with this I can assure, by my own experience that MMS works.

Summary

A retired teacher from Thailand gives an update after a previous 2013 video about using MMS. He says he stopped taking MMS for about two years after feeling better, but later discovered that his melanoma had returned with serious tumors, severe anemia, weight loss, abdominal swelling, and extreme fatigue.

He describes undergoing hernia surgery, later getting a CT scan, discovering a large tumor in his lower intestine plus additional tumors, and then having major surgery to remove the large tumor and part of his intestine. After recovering, he says he resumed MMS and MMS2, later feeling stronger, exercising again, and seeing tumor shrinkage on a follow-up CT scan.

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Transcript

Hello, everybody.

This is another update on my last one. I did another video in, I think it was March of 2013. I’m that teacher from Thailand. I’m no longer a teacher. I’m retired.

But in the interim, I got another… I had another problem with cancer.

I did… last time that you heard from me, I was steadily doing MMS. And because my health got better, and because I had no known symptoms from my tumors, I stopped doing it for about… I did it until about 2014 and I stopped. And I didn’t do it for about two years.

So we’re looking now at the beginning, middle of January… beginning of the year in 2000, middle of the… towards the middle of the year of 2016. Right now it’s 2018. So we’re talking about a year ago, basically. A little more than a year ago.

Anyway, I’m just going to give you a quick update what happened. Because it came back. It came back.

And as I said, I wasn’t doing MMS maintenance dose, and I should have been. I realize that now. And I wasn’t looking after my body and listening to the signs of my body and what was going on. So those are my bads. And so I advise anybody to not make that same mistake.

So here’s what happened. About the middle of 2016, I started getting bad heartburns. Heartburn at night. And I tried different things like peppermint leaves. And, you know, a doctor would give me some antacid stuff. And nothing really worked. I was just still getting them at night.

So I didn’t know what to do. And it wasn’t severe enough where I really wanted to delve in it deeper. I was just looking for like little band-aids. So that went on for about two months.

And in that two months time, so we’re talking maybe around August of 2016, I coughed one time when I had this kind of gas in my stomach from this, you know, heartburn. And I had a severe pain around my groin area. And it turns out that I had a hernia. That cough, which was very painful, caused a hernia.

I didn’t know about any of this at the time. So I went to see a doctor. He looked at me. Boom, he knew right away what it was. So he rushed me in. And they did a blood test. And they said, Oh, well, you’re pretty anemic as well. You’re very low anemia. I said, Well, I don’t know why that is.

So anyway, so he did the operation and successfully they got that hernia taken care of. Now I don’t know if you know this, but hernia is a kind of a painful operation. It takes a while to recover. And consequently, it took me a while to recover.

Now, during this time, I was having it was getting was causing me more tiredness. I was sleeping more during the day. And I thought that was a consequence of the hernia operation.

And I went back to the doctor and he said, Well, you should be getting feeling better by now. So anyway, this is about October now. And I wasn’t feeling any better. And I was still getting gas in my stomach, which was unrelated to the hernia, obviously.

So I went to the anemia lady. She did another anemia test and I had about one third a normal reading I should have for a normal anemia, right? So I was very deficient in red blood cells.

So she suggested that I go and I get I think it’s called colonoscopy, where they stick the tube down there and they take a look at your intestine. I’m not sure what it’s called, but it’s that it’s where they stick the little video camera down in your intestine and make sure there’s nothing wrong with you.

Because a lot of people that have anemia, very high anemia like I had, it turns out it’s a ulcer or something like that in their intestine. And that’s what they’re checking for. They didn’t find anything clean as a whistle.

So back to stage one. So I go and I just for the next month, I keep doing what I’m doing and it keeps getting worse. And then what happens is I start to get this big swelling in my stomach, like a like a beer gut. I’m not a big beer drinker.

And I went to the doctor again, the anemia lady, same lady. And she said, Oh, well, right away, she says, Have you ever had cancer before? I say, Yeah, I had I had cancer. She goes, I think you might have your cancer. I go, Well, I don’t have any other symptoms.

She goes, Well, let’s just check it out. Because, you know, now that I know you have cancer, I think the two are related. Sure enough, she goes in there and has me do a CT scan.

And I do the CT scan. And it’s bad. It turns out that I had a grapefruit size tumor in my lower intestine, which you can see very easily in the CT. And I had a bunch of look like the hanging gardens of Babylon. You know, all the little trees and stuff.

They were like grape size. They were probably about eight or nine, maybe 10 grape size tumors. And they were still kind of small. But there were a lot of them. And I had another tumor.

So once inside my intestine, and I had another one on a vein that was probably about this big.

Now that when I found out about this, I knew that the really big tumor, which is about six, six centimeters at the time, I knew that needed to come out. Okay, I knew it needed to come out.

Now, you’d ask, why not just take MMS and try and get that tumor down? Well, as this tumor was growing, it was starting to grow at a very rapid rate. I was losing at the time that I had this CT scan done. I was losing about a pound a day.

So I went from virtually maybe 180 pounds down to 130 pounds in about a month, maybe, maybe a little longer, right? But I was losing weight at a rapid rate.

And I was also getting all that fluid, like I said, where they pumped out three liters of fluid from my chest, which is giving me the beer gut, three liters of fluid with that lady. So I knew I had some serious problems.

Now apparently that was, she suggested that was a complication from the big tumor. I don’t know. That’s what she said. And I believe it. So anyway, I was in pretty bad shape.

Another side effect, and everybody should be aware of their body, is that I was really tired. Now I was also tired from the anemia, because that’s what anemia is basically, but I was really tired all the time. And that was from the tumor. So really the anemia was caused from the tumor. That’s what I think.

So anyway, so then I thought, well, talk to my wife, and we had to go see a doctor about a surgeon. It turns out that this lady’s husband was an oncologist, and she wanted to have him look at me. But I said, not not having any of that.

Because as I’ve said on my last video, I don’t believe in doing the whole chemo nor radiation. I think they’re a waste of time. But everyone’s got their own opinion, but I wasn’t gonna do it.

So anyway, so I went to see some doctors, and I was blown away because they wouldn’t respond well. They said, oh, no, your anemia level is way too low. We don’t want to do this.

So I got knocked back about two or three times from people just saying, no, your tumor is too big. Your anemia is too bad. We’re not going to operate because we think you’re going to die on the table.

At the meantime, this this oncologist is trying to contact me and say, well, come see me and I will I will help out with the pain. So they’d written me off, basically.

So I couldn’t find a doctor to operate on me. Finally, we went to a local hospital here, and we had some good hospitals, and it was a good local hospital. I found a guy really good doctor who said, yeah, I’ll operate on you.

OK, that’s great. So he saw my CT scans. He knew what he was getting into. And he was OK. He was game.

So OK, let’s go. So this is about November, I guess, maybe early December. And we’re getting all set. And it turns out that he’s got a week conference. So that pushed everything back a week. And this tumor is getting bigger.

I can feel it because my stomach’s getting more extended. And I know it’s getting bigger. And it was big to start with. Like I said, it was the size of a grapefruit to start with.

So my energy level was nil. I was on the ground. I couldn’t because I lost so much weight. I couldn’t really sit in a chair because my my backbone would would hurt so much because I was sitting on my ass bone. Right.

And when you lose all this weight, it you’re right on your spine and you can’t really sit for long. So I had to lie down. So consequently, I was lying down every every 20 minutes, every half hour, basically falling asleep because my energy level was flat.

So I knew at the time I had maybe two or three weeks to live. I’m positive. That’s my gut level. I’m really sure that that’s what would happen. Now, this was confirmed after the operation, but that I’ll get to that.

So anyway, we get we’re at the hospital. We’re getting everything set up. I’m going to be going into the operating room in 20 minutes. And, you know, when you’re getting ready to go on operation and it’s a life threatening operation, you kind of get psyched out.

And I didn’t know whether that’s going to die on the table or not. You know, I was really kind of upset about it. But what can you do?

And then so I psyched myself up. I’m getting ready for this operation. The doctor comes in and he says, we can’t do the operation.

I said, what do you mean you can’t do the operation? He says, well, the anesthesia, anesthesia, whatever the person does, the noxia out anesthesia, I think it’s called.

She has decided that you’re too. It’s too risky. She’s the only one. She’s not going to do it. Not until we can bring up my iron levels.

So anyway, then I had to go and get some pints of blood. So she stuck three pints of blood in me and it brought the levels up a little bit. But anyway, I guess not enough for the anesthesiologist.

So anyway, I said, listen, I’m either going to die on the table or I’m going to die from this tumor because I just knew in my gut. Literally in my gut.

So anyway, so like I said, it was in the lower part of my abdomen and in the intestine. So anyway, finally had to sign a lot of papers and and they said, OK, you’re cleared.

So they rushed me up to the operating room and they did a really long operation and they pulled what looks like just a massive blood and fat out of my intestine and they cut out a foot.

So I lost if I I’m operating on a foot less intestine than most of you, which doesn’t really have an effect. I guess maybe I got to eat more, a little more food to get the nutrients. I don’t know. But it’s to me, I don’t really notice any effect.

So I have a little bit less intestine. So it was a major operation.

I went through eight pints of blood during the operation and I woke up in ICU with a bunch of tubes down my throat breathing for me. You know, the ventilators, which was the worst experience I’ve ever had in my life, actually.

But after about two hours in ICU, I could breathe. They let me breathe again on my own. I got a big scar from where they pulled the tumor out.

And then after six days, I came home from the hospital. OK, after I could prove to them that I could walk for, you know, 20 feet or whatever.

So anyway, I came home and that was a huge bonus. And I went straight into the MMS, straight into it because I knew that’s what allowed the tumor to build over those two years. Maybe I have a bad DNA. I’m not sure what it is, but I got it again.

OK, and I knew I put all my faith in MMS because I didn’t know anything else. I knew chemo wasn’t going to work. I knew radiation wasn’t going to work. I knew I wouldn’t be here now. And I said it’s just all or nothing.

So I’ve been just in this past week was the year anniversary of basically doing MMS that whole time. And I do my protocol right now is probably I do eight drops at a time, maybe six, seven times a day.

So I’m getting in maybe eight sixes or what? 48. Yeah, maybe 50 drops per day of MMS. I’m doing MMS2 as well. OK, the calcium hypochlorite, I think that’s called. I’m doing that as well.

So that’s my protocol. And I’m doing great. I’m doing great now. OK, like I said, I was very close, but I’m doing fine now. I don’t know. I guess I look healthy. I don’t know my colors back.

I’m riding a stationary bike. I’m doing today. I did 10K. So I do that three times a week. And I’m just eating normal. I haven’t changed my diet at all. I eat pretty well.

I don’t eat a lot of junk food. We eat a lot of rice. That’s probably the worst thing we eat. But I’m feeling good.

I got a little bit of a cold now, which I’m surprised because usually when you do MMS, you don’t get a cold. But I got a little bit of a head cold, but nothing major. A little phlegm, which I’m probably going to do the gas method to get rid of.

But other than that, I feel good. Real good.

So that’s kind of my message. My message to you is don’t let something carry on long enough before you get a CT. Because CT scan, or maybe even a PET scan, pretty much tells it all. They’re pretty good tests.

And I kind of got fooled, like I said early on, because of the hernia operation. And that threw me back. And I thought that’s why I had the anemia, blah, blah, blah.

So that was my screw up. Hopefully you won’t screw up. Just follow your body. If you start to get really tired and things like that, go see somebody that’s going to give a CT exam. Or I don’t know if an MRI would work. I know a PET scan would tell you as well.

I’ve had blood tests at hospitals and I’ve had where it showed negative, no cancer. But it turned out I ended up having a tumor in my lung. That’s from the last story. So I don’t really rely on a blood test.

I think CT scan, they can see it. Now, you probably ask, well, don’t you have those tumors still inside you?

Well, I did a CT exam about four months after my operation. And the doctor looked at it and said, yeah, you’ve maybe lost about 30 percent of your old tumors.

Now, you still have the one on the vein, which was one of the tumors. It was pretty big. That shrunk, once again, about 30 percent.

So they’re not all gone. But they’re definitely a lot better than before.

So do I still have some tumors in my body? Yeah, I probably do. But I don’t think they’re very big. And I might not even have some tumors. I don’t know. I haven’t had a test for a while because I don’t have insurance right now. So it can be expensive due to CT tests.

But I’m judging by my health. Can I pedal a bike at double my heart rate for 30 minutes without any issue? Yeah.

Am I feeling good? Am I eating good? Am I sleeping well? All these positive health effects I’m finding are what I’m experiencing now. So I think I’m pretty good.

I’ll get a test in a while. I was going to do it for a year, you know, after a year of being on MMS. But I just haven’t gotten around to it because honestly, even if I don’t have any tumors in there, I’m going to keep doing MMS because I’m scared.

I’m scared that the cancer is going to come back. This was the third time I had this cancer. Melanoma. And I’m scared it’s going to come back.

So I don’t really care. I’m just going to keep doing MMS no matter what. So it really doesn’t matter if I do another test and I have little tumors in there. I’m not going to change what I’m doing. I’m going to keep doing MMS.

Now, the only other thing I would suggest that I would do, at least from my research, is if I could ever get a hold of it, I’d probably do some cannabis oil too. But that’s another subject.

If you’re going to do MMS, don’t make the mistake of stopping completely. That’s what I did. I thought I was over it. Obviously, I wasn’t.

And I think once a day, three drops or something like that, or maybe it’s three times a week. I’m not sure what exactly the protocol is.

You know, I wish I had did that because I think probably it wouldn’t have gotten a handle on me again, this cancer. But it did. I had those experiences. They’re not good experiences. But I survived it. And here I am.

So, just as an aside, what I do is I do the eight drops. I hold my nose. I drink it. And then I still am holding my nose. I drink just a little bit of chocolate milk.

And I find that if I swirl that chocolate milk in my mouth, it completely gets rid of the taste.

Now, you might ask, well, what are you using? Are you using citric acid? Are you using hydrochloric acid? I’m using the 4% hydrochloric acid.

So, yeah, there is still some taste when you do that protocol. But I find that the chocolate milk is just amazing the way it gets rid of the taste. And I haven’t had any real issues on that front. Not at all.

The general feeling I wanted them to get out of that is that, check your body. I didn’t do that. I mistakenly thought it was from my anemia and my tiredness. It was from my operation. That’s where I screwed up, from my hernia operation.

I wasn’t listening to my body. I didn’t get a checkup. I just assumed. And you know what happens when you assume stuff, okay?

Am I still sold on MMS? Absolutely. Am I going to keep doing it probably until the rest of my life? I’m 59 years old now.

When I have good experiences through doing MMS, which I’ve had lots of, I want to share these with other people. And what I find is that they’re very optimistic when they talk to you.

And they say, oh, well, you know, you cured cancer with it. And I say, yeah. And they say, yeah. You know, how did you do that? Blah, blah, blah. I tell them the whole story. And they’re very psyched.

Now then they go home and they get on the Internet. And then they come across these articles that say, MMS is bleach or MMS is going to kill you and blah, blah, blah. And they end up not taking it for whatever reason.

And that’s fine. That’s their choice. It’s always their choice. But I’ve found if they’re pretty religious about how they take it and they take it in the proper dosage, in the proper timing, we’ve had people from having, you know, stage two diabetes to people that have had all kinds of stuff wrong with them.

And it, you know, headaches. My wife was getting headaches regularly. She did the MMS protocol. Boom, headaches gone.

And there’s been lots of other experiences like this. Someone had really bad… Lady in Perth, Australia had really bad liver failure. And she started doing MMS and her liver test just went through the roof as far as being positive.

So if you do it correctly and if you, you know, you don’t have to be exact, exact. But if you do it close, you know, like every hour to every hour and a half, something like that, you should find good results.

But when they start getting on the Internet and believing everything they read, well, that’s another story because then they just don’t want to know about it.

So ask people to be informed. Don’t believe the first thing they read when they get on the Internet. Have them look at some of the videos and there have been some good ones.

There’s a lot of people. This is a big grassroots project. And there’s a lot of people being helped by this stuff. And, you know, you can’t… there’s just so many ways it’s helping people. I can’t even name a fraction of them.

But try it. Try it.

Because when I… Well, my experience with allopathic medicine is that they want to get you under the knife, radiated and chemoed as quick as possible when they find cancer in you.

And as I said in the last video thing we did, if you do that, that quick, without doing any research, I don’t think you got a lot of chance. I don’t think the odds are good doing the chemo and the radiation.

Just check it out. Other things. Try other things. You usually have a lot more time than you think. They’re going to tell you, the doctors are going to tell you, you got to do this yesterday.

That’s what they’re going to tell you. You got to go upstairs right now and get some chemo in you or radiation or whatever. I mean, it’s like leading cattle to a slaughter. It really is.

And part of my advice is, you usually got a little more time than you think. Research it. Check it out. Try different things. There’s lots of alternatives. MMS is one that I think works well. But you might want to try something else.