The following testimonial is excerpted from pages 419-422 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 now 8-year-old daughter was dx with autism at 18 months old. Started GF/ CF diet and started with a DAN! She slowly made progress with speech, had a few words, a few 2 and 3 word sentences, and despite having autism, she was always a happy, calm, sweet little girl. Shortly after her 3rd birthday, she “changed.’ She became more of a Jekyll / Hyde personality, and all progress in speech and improvements in eye contact and sociability started to fade. Seemed like everything we did was just like yo-yoing back and forth between improving, and then crashing yet once again.

Last year at this time, we had just left the doctor we had been taking her to. For years she was on antivirals, antifungals, antibiotics on and off, SSRI’s, Tenex, and when her violent SIB had become so bad the second year into treatment with him, he put her on Abilify. SSRI’s and the Abilify did nothing for her except make her behave worse. Neither did any of the other things he had her on. The first year she was doing pretty good, but possibly because the antivirals were acting as an anti-inflammatory. She always had chronic constipation with loose stools/ diarrhea. Nothing helped that either. We finally left that doctor who yelled at us in his office for 20 min straight, in front of my daughter, because he did not like that I had been challenging him on all of this for the past 6 months. I was no longer going to let him put the blame on us and everyone else… that her ABA and speech therapists didn’t know what they were doing, and telling us she acted out this way because we didn’t know how to give proper time outs or how to correctly give “pep talks” at bedtime. I was convinced that she had PANDAS/PANS and/or parasites that were causing her ever increasing SIB, loss of all progress she had made in speech over the past 4 years, and the fact that she had not grown in 4 years…did not gain 1 pound, feet did not grow at all, and she only grew 1/2 inch in height in that 4 year span. We had taken her to a very well respected endocrinologist the previous summer who ran all the tests. Could find nothing wrong as to why she wasn’t growing. But he decided to put her on HGH anyway. Thankfully, we left and decided not to give her the HGH. We also took her to one of the best Ped Psychiatric doctors at UCLA who specialized in autism that summer. He observed her, her SIB happened right there in his office for him to see. He said her SIB is coming from pain, discomfort, something medical going on inside, most likely stemming from her gut. He suggested we get her scoped upper and lower. So we did. The only thing that came up was on the upper endoscopy, and that was that she had esophageal gastritis. So the GI dr gave her Nexium.

All the parasite stool tests we had done over the years had always come back neg except for one at age 3 came back with Giardia. But that was it. So last January, when we had finally left that her doctor of 3 years, her liver AST and ALT were at 130 and 135, her Creatinine (kidneys) were severely elevated at a dangerous level, she now had hypothyroidism, and after testing her cortisol thru blood and saliva we discovered she was barely making any at all. She had dark circles under her eyes, grinding her teeth for 3 years now, and agitated beyond belief ALL the time. Mind you when we started with him 3 years prior, her thyroid, liver, and kidneys were all in normal range. She did have dark circles, many many food allergies, some SIB, but nothing compared what we were dealing with now, or what was to come.

So now, what to do. We took her to a very highly recommended Pediatric GI in Los Angeles who was very nice. Listened to what we had to say. Ran the most sensitive and comprehensive stool analysis. Came back with nothing at all. Then took her to the head of pediatric Infectious Disease at Cedars Sinai. She obviously had her mind made up before she even walked in the door. She saw the word AUTISM on my daughter’s chart, and that was it. I showed her every blood and stool test, explained the not growing at all for 4 years despite all the endocrinology labs said everything related to growth was in normal range, her severe SIB. She said to us…”I know you want to help your child. You want to find something “medical” that has caused her autism so you can fix it. But the truth is, your daughter has autism. You need to accept that, and take her to a pediatric psych dr who can help her with these SIB’s. There are lots of meds that can help her be calmer.” Had she not listened to one damn word I told her!!! All the meds we had tried in the past did nothing, already took her to a psych dr who specialized in autism telling us something internal was wrong. She would not run any blood tests, or any other kind of Infec Disease tests. So with that, my husband, my sister, and I completely dumbfounded started to walk out. The dr then had the nerve to say…”She hasn’t been vaccinated since 18 months (she was 7 here) Let’s get her caught up right now before you go. I can give her 6 vaccines today.” I looked at her and said you have got to be crazy! I am not giving my very sick child vaccines full of the poisons that did this to her.”

So a month later we started with doctor who “gets it.” Who listens, and treats parents with respect. Values their opinions. And the networking I had been doing for the past 6 months on a few different bio-med autism groups with other moms was paying off. The moms are the ones who KNOW!!! That’s how I found my daughter’s current doctor and how I found Dr Maile Pouls last June to help her with nutritional and metabolic healing. Dr Pouls ran a $100, 24 hour collection urine analysis, and we found out she had severe malabsorption, Ph was too Alkaline, she was catabolic, extremely electrolyte and mineral deficient, severely Vit C and D deficient, and had severe bowel toxicity. Working with Dr Pouls and her new doctor lead them to suspect parasites/worms. I was encouraged to look into mms, but of course I had heard nothing but bad things like it’s bleach. I was very hesitant to try it, but I researched it, and sought out other moms on Facebook who were doing it. The toxins from the parasites had completely taken over her body and brain. She was SIB almost all day, every day by now. It was pure hell. We thought we were going to lose our minds it was so bad. We had stopped taking her anywhere but school and dr’s appointments for the past 2 years because she would just suddenly out of nowhere, for no reason, violently freak out and there was no way to help her calm down. Her doctor said she’s so toxic, and her body is so sick that she can’t detox. That the mms will not only help kill, but will neutralize the toxins and help her calm down. So we started mms, and I could not believe how much calmer, happier, and more present she was in just a week. MMS is literally saving her life, and bringing her back to us. Before starting mms, we did just parasite meds like Alinia and Mebendazole. The parasite meds alone did not help her, even though she was dumping worms, but she was still completely psychotic, and getting more crazy and manic every day. Since starting mms she has dumped hundreds of worms, some 10-12” long, ascaris eggs, TONS and TONS of the shedded skins of the worms, tons of liver flukes, and hundreds of tapeworm segments. We had not done any PP yet. This had all been with MMS only! We actually started Albendazole for treating tapeworm about a month ago and saw immediate improvements with it. It really seems like this is her biggest beast right now to deal with.

These are her labs from before MMS, and after starting MMS:

2/7/2012 – one month after leaving scumbag dr of 3 years

AST = 79 ALT = 108 Creatinine = 1.24 EOS = 11.2 Sed Rate = 9 ~ Started MMS 11/23/2012 ~

12/4/2012

AST = 73 ALT = 64 Creatinine = 1.32

1/15/2013

AST = 61 ALT = 60 Creatinine = 1.30

2/27/2012

AST = 51 ALT = 42 Creatinine = 0.92 EOS = 5.1 Sed rate = 12 Ref Range for AST is [15 – 46] ALT is [3 – 35]

Ref Range for Creatinine (kidney) is [0.60 – 1.20] Shows how well kidneys are working. Anything close to or over the 1.20 is considered to be of serious concern

Ref Range for EOS (eosinophils) is [0.00 – 3.0] * High EOS are always seen with parasites

Ref Range for Sed Rate (marker for inflammation) is [0 – 10]

Her doctor said her Sed Rate is likely high because when killing off pathogens and detoxing, inflammation will go up temporarily.

So I say never give up. Don’t listen to doctors who don’t listen to you. Kerri, thank God you saw those bottles of MMS at the clinic that day and asked what they were. And that you bought some out of curiosity and tried it. And that you selflessly have taken what you’ve learned and experienced, and shared it. Given so much of your time to help others, to help heal and recover their kids. You are truly an amazing person. We finally have the answers to our daughters autism after almost 7 years of numerous doctors and specialists, so many tests, so much money and valuable time wasted… and now we finally have real hope…real results. We know without a doubt she is going to get healthy, which will in turn

give her the happy joyful life back that she once had before she got “autism.” ~

xoxo

Summary:

Sue describes her daughter Natalie’s lifelong health struggles, including mitochondrial disease, repeated infections, hospitalizations, cognitive regression, autism diagnosis, aggressive behavior, immune problems, and seizures.

After years of medical treatments, DAN doctors, special diets, immune globulin therapy, and rotating medications, Sue says she discovered antiparasitic treatment and later the MMS protocol connected with Kerri Rivera. She reports rapid signs of calmness and awareness after the first very small dose, followed by gradual improvements, reduced medications, lower ATEC score, and longer seizure-free periods.

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Transcript:

My name is Sue and my daughter has been very ill all her life, from birth actually.

She started, gosh, she started getting really ill at about two weeks of age. Pneumonia, different things happening to her, many hospitalizations, ear infections, many hospitalizations.

At any rate, we were told to get a muscle biopsy and we learned through that muscle biopsy that she has mitochondrial disease.

So we of course sought out the best doctors that we could seek at that time, that we could find at that time, excuse me. And we employed many, many different medical treatments on my daughter to try to help her feel better.

And part of those treatments were a lot of antibiotics, a lot of antibiotics over the years. And also the mitochondrial specialists at the time were telling us that you really should make sure that every single year you give that girl a flu vaccine and your entire family. Because, you know, she has mitochondrial disease and so she’s going to be more susceptible. She’s, you know, going to want to protect her.

So we did this. And every single flu vaccine that she was given, she ended up in the pediatrician’s office the day two later. And she somehow bounced back, you know, a little bit. But she was always weak, always fragile, always sick.

Ear tubes, always occupational therapy, speech therapy, you know, everything. She started to kind of get a little bit better with a lot of in-home nursing care and my quitting my job and a lot of care.

Somewhere around 2003, and we were getting more help for her. We were really excited. 2003, 2004, like, hey, she’s getting prepared to go into kindergarten, a special needs type of kindergarten, one for mildly cognitively impaired children, but nonetheless, a kindergarten in a general ed setting. And she was happy.

And we gave her another flu shot in 2005.

[Crying]

She regressed so rapidly. She went from being, you know, mildly cognitively impaired, I’m sorry, to severely, multiply impaired classification in the school.

Sorry, I wasn’t prepared for this. Severely multiply impaired. She could no longer be in that mild kindergarten anymore. Mildly impaired kindergarten anymore. She could no longer be integrated with normal children. Not even the least bit.

She had to be moved to an autism classroom. And it was, you know, a classroom of five children and three adults. And she was the worst one in that group of five children. She could not function at all. Barely at all.

So everything fell apart. And this happened, it was September of 2005, she got that flu shot. And she was rapidly degressed. By October, November, December, she had fallen apart within a couple months.

And the school systems take a while to make the adjustments. But by that April of 06, they did make the adjustments to that very heavy, intense need for her supports. And in 06 of April, we got an autism diagnosis.

So we had the medical side and we had the school side of her deterioration.

So of course I sought out the DAN doctors and we went that route for years, very diligently for years. And actually I started the gluten-free diet in 05 because I was already sensing and researching, you know.

And so gluten-free, casein-free diet in late 05 and then 06 became all the DAN supplements folded in and all that, you know. And, you know, there was some improvement initially, but then it just seemed like over the years things weren’t improving. They were getting worse and worse and worse.

07, 08, more aggression, more irritability, not only towards the caregiver myself, attacking kids at school, attacking them, attacking para-educators. My little, at that time, probably roughly 45-pound little infant girl, excuse me, infant girl, was attacking like an animal and could barely stay in school.

We had to switch school systems to try to find even more support for her. So I was really frustrated.

Things degraded even more to the point where she needed immune globulin therapy every four weeks. She’d get an injection of immune globulin into her vein to try to give her some immune support to try to combat these illnesses that kept on reoccurring in her.

And then the DAN doctor at the time, very generous and kind man, he was trying so hard for her, he said, well, let’s try every three weeks now. That still didn’t do it.

So we made another change. We said goodbye to that doctor, thank you for all your efforts. We made another change to the local hospital because we felt that we needed the local hospital support in case things continue to get worse for her.

[Crying] Excuse me.

We got her with an immune specialist and he put her on weekly immune globulin, which is subcutaneous. It’s less invasive. You don’t have to find a vein. You just go under the skin. So then weekly therapies.

Still didn’t do it. She was still attacking. She was still uncomfortable, still not sleeping well. She was not having a quality of life at all that she deserved.

And I was on Facebook, not on Facebook, on email, a Yahoo group, a support group of moms that I try to research like all autism moms do. And this one gal was talking about the moon.

She seems like she’s lost it. I mean, I thought I had already lost it. And she’s talking about the moon. Okay, whatever. And I’d see her emails periodically.

And one time, there was this one evening that Natalie had such a bad evening of weird crying, weird crying in a way that we had never heard before. Almost like a possessed kind of cry before bed.

And I looked at her dad, my husband, I said, this is weird. Something’s weird. And that email I had just read, again, the earlier in the day, I ran down to my computer at that very moment. And I went to Farmer’s Almanac.

And it’s full moon. It’s full moon. And that’s that crazy, crazy laughter. And it’s full moon. I knew that that crazy lady, that crazy mom wasn’t so crazy.

So then I knew what I was dealing with, at least to some degree. And I contacted her doctor. And I was emphatic.

Her pediatrician, I said, we need to, we need to give her an antiparasitic. This is what I think is going on based on all the research I had done. Give her an antiparasitic medication.

Things started to improve. Reports home from school. Natalie did this or Natalie did that where she hadn’t been doing things before. She hadn’t had behavior of hitting or pulling someone’s hair or biting or pinching or kicking. Oh, I could name the behaviors.

So we were onto something. I was really pleased. And we kept on with these antiparasitic meds. We’d rotate very various ones.

I was lucky enough to have found a doctor who was willing to see my passion and trust me. And I told that doctor, I will bring her in for as much blood work as you want me to bring her in. You have to do this for me.

And so there was a relationship where he allowed me to rotate various antiparasitic and sure enough, she improved.

But there was still some strain there. And I couldn’t figure it out what it was. Why? Why it was still going on?

Well, of course, she was still on antifungals daily, antibiotics daily, antivirals daily, and now an antiparasitic daily, rotating whatnot. So she had very complicated medical life.

And I ran into a friend of mine at Costco, an acquaintance who also had a special needs child with autism. And we were just chit-chatting back and forth over the Costco shelves.

And I told her, I said, no, we’ve been doing some antiparasitic on Natalie and they seem like they’re helping. I said, but I was expressing to her, you know, that some kind of strain is still there. I can’t.

And this friend of mine explained, she said, you know, maybe they’re having a hard time coming out. I didn’t really know what that meant. Because I hadn’t had that much time to research coming out.

She goes, you know, coming out, coming out of, you know, in the poop.

So I said, well, she goes, you know, there’s this, this, this woman who I’ve connected with Sue on the computer and she’s from Mexico.

I’m like, I said, I think, I think I know who you’re talking about. I said that to my friend, because I had just again been on Google and I was looking for mineral water, because I felt like, well, maybe this missing piece is maybe Nellie’s not getting enough minerals supplementation.

You know, you’re on the gluten-free diet. You don’t know. You want to make sure that she’s safe.

And I had Google mineral water and up pop Andreas Kalcker video. And I watched these videos. One, this was, this would have been November of 2011.

And I watched these videos around Thanksgiving and I saw this Andreas Kalcker talking and talking. And everything he was saying was making sense to me somehow, even though I didn’t understand the science. It was making logical sense to me, but I didn’t know, can I put, employ that, that technique, that product on someone so sick as this little girl, so sick? I didn’t know.

And I had actually again Googled again on a different evening, sometime around November or early December timeframe of 2011. Mineral water, because I thought, I want to look into that a little bit And Kerri Rivera popped up.

And she was, she had a tropical background. It was a nice, she was pouring and mixing and showing, displaying how to mix this product that Andreas was talking about. I didn’t know that they knew each other necessarily at this point, because I was still learning.

But when my friend at Costco said to me, hey, I know this woman. I said, is she, she has this beautiful face and she’s smiling like this in her video. She goes, yeah.

I said, and she said, Kerri Rivera. I said, yes, that’s who I was talking to, or who I saw in the video.

Anyways, within a week, that friend at Costco got me connected with another friend who had some spare MMS. And I went over to her house and she showed me how to mix the first drops.

And it was July 9th of 2012. And I’ll never forget it, because I’m sorry.

One eighth of a drop. One eighth. She took that afternoon at my friend’s house and we came home.

And I was in the kitchen getting ready to prepare dinner. And Nellie was watching me. She was watching me. Sitting there calmly, calmly sitting and observing me.

And I had never, never witnessed that ever in my life from her. And I knew, I knew from that moment, that moment I saw her, I said this, there’s something to this.

And we found a way to help my daughter finally feel better. I knew.

Anyways, the shock of it all, but delight too at the same time. She went and I had her go jump on the neighbor’s trampoline like she always liked to do. And she jumped.

But it was different. I was watching her from the kitchen, you know, and make sure she was safe and netted trampoline, of course. She stopped jumping.

She was looking around and she looked in the neighbor’s house. She looked up at the birds. She looked down at the grass. And it was different. It was different. Ken, this is just one-eighth of a drop.

Normally, on the trampoline, she would just be constantly bouncing, constantly flapping, looking, you know, never ever ability to focus, not one iota. You know, she could never attend to occupational speech therapy very well, hardly at all, because of that too, you know, in her past.

But yeah, so she came in from the trampoline. I said, Natalie, what are you doing out there?

Because I did see her doing a little bit of what is referred to as tick spitting. She has a little, you know, so I did see that she would kind of spit towards the sunlight, but it wasn’t consuming her, which was amazing.

She came, I said, I said, what are you doing out there? She goes, it’s sensory. She said to me about the spitting. It’s sensory.

Sensory. So what this tells me is she, all those years, and I’m talking with occupational therapists or teachers and trying to explain to people that all that spitting thing is a sensory input thing. She needs that, you know, visual stimming and oral stimming. And it’s a sensory thing.

She’s, you know, she was hearing me all those years. And she told me, it’s sensory, mom. Never had she ever said before. Anyways, more confirmation.

So from there, the story continues, of course, that I employed the MMS protocol of Kerri Rivera’s. I took out all the antioxidants from the DAN protocol. It was basically you’re doing a 180 away from DAN to the Kerri protocol and took some time.

This takes time, especially with a fragile one, as fragile as my Natalie. And we started seeing more, more good reports coming from home.

It’s a little rocky because with someone so sick, you have to move very, very slowly up on the drops. I could only go up, you know, I couldn’t go up as fast as some children could go up.

But I was able to go up and, you know, pretty fast and correlate it with the parasitic protocol and adding those also in slowly.

She started July 9th was the first drop and her ATEC was a 79, I believe it was. And she’s still a work in progress. And it is currently, what is it, May 25th of 2013.

But she hasn’t had a full year because it was such a slow ramping up. She has not had that many parasite full protocol rounds yet. But she’s already at about a 40, I think the last measurement was a 46, I believe, ATEC, somewhere around there.

She is off of antifungal med. Again, she used to take it daily. She is off of antibiotics. Again, she used to take them daily and rotate them because they weren’t working.

She is off of antiviral. She is off of low-dose naltrexin, which is an immune modulator type technique …that is employed by the DAN [protocol]. She’s off of that.

She is… her seizures used to happen grand mal tonic-clonic, which is a very dangerous kind of seizure. They used to happen every two and a half to three weeks. Terribly dangerous.

She has had seizure-free days now. Her largest streak of seizure-free days was 105 days. Then she had a seizure, but we know what it was related to. It was related to a stop in an antiparasitic med that was too fast.

But now she is, again, ramping back up. She’s at seizure-free day 69 right now. And she’s going to continue to go. I feel pretty good about that.

We are lowering her seizure med. We have to go very slow. But the dream is that she will be off that seizure med next too. And then the dream after that is that someday maybe she will be off that immunoglobulin therapy, which would be awesome for her.

So she’s a very complicated case. And being 14 years old and highly compromised in many ways, highly infested. Well, whatever.

She takes a lot of time, but she’s getting there. And so we’re really excited and really hopeful now. We’ve never had this before in our life. Never thought we would ever see her feeling better and coming off of all these medications like this.

So that’s my story, and I’m sorry for crying so much.

I started taking MMS drops in 2020 to prevent getting covid or whatever it is. Anyway, at that time I had gout, sciatic nerve pain to the point I couldn’t even cook a meal with that holding on to the drain board to get through the process. I was actually using a walker in the house I live in I almost didn’t buy 4 years earlier because it had a sunken living room and I knew I was going to end up in a wheelchair. Thank goodness a friend was with me that is a construction contractor he told me that I would be able to put a false floor in if I need to use a wheelchair.

I had an MRI done on one of my knees and it came back saying that there was arthritis, a torn and ripped meniscus, a bone spur and I thought that was my good knee. Both of my knees were so swollen that they were square and my feet were swollen as well. When you can’t move because of the pain then you gain weight and I was very overweight.

I took the MMS drops for 3 years straight I did not use any protocol. I just started with like 3 drops and went up to 12 in time and then I went back down to 8. I would activate it put it in a large glass of water and I would just drink it probably within 15 minutes every day. Jim Humble’s book was sold out when I started this. After getting the book, I changed the way I drank it and I would drink it in a 4-Hour period.

Everything I mentioned above has gone away the only exception is if I get up on a ladder I will have sciatic nerve pain. I believe this has cleaned out my body of all kinds of heavy metals, toxins and parasites. I have also lost 74 lb with no dieting. I had a knot from a car wreck on the back of my neck that is almost gone away. I have seen warts and moles disappear I had a knot in my inner thigh from an ingrown hair when I was real young that’s almost completely gone and it was the size of a golf ball. I also think that this dissolved scar tissue if there is such a thing.

One time I got a illness that had my sinuses and lungs all congested. I did one drop of each and put it in a little water and used a nebulizer several times a day for about 5 days and since then my sinuses and lungs have been really clear and it got rid of cough that I had all of the time.

I believe that the heavy metals, toxins and parasites are the main cause of muscle pain and fatigue. Let me tell you why. I bought a 10 speed bike and I rode it 2 1/2 miles a couple of years ago. My legs were shaking so bad by the time I got back that I had to walk the bike 1/10 of a mile to get back home. I didn’t even know if I would be able to walk the next day since I had not rode a bike in over 40 years. The next day not only could I walk but I was not sore at all.

I am 64 years old now and I feel better than I did when I was 35! I have a little 3 acre farm that I take care of honey bees, goats, chickens, sheep and pigs. I have three different garden areas and I manage all of it by myself. I know I’m missing some of the repair that has happened to my body but all I can say is if you have anything wrong with you give this a try because it really is a miracle mineral. Thank you to all that have done the research and put the information out help save people from an agonizing life.

Transcript translated from Spanish:

For the same reason as she did, I want to give my testimony because I am also here now.

I was diagnosed with diabetes about 17 years ago. When they diagnosed me, my blood sugar was 350, which means the diabetes had probably been developing for years already. We started with pills, but after some time my blood sugar reached 500 and they put me on insulin. I have been on insulin for four years, but I could never accept the idea that one day my pancreas simply stopped working. I just could not get it into my head that I had to be diabetic for the rest of my life. No matter how many times they insisted, it never made sense to me.

Two months ago, through the son of a very good friend of mine, I received a video from Andrés. As soon as I heard it, I said to myself, “This is for me.” The next day I ordered the book by Jim Humble without hesitation, and within weeks I was already taking MMS.

Since I’m a bit of a daredevil and I’m tired of so much nonsense, I started quite aggressively. Yes, I had my vomiting and everything that comes with it, but I kept insisting and continuing. About two weeks later I also did a parasite cleanse, and I passed some worms that were really something to see.

After about one month of taking MMS, my blood sugar levels began dropping dramatically. Before that I had to inject 18 or 20 units of insulin in the morning, 18 at midday, and 20 at night. Today I no longer inject insulin at midday. In the mornings I take only 4 units and at night I take 6. I cannot say my illness is completely gone yet, but it has improved tremendously.

Something very important also happened. After about 6 or 7 days of taking MMS, the diabetic gingivitis in my mouth disappeared. After about 8 or 9 days, the numb padded feeling that some diabetics get in their feet also began to change. The first thing that disappeared was the pain, and little by little the numbness faded away. Now I can feel my feet touching the ground again, something I had lost before. Conventional medicine has nothing for that.

So it not only improves diabetes, but it also corrects many of the complications caused by high blood sugar.

I thought it was important to talk about this because if there is a plague in our countries today, it is diabetes. Many people are condemned to live with something that, with proper parasite cleansing and taking a few drops regularly and with discipline, could possibly be solved. We do not necessarily have to be diabetic our entire lives.

There is a huge business built around us — tests, pens, strips, insulin, pills — things meant to keep us dependent for life. And that is all I wanted to say.

The following testimonial is excerpted from page 414 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 husband and I were on the couch having our morning coffee and my son came bolting out of the room and ran up to my husband’s face and said…”Oh Hi Daddy, I’m back!” And then ran back to his room…this is our once in a while “word” little man.

After 3 non-progressive PPs (parasite protocols) the 4th one was a charm. A nightmare, but quite an eliminator… Lots of Worms Gone! And he is slowly coming back…we are seeing it in fact he is even reassuring us that he “is back”.

The previous email was accompanied by an ATEC drop from 95 to 35 in 6 months.

The following testimonial is excerpted from page 436 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 severe autistic boy has been now doing wonderful!!! This protocol has completely changed my life!! He’s been dumping tons of parasites since we started MMS about three months ago we’re now in the second pp…he’s now much calmer more happier!! His ATEC dropped down from 80 to 48 in three months only…that was truly amazing he is now gaining weight, I feel like I’m getting my child back to normal again!! I wish I could tell the whole world how Kerri Rivera has changed thousands of people’s lives!!! God bless u Kerri for all your hard work to help others!!!

Note: There was a note that this is Part 2. We will add Part 1 if we locate it.

Transcript:

Tens and tens of tread marks just like covering my back. It seemed like they were just like running from the MMS like that Tasmanian devil or something, just chasing these mites at like trail marks under my skin of these parasites like darting.

It was insane. It was kind of scary. I was like whoa.

And then an hour later I would do my arm and then my other arm, and then my leg, my behind, my everything. And I was kind of… my back was just the most profound. So I wanted to do my back more often.

So before I got to that part again I actually did my back again just so I could get those guys. And I learned from that mistake because what happened was it kind of burned my skin and I couldn’t sleep on my back. It was insane from doing it too much.

So for three days I did that. My skin was just a mess.

And like what they say after you do this procedure you wait four days, let your skin heal, and then you start the procedure over again. There was no way I was going to do this again because it took more than four days for my skin to heal from as often as I put it on areas too much and too often.

So after the third day of doing this procedure the itching was… I thought that they were gone. However my skin was such a mess I didn’t know what itch was what so I just waited.

But I had a great feeling that the procedure actually worked and it actually did.

And what happened was a week later, probably ten days, my skin was completely healed. And I did a final test where I did that MMS DMSO mixture. I did it on my back again and there was no tread marks. They were just gone.

And this was months ago. So you know I’m just really excited. It was one of the most treacherous moments of my entire life and it was quite embarrassing.

I didn’t want to come public with that. Oh Matt Monarch has scabies and da da da da. I wouldn’t have gone to any festivals or done any events in that case and luckily I got rid of it so I could do those things.

But yeah that was a big thing for me and that’s the big secret.

I do feel that MMS is an awesome product.

Below is the article that I’m going to be putting in my next newsletter.

And MMS is supposed to help a lot of people with different things. It did help me. It’s just going to help you out with your procedure.

But what I recommend is seriously studying it. Typing in MMS with any type of issue that you have.

I feel everything. If this doesn’t work, there’s something else out there that will. You just got to keep looking for it.

That’s what I was doing with these canine scabies. It was one thing after another and finally I found the cure.

I feel extremely lucky that I found a natural way to heal myself.

My last resort would have been, if I was going on with dealing with this for a long period of time, I would have had to go and take chemicals somehow.

I could have simply gotten this taken care of in a minute by putting these antibiotic chemical drugs all over my body.

Now, if I were to do something like that, I would seriously be risking my health because of how sensitive I am as a 100% raw food eater doing this for over a decade.

Something you might want to think about. About sensitivities.

Imagine if you have scabies or human scabies or something like that and you’re really sensitive and you can’t take drugs like this.

It’s just something to think about.

Being 100% raw and this sensitive is not necessarily something to brag about.

So that’s my big secret.

It’s over. It’s gone.

Very excited about that. Life is so good.

This is Matt Monarch with the Raw Food World TV Show and we’ll see you tomorrow.

I am a man in my 50’s and a few months ago I thought I had an ingrown hair on my scrotum. Before long I had a grossly swollen, painful, inflamed scrotum. Within a couple of days my chest erupted into a rash.

Within two days this rash reddened into what looked like a large burn and rapidly moved from my sternum all the way to my elbow, including my armpit. The rash produced a scalded appearance and then erupted into sores. The pain and exhaustion were unrelenting and I could not rest. I was racked with pain and malaise.

Soon an itch started on my calf and there began the third location. I tried every topical essential oil that could be beneficial and was losing ground, so I went to my physician. He started me on antibiotics and ordered lab tests.

I went to the lab, they took scrapings and blood samples, and almost three weeks later the state lab reported that I had MRSA staph and an unidentifiable gram-positive bacterial infection that turned out to be strep.

As a side note, I had also been unable to breathe through my nose for many months. It was so occluded that I had to breathe through my mouth, which created shortness of breath when I ate and caused severe sleep apnea. I was already in a state of exhaustion before the infections set in.

I had been fighting a long-term battle with mycoplasmas and would take doxycycline for that, which is the only drug that would keep it in check. I was also plagued with prostate problems and had the resulting urination difficulties.

My doctor prescribed sulfa, cyclines and cillins to be staggered to hit the staph and the strep. Topically I used colloidal silver, essential oils including oregano, tea tree, lavender and chaparral, fresh aloe vera, hydrogen peroxide, goldenseal, slippery elm and lidocaine for the surface pain. Internally I used probiotics, olive leaf, goldenseal, aloe vera juice, digestive enzymes, amino acids, vitamin B’s and other supplements, along with pain medication.

Although I was holding my own, I was not returning to good health. I was becoming depleted, sleepless and fatigued, had chills and what felt like fever. I had to continue to work. The infection seemed to go away, although now I know it was only in remission.

During this remission time I had a muscle spasm in my other leg that caused me to fall, injuring my muscles, ligaments and tendons. The infection invaded the damaged tissue and became another site of infection and I had another 8-9 weeks of severe illness.

Later the outbreak returned on my face, primarily my nose. The second site was chest and armpit and the injured leg became painfully swollen again.

I enlisted the assistance of the QX system of bio-radionics. There was an identification of mycoplasma pneumoniae, MRSA staph and Group A strep erysipelas.

At this time two friends brought MMS to my attention. A friend brought me a bottle and the book. Thoroughly understanding the chemistry, I started taking it immediately. Since I was so seriously ill I did not start gently.

I started with 12-15 drops three times a day.

Results:

Reduction of swelling of the prostate and increased urine flow without pain. Sludge-like material passed in urine.

Complete clearing of nasal and sinus congestion that had plagued me for months. Puffiness in my face around my eyes went away.

Sharp stomach pains and nausea occurred. Despite warnings in the book I did not reduce the drops. I began vomiting on day three. On the third day of vomiting I passed what I believed to be a parasitic infection which took three more days to pass entirely.

The treatment stabilized the sores and swelling and prevented the advancement of the infection.

Edema and inflammation in extremities cleared, including severe leg and back spasms.

I was able to reduce pain medication due to the reduction in inflammation.

The whites of my eyes became extremely white and my vision somewhat improved.

My skin healed and re-formed. The new skin on my nose and face was smooth and healthy.

Inflammation throughout my body reduced significantly and my swollen calf returned to normal by day three.

I stopped taking MMS after two weeks as I was feeling so well. The following week after a minor injury to my thigh the infection appeared again, this time localized to my thigh.

I resumed MMS at 6-10 drops once every 24 hours and gradually increased the frequency to twice per day.

I believe MMS has been helping my immune system tremendously. Although another outbreak occurred, it remained localized instead of spreading as before.

I am recovering and very grateful to Jim Humble and the work he has done.

Rick