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.

The following testimonial is excerpted from pages 412-414 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.

My wife and I have always been fond of traveling, getting to know different cultures and people, this is why when we had our little one we decided to keep traveling but to adapt to his rhythm.

When he was 9 months old he went on his first international journey. Everything was perfect, he was the happiest baby on the plane, he played with the people in the seats behind us, the stewardess wanted to stay with him to play, all the plane ride went along perfectly.

Something happened between his 15th and 18th month, his smile was gone, we no longer had happiness in our home, only nerves and less language. Maybe the excessive vaccines were destroying his immune system and leaving the door open for parasites to take hold.

When he was 18 months we went on a second trip and it was an absolute nightmare. He wouldn’t stop crying and screaming on the plane, he didn’t want to play with anybody. We spent a few days getting to know this new place while our baby fell further into this abyss in front of our astonished eyes.

Something was wrong, and after an episode of auto aggression we knew that this was not normal. After watching a couple of videos on the Internet we started to understand, and we went to a psychologist who didn’t give us a diagnosis because our son was so young.

Later on we went to a neuro-pediatrician who also used the excuse of our son’s young age to dismiss us, and finally a last doctor who didn’t explain anything either.

Not even our family listened because they thought we were exaggerating. We were left alone and our biggest ally was and still is the Internet.

After the medical failure and their “anti-diagnosis” we took the best and most important decision of our lives, that was not to listen to any of the diagnoses, or to wait another 6 months to be called by the neuro-pediatrician again. We started down this road without an official diagnosis but with all the symptoms and behaviors that define autism.

We started with the casein, gluten and soy free diet with no experience on how to do it and our baby suffered awful withdrawal symptoms. We couldn’t believe what we were seeing, his nervousness and aggression took us to our limits. After a few days on the diet his tantrums went down little by little until he was stable. But we needed something else because everything was out of control; this is when we went back to the Internet.

After three months of false doctors and pseudo medical experts we found Kerri Rivera.

She gave us hope, and filled us with confidence, but most importantly she was clear with us from the beginning. Everything she told us was logical and everything made sense as to why it was done so we trusted her without a moment’s doubt.

He got better and better everyday. Kerri told us how to do the ATEC and what it meant. Our first result was 57 points when he was 2 years old, which was very high for us because of his young age.

We have been doing everything Kerri suggests, improving the diet, and using everything she recommends, and the results have been spectacular, right now he is 2 years and 10 months old, his ATEC is 8 and he is doing great. Our goal is to have him at 0, and I’m certain that once we free his intestines of all the parasites, he will be a strong, healthy and happy boy.

He doesn’t have any behaviors like the ones he had one year ago, now he smiles again, he talks and asks for things, he plays a lot and he is happy.

This was possible thanks to his Godmother Kerri.

Kerri, you have done and given us everything in exchange for nothing, and that is your defining quality as a human being and as a person.

Every day you give hope to all that YES WE CAN defeat Autism and now we have a lot of puzzle pieces to complete our puzzle. We may find a new one soon because there are a lot of people investigating and that makes us feel alive, to fight against the entire circus that has sprung up around this problem.

I would recommend that if anyone is not seeing progress in their children, to come to Kerri, and try everything she says word for word. She has done it all and has the best investigators and doctor on her side. The ones that aren’t intimidated by the absurd laws of the upper echelon, those who only want our children to be sick all their lives so they can sell medicine to us.

We will keep up the fight.

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.

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

The following testimonial is excerpted from pages 432-433 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.

Luca came into our lives July 26, 2010. He was premature, but all my kids were born in week 35, so I was not surprised. He was perfect. I have thousands of videos of him looking into my eyes, smiling, playing with his sisters, following daddy to the door when he was ready to leave for work and saying bye bye. He walked at one, and was a perfect little baby.

It is hard to know exactly when he changed, but I can tell you when I started to get worried and saw him behaving differently. I had a neighbor the same age as my son, and when they got together to play I was surprised at how my neighbor’s son followed simple directions and looked into my eyes every time I called his name. When I had play dates with my friends, all the moms were so relaxed, and while they were talking and kids were playing with toys, I was always chasing Luca and trying to keep him in the same room because he was not interested in toys or playing with other kids.

My first trip to the zoo with my three kids was a disaster. Luca didn’t want to move from the monkeys’ area and had his first meltdown, all over the floor screaming and crying. I remember seeing all the families with kids the same age as my son, and seeing how they understood and paid attention to what their mothers or fathers were saying. For me that was enough to feel for the first time something was not right, and it was not that I was a bad mother. I knew deep in my heart it had nothing to do with discipline.

I enrolled him in a school thinking that would help. The first day when I picked him up the teacher said they needed to move him with the babies because he was not ready for the 2-year-old class. That day I came home just knowing—and despite all my family, friends, husband, and pediatrician thinking I was crazy, we got him evaluated and the rest is history. On November 15th, 2012 it was official and we got the papers. Classic autism. By that time we had read so much, watched hundreds of videos, and searched every day on the internet for interventions, schools, therapy, etc.

I remember I wanted to start ABA the same day that I got the diagnosis, but the waiting list was really long and we would have to wait. So we waited and started an early intervention program in the Kent District. Surprisingly, I think we took the diagnosis really well; we just wanted to help him as soon as possible.

After the first month I stopped asking for a miracle or cure. I even asked all family and friends to do the same. I needed to accept it!!! My miracle was already here. My husband wanted to do the gluten-free diet and I was not even 100% in agreement…why??? He is such a blessing; let our miracle eat whatever he wants!!! I agreed to do the diet anyway, but wasn’t really interested. I just had the feeling my husband was not “getting IT” or accepting autism = our new precious miracle.

Now I can recognize and see clearly I was in total denial too. I was so afraid to let anybody know, even myself, that I didn’t want this for Luca. I tried and tried and tried, but a voice inside of me was not in peace. I spent a lot of time crying and looking for recovery videos on YouTube, imagining Luca being one of them, and was fascinated with those stories.

Then one day I found Kerri Rivera’s conference in Bulgaria. It was a “Godcidence” (like my father always says). I wasn’t looking for MMS. I didn’t know anything about that. I remember I watched the conference 3 times, and I felt butterflies for the first time since I got the diagnosis. It was like that voice was finally quiet and listening to every single word. “I want this.” 

I did my homework and found a lot of negative information about MMS, but I did not care…that voice was so strong that I knew, the same way I knew about Luca being autistic, that this was something I needed to explore. I looked for her on Facebook and to my surprise she answered me in minutes. When I asked her about the testimonies she connected me with some moms with recovered kids, real moms that decided to believe too.

After I saw pictures from before and after and reading about their journeys I felt hope!!! I knew deep in my heart this was the way and the path we should take. So I got my case together and when I was ready I talked to my husband about it.

It was easier than I expected. We wanted so badly to recover our son!!! It was not an easy process but finally after almost 3 months I GOT IT…WE GOT IT…THERE IS NOTHING WRONG TO WANT THIS. That is ALL we want for Luca!!!!

For the first time I recognized my kid’s autism was not a blessing, he was sick; GI problems, extreme constipation, food issues, sensory problems… and that voice (God voice) sounds really clear and loud: I NEED TO HELP MY KID TO RECOVER!!!!!!

On February 18th we started a dietary intervention with all Kerri’s recommendations. The diet that we were doing was full of sugar and carbohydrates, so we started to be really serious about all the food choices. We kept a very detailed food diary and ordered the MMS.

By March 12th when our bottles arrived at our doorstep we were ready to start Kerri Rivera’s Baby Bottle Protocol. March 13th we did our first bottle and that same day I asked Luca to look for a ball in the other room and give it to me—and he did.

It was like he was sleeping soundly, and then he woke up. He was extremely alert and he was looking in a different way. At first I thought I was crazy, but then my husband noticed it too and the changes kept coming. He improved dramatically in all his therapy sessions—his waiting time, sitting at the table, responding to commands, pointing, eye contact—everything improved!

Kerri recommended doing an ATEC when we started back on February 18th, so I did. His score was 64 points. By April 1st he dropped 20 points! He now follows simple directions, plays with his sisters, recognizes them by name, hugs me and says mommy and daddy, has close to 200 words, and every day is a surprise for us.

I’m proud to say my son is on his way to recovery AND HE WILL RECOVER, HE WILL BE RECOVERED!!!!!!!!

I’m loving Kerri Rivera’s protocol. I’m loving my kid dropping 20 points in his ATEC in a month. I’m loving searching his diaper and inspecting his poop finding parasites. I know it seems impossible but I truly get excited (probably some mothers would understand).

I’m loving this side of the picture FULL of hope. HOPE. I don’t think I can leave this road now. I don’t think I want my son to live in his “perfect” world and not in mine.

I’m a fighter and thanks to Kerri I’m a believer…THAT is the blessing right there. HOPE AND FAITH IN GOD IS ALL I HAVE AT THE MOMENT.

Luca is really special, but it’s not the autism that makes him special—autism sucks!!! Overcoming it and all the obstacles he encounters every day, and doing what he is doing now is what makes him the most special kid on the planet.

He always will be special to me no matter what, autism or not. I see it in his eyes now. He is a fighter like me. He is telling me what to do. Recovery is sooooo in the picture!!!!!! I can actually see it!!!!

I’m a HAPPY Mom!!!!!!!!!!!!!!!!!!!!!!!!

—Alma

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!

The following testimonial is excerpted from page 407 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 had first formed stool at 4 drops. It was so inspiring.

Since then somedays we have formed stool, some days we have loose stool but I relate this to detox – I can clearly see his gut healing.

His expressive speech hasn’t changed yet but he obviously understands much, much better and is able to follow complex commands like “come and give me one teaspoon from the drawer” or “go and put this in the dishwasher” or “wait for daddy to get out the baby from the car and then you can lock the door and put on the alarm”.

Things like that, that were unthinkable before. I hope he will go beyond his few words soon and will begin to talk.

Although speech is the thing that interests me most of all, perhaps the most impressive thing that MMS brought to us all of a sudden is the sense of smell – our boy never seemed to feel any smell, good or bad, in his entire life.

He got this sense a week ago. We are thrilled – something is waking up in his brain, perhaps some pathogens in some part of his brain or in his nose or whatever died and now he is able to sense a smell. Things are getting moved.

Thank you Kerri.

The following testimonial is excerpted from pages 425-426 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.

Drum roll….

I have been dying to share…

Been off MMS for a few weeks…AND HOLY SMOKES we are ALLLLL GOOD!!!!!!!!!!!!!!!!!

Summary…

My daughter—PANDAS—MAJOR sleep issues—fluctuate between diarrhea and constipation

Me—Acne—horrible—and nail fungus

ALL GONE. ALL.

NOBODY could EVER, ever, ever tell me why I broke out so much esp. with our squeaky clean diet.

First PP, OMG it was REALLY bad—worst ever—and became cystic—painful— so for SURE worse before better in my case BUT believed in protocol and KEPT GOING.

By month 4, GONE and yet to return

Fungus—gone in month 1, never to return

My daughter:

Well, you know, AMAZING!!!!!

YOU, Kerri, YOU helped me figure out FINALLLLLY after a zillion docs, WHY MY KID could NOT SLEEP! EVER! 7 LONG years… long long—exhausting years—and it was PARASITES NO DOUBT in my mind! Month 1 of PP, literally like a light switch, SLEEPING —falling asleep ON HER OWN—(not with a circus routine to “get her to sleep”) AND staying asleep ALL NIGHT LONG! UNREAL! This is HUGE!

AND bye bye PANDAS (Silver/Aloe nipped it, MMS maintained her gains, BEAUTIFULLY!) SO I do believe in our Silver Aloe protocol for PANDAS, 100% worked for us! AND MMS. Both.

AND since OFF MMS, my daughter is 100% pooping NORMAL—OMG first time in her WHOLE LIFE!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! (on MMS it was still fluctuating…) AND she is eating things she would have NEVER ever touched! EVER! Raw veggies, nuts, trying EVERYTHING I make… unreal… this is HUGE too… the “healthier” you get, your tastes DO change… and one becomes less “picky”

I have learned that SOME probiotics can literally throw a child into a PANDAS rage—and also brought back MY symptoms—literally within 12 hours of consuming. (Like “Regarding Caroline” posted) This clearly happened to us. Mental note: NOT all prob’s are appropriate for everyone. We react to fermented food—so I am going to experiment with no prob’s and with THeralac __ONLY THeralac BTW

Now,

We are back to silver/aloe, daily, as prevention

We will still take DE (prevention)

Vit D3

Trace Mineral Drops

Enemas as needed

AND I am going to go BACK to the herbs for 3 months around full moon “just in case”—

I CANNOT WAIT to meet you in person, THANK YOU, and share our story with EVERYONE that will “hear me”.

Again, my daughter did not have ‘autism’ per se, but autoimmune issues, meaning that, perhaps, her treatment protocol is ‘shorter’ then someone who is “more sick’ etc. if that makes sense.

We also did a boat load of work prior to this. Meaning diet in place, for instance, for 4 years already—so healing began. This was the final layer for us. The frosting on the cake!!!!!

I have 2 brand new bottles of MMS in my cabinet 🙂 AND will ALWAYS have it on stock!

With MUCH LOVE and respect to you Kerri. -Jeni, IL, USA

The following testimonial is excerpted from pages 415-417 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.

Puerto Ordaz, November 4th, 2011

My name is Carolina Moreno and my husband is Rafael Colmenares. We are the lucky parents of a little 6-year-old whose name is Ana Victoria. She came to this world to give us the world’s greatest lesson. Through her we have learned the real value of life, to be steadfast and brave. We learned that it’s our job to fight for our dreams if we want to accomplish them, and above all we’ve learned that God is who holds us up and gives us the strength and tools to move forward.

My journey with Autism began on the 27th of March of 2007. My daughter Ana Victoria was 23 months old. Her initial development was normal, but little by little she stopped talking, she didn’t understand anything, she didn’t miss her parents, she didn’t play with other children or even her toys, she didn’t like to be kissed or hugged. She acted as if she was deaf, but we didn’t know that all this were symptoms of Autism.

It wasn’t until the day that we went to a neurologist in our area that someone told us that this was Autism, an incurable condition, and that our daughter would have it all her life. It was a very hard moment for us. All of our plans to be a happy and healthy family went down in a matter of hours.

As parents we didn’t want to give up. After recovering from the horrible news, we began looking for information on how to help Ana Victoria. In our country of Venezuela there were 4 specialists in Autism and they were all using the gluten and casein free diet, vitamin therapy, as well as expensive tests performed in the United States to check candida and bacteria. Thanks to them I learned how important the diet was to get Ana back from Autism. Without it, recovery would be impossible.

We did some testing through Great Plains Labs, and the results indicated candida, bacteria, inflammation and much more. We started with Ketazol and Flegyl. My daughter was taking up to 400 mg of Ketazol even though she was barely three years old. Now with everything I’ve learned I cannot believe that a physician could prescribe such a high dose to a child who is only 3 years old and weighs only 16 kg. That alone should be punished and criticized.

However, I felt that I wasn’t doing the right thing. Years passed. Ana Victoria was 5 and her comprehension and attention levels were very low. My husband always thought there had to be something else we could do.

One day my dear friend Carolina Garcia talked to me about Kerri Rivera’s blog. She told me that it explained the reason for the supplements and the hours they had to be taken, for example that the antifungals had to be given away from food and the probiotics worked better if they are given at night. After I read her blog and visited her website in July 2010, I called the Clinic Autism02 and Kerri Rivera herself answered me. I explained my daughter’s case, and she asked me to give her an opportunity to help, and if in 2 months we didn’t see anything different with our daughter we could continue doing what we always did.

I told my husband and we agreed to try. I felt a great sense of peace when Kerri told me, “I’m here, and I promise I will walk with you until we recover your daughter.”

In August Ana Victoria was on Kerri’s full protocol and in November God gave me the opportunity to go to Puerto Vallarta, México. An entire month in this city where my daughter received hyperbaric chamber treatments. We started with MMS, plus we got together with Kerri at her home every night with pen and paper. She explained to us step by step how we could heal our children. From that moment a beautiful friendship was born between Kerri and I.

This is when I understood that Autism is caused by a weakness of the immune system and this brings as consequences viruses, bacteria, candida, intestinal and brain inflammation, food allergies and contamination with heavy metals, and that it is necessary to attack every aspect to be able to heal Autism.

On the 23rd of November Ana Victoria started to take MMS, and in 30 days of treatment we noticed the first changes. My daughter’s stools were consistent; there were no food residues or foul smells. When I came back from Vallarta I was full of new knowledge and a lot of MMS bottles. Ana Victoria already had a very well defined protocol, and the best thing was that it wasn’t a long list of supplements, only 7, MMS and Theralac.

Everyone in my family noticed a great change in our daughter: better eye contact, controlled hyperactivity. She started saying her first words with sense and purpose: “I want park please,” “I want food please,” “I want to sleep.” She was doing much better in therapy and at school. Anita had begun her way back to the world she left when she was 1 and a half years old.

When I saw this improvement in my daughter I decided to share my experience with other members of my community. It was there with my dear friend Yamileth Paduani and her husband Alejandro Teran that Fundación Venciendo el Autismo was born.

Mr. Alejandro asked if Kerri could come to Venezuela and talk to parents in a simple way so everyone could understand that Autism is curable. Kerri was delighted to accept the invitation and in only 7 months of work we had 2 conferences and many evaluations. Nowadays there are 700 kids on Kerri’s protocol that is: casein, soy, gluten and sugar free diet, some supplements depending on every child, MMS and Theralac. The results are very positive and there are hundreds of families that have started with their children’s recovery.

Then came the great discovery of the parasite protocol. For me, it was the missing piece in my daughter’s puzzle. The first few months were severe (fever, laughter, hyperactivity) and many worms in her stool. However, after all these worms came out I saw how her mind cleared, and month by month we waited for the full moon to deworm.

Ana Victoria is now improving very quickly. She is a girl that enjoys being with her family, the park, and going out. She goes to school and tells me that she now does her work in silence without crying. When I arrive home she greets me with a smile, runs to me and calls me Mom. She tells me what she wants and what she doesn’t. She can use the computer like an expert. She takes her own shower and dresses herself, she even picks out her clothes. She knows when Christmas is coming and that there will be gifts. Her therapists and her shadow teacher are really happy to see how Anita is progressing day by day.

Yesterday we were all at the table eating lunch and she pointed with her finger: “Papa’s food, Mama’s food and Ana Kikota’s food… yummy… heeheehee.” My husband and I were laughing with excitement and happiness. Some time ago we felt that speech would be nearly impossible for Ana Victoria.

My advice: do not be afraid of MMS… be afraid of Autism; that which is unforgiving and has the power to destroy lives and families if we don’t attack it on time.

We are grateful to God because He has never abandoned us and has always given us the strength and tools to fight and to believe that it is possible to recover our children. We thank God for putting Kerri in our path and we ask God to bless her every day for having such a big and noble heart, she who is always helping others in a selfless way. We also thank Jim Humble and Andres Kalcker for helping us find the missing piece in this great puzzle that is Autism. We can do it!!!

To all of you, many sincere thanks for helping the children in my country. Blessings,

Carolina Moreno
President of Fundación Venciendo el Autismo (The Defeat Autism Foundation)
Venezuela