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 page 358 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 son with autism is 31 years old. Although he is fully verbal, he had a lot of issues: SIB, aggression, he was not able to sleep.

We have been trying different kinds of protocols since he was 3 years old, unsuccessfully.

I heard about Kerri Rivera and the CD protocol last September. We started right away. We were continuously in touch with Kerri who kept giving us the faith, that even at that old age it is possible to heal and even recover.

In September, when we started CD he had an ATEC of 87, 4 months later we measured 63, and now, after 8 months, he has an ATEC of 28.

There are some SIB’s and aggression left, but it happens only rarely. If we could get rid of it, my son would be recovered.

He became an interested young man, his memory improved. He keeps giving proper answers to my questions, something he never did before.

I can see his real personality now: he became a nice, lovable, open-minded young man from a very sick raging, roaring, screaming, suffering boy.

There are no words to say thank you to Kerri to show us the end of the tunnel.

I think I’m on the best way to recover my 31-year-old son!

Mark, 31, Hungary

The following testimonial is excerpted from page 400 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.

From the ATEC at www.autism.com

Total Score: 5

I. Speech/Language/Communication: 1

II. Sociability: 1

III. Sensory/Cognitive Awareness: 2

IV. Health/Physical/Behavior: 1

Started at 56 score in March.

I’m still having problems in environmental awareness, because in his mind sometimes he is Super-Hero (he wants to help all the people in disasters, his own words). Sometimes he is eating portions like me, not such big portions but he is burning calories in the swimming classes. His meals are so healthy.

So, my homeopathic doctor told me (and recommends me) to wait until January next year to start the PP. He wants to see the effects of MMS, Probiotics and some homeopathy that he will provide at the end of this month.

We continue using as I said MMS, Theralac, GFCFSF diet, NAET and A.B.A therapy. I am so happy to share it with you.

Hugs my dear God Mother

The following testimonial is excerpted from pages 409-410 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.

Our 10 year old son, Ben, showed symptoms of autism since he was an infant. Until he was 6, he never connected normally with family or peers. As his mother, I ached for a hug, to be called “Mommy,” or for a lingering look of love. I never got them.

Until he was diagnosed with autism at age five, I was utterly befuddled. What had I done? What was wrong with Ben? Why didn’t he want to play with other children? Why did he drool endlessly, laugh constantly for no reason, and bolt from play dates and parties with no warning? Why was he constantly lethargic, to the point where we called him “the playdough boy?”

Ben was always happy, dwelling far from us, in his own perfect little heaven. My husband and I were depressed, even despondent, despite attempts at gluten-free, casein-free diets, ABA therapy, and many supplements, because we saw no substantive and lasting changes in our child.

Finally we found the Son-Rise Program, which brought Ben back to us. After three-plus years of a mostly full-time Son-Rise Program, Ben became highly interactive, engaged, and interested in his peers. That alone was a palpable miracle. As we say in Hebrew, Dayeinu! That would have been sufficient. But we constantly experienced regressions back into autistic symptoms. For no apparent reason, and despite endless biomedical interventions, including the DAN! protocol—to the tune, I might add, of tens of thousands of dollars, multiplied over four to five years—Ben would suddenly revert to autistic behaviors, and we would lose contact. He became once again non-responsive, uninterested in family or peers, and seemingly unable to connect. Only the day before, he had been totally connected.

After being on the SCD and GAPS diets, and finding even them ineffective to alleviate these regular and devastating returns to autism, we were advised by Dr. Campbell-McBride that it sounded to her as if Ben had parasites. A friend of mine who was also a Son-Rise mom had mentioned to me that she and another Son-Rise mom friend of ours were trying something called “MMS.” When I heard the words for which the acronym stood, I gave an internal scoff. “Master Mineral Solution? Is this a joke?”

I can tell you, in all seriousness, that now, five and a half months into our MMS autism protocol, MMS is definitely no joke. Since starting MMS, we have seen nothing but progress in Ben. We are still doing GAPS, but avoiding foods we know Ben cannot yet digest. Ben’s ATEC score has dropped from 43 when we started MMS to a startling 20. We are seeing sustained, natural, unsolicited and consistent eye contact, like never before. Ben is consistently responsive, certainly on par with most 10 year old boys. He is playing hockey in our driveway with friends. He is solicitous of others, and compassionate when others are hurt in any way. He is funny, expressively loving, and eager to please and be loved. It makes me cry to write this. I wanted this so badly, and now, with MMS leading the other interventions, I have what I prayed for.

We are not perfect on the MMS. Ben is in his first year of school post-Son-Rise, and dosing during the school day is not easy. But we are tremendously hopeful and excited.

I truly believe, as Kerri Rivera has often said, that parasites are the missing piece of the autism puzzle. Like so many other warrior parents, we have done everything. But everything minus one was not enough for Ben. Now, I think we truly have the tools, and it is only a matter of time, faith, and love, to fully and permanently recover our beloved Ben.

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 422-423 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.

Dear Kerri and the readers,

I would like to say that we started giving MMS to my son Filip, autistic/PDD NOS, when he turned 5 years old, after having tried lots of things (diet, many different supplements, HBOT, some sort of behavioral therapy Teach and ABA), we have seen enormous changes already in the first month.

I had heard about MMS from a mom of an autistic child. I started reading about it, but was not impressed by the comments I read on the internet. I contacted a few mums that I knew from the Son-Rise programme in the US and they have reassured me that it works miracles.

I was however very sceptical of MMS, as I have read so many “negative” comments on the internet. This is why I decided to start it myself for a few months to see what would happen to me. Also, I had to figure out how I was gonna dose MMS 8 – times a day, when I am working 10 hours a day and Filip is going to the kindergarden.

In fact, I was just feeling great when I started using MMS.

I wanted to start with my son when on holiday, but my husband displaced MMS bottles by mistake. I was so mad. I have only found them the last day when we were returning home. I have immediately decided to give one drop to Filip before we started to drive. I need to underline that my husband was very sceptic. Filip would at that time speak, but it would mostly be scripting and rarely would he say things in context. Otherwise he also had other autism symptoms- tantrums, no friends, low muscular tone, no drawing, obsessive occupations ( in Filip’s case watching cartoons and reading books), no sense of danger, wandering out, nose picking, scratching but, toe walk etc. But suddenly Filip started commenting everything in the car, asking questions, observing the things he would see from the car etc. Me and my husband looked at each other and my husband commented “ Maybe it is working after all”.

Filip’s ATEC was 48 at the time we started. At start, my mother-in-law helped out in dosing and we were able to dose 8 times a day. Filip’s ATEC fell to 32 the first month. Unfortunately, my mother-in-law read some horrible stories on the internet and the FDA’s advice was detrimental for her decision to stop dosing Filip, even though she was seeing wonderful results, she was scared and said that she is only believing the official medicine, admitting that the official medicine has nothing to offer our son.

I was very disappointed, but continued to dose as much as I could, however not reaching the recommended 8 times a day. I was therefore only able to dose 4-5 times a day. I started telework on Friday’s in order to at least get 8-10 doses in on Fridays, Saturdays and Sundays and 4-5 doses the rest of the week. My son was great in November (the volunteers working on Son-Rise with Filip were commenting on unprecedented success), but his ATEC only fell to 28, I would say due to low dosing the progress was slower. Filip was having some hard times in January, when he was more hyperactive. At that time we have also introduced the GcMaf injections, which could have added to Filip’s hyperactiveness.

But since two weeks now Filip is back to his shape. He is so communicative, uses unseen vocabulary, amazes us every day, he started drawing without being prompted, communicates with everyone, was invited to a birthday from a girl at the kindergarden, started to dress without prompting, started to tell me: “Common mummy, hurry up, let’s go.” or “Where are you mummy? What are you doing?” or when he occasionally wakes up during the night “Is it day already?” or “I should not go on the street, because a car can hit me” or “Daddy, you are not sad, you look angry” or just yesterday when he draw a picture in the kindergarden he said to his teacher “I want to show it to my mum”. The list goes on and on and every day I have to thank the all mighty for having led me to Kerri and to the MMS protocols. I know we are on the right path to recovery and I am not scared of the future any more. And, finally, i just did his ATEC to check out his ATEC- it is 16!!!!!! LOVE IT! LOVE IT!!!!!!

Kerri, thank you!!!!!!!!!

The following testimonial is excerpted from pages 426-428 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 daughter was born Sept 9 2010 and she had pretty good health until she was 15 months, she was able to say five to ten words by then, she had all her vaccines on time as recommended by our pediatrician, and she was really lovely and happy but suddenly everything started to change slowly.

We noticed she started losing the words she had learned, she used to wave people saying hi, and suddenly she was not interested on waving anymore and she started to isolate herself little by little to the point she stopped being a happy girl, she barely looked at us and we started to worry about it, anyway, I believe the first thought every parent may have think in this very same situation is that her personality is different than other kids and is something temporary.

When she had 18 months we went to the regular doctor check and they asked us to get the opinion of a developmental pediatrician since her social and language skills were behind the expected, and this started the worst nightmare ever.

It seems like every single developmental pediatrician has a waiting list huge enough to have more than a couple months totally scheduled, we called on May and the first available appointment was 4 months later, we called like 4 or 5 of the recommended pediatricians and institutions but it was all the same thing, but we finally got a pediatrician, not from the recommended list, but he made room for us in a couple of weeks and we were able to see him in a couple of weeks.

The diagnosis was mild autism, the recommended treatment was ABA therapy and the follow up was going to be 1 year later since he did not have many expectations of positive changes in the next 6 months, we were devastated by this, my wife was in denial, and I started our journey to recovery the very same day, I started researching and suddenly I found tons of information about autism and people who claimed to have recovered their children from autism.

I sent emails everywhere and I never imagined I would have such a great response from every person I wrote extending me a helping hand on all my doubts with the most sincere and honest recommendations, 2 or 3 days later I found Autismo2.com website and I saw all the videos available.

I bought 3 or 4 books on amazon, I saw many hours of recordings and seminars in Spanish and English, and I was amazed about some kids losing their diagnosis, but also about how they were affected by heavy metals, bacteria, viruses and all sort of things.

At the beginning I thought my daughter could not be sick, she has never had a single cold, how come? but a home heavy metal screen test gave us the first clue, and some lab tests confirmed the very same problems all our kiddos share, mercury levels on the roof, candida, yeast, you name it.

I started the GFCFSF diet the first weekend after her confirmed diagnosis and just one week later we started noticing changes, then I started with baths with bentonite clay, and noticed more improvements, we also started ABA on July, and little by little our daughter started to improve, later on we introduced MMS baths, Quinton water, DE, probiotics, and she improved every day.

I honestly believe that the early diagnosis and prompt reaction from our side played a big role on her fast recovery, It happened that we never canceled the first appointment that was made with the most recommended developmental pediatrician, by then we were looking for a second opinion and a new evaluation due to her huge improvements, we never imagined this pediatrician will say what.

Although my history with this disease or condition has been very short nobody knows how much pain, stress and suffering had caused to our family, we now enjoy our daughter more than ever when we see her playing with her older sister and taking away every single concern we had, we continue keeping an eye on her development but she is doing really well, I wish nothing more than every single mother I have heard on the discussion groups I follow have the very same results we have had with all the guidance from such smart and courageous parents like Kerri Rivera and many others that shed us the light on our darkest night.

I am more than grateful with all of those parents, I would do anything on my reach to help them, we need to help every single kid and family that goes through this disease to recover our kids.

UPDATE:

I’m very happy to forward the last ATEC from my daughter, today we came from her 2 year check up with the new pediatrician and she found her pretty well, she just told us” It’s pretty hard to believe she was diagnosed with mild autism keep doing whatever you are doing, since I would say she is acting like a regular kid for her age.”

I would say that keeping in mind that most of her ATEC score is on the Language section, for a 2 year old and from what we came from she is on her way to full recovery (Previous ATEC was 55, at this writing was a 23)