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 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 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 434-435 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 now in our 7th month of using MMS (CD) and in our 4th year of treating B.D., our son, who was diagnosed Autism.

Our first week of MMS (CD) brought on a skill that we had spent years trying to accomplish, overnight potty training. Week 1 of MMS (CD) and B.D. was out of pull-ups and in underwear. We weren’t even close to full dose and already seeing positives. We knew we were on to something big at this point.

One month later, we all witnessed my son blow out his birthday candles and open birthday gifts. Probably the first time he knew this event was a birthday and it was meant for him. As a gift to him, we took a trip to Disneyland. Not only did B.D. walk the entire park at our side, but he never once cried, whined, or objected to anything on the trip. Prior to this, he had to be in a stroller or wagon at all times.

B.D.’s skills continued to flourish over the next few months. We enrolled B.D. in swimming lessons hoping he would feel comfortable without a life jacket on and clinging to an adult. This hope turned into a major accomplishment. B.D. has passed all Beginner levels in swimming and is now on to Intermediate. He is now swimming unassisted in the deep end of the pool!

I used to hold my breath during his sessions hoping he wouldn’t do anything that would scare the other kids in the pool. I still hold my breath, but now I’m at the end of my seat recording him as he’s giving every single bit of effort to learn from his instructor and pass another level!

Just the other day, we went to a birthday party that was held in a warehouse full of screaming kids, loud music, inflatable jumpy houses and slides. This place can over stimulate just about anyone! In the past, my son would vocally stim, cover his ears, run behind the jumpers where the generators are (trying to turn them off) and require me, or his Dad to keep him engaged with the rest of the kids.

Well, not anymore! He blended right in with the rest of the kids! Not a single stim, didn’t cover his ears, stood in lines, listened and followed the rules and instructions, stood in lines and PLAYED with the other kids.

His Dad and I were able to hang out with all the other parents, watching him run and whiz by with all the other kids as if that is how it has always been. Only it hasn’t.

He has come so very far in the past 7 months. We have a 6 year old son who no longer has sound sensitivity, loves to eat whatever is placed in front of him, DRINKS tons of WATER, has manners, shows empathy, is careful and aware of other kids (especially babies and toddlers), making progress academically, and so very affectionate.

B.D. isn’t recovered… YET, but we expect it to happen now more than ever. We have to put our shades on because the end of the tunnel just got closer and brighter!

The following testimonial is excerpted from page 435 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 third child (K) was diagnosed with moderate autism at 21 months of age. K was very ill. He suffered from vomiting and diarrhea mixed with severe constipation for years. At first, we began every intervention we could afford. The first step was removing all gluten, caseine and soy. We saw a decrease in stimming behaviour and an increased ability to learn. We implemented many vitamins and B12 injections, cranio sacral therapy, anti-fungals, HBOT and an even stricter diet removing all artificial colours, flavours, preservatives and most sugar. Our son was making slow but steady gains. ABA therapy continued from when he was two until just this past March (4.5 years). K was seeming much better but despite these gains, was never close to “normal”.

In July of 2012 a friend suggested MMS. I did my research and so it began. In three days K started to sleep through the night. After less than one week at a very low dose, K stopped the constant verbal scripting and obsessive speech- his most evident sign of autism. In that same week he began dressing himself independently. In the coming months, K’s ATEC began dropping steadily. He began to make jokes, initiate social interactions, show empathy, cope with noise and busy places and best of all- understood safety. The risk of him running away was a memory. We could go places and he would stay near us. Teachers and Educational assistants were raving about his progress, unaware of the protocol we had begun. His most significant changes happened after a three months of the Parasite Protocol, using mms, Vermox, rompepiedras, neem and diatomaceous earth. Through enemas, he expelled worms as long as 24 inches to my husband and family doctor’s disbelief. What K expels in his stool now looks normal and ordinary.

His ATEC in July 2012 was 46. Ten months later he has a score of 6.

He is undecipherable within his classroom and amongst his peers. He laughs, plays and acts like any other child his age. His academics are at par with his peers. Our son does not appear to have autism anymore and only a trained eye would suspect that he ever had it to begin with. We thank Kerri Rivera, her Facebook group for all their support and MMS for being the final, and most significant leg in our sons’ journey to recovery.

Maria A., Ontario Canada

The following testimonial is excerpted from pages 436-437 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.

After 7 years of biomedical treatments, numerous therapies, and more doctors than I care to think about, our son, who was diagnosed with autism, could speak a full sentence, was potty trained, and could finally go to the mall and movie theater without screaming and putting his hands over his ears.

Victory??…yes…however, we knew we had so much farther to go. You see, as your child gets older, you realize that he is missing the key things in life that are crucial for independence. Our son had become “stuck” if you will, he was not socially maturing, and still lacked empathy, mature connections with peers, and proper communication with teachers and the other adults in his life. He would still yell when he didn’t win a game, and he did not always react in an age appropriate manner, if something did not go his way.

My research went on as always…searching, searching, searching…we were not getting anywhere with his current doctor, and I knew that we had to change our current plan for treatment.

A good friend of mine called me to tell me about a new product that some of our warrior mom friends were trying. The letters MMS were spoken to me for the first time in March of 2012. My son was 11 years old and I was desperate for help. The first thing I asked was, “How much does it cost?” $25.00…what?? It can’t be! We have spent our life savings, and now I am looking at something that cost less than a night out for dinner?? I decided to check it out!

I emailed Kerri Rivera and told her that I wanted to start the MMS autism protocol, and I’ll never forget her quick response…”YIPEE”, she said, let me know if you have any questions, I am here for you.

I read, studied, and called my friend about twenty times over the next couple of days, and then we began the next chapter in our journey.

About three weeks into the protocol, our son seemed calmer, as well as aware of others on a more mature level…we were excited! Once he was at full dose, we began, baths and enemas, and he continued to improve. Our next move was to try the 72/2 protocol, which is giving MMS every two hours around the clock for 72 hours.

Well, it was as if someone had kicked our sons maturity clock into high gear. We saw HUGE gains!

“Hey mom, I like your dress…you look really nice today”….WHAT??

“I’ll try that new kind of chicken for lunch”…WHAT??

“I feel like I’m beginning a new life”…WHAT??

“It’s OK that I didn’t win the race, I had fun”…WHAT??

I wanted to call the Good Morning America Show and say, LOOK AT WHAT MY SON IS DOING!

He also began to grow and put on weight for the first time in three years! He put on 10 pounds and 2 shoe sizes in about 2 months!

The gains continue to come, and our boy is coming alive…recovering…finally it’s here! My eyes well up with tears as I write these words…the words I have dreamt about for eight long years.

He celebrated his 12th birthday on January 3rd, and has told us that 2013 is going to be the best year of his life…YES…it is!

He is our angel, our fighter, our miracle. Thanks be to God for MMS! We are blessed and forever grateful~

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.

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.