A Long Journey Through Autism

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!