The Right Autism Supplement For Speech Recovery

A video greeting from Kerri Rivera:

Many of the families I consult with who have children who are either non-verbal, or who speak, but not in the appropriate manner, have reported excellent results with this product.

Speech Problems Common For Autistic Children

Your autistic child does not have to be completely “non-verbal” to benefit from supplements that have shown to augment the development of speaking skills.

Speech problems for autistic children can present in a variety of ways:

– No speech at all

– Stuttering, stammering, grunting

– Limited vocabulary

– Do not speak in full sentences

– Echololia – repeating phrases, scripting

– Odd tonality – too high, nasal, or other “unusual” or “affected” speach

– Sentence construction not as robust as peers’

– Elocution: under- or over-pronouncing certain words or parts of words

– Difficulty gathering thoughts before beginning to speak

Have you noticed your child with autism speaking differently than his peers?

If so, you might want to consider adding Breakthrough Vitamin D with Chondroitin to your daily routine.

Where To Find BreakThrough Vitamin D (with Chondroitin Sulfate) – An Affordable GcMAF Alternative

Breakthrough Vitamin D with Chondroitin is based off of the scientific ideas behind GcMAF (which I recommended in my book (Healing The Symptoms Known As Autism) and RERUM. Both of these are wonderful products, but very expensive. The Breakthrough Vitamin D – Chondroitin Sulfate, is available through my webstore at a fraction of the price.

Try it, and if you like it, buy a case and just use as much as you can afford! It is relatively cheap and excitingly effective.

Big picture, this supplement is believed to activate macrophages which helps support the immune system. Along with the rest of my protocol, it has been very effective when taken with high frequency, for helping improve speech quality.

Click here to learn more.

– Kerri Rivera
Doctor of Homeopathy


None of the products or statements on this website have been evaluated by the US Food and Drug Administration and are not intended to diagnose, treat, cure or prevent any disease or condition. If you suspect you may have a disease or condition, you should consult a licensed healthcare practitioner.

El Suplemento Adecuado Para La Recuperación Del Habla

Un video de saludo de Kerri Rivera:

Muchas de las familias con las que consulto que tienen niños que no son verbales o hablan, pero no de la manera apropiada, han reportado excelentes resultados con este producto.

Problemas del habla comunes para niños autistas

Su hijo no tiene que ser “no verbal” para beneficiarse de los suplementos que han demostrado aumentar el desarrollo de las habilidades para hablar.

Los problemas del habla para niños autistas pueden presentarse de varias maneras:

– No habla en absoluto

– Tartamudeo, tartamudeo, gruñidos.

– vocabulario limitado

– No hablar en oraciones completas

– Tonalidad extraña: demasiado alto, nasal u otro discurso “inusual” o “afectado”

– La construcción de la oración no es tan robusta como la de sus compañeros.

– Elocución: pronunciar en voz alta o baja ciertas palabras o partes de palabras

– Dificultad para reunir pensamientos antes de comenzar a hablar

¿Ha notado que su hijo habla de manera diferente a sus compañeros?

Si es así, es posible que desee considerar agregar este suplemento a su rutina diaria.

Dónde Encontrar Vitamina D Revolucionaria (Con Sulfato De Condroitina): Una Alternativa Asequible A GcMAF

La revolucionaria vitamina D con condroitina se basa en las ideas científicas detrás de GcMAF (que recomendé en mi libro (Sanando Los Síntomas Conocidos Como Autismo) y RERUM. Ambos son productos maravillosos, pero muy caros. La innovadora vitamina D – sulfato de condroitina, está disponible a través de mi tienda web a una fracción del precio.

Pruébalo, y si te gusta, ¡compra un estuche y usa todo lo que puedas! Es relativamente barato y emocionantemente efectivo.

En general, se cree que este suplemento activa los macrófagos que ayudan a apoyar el sistema inmunológico. Junto con el resto de mi protocolo, ha sido muy efectivo cuando se agrega con alta frecuencia, para ayudar a mejorar la calidad del habla.

Pulsa aquí para saber más.

– Kerri Rivera
Doctor of Homeopathy

Descargo de responsabilidad:

Ninguno de los productos o declaraciones en este sitio web ha sido evaluado por la Administración de Drogas y Alimentos de los EE. UU. Y no está destinado a diagnosticar, tratar, curar o prevenir ninguna enfermedad o afección. Si sospecha que puede tener una enfermedad o afección, debe consultar a un profesional de la salud con licencia.

Autism Recovery Update – The GAPS Diet and MMS

Here’s another Autism Recovery Update from Autism Warrior Mom Laurel.

Here autism mom Laurel discusses several important issues that she observed in treating her son, both before and after the Kerri Rivera protocol, which she began to implement in July 2018.

Timeline of Jeremy’s Adult Autism Recovery Journey

1) Jeremey was already experiencing autism symptoms as a child, but they got worse – in that he started experiencing seizures – after the tDap vaccination he receieved as a teenager. He also became extremely aggressive after being vaxxed.

2) The family tried seizure medication under the supervision of a doctor. The doctors kept changing his prescriptions because the medication wasn’t working. The seizures were getting worse and Jeremy would sometimes fall down and hit his head. One of his seizures lasted 22 minutes. It was a miracle he survived. It was a dangerous, untenable situation.

3) In 2009, when Jeremy turned 18, Jeremy went on the GAPS diet and moved into a residential care facility. He was not on any anti-seizure medications at this time, due to lack of efficacy. After starting the GAPS diet, the seizures became less frequent and severe.

4) In 2010-11, the adult-care facility reported he was still having occassional seizures a few times per month. The rate had declined from 20 seizures per week, to 5 per month, approximately.

5) Jeremy left the residential care facility and returned to living with his mother, Laurel, at the end of June 2018.

At that point, when he came home to live with his mother, Jeremy began the MMS protocol. (Kerri refers to this substance by its chemical name, Chlorine Dioxide.)

The Rate Of Seizures Declined Once Jeremy Started Taking CD

Prior to June: 5-6 Seizures per month at in-patient center

July: 4 Seizures

Aug: 3 Seizures

Sept: 1 Seizures

Oct: 1 Seizure

6) Now – one year later – October 2019, Jeremy has not had any additional seizures.

Laurel points out that they saw significant improvement from the change in diet, but that the seizures were not eliminated until the CD protocol that Kerri recommends was implemented.

If you would like to learn more about Laurel and her battle to help her son, please visit her Youtube Channel:

And her GoFundMe Page where she is raising money for legal fees:

Make An Autism Recovery Resolution!

A video greeting from Kerri Rivera:

If you’re on my email list or reading my website and have not yet taken action to implement my autism recovery protocol, I invite you to take part now, and join me in making your own Autism Recovery resolution.

Book a consultation, and let’s get started! I will help you.

How To Book An Autism Recovery Consultation With Kerri Rivera

Let’s get clear on what you need to do if you are ready for an Autism Recovery Consultation.

1) First, everyone begins with an initial consultation where I can get to know you, your child, and his medical history.

You simply pay for the consultation online, and then email me to schedule a time to do our Skype call. I work with people all over the world and speak both English and Spanish.

I do keep these affordable for everyone, as much as possible.

2) Then, as I mentioned in the video, it’s a great idea to have a follow-up consultation in 4-6 months so we can see how everything is going.

I find that at the follow-up, many families need to:

– Adjust servings of supplements

– Add or remove supplements

– Re-motivate themselves to follow certain parts of the protocol

– Celebrate progress!

In addition to just re-motivating you to stay the course, it’s great to have someone (like me) outside the family, who can help you ascertain how much progress the child is making and what areas still need support.

It’s easy to fail to notice all your successes. Some parents gloss over progress as they quickly adapt to the “new normal” and then raise the bar for the child, looking for the next big win.

It’s also easy to “get used to” things that may need improvement. We all have idiosyncracies and sometimes we forget that the “cute thing” that the child does is no longer developmentally appropriate for his age.

Click here to book a follow-up consultation:

I can help you with all of this and create a customized plan for you and your child. Join our growing list of success stories and begin your own autism recovery journey!

– Kerri Rivera
Doctor of Homeopathy


None of the products or statements on this website have been evaluated by the US Food and Drug Administration and are not intended to diagnose, treat, cure or prevent any disease or condition. If you suspect you may have a disease or condition, you should consult a licensed healthcare practitioner.

¡Haga Una Resolución De Recuperación Del Autismo!

Un video de saludo de Kerri Rivera:

Si está en mi lista de correo electrónico o está leyendo mi sitio web y aún no ha tomado medidas para implementar mi protocolo de recuperación del autismo, lo invito a participar ahora y unirse a mí para tomar su propia resolución de recuperación del autismo.

¡Reserve una consulta y comencemos! Te ayudaré.

Cómo reservar una consulta de recuperación del autismo con Kerri Rivera

Aclaremos qué necesita hacer si está listo para una Consulta de recuperación del autismo.

1) Primero, todos comienzan con una consulta inicial donde puedo conocerlo a usted, a su hijo y su historial médico.

Simplemente paga la consulta en línea y luego me envía un correo electrónico para programar una hora para hacer nuestra llamada de Skype. Trabajo con personas de todo el mundo y hablo inglés y español.

Los mantengo al alcance de todos, tanto como sea posible.

2) Luego, como mencioné en el video, es una gran idea tener una consulta de seguimiento en 4-6 meses para que podamos ver cómo va todo.

Encuentro que en el seguimiento, muchas familias necesitan:

– Ajustar porciones de suplementos

– Agregar o quitar suplementos

– Volver a motivarse para seguir ciertas partes del protocolo

– ¡Celebre el progreso!

Además de motivarlo nuevamente para que mantenga el rumbo, es genial tener a alguien (como yo) fuera de la familia, que pueda ayudarlo a determinar cuánto progreso está haciendo el niño y qué áreas aún necesitan apoyo.

Es fácil dejar de notar todos sus éxitos. Algunos padres pasan por alto el progreso a medida que se adaptan rápidamente a la “nueva normalidad” y luego elevan el listón para el niño, en busca de la próxima gran victoria.

También es fácil “acostumbrarse” a cosas que pueden necesitar mejoras. Todos tenemos idiosincrasias y, a veces, olvidamos que lo “lindo” que hace el niño ya no es apropiado para su edad.

Haga clic aquí para reservar una consulta de seguimiento:

Puedo ayudarlo con todo esto y crear un plan personalizado para usted y su hijo. ¡Únase a nuestra creciente lista de historias de éxito y comience su propio viaje de recuperación del autismo!

– Kerri Rivera
Doctor of Homeopathy

Descargo de responsabilidad:

Ninguno de los productos o declaraciones en este sitio web ha sido evaluado por la Administración de Drogas y Alimentos de los EE. UU. Y no está destinado a diagnosticar, tratar, curar o prevenir ninguna enfermedad o afección. Si sospecha que puede tener una enfermedad o afección, debe consultar a un profesional de la salud con licencia.

“When The ATEC’s Dropping – Kids Start Talking!”

Hello friends, just another wonderful testimonial to share with you. This one is from Dane’s mom. She is excited that he has begun speaking!

Many of our parents wonder if their non-verbal children with autism will be able to recover their speech. This is so important because it helps children communicate with family about their moods, desires, and how they are feeling.

Words also help parents feel like they are better able to connect with their children. Speaking is a big sign of progress and a major milestone in any autism family’s recovery story.

Here’s what the mother has to say!

“Just a quick update on my Dane.

“He has started to say several words… such as; red, three, purple, doctor, pickup truck, applesauce, apple tree, kitty cat, Peppa Pig, mom, dad, and WOW.

“LOL I redone his ATEC and we have dropped from 74 to 61. Then from a 61 to 52. 52 was yesterday’s score!

I was able to account for some language now. Yay!”

This is a big win and we are so happy for her and Dane!

Not everyone recovers speech at the same “level” of ATEC score, but if your child is not speaking yet, make sure you schedule a consult with me so we can get him on the right course of action.

Looking forward to hearing from you … and your child!…

– Kerri Rivera

PANS/PANDAS Symptoms Improved When We “Got Serious” About The Protocol

Dearest Kerri,

I am excited to write you that our child’s ATEC is at 18 after eight months on your protocol.

Our child is 12 now, but at the age seven, the ”shadow-syndrome” that had been driving his behavior introduced itself to us in a dramatic way. Our child has PANDAS/ PANS. We could no longer attribute his over-the-top behavior to his age, maturity or gender. What looked like ADD, ADHD, and ODD (oppositional defiant disorder.), selective hearing, and nervousness (mixed with the sweetest and most loving personality a parent could ask for) changed 36 hours after his 7th birthday party. He could no longer hold a pencil without his hand shaking. He could no longer write. (His hand and head were shaking constantly.) He had non-stop motor and vocal tics, separation-anxiety, bed-wetting, night terrors, and everything that PANDAS/ PANS inflicts on a child and family. (The list of symptoms is absolutely endless and sadly, he had ALL of the symptoms.)

We had our church elders pray over us as a family. I believe that THE LORD heard our prayers and gave us an extra measure of strength and tenacity to get through the last five years. He also guided us to you.

After years of “managing” his illness with many alternative options, including (predominately) homeopathy and (later) the Buhner Protocol, some things were better, but his OCD symptoms were getting worse BY THE SECOND. We contacted you after the OCD rituals and compulsions become so bad we could only operate at the most basic level.

We purchased your book in the spring of 2015. We measured his ATEC in the spring of 2015 and forgot about his score as we pursued many rabbit trails. At that time, his score was 34 (28 points were in the behavior category).

After our consult with you, we measured his ATEC again. We were SHOCKED to realize that his ATEC had not dropped AT ALL since we took his score in the spring of 2015. This revelation was SERIOUSLY eye-opening for me. The ATEC score provided concrete proof that despite my best efforts, we were only “treading-water”. Thank God, his score did not get worse. But for all our efforts, we should have seen a full recovery and this was not the case. In fact, his OCD had gotten much worse.

As of September 2019, his ATEC score is 18 and his behavior category has now dropped to a “10”. He still has all of his OCD symptoms, but the intensity is less. Everything else is improving on a daily basis.

He can finally get through a full day of school. He understands verbal instructions and he is getting his confidence back. He has developed three new friendships with other children. He is able to read a book and understand the content. His focus is improving every day.

He enjoys being updated each time his ATEC drops a little. (It’s been a yo-yo.) The biggest ATEC decreases came (recently) after adding CD doses throughout the night (2 or 3 one-ounce doses every night from midnight to 8am~ 16 doses total in any 24 hour period), removing sugar, adding “Roby”, and month-long Mendendazole. We just added the ionic foot bath and we are seeing smaller pupils after ONLY two 15-minutes sessions.

I keep looking at my sweet child and smiling. I see the intensity leaving his body. This illness is devastating to a child’s development in EVERY possible way. It is devastating to families. Our world collapsed every day, year after year. Eventually, we made few (if any) plans to go anywhere and we just survived what each day brought.

In the last few months, I am seeing glimpses of freedom. I am able to sit down for a few minutes and NOT read a medical book. I am catching up on some housework. It’s nearly impossible to manage a household with PANDAS/ PANS. You never know what the next minute is going to bring.

The knowledge you share is priceless. The videos and testimonials are priceless. I have watched, listened and read them over and over again. I have followed your work since 2015. I only wish we had started the protocol sooner. But thank God, we are doing the protocol now. I look forward to writing you again when we achieve full recovery.

Kerri, I am thankful for you every day. May the Lord richly bless you and your work and may the Lord keep you and your loved ones in the palm of his hands.

Our moms need your help

Last week, we relayed a report from Laurel Austin whose son Jeremy has been suffering from autism since the age of 3 after a series of vaccinations. His MD reported one of his injuries to the Vaccine Adverse Event Reporting System.

Jeremy’s autism is severe. He lost speech entirely along with the ability to interact with others; he became agitated frequently during the day and sometimes dangerous to others and he was self-harming.

Jeremy is now 28.

The medical myth – the one promoted by pharmaceutical companies that would like to put people like Jeremy on a lifetime of powerful psych meds – is that such cases are beyond hope.

The reality is that very often meaningful improvements can be made at any age with the CD protocol and Jeremy is a living example of this.

Jeremy now has six words – “no”, “mom”, “more”, “bye”, “hot” and “please.”

Six words – when for the last 25 years he had none.

Needless to say, normal people receive this news with great happiness for Jeremy and his family.

Anyone with severely autistic children recognizes what huge gains these are and what a big difference they make in the life of a child and his family.

Unfortunately, we live in a sick world with some sick people in it.

After posting the story last week, Jeremy’s family has come under organized attack by a sadistic ring of Internet trolls who take delight in tormenting families with autistic children.

I know this may be shocking, but I also know that hundreds, if not thousands, of people reading this are either aware of this group and some have even been attacked by them as well.

Who are these people?

Let me name some of them by name:

* Emma Dalmayne (UK)

* Fiona O’Leary (Ireland)

* Amanda Seigler (US)

* Melissa Eaton (US)

* Lindsay Mohler (US)

They have also managed to rope in an NBC reporter named Brandy Zadrozny who, in addition to attacking Laurel and other families, is an advocate for rights for pedophiles.

(Yes, you read that right and if you write me I will send you a link to one of her NBC-approved articles on this subject as well as documentation of every other claim in this letter.)

Here’s what we know about these individuals:

1. They have no training is science, medicine or health care.

2. They have no understanding of basic chemistry and have no interest in clearing up their moronic confusion on the subject.

3. They have absolutely no interest in the truth. They manufacture “facts”, misrepresent basic science, make up injury stories and fabricate injury statistics.

4. They not only attack families who use the CD protocol, they attack anyone who calls for vaccine safety, anyone who researches treatments for autism, any families who seek treatments for autism, charities that support families with autistic children, and MDs and other health care professionals who seek to help children with autism.

5. They openly mock mothers with autistic children calling them “martyr moms” and telling them to “get over it.”

6. None of them seem to have a reliable source of earned income, yet they’ve been able to devote full time and near full time effort to harassing people online for years.

7. They claim to care for the rights of autistic children, but have NEVER in all the years that they have been harassing families with autistic children ever once spoken out against the common practice of institutions putting autistic children on powerful and dangerous psych meds to make them “easier” to manage.

In other words, they are uniformly friendly to the interests of pharmaceutical companies and hostile to anyone who challenges their business practices.

As crazy as this sounds, all you have to do is search any one of the names listed above with the word “autism” and you will uncover a cesspool of abusive, unhinged raving and invective directed at families, their health care practitioners, and scientists doing research in the field of autism.

Even more crazy than their behavior is that companies like Facebook, Google, Twitter and YouTube that are usually in a rush to shut everyone down, allow these vicious people to spew their venom without limit.

One of our new families explained the facts of life to us:

“Facebook, Google, Twitter, YouTube and the other services do NOTHING to protect the public from people like this…unless they receive complaints about them.”

Here’s how you can help shut these people down and put an end to the terror campaign they’ve been waging against doctors, charities, families, patients and moms like Laurel.

Step 1. Make a contribution to Laurel’s legal campaign against these people.

(Your contribution can be made anonymously to protect yourself from harassment by the trolls.)

Laurel is willing to put herself on the line for all of us. Helping her is the least we can do.

The minimum contribution the system will accept is $5. Give more if you can.

Step 2. AFTER you make an ANONYMOUS contribution, please copy and paste your confirmation and mail to this address:

We have someone at this address who has volunteered to coordinate unified action against these online harassers and you will be told about ways you can help.

Your identify will be safeguarded.

Our goals are very simple:

1. To protest the demented behavior of these harassers to all the social media platforms they are currently abusing and get them delisted.

2. To petition legitimate news outlets and legitimate journalists to shine a light on these people and their activities.

We need your help.

Families should be allowed to seek care and care for their autistic children in peace without being subjected to vicious personal attacks online.

It’s a sad reality that many families and doctors who’ve experienced great success with the CD protocol are afraid to come forward and tell their stories for fear of being victimized by these people.

Enough is enough.

Go here and contribute a minimum of $5 to prove you’re real and not a troll (Trolls can’t fake credit or debit cards the way they fake Facebook profiles.)

You can do this anonymously.

Step 2. AFTER you make a contribution – you can do it ANONYMOUSLY to protect your identity- copy and paste the email confirmation you receive from GoFundMe and mail to this private secure address:

And await further instructions.

Next week:

Back to the important business of helping our kids…hopefully some day without fear of harassment from sick pharmaceutical industry subsidized trolls.

– Kerri Rivera

La semana pasada, transmitimos un informe de Laurel Austin cuyo hijo Jeremy tiene estado sufriendo de autismo desde el edad de 3 años después de una serie de vacunas. Su médico informó de una de sus heridas. al informe de eventos adversos de la vacuna Sistema.

El autismo de Jeremy es severo. Perdió el habla completamente junto con la capacidad de interactuar con otros; se agitaba frecuentemente durante el día y a veces peligroso para los demás y se hacía daño a sí mismo.

Jeremy tiene ahora 28 años.

El mito médico – el promovido por compañías farmacéuticas que quisieran poner a gente como Jeremy en una vida de poderosas medicinas psicológicas – es que tal los casos están más allá de la esperanza.

La realidad es que muchas veces tiene sentido Se pueden hacer mejoras en cualquier edad con el protocolo de CD y Jeremy Es un ejemplo vivo de esto.

Jeremy ahora tiene seis palabras: “no”, “mamá”, “más”, “adiós”, “sexy” y “por favor”.

Seis palabras: cuando durante los últimos 25 años él No tenía ninguno.

No hace falta decir que las personas normales reciben esta noticia con gran felicidad para Jeremy y su familia.

Cualquier persona con niños severamente autistas. reconoce qué grandes ganancias son estas y qué una gran diferencia que hacen en la vida de un niño y su familia.

Desafortunadamente, vivimos en un mundo enfermo con algunas personas enfermas en el mismo.

Después de publicar la historia la semana pasada, la familia de Jeremy ha estado bajo ataque organizado por un anillo sádico de trolls de Internet que se deleitan en atormentar familias con niños autistas.

Sé que esto puede ser impactante, pero también saber que cientos, si no miles, de las personas que leen esto son conscientes de este grupo y algunos incluso han sido atacados por ellos también.

¿Quienes son esas personas?

Déjame nombrar algunos de ellos por su nombre:

* Emma Dalmayne (Reino Unido)

* Fiona O’Leary (Irlanda)

* Amanda Seigler (Estados Unidos)

* Melissa Eaton (Estados Unidos)

* Lindsay Mohler (EE. UU.)

También han logrado cuerda en un reportero de la NBC llamado Brandy Zadrozny quien, además de atacar Laurel y otras familias, es un defensor por los derechos de los pedófilos.

(Sí, lo leíste bien y si escribes yo te enviaré un enlace a uno de ella Artículos aprobados por la NBC sobre este tema así como documentación de todos los demás reclamo en esta carta.)

Esto es lo que sabemos sobre estas personas:

1. No tienen entrenamiento es ciencia, medicina o cuidado de la salud.

2. No tienen conocimiento de química básica y no tengo interés en aclarar su confusión idiota sobre el tema.

3. No tienen absolutamente ningún interés en el verdad. Fabrican “hechos”, tergiversan ciencia básica, historias de lesiones inventadas y fabricar estadísticas de lesiones.

4. No solo atacan a las familias que usan el protocolo CD, atacan a cualquiera que pide seguridad de la vacuna, cualquiera que investigue tratamientos para el autismo, cualquier familia que busque tratamientos para el autismo, organizaciones benéficas que apoyan familias con niños autistas y médicos y otros profesionales de la salud que buscan Ayuda a los niños con autismo.

5. Se burlan abiertamente de las madres con autismo niños llamándolos “madres mártires” y diciéndoles que “lo superen”.

6. Ninguno de ellos parece tener un confiable fuente de ingresos ganados, sin embargo, han podido dedicar tiempo completo y casi a tiempo completo acosar a la gente en línea durante años.

7. Afirman cuidar los derechos de niños autistas, pero NUNCA han tenido los años que han estado acosando familias con niños autistas que alguna vez hablaron en contra de la práctica común de las instituciones poner a los niños autistas en poderosos y medicamentos psiquiátricos peligrosos para hacerlos “más fáciles” administrar.

En otras palabras, son uniformemente amigables con el intereses de las compañías farmacéuticas y hostiles a cualquiera que desafíe sus prácticas comerciales.

Tan loco como suena, todo lo que tienes que hacer es buscar cualquiera de los nombres enumerados arriba con la palabra “autismo” y lo harás descubrir un pozo negro de abuso, desquiciado delirante e invectiva dirigida a las familias, sus profesionales de la salud y científicos haciendo investigación en el campo del autismo.

Aún más loco que su comportamiento. es que compañías como Facebook, Google, Twitter y YouTube que suelen ser en un apuro por cerrar a todos, permitir estas personas viciosas para vomitar su veneno sin limite.

Una de nuestras nuevas familias explicó el hechos de la vida para nosotros:

“Facebook, Google, Twitter, YouTube y los otros servicios NO HACEN NADA para proteger al público de personas como esto … a menos que reciban quejas a cerca de ellos.”

Así es como puedes ayudar a callar a estas personas abajo y poner fin a la campaña de terror han estado luchando contra doctores, organizaciones benéficas, familias, pacientes y madres como Laurel.

Paso 1. Haz una contribución a la legal de Laurel campaña contra estas personas.

(Su contribución puede hacerse de forma anónima para protegerse del acoso de los trolls.)

Laurel está dispuesta a ponerse en la línea para todos de nosotros. Ayudarla es lo menos que podemos hacer.

La contribución mínima que aceptará el sistema es de $ 5. Da más si puedes.

Paso 2. DESPUÉS de hacer una contribución ANÓNIMA, por favor copie y pegue su confirmación y envíela a esta dirección:

Tenemos a alguien en esta dirección que se ha ofrecido como voluntario. coordinar acciones unificadas contra estos acosadores en línea y se le informará sobre las formas en que puede ayudar.

Su identidad será salvaguardada.

Nuestros objetivos son muy simples:

1. Para protestar por el comportamiento demente de estos acosadores a todas las plataformas de redes sociales que actualmente están abusando y sacarlos de la lista.

2. Solicitar medios de noticias legítimos y legítimos periodistas para arrojar luz sobre estas personas y sus ocupaciones.

Necesitamos tu ayuda.

Se debe permitir que las familias busquen atención y cuidado para sus hijos autistas en paz sin ser sometido a ataques personales viciosos en línea.

Es una triste realidad que muchas familias y médicos que han experimentado un gran éxito con el CD protocolo tienen miedo de presentarse y decirle a su historias por miedo a ser víctimas de estas personas.

Suficiente es suficiente.

Vaya aquí y contribuya un mínimo de $ 5 para demostrar que eres real y no un troll (Trolls no pueden falsificar tarjetas de crédito o débito de la forma en que falsos perfiles de Facebook).

Puedes hacer esto anónimamente.

Paso 2. DESPUÉS de hacer una contribución – puedes hacerlo de forma ANÓNIMA para proteger tu identidad- copie y pegue el correo electrónico de confirmación que recibe de GoFundMe y envíe por correo a esta dirección privada segura:

Y aguarde más instrucciones.

La próxima semana:

Volviendo al importante negocio de ayudar a nuestros hijos… ojalá algún día sin temor al acoso de industria farmacéutica enferma trolls subsidiados.

– Kerri Rivera

Celebrating Another Autism Recovery

I can’t begin to tell you how happy I am when a family who is using our protocol tells me their child has recovered from autism. This is why I do the work that I do, and I celebrate each and every one of these victories.

Today’s success story comes from a family I consulted with. If you would like to consult with me regarding your child’s autism recovery, please let me know via email!

As referenced in the story, we use the ATEC score (Autism Treatment Effectiveness Checklist) to track the severity of children’s autism symptoms. The higher the score – the more the child is impacted by the symptoms of autism. A score below 10 indicates the child’s symptoms are below the diagnostic threshold for autism and that child is considered to be recovered. Click here to learn more about ATEC scores.

This mom writes about her son’s autism recovery:

# 501

Kerri my boy is recovered fully – not sure if you added him.

I’m sure his ATEC was about 52 when I spoke to you on that video call and he was non-verbal and in nappies [diapers] (aged 3.5). I checked his ATEC about a week ago and it was 6.

He is absolutely loving school, which started a few weeks ago – aged 4 and is at a gymnastics and athletics club too. He loves kids parties (used to hide under tables due to being overwhelmed).

I don’t even know if he would be speaking now if it wasn’t for your help.

Love and hugs to you xx

Thanks again to this brave and committed mother for writing in to share her story.

I hope you are inspired to take action as well.

If there is more that I can do to help you in your journey, please don’t hesitate to write in and let me know!

– Kerri Rivera
Doctor of Homeopathy


None of the products or statements on this website have been evaluated by the US Food and Drug Administration and are not intended to diagnose, treat, cure or prevent any disease or condition. If you suspect you may have a disease or condition, you should consult a licensed healthcare practitioner.