Families for Autism and Immune Recovery

04/24/2026

Prayer Requested ✨

Collin’s precious pups are waiting for him to return.
🐶🦊🐶🦊

Many parents experience their kids riding around with friends when they are 16 and exploring their world around them as a passage of time.

Patents like me often don’t experience these developmental stages at regular time frames and many never do.

I’m so elated that this is now happening. It’s such an amazing blessing; however, the worry is so raw and real. It’s such a mixed bag of emotions - mostly happy thank God. ✨

Please pray for his safety, wisdom and judgement as he progresses forward creating the life he’s worked so hard for and dreamt of.

Vaccine injuries can’t and won’t destroy us!

We are over-comers and will always reach for the stars! ⭐️. Because, if you shoot for the stars, you may just land on a cloud. 😀⛅️

🧡🧡🧡

04/19/2026

The Power of Love and Healing ❤️‍🩹

Collin and I became the first mother-and-son team to travel together to Panama for stem cell treatments. Our lives were incredibly delicate - every day was a fight for survival.

Collin, with severe vaccine-generated autism, was having 3-hour meltdowns daily, struggling with gut issues, behavioral challenges, and constant stimming. I was battling Lyme disease and its devastating effects. As a single mom, I carried it all alone. His father offered no support—in fact, he once told me that if I died, he wouldn’t even house our son. The pressure was unreal.

Many people told me it was too late, that the treatments wouldn’t work. But I knew better. After 30 years of researching what actually makes sense and works—running clinics and never giving up - I took the gift of life that God entrusted to me seriously. Collin is my beautiful boy, and I was determined to be his light.

The only things that kept me going were our deep faith and the unbreakable love for my son. Today, I’m sharing our story to encourage every single one of you:
Never give up.

You are NOT your disease.
Hold your faith tight.
When they say “it can’t be done,” keep going and tell them to suck a duck! Be a force to be reckoned with.

The ingredients for overcoming are persistence, belief, and relentless love. ❤️

If you’re walking a similar path with chronic illness, autism, or immune challenges, reach out. I’m a patient, a survivor, and a passionate advocate. I’ll soon be launching my new sites with in-depth info on the best diagnostics and treatments from around the globe.

In the meantime, you can connect with me here on my page Bioresetcode, or through my nonprofit Families for Autism and Immune Recovery.
Let’s heal together. You’ve got this.

03/04/2026

Stem cells are not created equally

Not all stem cells are created equally.

The US is regulated which means that stem cells can ONLY be minimally manipulated.

In Mexico and in a few other countries they are not regulated so they can culture expand and target their cells - making the cells and treatments exponentially more powerful and precise. Not all stem cells are the same.

Then you have to worry about viability - many stem cell groups do not give you all the cells that they say - it’s only a percentage. There are ways to ensure the cells are viable and that you will get the correct number of cells.

Cells that are womb temperature and that are not cryofreezed are best. There are stem cell counters for accuracy that only certain clinics use.

Most importantly, the concern is did the cells come from a healthy donor / they can not have had the MRNA shots. That would be detrimental.

There are so many things to consider. I’ve traveled the globe to get treatments for both me and my son and have even done pig stem cells, plant and other cellular technologies. I’ve also traveled the globe with a friend that is a stem cell researcher and doc. We would investigate stem cell companies. He later started a clinic. Before that, he helped me along the way choose the best groups for our care. Both my son and I were incredibly blessed to both get substantial gains each time.

Additionally, stem cells are only a layer that is needed to heal. It’s in the proper order and stacked treatments that the real transformations occur. Exosones are very powerful communicators that can be grown in such a way to better target very specific disease processes. This is very important and a complex process that not everyone does or does well. They and other cell types and integrative stacked treatments along with frequency based treatments, etc. when done in a very structured way create the absolute best results. Akeo, there are different stem cell types to choose from. Basic mesenchymal cells are good but are not best for neurological disorders compared to other types. There are places that just throw stem cells in your arm and charge a fortune. That’s why you have to know exactly what you are getting. Pricing can vary so you want the most targeted and potent treatments for your particular need / illness.

You also have to prep the body to ensure the cells have an optimal environment. Just dumping cells into the body is not the best course of action. In addition, it’s important to address other organs during your care. So, when shopping for treatments you must compare apples to apples. So, no not all stem cell groups are created equally. What I have found is we get more for our money and more precusion care at the clinics that we choose.

I’ve been in this arena for decades and have learned a lot.

If you’d like more info feel free to dm me.

08/23/2025

How I Recovered My Son with Autism:

Genetic testing, purposeful nutrients, vitamins and supplements customized based on genetic testing, allergy testing, food avoidance and specific diet, chelation, integrative medicine, regenerative medicine (stem cells and other technologies), cell communicators, therapies ( speech, OT, PT, cranial sacral, behavioral, music, rec) one-on-one tutoring and teaching, vaccine avoidance, counseling, one-on-one school aids, breathing equipment, neurologist, PhD psychologist (with her specialty in ASD, DAN doctor, hypnosis, college aids, tutors, signing him up on every autism specific program possible, energetic / Quantum healing, neuropsychological comprehensive testing, nursing, classical music, Advocating at ARD meeting ensuring EIP and BIP were executed and followed, Disability Rights Advocacy, prayers, affirmations, law of attraction, meditation, Sunday school with an aid, becoming a devoted researcher, at home labels and behavioral strategies for the entire family and globalizing each goal with the team - all people working on very targeted goals. Family education and counseling, EMDR trauma therapy (PTSD is real with parents of ASD kids - moms and dads near care too. Lots of bubble paths, hypnosis, counseling, reading, goal setting for me (mom), positive reinforcement and time out ( no spanking). I’ll be writing an ebook at some point. This is just some of the trenches we’ve walked through to get to where we are! It’s a marathon not a sprint.

11/17/2019

I want to scream from the rooftop ..

My inflammation is gone!!!!

My energy is way up and life is so much brighter.

💃🏻💃🏻💃🏻💃🏻💃🏻💃🏻💃🏻💃🏻💃🏻💃🏻💃🏻💃🏻

I’ve had so many ups and downs with inflammation since 2009 and the only thing that worked was expensive stem cell and oxygen treatments and IV chelations and more. I’ve spent so much the past 10 years I could out right pay off my own house.

I’m a big believer in systemic healing and recovery. I have been working on starting a stem cell company - which I did form a Delaware C-Corp which is on hold due to legislative issues with stem cell laws (helping with Neurodegenerative diseases / crossing the blood brain barrier is not allowed in the states).

My hopes and dreams have been crushed in many ways but my nature is to keep going and seek things that work which I have done since I’m still alive from a myriad of dreadful disease processes occurring simultaneously throughout my body. I’ve never quit finding ways to help both my Son and myself.

However, I was running out of money and ideas. I had been researching cell communication and repair technologies and in a crying mode of desperation I pulled the trigger and ordered the one I had been researching for over a year. I do a lot of due diligence before I decided on something. I was at wits end and about to go into savings to get a lot of IV’s and jump back into the hyperbaric chamber as the fatigue, pain, digestive issues and sleep deprivation were winning.

I am now more than pleased (I even want to pinch myself as I’m waiting for the other shoe to drop because I’m out of pain, energized, moving things along and sleeping better!!!

My hopes and dreams are also coming back to life. I prayed in solitude as my hope was lacking to be honest and I was not sure I could keep doing all I need to do to hold down the fort for my Son and family.

It’s only been approx. 4 weeks with my new find (cell signaling molecules).

I’ll keep you posted! Collin starts it soon!!!!!

08/23/2017

http://kerrymagro.com/i-have-autism-and-am-getting-a-college-degree-in-computer-science

Collin CarabineNEEDS LIKES FOR AUTISM SCHOLARSHIP!
He wrote an awesome essay that's now live online; the more interest in his page - shares, likes, clicks, etc. - the better his chances at being awarded the scholarship

Please click on the photo below to view :-)

This guest post is by Collin Carabine, a young man on the autism spectrum. Collin attends Huston Tillotson University. Collin is applying for our Summer 2017 Making a Difference Autism Scholarship via the nonprofit KFM Making a Difference. You can read more about the organization and how to apply fo...

08/19/2017

The big day! Our procedure day - when they take the bone marrow extraction and then take it to their lab, prepare the stem cells and other necessary cells, etc. and transplant them into the spine - intrathecal as well as in an IV push for our protocols - autism and immune.

We where their from 7 until 2 - mother and son back to back. They sedated Collin for both procedures and me for the first one when they extracted the bone marrow. When they put the stem cells in me, I was awake because I am used to spinal treatments as well as iv's and I was very relaxed.

The doctor was there to explain everything and was very compassionate, loving and caring with Collin and myself. I was able to see the cells prior to them being implanted in my spine as well as and placed in an IV push.

Every individual creates a different amount of cells and they will be counted after the procedure and you will be told what that number is a few days after. It will be in the millions. There are four cell types that they use and going through the spine for kids with autism in adults is very effective. This clinic has done a lot of of research and has treated many patients with great success with no spinal injuries.

They explain what the common side effects are (headaches, nausea, fever, chills, vomiting) because anytime you enter the spine there could be side effects whether you go here or Panama or wherever you go. The doctor has made her self available by phone and would even visit your own apartment or hotel if needed. She is very hands-on and caring. This is her specialty.

After getting home, they say to lay flat for two days because the stem cells are very heavy and they need to travel to the brain through the spine. Side effects differ for children six and under where they have a lot of vomiting and dizziness and nausea. They do not usually have pain. Children nine through teens and early 20s experience headaches and pain mostly. Collin experienced fever and chills, achiness and headaches.

The doctor says as the cells awake in the brain that there could be pain. I on the other hand did not. I felt soreness in the areas where they took the bone marrow and some pains here and there.

Having symptoms post procedure does not indicate whether the stem cells are working or not.

We are now looking forward to gains and need to give it time. We will be keeping you all posted as the miracles begin!

04/02/2016

Let's get FAIR back up and make a difference for a child with Autism. We have been blessed to have had a success with our first big fundraiser and are looking to ramp up and help more families with Autism / Immune Disorders.

Seeking Advisory Board Members with the following talents:

- Grant Writing
- IT
- Fundraising
- Multmedia
- Writers
Etc.


org

Message me or Carlton Caudle if you are interested in becoming a part of our team!!

Thank you dearly in advance

03/12/2016

STEMCELL UPDATE: 10.5 months .. This is just good stuff!!!

Collin with Autism... Went at 19 😇. He is now 20. Yes, the cells from the Panama clinic have been great! My son still focuses better, has less meltdowns and when he does have them he owns them (Instead of blaming others which is huge). He even apologizes and they don't last near as long. He can calm his nerves better and feel like "he's not going to hyperventilate". He feels they helped him 35-40% overall. He would want to tell others "that it helps at a certain level .. It doesn't fix everything, but it definitely helps make a lot of things easier".





Families for Autism and Immune Recovery
org

Here's to your health!

09/01/2015

A huge HEARTFELT ... THANK YOU to all of you who participated in Families for Autism & Immune Recovery's (FAIR's) FB fundraiser!! 🌎
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We raised $9,430.00!!!!

Now let's use that money for another event and make it double and send a child with Autism to get medical care!!!

Thank you Jane Allen CPA, PC and team for your generosity!!!



Heidi Carabine's photo.

08/27/2015

Looking for creative minds... let's brainstorm together for a mission for our children.

What is THE most creative name for a stem cell company?

Winner of "BEST NAME" wins a $50 gift certificate to Amazon.

Let's do this!
:-)

04/17/2015

TODAY is THE DAY!!! Our Filmmaker turns in our Film for Families for Autism and Immune Recovery!!!! We entered the "2015 Film Frenzy for Change" and we blessed to a part of this contest. What a good time to get chosen during AUTISM AWARENESS MONTH!

A few details...there are 10 Non-profits matched up with film teams going head to head to create a valuable film to help each organization with their mission!

What a cool contest!!!! We want to thank all of the people who participated in our film as well as those who worked hard to put on this great event. Because... it rocks! And, I can't wait to see our fantabulous film collaboration headed by Michael Goodman!

FAIR's film will be showing this Sunday, April 19th at 5:00 at The Movie House in Austin, TX - on the Big Screen at 5:00 p.m.

Click below for tickets or to support this great cause with Lights. Camera. Help. Ticket sales first go to the filmmakers and then support Lights Camera Help!

Thank you

Mat Hames, filmmaker for the Austin History Center Association, shoots on location for the Reel Change Film Frenzy