The Mad Max Foundation is dedicated to supporting, educating, and providing resources to families of children in the SCN8A and other special needs communities.
Meet Max
My name is Max and I was born on October 13, 2014. I was diagnosed on January 5, 2015 with Infantile Spasms and then subsequent genetic testing revealed the I had a very rare genetic mutation known as SCN8A
(there are currently ~550 reported cases in the world).
Meet the Family
We are the Cabreras… a small, but mighty family. The first militia in the Mad Max campaign.
Our Vision
The Mad Max Foundation strives to create a compassionate community where parents, siblings, and caregivers are equipped with the tools, resources, and encouragement they need to navigate the challenges and celebrate the unique joys of raising a child with special needs.
Through tailored programs, emotional support, fundraising, and advocacy, we aim to foster resilience, build connections, and ensure every family feels empowered in their journey.
Your generous donation will help us kickstart this important initiative and fund our goals. Together, we can make a difference in the lives of those facing similar challenges.