Mad Max Foundation Corp

We are here to launch Mad Max Foundation and we need your help!

Our story begins with a remarkable little boy named Maximuus, or Max for short. Born with a rare genetic mutation known as SCN8A, Max faces significant challenges, as this mutation can lead to a variety of neurological conditions, including epilepsy, developmental delays, cognitive impairment, autism spectrum disorder, and movement disorders. Sadly, Max falls within the more medically vulnerable spectrum, having been hospitalized over 40 times in his 10 short years.

Navigating the complex world of rare medical conditions and special needs has been a profound journey filled with challenges. These experiences have inspired us to establish a foundation dedicated to providing support and resources for families caring for medically vulnerable children.

To launch our mission, we need your help. Your generous donation will help us kickstart this important initiative and fund our goals. A portion of our proceeds will support The Cute Syndrome Foundation’s Travel Grant for SCN8A families. This organization holds a special place in our hearts; since 2015, they have tirelessly raised awareness about SCN8A mutations, funded dedicated scientists researching this condition, and provided vital support to families worldwide affected by this disorder.

Together, we can make a difference in the lives of those facing similar challenges. Thank you for your support!