Join Us in Celebrating CACNA1A Awareness Day!

Thank you for your interest in supporting us on Awareness Day! CACNA1A is a rare neurodevelopmental genetic disease. Individuals with variants or mutations on their CACNA1A gene present with intellectual disability, autism, movement/coordination disorders, eye movement issues (nystagmus) which cause debilitating dizziness, stroke-like episodes that can result in coma (hemiplegic migraines), speech and language issues, and more. Currently, there are no targeted treatment options or a cure available.

As the largest non-governmental funder of CACNA1A research, we remain fully committed to advancing research even as some efforts face federal funding cuts. In this special year—our 5th anniversary—our goal is to raise $5,000 today to celebrate our progress and fund research focused on finding a cure.

Thank you for helping us reach our goal!

Every donation, regardless of size, brings us closer to life-changing treatments and, one day, a cure.