My Nonprofit Reviews

The Angelman Syndrome Foundation is an incredible organization that has truly made a life-changing impact on so many families, including my own. Their dedication to advancing research, providing vital family support, and raising awareness for Angelman syndrome is nothing short of extraordinary.

From funding groundbreaking scientific studies to helping families navigate the complexities of this rare genetic disorder, the Foundation is a beacon of hope in the Angelman community. Their tireless efforts to build specialized clinics, offer resources, and advocate for better care and treatments show just how deeply they care about the individuals and families they serve.

The community they’ve built is also remarkable. Whether through local walks, advocacy events, or online support groups, you never feel alone in your journey with Angelman syndrome. Their passion, commitment, and compassion are unmatched.

The Angelman Syndrome Foundation is an organization that is truly changing lives, and I cannot recommend supporting them enough!

I can't speak enough of the impact that the ASF has made on my family and I! From the second we received the diagnosis of AS, they have been there for us through family support, their clinical network and their steadfast work in research!