My Nonprofit Reviews

The AHCF has been extremely important in our life with our son who has Alternating Hemiplegia of Childhood. Living with a rare disease can keep you isolated, feeling alone constantly, but the AHCF keeps everyone connected, positive, and always hopeful for a cure!

Having a child with AHC is a world of confusing twists and turns, constant chaos, and unexpected chapters to turn next....but with the AHCF, I can breathe a bit easier day by day, and I always know where to turn for advice, wisdom, experiences, recommendations, etc. The AHCF has been a lifesaver for this mommas sanity and I am forever grateful!

CureAHC has been a miracle worker in our lives!! My son Tanner is 14 months old, diagnosed with Alternating Hemiplegia at 8 months old. I was thrown 3 papers from his doctor with his diagnosis and she left, leaving us with countless numbers of questions, worries, fears, struggles, unknowns. Cure AHC is there for me and my family whenever we need questions answered, advice given, ears to listen, and peace of mind that we are never alone. The amount of time dedicated to the families is unimaginable, and I am forever grateful for this organization!!!! Thank you, beyond words, to all!!! Brittany Rosebrook