Cure Ahc

Cure AHC founders, Jeff & Renee Wuchich, are the parents of 5 year old Matthew who is afflicted with Alternating Hemiplegia of Childhood (AHC), a rare and incurable children’s neurological disorder. Along with other parents, physicians, scientists and children’s rare disease advocates, they tirelessly work to meet this disorder head on to make a difference for all who suffer from Alternating Hemiplegia of Childhood (AHC). You can make a huge difference by participating in sharing information about Alternating Hemiplegia of Childhood and Cure AHC’s progress, events and efforts to raise desperately needed research funds. VISION STATEMENT Cure AHC envisions a world where Alternating Hemiplegia of Childhood no longer robs its sufferers of the chance to participate fully in life. We seek a time where no case goes undiagnosed for lack of awareness. We believe that collaboration is critical for those suffering now, and for those yet to come. MISSION STATEMENT Cure AHC was created in order to raise funds necessary to facilitate research aimed at treating and ultimately curing Alternating Hemiplegia of Childhood (AHC). We do this by partnering with physicians and organizations worldwide and supporting families who live with AHC every day. By bringing together donors, researchers and families we believe a cure for AHC is within reach.