About Cure AHC
AHC (Alternating Hemiplegia of Childhood) is a complex, ultra-rare neurological disease. The majority of cases (approximately 80%) are caused by mutations in the gene ATP1a3, as well as other potential genetic root causes, which Cure AHC funds active research to discover. The hallmark of this disease is episodes of temporary paralysis that alternate from one side of the body to the other, sometimes engulfing the entire body, lasting anywhere from minutes to days at a time.
Cure AHC is actively involved in finding ways to empower sufferers and their families to battle the complexities of living with this rare disease.
On Rare Disease Day, we share campaign visuals on our social media.