My Nonprofit Reviews

The AHCF is a priceless resource for parents battling this ultra-rare disease.

AHCF was a priceless resource when our daughter was diagnosed with AHC in 2019. I made an inquiry on their website, and I received a return call from a board member and AHC parent within a matter of hours. When every doctor you go to tells you they've never heard of AHC, even the diagnosing doctors, having the opportunity to talk to someone who has been walking this path for years is an indescribable comfort. Thank you, AHCF, for everything you do for those affected by AHC!