It is Rare Disease Day! The AHCF has been busy working on behalf of all AHC kids. This month’s newsletter outlines some of our recent work, and a few highlights to our future as a community. A message from Lynn, a large grant was received, fundraising is rolling along with great momentum, families are int he news, AHC researchers are awarded honors, 2nd mutation found, and more are in the issues.
Copyright © 2017 · All Rights Reserved · Alternating Hemiplegia of Childhood Foundation