Join My City Med as we celebrate the global rare community in a 24-hour marathon event you won’t want to miss in celebration of Rare Disease Day!
On February 28 at 1:00 p.m. Eastern Time, catch a panel discussion on Teaming up on Single-Gene Diseases: A Collaborative Approach to Treatment, featuring members of the KIF1A.ORG community:
- Luke Rosen, co-founder of KIF1A.ORG
- Wendy Chung, MD, PhD, Kennedy Family Professor of Pediatrics in Medicine & Chief, Clinical Genetics, Columbia University
- Stephanie Fischer, Rare Disease Patient Advocate & KIF1A.ORG Champion
Visit 24HoursOfRare.com to register for this and other events hosted by My City Med.