Byrds Fore A Cure-Cast
About This Show
Byrds Fore A Cure-Cast is dedicated to sharing the latest on SMA research as well as other topics of interest to our muscular dystrophy family and the special needs community. I am a parent of three children, two of whom have type 2 spinal muscular atrophy.
Most Recent Episode
Ep 14: MDA Camp + Summer Travel
Happy Summer, SMA community! In this episode I touch on MDA camp, SMA drama on Facebook, and air travel with a wheelchair. Also, a Spinraza update! (Spoiler: the twins still aren't approved for Spinraza.) Please like us on Facebook, and follow us on Twitter, Instagram, and LinkedIn!