| Experiences and stories

the story of shanna who has LGMD2C (or LGMDR5)

Sarepta Therapeutics

Leading up to Rare Disease Day, we're raising awareness of the 300+ million people living with a rare disease. People like Shanna, who has LGMD2C or LGMDR5. Watch and share her story to raise awareness.

watch the video

©2020 GFBONLUS.IT - GRUPPO FAMILIARI BETA-SARCOGLICANOPATIE
+39 328 0075986 This email address is being protected from spambots. You need JavaScript enabled to view it.

Via Civasca 112 23018 Talamona - SO  Italia

Made by Betsoft