Why I made the FSH Society a beneficiary in my will
[…] if not us, then who? by Deborah Schwartz, New York City I was clinically diagnosed with FSHD two years before the FSH Society came into being. Mine is a spontaneous mutation. […]
Our look is new. Our purpose is the same. Learn more about our brand evolution.
[…] if not us, then who? by Deborah Schwartz, New York City I was clinically diagnosed with FSHD two years before the FSH Society came into being. Mine is a spontaneous mutation. […]
Volunteers who are 18 to 55 years of age with FSHD are needed for a study to evaluate functional mobility. The principal investigator is Jay Han, MD, of the University […]
From our 2018 FSHD Connect conference, researchers present their work on therapies to suppress the toxic DUX4 gene. Two companies may be going into clinical trials in 2019. This is […]
[…] highlights include:Â -Jim Chin elected Chair of the Board -Announcing: Walk & Roll to Cure FSHD! -The DUX gene may have a starring role in biology -IRC & FSHD Connect […]
We are sharing this news release from Facio, the Netherlands-based biotech founded by FSHD advocates and business leaders with the sole mission of developing treatments for FSHD. In this story, […]