[…] a number of compelling similarities to the human disease. Ever since the genetic mechanism of FSHD, centered on the abnormal expression of the DUX4 gene, was published in 2010, scientists […]
A new DUX4 mouse with muscle disease
FY2017 Donor Report documents a year of change and growth
[…] to move closer to our collective goal of better treatments and ultimately a cure for FSHD. As we close the book on 2017, we have much to celebrate. Together, we […]
FSH Society launches national chapter program
Today, The FSH Society, the world’s largest research-focused patient organization for facioscapulohumeral muscular dystrophy ( FSHD), announced the launch of its national chapter development program to provide the opportunity to fund […]
NAD+ supplementation may help aging muscle
Could it be helpful for FSHD? BY AMANDA HILL, HIGHLANDS RANCH, COLORADO In the current absence of a treatment for FSHD, many patients experiment with a variety of lifestyle or […]
What’s in a name?
We’re now the FSHD Society Discerning readers will notice that we have changed our name and logo to align with how the rest of the world abbreviates facioscapulohumeral muscular dystrophy. […]