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[…] to accelerate disease treatment and care for rare diseases See PaLaDIn Launch Press Release The FSHD Society is embarking on an exciting international collaboration to speed up the development of […]
[…] nonprofit, patient-driven organization that supports research and education for individuals with facioscapulohumeral muscular dystrophy ( FSHD) and their families, today announced that it has awarded a $121,000 grant to co-principal […]
by June Kinoshita, FSHD Society Our mission at the FSHD Society is to find treatments and a cure for FSHD—and then make sure everyone in the world who needs it […]
Celebrate World FSHD Day on June 20th What is World FSHD Day? Observed on June 20, World FSHD Day is a global movement to raise awareness of Facioscapulohumeral Muscular Dystrophy […]
[…] years, scientists around the world have begun to investigate the role of oxidative stress in FSHD. A 2018 study reported that muscle biopsies from people with FSHD had greater levels […]
