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Members of the international team that discovered the cause of FSHD Type 2 Fueled by funding from the FSH Society, an international research team has discovered the genes that cause […]
[…] leaders in our community—activists, celebrities, scientists, doctors, people doing awesome things—to raise worldwide awareness of FSHD. Their stories were utterly compelling, and the sense of optimism for a treatment in […]
Boston, MA / January 24, 2013 Facioscapulohumeral muscular dystrophy ( FSHD) is a disease most people have never heard of, even though it is one of the most common forms […]
[…] leaders in our community—activists, celebrities, scientists, doctors, people doing awesome things—to raise worldwide awareness of FSHD. See our interview schedule below. How can you help? Join us on our Facebook […]
by Amanda Hill, Denver, Colorado FSHD clinical researchers recently published what may soon become a standard battery of assessments for use in clinical trials, an exciting and essential milestone for […]
