FSH Watch Summer Annual Research Report 2011
Our 2011 annual review of scientific research funded by the FSH Society was published in the Summer 2011 issue of the FSH Watch newsletter. The issue includes a list of the top […]
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Our 2011 annual review of scientific research funded by the FSH Society was published in the Summer 2011 issue of the FSH Watch newsletter. The issue includes a list of the top […]
Highlights include: FSH friends for the journey FSH Society establishes collaboration with Stanford University FSH Society grants recently awarded End of tax season celebration for FSH muscular dystrophy raises $30,000 […]
Highlights include: Highlight of neuromuscular clinics that might be of interest to patients and their families From “children” to “strong adults”: a family’s journey with FSHD FSH Society annual donor […]
Our 2010 annual review of scientific research funded by the FSH Society was published in the Summer/Fall 2010 issue of the FSH Watch newsletter. The issue includes a list of […]
Watertown, MA–Daniel Perez, co-founder, President and CEO of the FSH Society and a 48-year-old patient with facioscapulohumeral muscular dystrophy (FSHD), the most common form of muscular dystrophy, hailed new findings, […]