FSHD Society
Non-Profit & Charitable Organizations · Massachusetts, United States · 11-50 Employees
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Overview
Headquarters
75 N Main St PMB 1073, Randolph, Massach...Phone Number
(781) 301-6060Website
www.fshdsociety.orgRevenue
<$5 MillionIndustry
About FSHD Society
FSHD Society Org Chart
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Debt
$150K
Debt
$285K
FSHD Society Tech Stack
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FSHD Society News & Media
The FSHD Society, SOLVE FSHD, and the FSHD CTRN Announce Launch of Industry Collaborative to Improve FSHD Clinical Trials
The FSHD Industry Collaborative is a first-of-its-kind, multi-stakeholder initiative designed to improve how FSHD clinical trials are designed, executed, and evaluated RANDOLPH, Mass. and VANCOUVER, BC, April 8, 2026 /PRNewswire/ -- The FSHD Society, a patient-driven organization...Organizations Join Forces to Map How Human Muscle Regenerates
Muscular Dystrophy Association-led research collaboration with FSHD Society, LGMD2L Foundation, and Parent Project Muscular Dystrophy to fund Abigail Mackey, PhD, at Copenhagen University Hospital to decode muscle regeneration. Muscular Dystrophy Association-led research collaboration with FSHD Society, LGMD2L Foundation, and Parent Project Muscular Dystrophy to fund Abigail Mackey, PhD, at Copenhagen University Hospital to decode muscle regeneration.Global FSHD Innovation Hub Expands Board to Strengthen Leadership and Impact
RANDOLPH, Mass., Nov. 24, 2025 /PRNewswire/ -- The Global FSHD Innovation Hub, an initiative by the FSHD Society to accelerate the development of therapies for facioscapulohumeral muscular dystrophy (FSHD), has announced the addition of four new members to its Board of Directors: Neil...VOLUNTEERS IMPACTED BY FSH MUSCULAR DYSTROPHY RALLY FOR NATIONAL FUNDRAISING EVENTS
The Walk & Roll to Cure FSHD brings communities together to raise funds and awareness RANDOLPH, Mass., Sept. 5, 2025 /PRNewswire/ -- This September and October, families, friends, and neighbors across the U.S. and Canada will gather for the Walk & Roll to Cure FSHD. These events unite...
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Frequently Asked Questions Regarding FSHD Society
Founded in 1991, FSHD Society is a grassroots network of individuals with FSH muscular dystrophy, their families, and research activists. The Society helps people through education and outreach; funds scientific and medical research; and advocates for increased government and industry investment in FSHD. The company is headquartered in Lexington, M... Read More