[…] 2017 – Today the FSH Society, a world leader in combating facioscapulohumeral muscular dystrophy ( FSHD), announced it has committed $541,133 in funding to five research projects that aim to […]
FSH Society Awards $541,133 in Funding for FSH Muscular Dystrophy Research
The FSH Society Issues Research Grant
[…] can evaluate electrical impedance myography (EIM) as a tool for quantifying the muscle structure of FSHD patients. Today, the FSH Society, a Massachusetts based non-profit that is a world leader in […]
A success for the virtual 2020 International Research Congress
by Jamshid Arjomand, PhD, Chief Science Officer, FSHD Society Our original plan for 2020 was to host the International Research Congress (IRC) in Washington, DC, in proximity to the FDA […]
Raise Awareness
Spread the Word! The FSHD Society is on a mission to raise the visibility and understanding of FSHD in order to further reduce the time to accurate diagnosis, increase empathy […]
FSH Society’s International Meeting to Bring Together Patients & Researchers From Around the World to Explore New Insights on Rare Disease
[…] charitable foundation that has transformed the science of a little-known disease, facioscapulohumeral muscular dystrophy ( FSHD), today announced its Biennial International Network Meeting. The meeting will be the one of […]