The Huffington Post hosted a live discussion around the 25th anniversary of the Americans With Disabilities Act. Our very own Kristin Duquette, a decorated athlete and activist, participated in the… Read More »
Kristin Duquette speaks about the 25th Anniversary of the Americans with Disabilities Act with Huffington Post Live
Hot off the press: FSHD care guideline
Evidence-based, if incomplete, new guideline is a major step forward. All too often, FSHD patients encounter doctors whose knowledge of the disease seems to be gleaned from dusty textbooks. A… Read More »
First-Ever FSHD Evidence-based Care Guideline Published by the American Academy of Neurology
From PRWeb Contact Information: Rosie Hale 617-779-1893 FSHSociety@shiftcomm.com Guideline is a landmark step forward for the diagnosis; comes as a result of FSH Society’s advocacy efforts over the past 20… Read More »
FSH Society sets all-time record in funding research
The FSH Society announced a new round of grant award recipients bringing the Society’s total grant awards to over $890,000 in 2015. This round of award winners were among a competitive… Read More »
FSH Society Awards New Round of Research Grants to Support Critical Research on FSH Muscular Dystrophy
From PRWeb BOSTON, MA (PRWEB) JULY 24, 2015. The FSH Society, the Massachusetts-based charity that has transformed the science of the little-known and incurable disease, facioscapulohumeral muscular dystrophy (FSHD), announced a… Read More »