Fighting FSHD
Mar 16, 2021
3 minutes
Bill Moss is a man on a mission. Diagnosed with degenerative muscle-wasting disease facioscapulohumeral muscular dystrophy (FSHD) at 28, the former Macquarie executive director and founder of the FSHD Global Research Foundation has spent more than a decade searching for a cure.
FSHD is a genetic muscle disorder that most commonly affects muscles in the face, shoulder blades, upper arms and abdominals. In some cases it can progress to the hips and legs, and the Muscular Dystrophy Association estimates that around 20 per cent of FSHD
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