Quest Winter 2015

January 1, 2015 - March 31, 2015

Cover Story

MDA Muscle Walk connects MDA families and raises critical funds for lifesaving treatments and cures. So are you ready to join us?

When Lizzie Chamberlain of Jacksonville, Ill., was 2 years old, her physical development relative to other children began to plateau — and then decline. Lizzie received a diagnosis of type 3 spinal muscular atrophy (SMA)


According to experts, reframing your perspective on life can help conquer the anxieties or depression that can accompany living with neuromuscular disease
Combating chronic pain in people living with neuromuscular disease requires a multifaceted approach
Meet Grace Pavlath, MDA's new scientific director


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Quest Extra

For one mother living with Charcot-Marie-Tooth disease, daily perseverance starts with redefining 'normal'