I help people through a neuromuscular diagnosis and whatever comes next

“I don’t even know what question to ask.” I’ve heard some version of that sentence hundreds of times. Sometimes it’s from a parent whose child was just diagnosed with Duchenne muscular dystrophy. Sometimes it’s a husband whose wife has been diagnosed with ALS. Other times it’s someone living with spinal muscular atrophy, Charcot-Marie-Tooth disease, limb-girdle […] The post I help people through a…