Does anyone know an effective treatment for Charcot Marie Tooth Disease (CMT)?
I was diagnosed with this heredity-based, degenerative neuromuscular disorder about 15 years ago but the symptons started getting progressively worse about 6 years ago. I’ve been to a neurologist with Muscular Dystrophy and his only treatment was Vicodin and we all know the problems that can cause. The pain started in my right foot but is now also in my left foot and both hands from the forearm down. I’ve been to an orthopedic Dr. but he had no solution. I have to wonder if this a disease stem cell research could help but I don’t want to get into that debate. I appreciate any available advice.
