Tamgerine, I don't live with Charcot-Marie-Tooth Disease but I think that some NeuroTalk members do - they will be able to offer you far more direct support than I can.

It comes in many forms, most of which have a strong genetic component.

The information here might help you when talking with your health care team; http://www.ninds.nih.gov/disorders/c...arie_tooth.htm.