Share this article on:

Pictures of You: Allison Moore, who has Charcot-Marie-Tooth disease

Levy, Annie

doi: 10.1097/01.NNN.0000415699.19477.fb
Departments: Photo Essay

A photo series of Neurology Now readers.

Allison Moore, founder of the Hereditary Neuropathy Foundation, on living with Charcot-Marie-Tooth Disease.



Allison Moore, who has Charcot-Marie-Tooth Disease (CMT) and founded the Hereditary Neuropathy Foundation.

What is CMT, and when were you diagnosed? CMT is an inherited disorder of the peripheral nerves that causes progressive loss of muscle and sensation in the arms, hands, feet, and legs. I started having symptoms in 1995, but it took two years to get a diagnosis.

What helps you live with your condition? Founding the Hereditary Neuropathy Foundation (HNF), which provides support for people with CMT and related diseases. HNF just launched the National CMT Resource Center ( with funding from the Centers for Disease Control and Prevention ( You don't feel helpless when you're doing something to make a change.

Is there a person, place, or thing that has been of great support to you? My husband, Robert. We were married less than one year when I was treated for a rare cancer with chemotherapy, which my doctors think exacerbated the CMT.

©2012 American Academy of Neurology