Tel: 0800 6526316 or 01202 432048
CMT UK was established in 1986, and is the support group for those people who have Charcot-Marie-Tooth disease (also known as peroneal muscular atrophy, and hereditary motor and sensory neuropathy), and their families.
A service of support, advice, and information is offered to all members and their families. All committee members are contactable by phone. Money is raised for research, both by the organisation and individual members.
Leaflets, both about the condition and the organisation, are available. A magazine is produced three times per year and a small subscription is asked for.
An annual general meeting is held each year. This is combined with a conference, when there are speakers and/or workshops.
Last updated on 21/07/2012
Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions. Patient Platform Limited has used all reasonable care in compiling the information but make no warranty as to its accuracy. Consult a doctor or other health care professional for diagnosis and treatment of medical conditions. For details see our conditions.