Tel: 0800 6526316
Web: www.cmt.org.uk
Best time to telephone: 9.30am - 3.00pm, Monday - Friday (answerphone at other times)
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.
The authors and editors of this article are employed to create accurate and up to date content reflecting reliable research evidence, guidance and best clinical practice. They are free from any commercial conflicts of interest. Find out more about updating.
Patient UK Hearing Impairment Survey
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Clicking here will take you to the foot of this page where you'll find a list of diagrams which are related to the topic you are currently viewing
Clicking here will take you to the foot of this page where you'll find a list of PatientPlus (detailed reference) articles which are related to the topic you are currently viewing
Clicking here will take you to the foot of this page where you'll find a list of UK Guidelines which are related to the topic you are currently viewing
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Clicking here will take you to the foot of this page where you'll find a list of Online Videos which are related to the topic you are currently viewing
Clicking here will take you to the foot of this page where you'll find links through to our interactive forum. Here you can follow a link to view existing patient experiences on this subject, or to add your own
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