Merchandise
Raise awareness and support us by purchasing CMTUK merchandise.
Welcome
CMTUK is the UK charity dedicated to supporting people living with Charcot-Marie-Tooth disease, the most common inherited neurological condition in the world, estimated to affect 1 in 2,500 people and related conditions (including HNPP and GAN).
We provide support, advice and information through; our help-line, email, Support Groups, Facebook groups/page, website and publications, including a magazine (ComMenT) for members.
CMTUK is registered as a charity in England and Wales, registration number: 1112370.
Coronavirus: COVID-19.
CMT Kids
CMT Kids runs events for children (age 11 – 18) with CMT.
Become a member
Join our growing membership and support CMTUK.
Help fund CMT events, charity days and vital research.
Karin Rodgers
We can confirm that Karin Rodgers has stepped down from her role as a Trustee of CMTUK, and from all […]
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CMTUK Conference 2025, 10th May 2025
CMTUK AGM & Conference 2025The Annual General Meeting and Conference 2025 will be held on 10th May in Stratford-upon-Avon. We […]
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Daniel Tanesse, Honorary President of ECMTF, 1941-2025
We are deeply saddened by the passing of Daniel Tanesse, a dedicated advocate for the CMT community, a key figure […]
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Open Letter to the Rt Hon Peter Kyle MP
Department for Science, Innovation and Technology Neurological conditions must be a research priority
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CMTUK London Support Group Face-to-Face Meet Up
Hello! We’re excited to invite you to the next CMTUK London Support Group Face-to-Face Meet Up! It’s going to be […]
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How we can help
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