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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Department for Science, Innovation and Technology Neurological conditions must be a research priority
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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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We’re excited to invite you to our next CMTUK Hampshire & Sussex Support Group Meeting! This is a fantastic opportunity […]
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Rare disease community: open letter – gov.scot
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In the UK, some 25,000 people are thought to have CMT (Charcot-Marie-Tooth disease), making it the most common inherited neurological […]
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CMTUK has relocated to: 7a Churchill Court, 33 Palmerston Road, Bournemouth BH1 4HN
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Research award 2023 We delighted to announce applications for our new research award for 2023 are now open. The initiation, […]
Continue ReadingA personal health budget is an amount of money to support your health and wellbeing needs, which is planned and […]
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ONLINE PATIENT INFORMATION DAY (VIA MICROSOFT TEAMS) SENSE TRIAL – Hereditary Sensory Neuropathy type 1 Published on behalf of Dr […]
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ATLANTA (March 2, 2023) The CMT Research Foundation (CMTRF), a non-profit focused solely on delivering treatments and cures for Charcot-Marie-Tooth disease (CMT)*, is […]
Continue ReadingLast Updated: Tuesday 7th March, 2023