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Charcot-Marie-Tooth Disease Virtual Information Webinar

Join us for our 2025 webinar! Learn about the latest research on CMT and gain insights on living well with this condition.

Sign up now

This free, informative, and supportive session will cover topics relevant to both adult and paediatric care. The webinar is open to individuals living with CMT, as well as their friends, family, carers, and healthcare professionals.

What you will gain 

  • Updates on ground breaking research and treatments.  
  • Practical advice for living well with CMT. 
  • The opportunity to have your questions answered by leading experts in the field.  

Our webinars are hosted on Zoom, making it easy to join from anywhere in the UK. Don’t miss this change to gain valuable knowledge directly from specialists!

The session will be recorded and made available via YouTube for those unable to attend live. 

What to expect

Hear from leading experts who will share insights on key topics related to limb girdle muscular dystrophy. The panel includes:  

  • Professor Mary Reilly – Professor of Neurology, UCL Queen Square Institute of Neurology.  

Key information 

The webinar will be recorded and shared with all registrants. Register even if you plan to watch it later.   

Together we are stronger. 

This webinar is kindly sponsored by PTC. They have no control or influence over the event content.  

Important note: Webinars are for informational purposes only and should not replace professional medical advice. Please consult your neuromuscular clinical team or health professional if you have concerns.  

We look forward to seeing you there! 

Details
Date Wednesday 5 November 2025 Sign up now

  

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Past webinars

Our free webinars offer you the opportunity to hear from expert speakers, share your experience and ask questions. They are held on Zoom so you can join from wherever you are in the UK.

Support and events

We know that talking to people with similar experiences is powerful. Our support groups are safe and welcoming places to talk to others affected by muscle wasting and weakening conditions, share experiences and meet people who understand what you’re going through.

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