Kathryn Simpson

Kath and Phil's Pass' Portes du Soleil MTB 2016 page

Fundraising for Charcot-Marie-Tooth UK
£1,329
raised of £1,000 target
by 69 supporters
Donations cannot currently be made to this page
Participants: Kath Simpson, Phillipa Long, Chris Long, Liz Leyland
What do we all want for future generations? A treatment or cure for CMT! Help us make it happen.

Story

Thanks for taking the time to visit our JustGiving page.

We'll be riding the Pass' Portes du Soleil MTB marathon at the end of June, along with Chris Long and Liz Leyland.  The 80km route takes in the spectacular scenery of the French and Swiss Alps.

Charcot-Marie-Tooth Disease is also known as Hereditary Motor and Sensory Neuropathy. Anyone who knows about CMT knows just how devastating it can be. It may not be a death sentence, but it is a life sentence in that every single task and every single thing we do is affected by it. This neurological muscle wasting disease causes muscle wastage in the lower legs/ feet and arms/ hands. It causes poor co-ordination, loss of balance and strength in the arms and legs as well as reduced sensations.  This degenerative condition affects individuals in different ways and whilst some may retain mobility throughout, many others sadly depend on walking aids and even become wheelchair bound.

Currently, there are no disease specific treatments to either halt the progression or cure CMT, but the condition is managed by physiotherapy, orthotics, occupational therapy, pain and fatigue management and when indicated orthopaedic surgery, speech therapy, etc.

Funding for research into effective treatments and eventually a cure is of vital importance to give future generations the chance of a normal life.  For more information on the condition and current research, please visit the CMT UK website.

About the campaign

What do we all want for future generations? A treatment or cure for CMT! Help us make it happen.

About the charity

Charcot-Marie-Tooth UK

Verified by JustGiving

RCN 1112370
Charcot-Marie-Tooth UK (formerly CMT United Kingdom) is the national support group for people affected by Charcot-Marie-Tooth Disease, aka Hereditary Motor and Sensory Neuropathy. We provide advice, support and information for people with the condition, family, carers and medical professionals.

Donation summary

Total raised
£1,328.75
+ £183.75 Gift Aid
Online donations
£1,254.60
Offline donations
£74.15

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