Welcome to the Scleroderma Society Website
The Scleroderma Society is a registered charity (No.286736) founded in 1982.
It is also an affiliate of the nonprofit International Scleroderma Network at www.sclero.org.
The society's aims are to
help and support people with scleroderma
increase awareness of scleroderma
fund scientific and medical research
Membership is open to anyone. Society members range from people who have the disease themselves, or have a relative or friend with the illness, to doctors and healthcare professionals with an interest in scleroderma.
There is a small annual subscription which covers the cost of a quarterly newsletter.
The society is managed and run by volunteers including our trustees who are elected by the membership every three years. Members join from all over the UK and we now have a number of regional groups that meet locally . Members keep in touch via a quarterly newsletter, Internet message board and our Scleroderma Society U.K. sub forum. We also exchange newsletters with other groups around the world.
We are very privileged to have Professor Dame Carol Black as our president and Professor Chris Denton and Dr Ariane Herrick as our vice presidents.
Please explore this website to find out more about scleroderma, how we provide help and support to those who have scleroderma and how you can support us by joining the Scleroderma Society or by making a donation .
It's quick and easy to support us by making a donation online
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Click here to make a donation online. |
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The Scleroderma Society is a company limited by guarantee and not having a share capital. Registered in England, company no. 01704872. Trustees K Fligelstone, S Saunderson,
S Hoare, A Thorpe, R Dodds, S Holloway (secretary). Registered address 37 Warren Street, London W1T 6AD.
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