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Scleroderma Society
PO Box 581
Chichester
PO19 9EW
Tel (advice line): 0800 311 2756
Te (general)l: 020 7000 1925
Web: www.sclerodermasociety.co.uk
Best time to telephone: 10am - 9pm
The Scleroderma Society was founded in 1982 to help patients who suffer from the disease and their families. Features of its activities are as follows:
- National group with regional groups in some areas.
- Meetings to exchange ideas and experiences and share advice.
- Small membership fee to cover administration costs. Membership is open to anyone with an interest in the disease.
- Leaflets are available which describes the Society, the condition and its various forms including 'localised scleroderma' and 'systemic sclerosis' which can be downloaded from their website.
- Quarterly newsletter.
- Website includes message board.
- Contact lists for members who wish to be in contact with others.
- Raise awareness.
- Raise funds for scleroderma research.
- Telephone advice line.
- Email contact.
The authors and editors of this article are employed to create accurate and up to date content reflecting reliable research evidence, guidance and best clinical practice. They are free from any commercial conflicts of interest. Find out more about updating.
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