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Scleroderma Society

PO Box 581
Chichester
PO19 9EW

Tel (Helpline): 0800 311 2756 (9am-9pm)
Tel (Office): 020 7000 1925
Web: www.sclerodermasociety.co.uk

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 international forum.
  • Contact lists for members who wish to be in contact with others.
  • Raise awareness.
  • Raise funds for scleroderma research.
  • 0800 Telephone helpline.
  • Email contact.
Checked: 29 Jun 2011
For the planned review period see the Data Creation and Quality Control Process.

Comprehensive patient resources are available at www.patient.co.uk

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