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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.
Checked: 24 Apr 2008

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









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Disclaimer: Patient UK has no control of the content of the above links. Inclusion does not imply endorsement by Patient UK.

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PS - Health and Poverty

Perhaps the biggest cause of ill health in the world is poverty. Help to Make Poverty History. For example, why not lend some of your money to disadvantaged communities to enable them to trade their way out of poverty through schemes such as Shared Interest.

See also MAKEPOVERTYHISTORY North East for details and links to campaigns against poverty.

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