Scleroderma / Systemic Sclerosus

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This page has been archived. It has not been updated since 18/11/2011. External links and references may no longer work.

UK sources of information and / or support

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Patient UK

Has a leaflet on Localised Scleroderma (Morphoea).

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Raynaud's & Scleroderma Association

The Association's aims include to create a greater awareness of Raynaud's and scleroderma and offer support, advice, and information to sufferers and their families.

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Scleroderma Society

A voluntary organisation based in the UK. Offers support to patients and relatives who can often feel isolated.

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Reliable information provided by Arthritis Research UK.

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The Circulation Foundation

Dedicated to raising funds for research and awareness of vascular (circulatory) disease. Their website includes information on various vascular diseases including scleroderma.

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Scleroderma and the Kidney

Information from the Renal Unit of the Royal Infirmary of Edinburgh.

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Morphoea / Localised Scleroderma

Information from The British Association of Dermatologists.

Further sources / more detailed information

Some non-UK sites

The following list popular non-UK health information sites with content aimed at the general public. They are mainly from the US. They have not been checked to see if information about the above topic is included but these large sites are comprehensive.

More detailed medical information

The following list online sources of more detailed medical information, mainly from the UK. These sites are mainly aimed at health professionals, but are of interest to all. They have not been checked to see if information about the above topic is included, but information about most medical topics can usually be found.

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