Scleroderma is a rare, chronic disease of the immune system, blood vessels and connective tissue. It is an autoimmune condition, meaning that the immune system becomes overactive and attacks healthy tissue within the body.

‘Scleroderma’ comes from the Greek, ‘sclero,’ meaning hard, and ‘derma’, meaning skin.

Scleroderma occurs when your body produces too much collagen, which is a strong, fibre-like protein. Collagen is useful because it provides a kind of scaffolding to support the skin and the body’s connective tissues. When you have scleroderma, extra collagen builds up. This can make your skin stiff, tight, thick or scarred. For some people, this build-up affects the blood vessels, joints and muscles, and internal organs.

There are many types of scleroderma and so everyone’s experience of scleroderma is different.

SRUK
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Types of Scleroderma

There are two main types of scleroderma: Localised and Systemic
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What causes Scleroderma?

The cause of scleroderma is still unknown, although medical professionals are continuing to carry out research
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Scleroderma in children

When your child is diagnosed with scleroderma it is important to have reliable information and support when you need it.
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FAQs about Scleroderma

Everyone has questions about scleroderma, and here we have compiled some of the most common questions we are asked about scleroderma.

Download our publications on scleroderma

Understanding Scleroderma

A longer publication all about scleroderma

Information

Learn more about scleroderma

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Signs & symptoms of Scleroderma

Everyone’s experience of scleroderma is different. It depends on what type you have, how severe it is, and what parts of your body are affected.
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Diagnosing Scleroderma

The first step to getting diagnosed is to book an appointment with your GP
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Newly diagnosed with Scleroderma

What to know when you have just been diagnosed with Scleroderma