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Whether you're newly diagnosed or have been living with it for years, we can offer support and information to help you on your Raynaud's or Scleroderma journey.
We have everything from in-depth booklets on individual symptoms to a helpline that operates 365 days a year. Not sure where to start? Click one of the buttons below
SRUK is dedicated to improving the lives of people with scleroderma and Raynaud's phenomenon
Our mission is to improve the lives of everyone affected by scleroderma and Raynaud's. We do this by investing in research, improving awareness and understanding of the conditions and providing information and support to all those affected.
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Monday 1st August 2022
SRUK supports the call on the UK Government to provide Evusheld - a preventative antibody treatment for COVID-19
Evusheld is an antibody treatment designed to prevent patients from contracting COVID-19, and can provide protection for immunocompromised and immunosuppressed people that haven’t mounted a proper response to the vaccine. SRUK is supporting the call for the UK Government to procure and provide Evusheld to patients in the UK. Find out about how you can help on this page.
Friday 15th July 2022
Six Months of STAR – the Symptom Tracking App for Raynaud’s
July marks six months since Scleroderma & Raynaud’s UK launched STAR, the Symptom Tracking App for Raynaud’s, which enables members of the SRUK community to track their Raynaud's attacks and directly contribute to essential scientific research into the condition. Here’s a breakdown of what we’ve learnt so far, thanks to the STAR community!
Wednesday 29th June 2022
Undiagnosed & Untreated: Realities of Systemic Sclerosis in Europe Today
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