Suzie's Raynaud's Story
Paramedic Suzie didn't know she had Raynaud's until a colleague mentioned the possibility.
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We are incredibly grateful to everyone who has shared with us their personal stories of living with Raynaud's and scleroderma. As well as continuing to raise awareness, sharing experiences and talking about all the various aspects of living with these conditions provides an essential resource that is always available when someone is looking for some information and support.
Could you share your story with us? Everyone's journey is different so whatever your experience, we would love to hear from you. Please get in touch with us if you would like some more information, and we will be very happy to help you.
Paramedic Suzie didn't know she had Raynaud's until a colleague mentioned the possibility.
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Steph has been living with Raynaud's since she was a teenager
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For Caroline, a 40-year-old veterinary surgeon from Milton Keynes, the winter months can be problematic.
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Teenager Amy talks about her fight with Raynaud’s
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William Bloodworth, Age 9, from Sheffield doesn't let his Raynaud's get in the way of his love of sports.
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Meet Chloe who has Raynaud's
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Read Chelsea's story of living with extreme Raynaud's.
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Claire and Lewis share the challenges of doing every-day tasks
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Share your stories of Scleroderma and Raynaud's.
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Diane's story of Secondary Raynaud's.
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Hear Lorraine's experiences of Raynaud's, and later developing Scleroderma.
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Our Community share their personal Scleroderma stories
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Deb lived with Raynaud's for many years before being diagnosed.
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Sharon is newly diagnosed with Raynaud's and Scleroderma and shares her story of how it affects her everyday life.
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Thursday 14th November 2024
SRUK launches first of its kind Raynaud's Citizen Science campaign - calling for 10,000 people to Be Part of The Answer to unlocking progress on Auto-immune conditions affecting millions
Wednesday 16th October 2024
Together, Heat Holders and SRUK can combine their expertise, passion, and resources to make a meaningful difference, offering practical solutions to those who are most affected by the cold.
Tuesday 23rd April 2024
Have your say on the way your services are working for your Rare Autoimmune Rheumatic Disease (RAIRD)