SRUK | Scleroderma & Raynaud's UK

Scleroderma & Raynaud’s UK is the only charity dedicated to improving the lives of people affected by scleroderma and Raynaud’s.

[Scarlett Prentice @scarlettrosep97]

So close to my target 💙🥰 Thanks to all the donations 🥰 Raising money for Scleroderma. This is an autoimmune rheumatic disease. That currently has no cure. All donations to this charity go along way. It’s also important to spread awareness @WeAreSRUK

https://t.co/AfwCnVRh2Z

[SRUK | Scleroderma & Raynaud's UK @WeAreSRUK]

@scarlettrosep97 You are most welcome : )

[Scarlett Prentice @scarlettrosep97]

I’m running the London Marathon 2026 for @WeAreSRUK 🇬🇧 🫶🏼 If anyone can donate anything at all or share my post it would be really appreciated 💙

https://t.co/Vd97bo0Wd0

[SRUK | Scleroderma & Raynaud's UK @WeAreSRUK]

“We are delighted that @ScleroForum is signposting clinicians to SRUK to help them further support their patients living with scleroderma. SRUK provides information and support for patients, funding research and improving treatment'' - Sue Farrington, CEO, SRUK

[Scleroderma Forum @ScleroForum]

We’re excited to announce our collaboration with @WeAreSRUK! 🎉

You can now find their site in the ‘useful links’ section of the Scleroderma Forum.

Check it out to explore valuable patient resources to enhance your clinical practice: 🔗https://t.co/25S47rBFXs

[Scleroderma Forum @ScleroForum]

We’re excited to announce our collaboration with @WeAreSRUK! 🎉

You can now find their site in the ‘useful links’ section of the Scleroderma Forum.

Check it out to explore valuable patient resources to enhance your clinical practice: 🔗https://t.co/25S47rBFXs

[Scarlett Prentice @scarlettrosep97]

So exciting all my fundraising merchandise has arrived, for my first London Marathon 💚 🇬🇧 for @WeAreSRUK Time to make a difference💙 #scleroderma #raynauds donate below or share if you can 🙏🏻 💪🏻 https://t.co/nm6jJRnTcu

[SRUK | Scleroderma & Raynaud's UK @WeAreSRUK]

🎓 Just 2 days to go until the SRUK Conference in Cambridge!
Join us for expert talks, community connection & the latest in scleroderma care.
🎟️ Tickets available: https://t.co/8HK3QU9zn4
💙 Thanks to our sponsors: @ZuraBioLimited @Boehringer, @JNJNews & Bristol Myers Squibb.

[SRUK | Scleroderma & Raynaud's UK @WeAreSRUK]

🎓 The SRUK Conference is happening this Friday, 26 July in Cambridge!

Proudly sponsored by @ZuraBioLimited, @Boehringer, @JNJNews & Bristol Myers Squibb.

Don’t miss this powerful day of learning, connection & community.

🎟️ Tickets still available: https://t.co/8HK3QU9zn4

[Scarlett Prentice @scarlettrosep97]

I’m raising money by running a marathon for @WeAreSRUK! Scleroderma is currently an incurable disease and isn’t known by many people. If you can donate anything at all or retweet my post it is really appreciated 🤍 https://t.co/Vd97bo0Wd0

[Scarlett Prentice @scarlettrosep97]

I’m running the London Marathon!! 🏃🏻‍♀️🇬🇧 for @WeAreSRUK Please click the link below to find out more. If you can donate anything at all it would be really appreciated or share to spread awareness🤍❤️

https://t.co/Vd97bo1u2y

[Melanie Prentice @MelaniePrentic2]

Take 2 mins to learn more of Sarahs story. Our beautiful friend & neighbour of 28 yrs

Please support our Scarlett in anyway possible for her London Marathon, donate if you can to this relatively unknown disease.

Retweets appreciated to raise awareness
@WeAreSRUK

[RAIRDA @RAIRDA_org]

The 10-Year Health Plan for England includes some welcome steps, but must go further to meet the needs of people with RAIRDs, and deliver the specialist care and support they need. Read our full statement➡️https://t.co/jx0aNA0Ts1

[SRUK | Scleroderma & Raynaud's UK @WeAreSRUK]

🧪 Have an autoimmune disease? Help shape research & educate doctors on flares, triggers & symptoms. 🗣️

🩺 Take this 45-min survey co-created by @Cambridge_Uni & top rheumatologists.

🎁 Prize draw: 4x £50 Amazon vouchers!
🔗 https://t.co/Lqi8I8FzlE
📅 Closes 14 July

[RAIRDA @RAIRDA_org]

Go an watch #SayScleroderma film if you haven't already. You can check @WeAreSRUK's website for more details. 🎦⬇️

[PAFLAR AFRICA @paflar]

"From Hardship to Hope: United for Scleroderma – Raising Awareness, Inspiring Strength, and Standing Together: https://t.co/LLClS2RBhn

[SRUK | Scleroderma & Raynaud's UK @WeAreSRUK]

Aberdeen student Mithi Ahmed-Richards thought her cold hands were just winter blues, but it was scleroderma, a rare autoimmune disease.

Her story is a reminder: don’t ignore persistent symptoms.

Read more👉https://t.co/mbP6lNTHsn

[SRUK | Scleroderma & Raynaud's UK @WeAreSRUK]

Have you watched our #SayScleroderma film yet? 🎥 Dawn Neill from Magherafelt is one of 7 people featured. She recently spoke to @DerryNow about living with systemic sclerosis & why raising awareness matters 💜

Read more 👉 https://t.co/8OoIPtgauE
#SclerodermaAwareness #SRUK

[RAIRDA @RAIRDA_org]

June is #SclerodermaAwarenessMonth. @WeAreSRUK is raising awareness with their short film #SayScleroderma. 🎥 Watch the film and learn more about scleroderma and ways you can support on their website ➡️ https://t.co/sxcqIj5eax
#Scleroderma