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For more detail on the challenges faced by people living with RAIRDs, read the Rare Care Matters report, released this week. The full report is available on our website: rairda.org/publication/re… Sue Farrington

I just nominated SRUK | Scleroderma & Raynaud's UK health.movementforgood.com/index.php?cn=1… #nominateACharity

Another great day at the BSR conference. Yesterday, Nick from our research team delivered a presentation to a packed house on how we help and support people with #scleroderma and #Raynauds. We'd also like to thank everyone who visited our stand!

Trisha Goddard reveals she’s now battling severe Raynaud’s syndrome, made worse by a year of chemo, sharing a photo of her bright red fingers as she sheds light on this often-overlooked condition. Read more: bit.ly/4keEPXV

I have this #SayScleroderma

Just to say ... I have this ... #SayScleroderma #SclerodermaAwarenessMonth Please RT to help raise awareness

June is Scleroderma Awareness Month. For people like me with this disease, if you can, please donate to this charity. It is the only charity for this rare disease in the UK, and SRUK helps keep people like me alive. x.com/WeAreSRUK/stat…

🎬 Our powerful new film is shining a light on scleroderma, a rare, life-altering autoimmune disease. Beth, 31, stars in #SayScleroderma to share her journey with systemic sclerosis and raise awareness. 📰 Read her story here: bit.ly/3HnkfpJ #SclerodermaAwarenessMonth

🗣️ “Early diagnosis is vital.” Dawn, 43, from Northern Ireland, shares her journey with CREST syndrome in support of #SayScleroderma, raising awareness of this rare autoimmune disease. Read her story 👇 bit.ly/3ZMAnaD #SclerodermaAwarenessMonth

Your health matters. The wonderful charity SRUK | Scleroderma & Raynaud's UK has an online #Raynauds test that takes just a couple of minutes sruk.co.uk/about-raynauds… 🧤💛 Get to know #AutoimmuneHealth visit their website to learn more #Scleroderma & Raynaud's UK - #SRUK #SclerodermaAwarenessMonth

Our Head of Research, Ula is at EULAR in Barcelona, kicking off with powerful insights on ILD, digital ischemia, GI involvement & more in systemic sclerosis. A vital reminder of how far we’ve come and what’s still to come. #EULAR2025 #SystemicSclerosis #Scleroderma

This Scleroderma Awareness Month join SRUK | Scleroderma & Raynaud's UK as it launches its #SayScleroderma film to help raise vital funds into research of the rare, autoimmune disease. 🎥 youtube.com/shorts/ZS4_SY4… #SclrodermaAwarenessMonth

Many people with an auto-immune condition such as inflammatory arthritis also have other auto-immune conditions, so we're always happy to help our friends at SRUK | Scleroderma & Raynaud's UK raise awareness of these. It's Scleroderma Month - we encourage you to find out more. #SayScleroderma

Highly recommend hearing Professor Chris Denton, VP of Scleroderma & Raynaud's UK - SRUK. Professor Denton was one of the first medical professionals who was involved with my #autoimmune journey. I’m ever grateful for his expertise and urge anyone who has the opportunity to

June is #SclerodermaAwarenessMonth. SRUK | Scleroderma & Raynaud's UK is raising awareness with their short film #SayScleroderma. 🎥 Watch the film and learn more about scleroderma and ways you can support on their website ➡️ sruk.co.uk #Scleroderma

🚨Patients with systemic sclerosis survey alert 🚨 Questionnaire on ORAL HEALTH 👄 needs of people with systemic sclerosis (on behalf of the SCTC Orofacial in SSc Working Group) docs.google.com/forms/d/e/1FAI… SRUK | Scleroderma & Raynaud's UK World Scleroderma Foundation EUSTAR Professor Francesco Del Galdo Alessia Alunno