Wednesday 22nd November 2023
SRUK asks the Chancellor to consider the impact of changes to disability benefits on people with scleroderma and we renew our call for more support with energy bills for those that need it most.
Tuesday 21st November 2023
Ahead of the Chancellor's Autumn Statement we are calling on the government to expand its Cost of Living Payment criteria to include people living with Raynaud’s Phenomenon.
Thursday 17th November 2022
Scleroderma and Raynaud’s UK (SRUK) has expressed its disappointment that people with Raynaud’s have been ignored once again by the government.
Tuesday 15th November 2022
“My Raynaud’s has definitely gotten worse this year. I used to have an attack a couple of times a week, particularly if I was outside in the cold, but now it happens every day, even in my own house.”
Monday 7th November 2022
SRUK Survey highlights the devastating impact of the cost-of-living crisis and high energy bills for people with Raynaud's.
Friday 4th November 2022
The Rare Autoimmune Rheumatic Disease Alliance (RAIRDA) which SRUK is a member of, has released a report highlighting ‘alarming disparities in the quality of care and treatment’ received by people living with rare autoimmune rheumatic diseases (RAIRDs).
Thursday 21st November 2019
SRUK has long recognised that detecting the conditions earlier is key to ensuring that people live longer and better lives, which is why we fund studies to improve our understanding of the early warning signs of the conditions.
Tuesday 19th November 2019
Here, we highlight some examples of research projects that have been funded by SRUK in the past which focus on improving quality of life for patients.
Monday 28th November 2016
SRUK will be supporting Rare Diseases Day February 2017.
