Thursday 12th July 2018
Mum walks 100 miles to find a cure for son’s rare condition
Jo Barry walked 100 miles to raise vital funds and awareness for SRUK.
Monday 24th July 2017
Sian talks about helpful hints for looking after your feet
Sian talks about helpful hints for looking after your feet
Tuesday 18th July 2017
Autologous lipotransfer utilises the patient’s own cells to reverse the effects of fibrosis
This pioneering and innovative new treatment option is to treat fibrosis of the face and other tissues in people with scleroderma. The technique is known as autologous lipotransfer and utilises the patient’s own cells to reconstruct facial tissue and reverse the effects of fibrosis and internal scarring.
Wednesday 12th July 2017
5 symptoms to look out for if you have cold hands or cold fingers
5 symptoms to look out for with your hands to tell if you have Raynaud's
Tuesday 11th July 2017
The Rare Autoimmune Rheumatic Diseases Patient Survey
This survey has been developed on behalf of the Rare Autoimmune Rheumatic Diseases Alliance (RAIRDA), a partnership that was formed in 2016 to improve the quality of life of people living with rare autoimmune rheumatic diseases.
Wednesday 5th July 2017
Charity research makes a difference
On average it takes 17 years for an idea for a medical product to be developed, tested in studies and trials, and become publicly available. Charities have an important role in supporting medical research that leads to breakthroughs, and ultimately licensed treatments.
Friday 22nd July 2016
Increasing Awareness
During June we launched our first public facing awareness campaign to highlight the signs and symptoms of Raynaud’s and the link between Raynaud’s and Scleroderma.
Thursday 21st July 2016
Charity Spotlight - OpenCity Inc
Thank you to OPENCITY INC for featuring us this month in their Charity Spotlight. Take a read of the article John Gregory wrote about SRUK.
Wednesday 6th July 2016
Afternoon Tea
Yun Wah Wan organised this amazing afternoon tea in celebration of the merger between the Scleroderma Society and Raynaud's and Scleroderma Association to for SRUK.