Scleroderma family day 2020

The scleroderma family day is an opportunity for patients, their families and friends to talk with the doctors who look after them, receive education and ask questions about the treatment of their disease.

Scleroderma Family Day - Saturday 02 May 2020 - Postponed to 2021


To mimimise risk to patients and families during the Covid-19 pandemic we are cancelling the 2020 Scleroderma Family Day. This is unfortunate but in line with our hospital policy of reducing potential exposure. It is disappointing but it would be difficult to celebrate the 25th Family Day in the way that it deserves. We will therefore postpone our anniversary Family Day to 2021. The raffle will still proceed, and winners will be contacted in due course.
 

2017 family day talks

Stem cell transplant: Prof Chris Denton roy
Lessons from Sjogrens Syndrome: Dr Elizabeth Price    

Previous family day talks

Vascular disease in the extremities: Dr Ariane Herrick
The gut in scleroderma: Dr Charlie Murray
Treatment of systemic sclerosis: Prof Chris Denton
Factor XIII in scleroderma: Dr Anna Gill
Foot pain in scleroderma: Dr Begonya Alcacer-Pitarch
Emerging therapies for lung fibrosis: Helen Garthwaite
Scleroderma and the kidney: Ed Stern
Research update: Prof David Abraham
Plastic surgery approaches for Raynaud's: Ms Sophia Opel
Stem cell transplant, part 1: Prof Chris Denton
Stem cell transplant, part 2: Prof Chris Denton
Scleroderma and cancer: Dr Voon Ong
International research collaboration: Prof Oliver Distler