Living with Scleroderma (Nicola Whitehill); European Rare Diseases Organisation (EURORDIS) Article

I am extremely honoured that EURORDIS (European Rare Diseases Organisation) have shared my 'living with scleroderma' story in their Jan 2016 e-newsletter, as well as, on their website homepage www.eurordis.org 

http://www.eurordis.org/news/living-with-scleroderma-and-raynauds-disease

~ Living the dream, in the hope for a cure, NOW.... 

PLEASE DONATE to the ROYAL FREE CHARITY, to help fund desperately needed MEDICAL RESEARCH at the SCLERODERMA UNIT, THE ROYAL FREE NHS HOSPITAL.  

 

#SclerodermaFreeWorld   #RaynaudsFreeWorld   #Research 

  

#Autoimmune #RareDisease  #LifeChanging