Wednesday, 20 January 2016

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 



~ 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


  



 

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