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FESCA
Mini newsletter from Fesca

Mini newsletter from Fesca

September 2, 2015 | News

Our latest newsletter, which is a mini newsletter on recent events involving Fesca is ready.

Recent news

  • Public access to medical records – why is progress so slow?
  • Kids get scleroderma, too!
  • Opinion article: The patient’s journey to a diagnosis
  • Testimony: António Pereira, music teacher
  • Testimony: Tânia Vieira, mother

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© 2020 FESCA. Federation of European Scleroderma Associations is an International Non-Profit Association registered in Belgium with Registration No. FOJ 15454