Your questions answered
To mark Sarcoidosis Awareness Month 2023 we have added an FAQs section to our website
ERS Virtual School of Sarcoidosis - educational event for healthcare professionals
Promote this event to clinicians you know who might want to find out more about sarcoidosis
Online mindfulness course can improve fatigue for people with sarcoidosis
A summary of research published in the Lancet Respiratory Medicine
Watch our webinars to hear about the latest European sarcoidosis treatment guidelines
Webinar recordings available in English, Spanish, Italian, French and German.
Registration open - Sarcoidosis Treatment Webinars (September 2022)
Join a webinar to find out more about sarcoidosis treatment recommendations: in French, Italian, German, Spanish and English
Launch of Sarcoidosis Patient Charter
Promote our international charter and help raise awareness of sarcoidosis to improve patient care
Understanding the new sarcoidosis treatment recommendations: patient webinar
A 1 hour webinar for patients and family members - Thursday 9 June 16:00-17:00 CEST
Have your say on the future of rare disease
Please complete the Rare Barometer survey on the future of rare diseases - available in 23 languages
Get involved in a new group to help improve diagnosis, treatment and care for COVID-19
We are looking for people from across Europe to join our new Patient Advisory Group to work with several research projects in this vital area.
A survey to help future sarcoidosis research studies for people with pulmonary sarcoidosis
Can you help the FSR-SCOUT study led by the Foundation of Sarcoidosis Research and the University of Liverpool?