In June 2022 we held the first ever patient webinar to help people with sarcoidosis and their family members to understand the latest treatment recommendations outlined in the new European Respiratory Society medical guideline for clinicians.
To make this information even more accessible and give more people the opportunity to have their questions answered, we held the webinar again in September in 5 languages: English, French, German, Italian and Spanish.
Each webinar included a presentation from a native sarcoidosis expert who helped develop the clinical guidelines. Participants had the opportunity to ask questions to the speaker.
The recordings of the event are available below (German to follow).
We are currently in the process of gathering the most frequently asked questions across the webinars to compile the answers to provide as an FAQ section. The link will be added to this event page.
This document explains the recommendations in the European Respiratory Society (ERS) clinical guideline for the treatment of sarcoidosis. It is aimed at people living with sarcoidosis, or their care givers.
Available in: Danish, Dutch, English, French, German, Italian, Serbian, Spanish and Swedish.
ELF does not charge for its events and materials. We want to make sure they are available to anybody who wishes to join or use them. To ensure we can keep doing this we ask that those who can afford to pay to make a donation. We are grateful to everyone who supports us in this way and helps lung health patients to understand more about their condition and have their voices heard.
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