For people with sarcoidosis and their family members to hear about the latest European sarcoidosis treatment guidelines
This 1 hour event is for people with sarcoidosis and their family members and caregivers to hear about the latest treatment recommendations outlined in the new European Respiratory Society medical guideline for clinicians.
You will have a chance to ask questions in a range of languages to the medical experts who developed these evidence-based recommendations.
The event will be in English but the main presentation will be pre-recorded in a range of languages and made available in advance for attendees to watch. Languages include: Chinese (Mandarin), Danish, Dutch, French, German, Italian, Serbian, Spanish and Swedish. We will send a link to these to all attendees when they are available.
You can also join a breakout room during the event to ask questions in the above languages to the medical experts who developed the guideline.
We hope this event will help people affected by sarcoidosis to better understand sarcoidosis treatment and the latest guideline recommendations. We hope it will help you to ask informed questions about treatment to your own doctors.
Anyone interested in finding out more about sarcoidosis treatment is welcome to attend this free event.
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ELF is a non-profit organisation registered as a UK company (VAT no. GB 115 0027 74) and charity (no. 1118930).
Our Brussels office enterprise number is 0738.383.695
European Lung Foundation's TR ID number in the Transparency Register is: 094039644810-79
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