DEBRA International
@InterDEBRA
For a world where anyone with epidermolysis bullosa (EB) has support from a DEBRA group, and access to specialist treatments, healthcare, and social support.
ID:4322311276
http://www.debra-international.org 29-11-2015 21:59:35
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Day 3 of the #EBCongress2024 has kicked off with panel sessions from experts around the world who are discussing key issues in access and advocacy for rare disease patients.
Welcome to day 2 of #EBCongress2024 ! Today focuses on advocacy in EB with networking sessions, achievements and challenges of DEBRAs in the MENA region and worldwide, and the priorities of patients.
Opened with an informative introduction from DEBRA International president Ritu Jain.
Weโre here! The #EBCongress2024 is underway with emotional opening remarks from Yasmin ElSamra Foundation, DEBRA International and representatives from the National Research Centre and universities around Egypt ๐ช๐ฌ
Thank you Urgo Medical UK & Ireland for your support, and for allowing us to come together and learn more about EB. We look forward to welcoming you in Cairo soon!
Raise global awareness about the significant impact of skin conditions, and to urge health policy leaders worldwide to prioritize these critical issues. Join the Movement: It's About Our Skin, But It's Also About Our Lives ๐๐ข #NotJustMySkin
๐๏ธ notjustmyskin.org
๐๐๐ Thank you Krystal Biotech, we are very much looking forward to having you at the next EB Congress 2024 in Cairo!
Illumina โถ๏ธAlexandra Heumber, CEO of Rare Diseases International who has a deep-rooted conviction in patient advocacy, multilateralism and diplomacy to improve global health ๐๐
Plus many, many more! Take a look at our programme online for more details ebcongress2024.org/programme