UNESCO-IBE is organising a webinar on “Improving inclusion of children living with a rare disease through curriculum transformation”, co-organised with the Agrenska Foundation and Rare Diseases International and taking place on 28 November 2022 2:00-4:00 PM – Geneva time – (UTC+1).
Panelists:
- Yao Ydo – Director, UNESCO-IBE
- Anders Olauson – Founder and Chairman of Agrenska Foundation
- Flaminia Macchia – Executive Director of Rare Diseases International (RDI)
- Florence Migeon – UNESCO, Programme Specialist, Inclusive Education Expert
- Gunilla Jaeger – Senior Advisor Agrenska Foundation
- Carlos David Peña Aragon - Head of Social Networks, Federación Mexicana de Enfermedades Raras (FEMEXER), lives Gaucher disease (Mexico)
- Eda Selebatso - Founder of Botswana Organization For Rare Diseases (BORDIS) – Mother of two children living with different rare diseases (Botswana)
- Mark Rogers - Parent of a young adult living with DiGeorge Syndrome (New Zealand)
- Nikita Van Dijk - University student and patient advocate living with Ehlers-Danlos syndrome (New Zealand)
- Robin Yoon - M.D. Candidate, Georgetown University School of Medicine (USA)
- Sook Yee Yap and Jaden Lim - We Care, Journey – mother and son, Jaden lives with Growth Hormone Deficiency and Pituitary Microadenoma (15), and his brother lives with SMA Type One (Malaysia)
To attend the webinar, register here.
About Didier Jourdan
