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In line with the UN Agenda 2030 and its central promise to “Leave no one behind,” the webinar aims to raise awareness of the impact of RDs on children’s learning and the curriculum transformations needed to include them in education. The event is organized by and co-organised with the and .

Panelists

• HE Irène Esambo Diata, Minister Delegate to the Minister of Social Affairs, Humanitarian Actions and for Persons Living with Disabilities and Other Vulnerable Persons, Democratic Republic of Congo
• Yao Ydo - Director, UNESCO-IBE
• Anders Olauson - Founder and Chairman of Ågrenska Foundation
• Flaminia Macchia - Executive Director of Rare Diseases International (RDI) 
• Florence Migeon - UNESCO, Programme Specialist, Inclusive Education Expert
• Gunilla Jeager, Psychologist, Ågrenska Foundation
• Renato Opertti - UNESCO-IBE Senior Expert
• 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)