🌍 28 February 2026
💜 #EURORDISRareOnAir Stories return with Ahmed, who reflects on his global career and how living with #PCD has deepened his strength and purpose.
🎧 Listen to his inspiring story: https://www.eurordis.org/rare-on-air/
💜 #EURORDISRareOnAir Stories return with Ahmed, who reflects on his global career and how living with #PCD has deepened his strength and purpose.
🎧 Listen to his inspiring story: https://www.eurordis.org/rare-on-air/
Meet Mak, Linges, Micah, Ayça & Burak, our heroes showing what life is like for the 300M people living with a rare disease.
Full video 🎥 youtu.be/7J1oTfoIOGw
Let’s bring about equity in more ways than even we can imagine!
#ShareYourColours
Meet Mak, Linges, Micah, Ayça & Burak, our heroes showing what life is like for the 300M people living with a rare disease.
Full video 🎥 youtu.be/7J1oTfoIOGw
Let’s bring about equity in more ways than even we can imagine!
#ShareYourColours
On #RareDiseaseDay, we call for equity for 300M people worldwide 💜.
🔗 Explore the toolkit and join the movement: https://go.rarediseaseday.org/equity
On #RareDiseaseDay, we call for equity for 300M people worldwide 💜.
🔗 Explore the toolkit and join the movement: https://go.rarediseaseday.org/equity
How can you get involved? Learn more: https://go.rarediseaseday.org/rdd
How can you get involved? Learn more: https://go.rarediseaseday.org/rdd
But, did you know that over 300 million people worldwide are living with a rare disease? That’s 3.5%-5.9% of the world’s population.
💚Learn more at rarediseaseday.org
But, did you know that over 300 million people worldwide are living with a rare disease? That’s 3.5%-5.9% of the world’s population.
💚Learn more at rarediseaseday.org