💙 As we count down to #RareDiseaseDay, revisit our Capacity Building video series on enhancing accessibility in physical and digital spaces.

Available in 12 languages, it's packed with practical insights to help you build a more inclusive world. 👉 https://www.rarediseaseday.org/webinars/

🏆 Celebrate the people and initiatives making a difference in rare diseases.
Join the 15th #EURORDIS Black Pearl Awards on 24 Feb 2026, held in Brussels & online as part of #RareDiseaseDay celebrations.
🎥 Online participation is free.
👉 https://loom.ly/ClRoNdc
#RareDiseases #ERDERA

💜 #Equity starts with one simple truth: not everyone begins from the same place.

Equality gives everyone the same opportunities. Equity removes barriers so everyone can achieve fair outcomes. This #RareDiseaseDay, let's turn awareness into action.

We achieved #MoreThanYouCanImagine. But we’re still imagining more. 🌍

Millions came together for #RareDiseaseDay 2026 to raise awareness and call for greater equity. Now, we’re building on that momentum for 2027.

🔗 See what we achieved: https://go.eurordis.org/RDDArticle

🌍 Same goal: bringing #RareDiseaseDay into the classroom. Two different approaches.

Stories, games & student research
Family conversations, art & an exhibition

Our NEW case study shares how schools brought rare disease awareness to life: https://go.eurordis.org/ItStartsWithAConversation

What is #RareDiseaseDay? 💙

More than a day on the calendar, it's a global movement united by one goal: EQUITY.

Equity in diagnosis, healthcare, treatment, support and opportunity for the 300+ million people living with a rare disease worldwide. Join the movement: https://go.eurordis.org/RDD

What is a rare disease?

A rare disease is a condition experienced by fewer than 1 in 2,000 people. Yet together, more than 300 million people worldwide are living with a rare disease.

Rare diseases are rare. People living with them are not.💙

#RareDiseaseDay