Raising awareness for patients, families and carers around the world that are affected by rare diseases.
Rare Disease Day is an observance held on the last day of February to raise awareness for rare diseases and improve access to treatment and medical representation for individuals with rare diseases and their families. The website serves as a central hub for information, resources, and events related to Rare Disease Day.
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Find and share events happening around the world for Rare Disease Day.
Access a wide range of resources including guides, reports, and educational materials.
Learn about ongoing campaigns to raise awareness for rare diseases.
Discover ways to participate, from volunteering to organizing your own event.
Read personal stories from individuals and families affected by rare diseases.
Stay informed with the latest news and updates related to rare diseases and Rare Disease Day.
Connect with the community through integrated social media platforms.
Download or request educational materials to spread awareness.
View a map showing global participation in Rare Disease Day events.
Find support groups and advice for dealing with rare diseases.
Rare Disease Day is coordinated by EURORDIS (European Organisation for Rare Diseases) and 65+ national alliance patient organization partners.
Rare Disease Day is observed in over 100 countries, making it a global movement.
The main objectives are to raise awareness amongst the general public and decision-makers about rare diseases and their impact on patients' lives.
The symbol for Rare Disease Day is a hand with a painted zebra stripe, representing the uniqueness of rare diseases.
Collaborates with various organizations, healthcare professionals, and researchers to advance the cause.
Funded through donations, sponsorships, and grants aimed at supporting rare disease research and awareness.
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