28 Februaryis Rare Disease Day

Raising awareness and generating change for the 300 million people worldwide living with a rare disease, their families and carers.

Share your colours Download materials
92
days
to go

300M

people with rare diseases

600+

events worldwide

106

countries involved

Share your colours

Join the community. Help us build awareness. Share your photos, videos and experiences!

Read our stories

Vincent’s Story

In 2016 my son Vincent was born. Weeks after he was born he started experiencing symptoms of sweating, shaking, paleness and blueness in the lips… Continue reading Vincent’s Story

Read full story

Friends that Care are Rare

“Not Too Rare to Care” Did you know that millions of people are diagnosed with rare diseases and unknown disorders everyday, especially women? According to… Continue reading Friends that Care are Rare

Read full story

Living with Batten Disease: Anthony’s Story

Meet my son Anthony, he was diagnosed with Neuronal Ceroid Lipofuscinosis Type 7, also known as Batten Disease. Batten Disease is a rare, terminal genetic… Continue reading Living with Batten Disease: Anthony’s Story

Read full story
What's your story?

Be part of Rare Disease Day by sharing your story with others and sending a message of solidarity!

Share your story

Listen to our stories

Subscribe

Thousands of events
in over 100countries

Every year, thousands of events are
organised across the world.

In the news

Thumbnail with a pink and blue painted background. Five people (3 women, 1 man and 1 child) are featured. The text reads "Rare Disease Day. More than you can imagine. 28 February 2025"

Today, 20 November 2024, marks the official launch of the Rare Disease Day 2025 global campaign, beginning the 100-day countdown to 28 February 2025. This… Continue reading Launch of the Rare Disease Day 2025 Campaign

A photo with two men and one woman sitting. The man on the right is in a wheelchair and smiling. The other man is on the left, his back to the camera, and is handing the woman a juice bottle. She is in the middle facing the camera and smiling.

Imagine a world where everyone can access the spaces and resources they need to thrive, regardless of their condition. As Rare Disease Day approaches, join… Continue reading Enhancing Accessibility in Physical and Digital Spaces

Pink spots on purple background. The text reads "Upcoming Webinar; Driving Awareness by Amplifying Young Voices In the Rare Disease Community; Thursday Feb 8, 2024, 2pm (CET); Follow for more; rarediseaseday.org"

On February 8 at 2PM (CET) the Rare Disease Day team is hosting a webinar on “Driving Awareness by amplifying young voices in the rare… Continue reading Learn to engage your young community

EURORDIS has received funding for this website under an operating grant from the European Union’s Health Programme (2021-2027). Views and opinions expressed on this website are however those of the author(s) only and do not necessarily reflect those of the European Union or HaDEA. Neither the European Union nor the granting authority can be held responsible for them.