Rare Disease Day
29th February
Rare Disease Day is the globally coordinated movement on rare diseases, working towards equity in social opportunity, healthcare, and access to diagnosis and therapies for people living with a rare disease. Since its creation in 2008, Rare Disease Day has played a critical part in building an international rare disease community that is multi-disease, global, and diverse– but united in purpose.
The International FOXP1 Foundation is working to encourage research to better understand how FOXP1 gene mutations affect the health and development of our children.
Please Donate Today to support FOXP1 Research
Ways you can raise awareness and generate change for FOXP1 Syndrome and Rare Disease Day
200+ Sterk voor RareX
Doe mee aan de uitdaging om RareX Data Collection te krijgen
bevolkt met meer dan 200 vossengegevens door Feb 29e
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200+ vossen geregistreerd bij RareX
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200+ genetisch rapporten uploaded
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200+ opheel eenantwoordde
Heeft u uw RareX-registratie en gegevensinvoer voltooid?
Schrijf je in of log inHer om je zeker te maken help om onze te bereikendoel
~200+ inzendingen zullen onderzoekers aanmoedigen om FOXP1 te bestuderen
Everyone can participate in the Global Chain of Lights and Share Your Colours!
In an effort of global solidarity, you are invited to light or decorate your home with the Rare Disease Day colours at 7 PM your local time on 29 February 2024. You can use garlands, social media filters, candles, disco lamps, colourful decorations… Let your creativity shine!
You could create your own window display with coloured lights, painted pictures, tissue paper colages or your drawings. However you like to get creative, share your colours!
Light up for Rare
Write your city or town council and ask them to Shine the Lights for FOXP1 Syndrome on Rare Disease Day.
Download multi media frames and filters here
Be part of Rare Disease Day by sharing your story with others and sending a message of solidarity! link
Find an event near you. Check out all the events and activities happening around the world.
~~ 100% of your donations will fund research on FOXP1 syndrome ~~