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Join 300 of the greatest minds in rare disease
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Available for 30 days until 7 Nov
DOWNLOAD the full RARefest20 review
Delve into this beautifully illustrated and fascinating review of the RF20 highlights from 28 Nov 2020. A truly collaborative review with a wealth of feedback, event reports written by attendees from around the world.
“This was a fabulous day; very well organised and thought provoking!”
Noonan Syndrome Association
Over 25 young people did live quizzes, demos, performance and panel discussions. Dana, Cookies4Cures founder from the USA, joined us for a live cookie decorating demo and to talk to us about how she’s raising funds for rare disease research, giving hope one cookie at a time. Meet all of the 36 speakers who took part.
RAREfest20 took place on an interactive virtual platform. Images from the festival atrium and auditorium
21 science, technology, advocacy and arts organisations from the UK, Europe and the USA hosted exhibition stands with interactive content, fun experiments, cool facts and information and opportunity to chat to the experts behind the stand.
Catch up on RAREfest20 live
Watch RAREfest20 talks, demos, panel discussions, and quizzes recorded from the live event.
thought the organisation was very good or excellent
thought RAREfest20 was very good or excellent
made good connections which could prove fruitful in the future
are more interested in rare disease after RAREfest20