RAREfest20 | Reflections
“This was a fabulous day; very well organised and thought provoking!”
Noonan Syndrome Association
Over 25 young people did live quizzes, demos, performances 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.
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.
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