RT @Prof_Marciniak@twitter.com

Having fun at #RAREFest22 with @TheCIMR@twitter.com @dgershlick@twitter.com https://t.co/EhnAW7Bmas

RT @SuttyEmma@twitter.com

“For us, rare disease day is every day.”
Mum of Tristan who has Russel-Silver Syndrome.
We are listening.
#RAREFest22

🐦🔗: https://twitter.com/SuttyEmma/status/1596492292260593669

RT @SuttyEmma@twitter.com

Two lectures in at #RAREFest22 and already my mind is blown by the phenomenal mix of science, art and sharing how we find solutions for people living with rare conditions. Another outstanding event from @camraredisease@twitter.com BRAVO!

🐦🔗: https://twitter.com/SuttyEmma/status/1596468807777804294

RT @camraredisease@twitter.com

A huge thank you to Sobi, gold sponsors of #RAREfest22 for helping put #RareDisease in the spotlight at this inclusive event in Cambridge on 25/26 Nov.
RAREfest is for everyone from curious kids to professionals!
More info & book your tickets here: https://bit.ly/3uFhKWu

🐦🔗: https://twitter.com/camraredisease/status/1595054774226911232

Hello! Todays our first day in the new world of @Mastodon

Some stuff we love, are interested in and do 😊

#RareDisease
#RareFest22
%RareSummit
#UniqueFeetCam
#RareBearLife
#PatientVoice
#Cambridge

Give us a follow. Come to our #science #twcuology #community #arts festival RAREfest22 next weekend!

Bit.ly/RAREfest22 It’s free and gonna be awesome!