Yesterday, we were delighted to be a part of the Royal Holloway University of London’s Rare Disease Day event.
Neil and Helen were inspiring the next generation of researchers and clinicians with interactive experiments and demonstrations (not unlike what you could expect to take part in at the Science on Tour events!).
We have been waving the flag for Duchenne muscular dystrophy, and celebrating Rare Disease Day together with the international community.
Find out more about the Duchenne research we are funding at Royal Holloway.
Rare Film Festival
