Fighting Covid With Creativity

To overcome the lockdown, I have partnered with a local pianist to create daily Jams. Each day he sends me a song and I go through my archive of footage captured around Cambridge to make a short little digital postcard for social media. We call them jams as there is not to be any forethought

Revisiting Families 5 Years later

In 2015 we went out with F.A.S.T to create a series of filming highlighting the complex diagnosis of Angelman Syndrome. You can view the project here. Five years on we revisited the families plus a whole lot more to understand what changes have happened, what new support there is and how far the science has

A theatrical Journey to the Centre

The Freezer version of Jules Verne’s Classic tale of the journey to the centre of the earth is a high tempo, hilarious carnival of musical theatre, performed in english. The cast of 21 performers take the audience on an unforgettable theatrical adventure of song, play and dance, where the full spectrum of theatre magic is

Raising awareness of a rare disease

The Foundation was founded by parents of Angels, a term for to people with Angelman Syndrome, a condition discovered by Dr. Harry Angelman. They have been on a quest to find therapeutics to help support families with Angels. Angelman Syndrome (often abbreviated AS) is a severe neurological disorder characterized by profound developmental delays, problems with