About Vicki Cowell

I joined Seriously Ill for Medical Research (SIMR) in 1992 and was Chair of the organisation for eight years. Following the untimely death, in May 2002, of SIMR’s Director and Founder, Andrew Blake, I was appointed the new Director.

Originally involved in the world of public relations and advertising, I developed a keen interest in the world of medical research when my only child was diagnosed with cystic fibrosis (CF) in 1985. My daughter Laura (now nearly 20) is also involved in the work of SIMR, as a member of the management committee. 

Laura and I have also undertaken a lot of publicity work for both SIMR and cystic fibrosis research. We both firmly believe that patients suffering from serious, often incurable illnesses and genetic conditions, have a right to the best medical treatment that modern research can offer. We have never been frightened to voice their opinions and over the past 13 years have engaged with anti-vivisectionists in numerous radio and television debates.  

I am Editor of HOPE, SIMR’s quarterly newsletter, am a member of the Human Genetics Committee Consultative Panel and Deputy Chair and a Trustee, of the Genetic Interest Group (GIG).

I have worked in the theatre (in a previous life!) promoting a West End production and working on the organisation of a young writers’ festival. Before joining SIMR I was also an active member of an amateur dramatics company.     

http://www.simr.org.uk/

	This production tours the UK in Autumn 2007 for further information, Martin Ball