Susan Morris

Executive Director

Susan joined the Lynch syndrome team in 2014, driven by her own experience with Lynch syndrome and that of her family over four generations. She wants to help improve understanding of this condition amongst the medical profession and the general pubic and to advocate on behalf of all those living with Lynch syndrome who face myriad medical, social and financial challenges. 
 
Susan has many years’ experience in communications, public relations and corporate social responsibility in the UK, Europe and in Australia and is determined to make Lynch syndrome a mainstream and widely understood inherited cancer condition and to establish accepted standards of care and surveillance for those with this genetic disorder. 
 
Susan has a BA (hons) in Combined Arts and a Master of Arts in Strategic Communications. She also speaks five languages, none of which, unfortunately, helps her understand research studies on cancer genetics!