Graham Slater

4 May 2013

EAT and its member organisations are very dear to my heart. In 1953 I was born in England with OA/TOF and I am fortunate enough to be one of the very earliest survivors of the condition not only in England but anywhere in the world. When I was born, and even by the time I was a young adult, there were no such support groups and neither my parents nor I had the benefits which EAT and its member organisations can now bring to the families of children and adults born with this condition. Indeed such groups still do not exist in many countries and one of EAT’s objectives is to encourage the creation of such groups in other countries