Connie Dickason was born in Cambridge on 14 March 2010, Mother's Day. She was diagnosed with Edwards Syndrome at just 9 days old. Edwards Syndrome is a life limiting genetic condition with no cure. Despite the odds against her, she stayed with us for 21 months and was an inspiration to all who met her. She is much loved and missed by her family, friends and everyone who knew her.

The family and EACH have created the following film of Connie's life to highlight the services that they all received during Connie's life.  Please take a look:

https://www.youtube.com/watch?v=DQkkkC6OOuA