Being diagnosed with Turner’s Syndrome can be a terrifying experience. Our support groups aim to be a place of comfort and discussion away from the doctor’s waiting room where TS girls and their families can learn to come to terms with the condition, the health checks required and the social aspects of what lies ahead. Being available at the earliest possible stage is priority because we aim to support TS girls in living the best life possible.
The condition occurs in about 1 in 2500 live female births across the globe and yet there are still so many who have never heard of it. We feel that it is important to raise awareness so that more attention can be given to research into the condition as well as giving TS women the opportunity of the best care and support possible.
With your generosity we can expand our awareness campaigns and extend our reach further.