Alex’s Wish is a charity organisation raising funds and awareness to help find a cure for Duchenne Muscular Dystrophy. Andy and Emma Hallam and his family founded Alex’s Wish in 2012 shortly after their son Alex was diagnosed with Duchenne. Since launch, the team has grown to include 3 voluntary Trustees and a part-time member of staff to support areas of Events, Marketing and Administration.
We are a positive/upbeat team with one goal to end Duchenne for all and as quickly as possible. All our funds raised goes directly to research projects and clinical trials that will benefit all children and young adults who have Duchenne Muscular Dystrophy. Andy and Emma are hugely dedicated to doing everything they can to save their son and to prevent others from suffering as they do. The support we get from our team helps the charity grow from strength to strength.
We are always looking for new trustees and volunteers to join our cause – if you think you could dedicate some time – please get in touch with us today by contacting Emma on 07903 349475 or firstname.lastname@example.org we would love to hear from you.