Undiagnosed Children’s Day - Jemma’s Story
SWAN UK (syndromes without a name) is a support network for families of children and young adults (up to 25 years old) with undiagnosed genetic conditions.
Meet SWAN UK member Jemma and her son, Atticus, who has an undiagnosed genetic condition. In this video, Jemma discusses the challenges this brings and what a diagnosis would mean for her and Atticus. This video was made for our seventh annual nationwide awareness day, Undiagnosed Children’s Day.
You need to login to vote for your favourite videos.
Login using your existing social media account:
Register by email
If you don’t have an account, please register using the form below.
Why are we asking you to register to vote?
This helps us to stop voting abuse and also enables us to communicate the short-list and winners to everyone who voted later on. We will not pass this information on to anyone else.
If you have an account, please login using the form below or click here if you have forgotten your password.
Promote - Donate - Celebrate
Increased exposure for charity video content
Donations made directly to good causes throughout the campaign
Celebrating the success of film in fundraising