UK NHS Lymphoedema Network Wales specialists and patients have created these short films to help you understand the impact of lymphoedema on families. However, if you have any concerns or worries you should of course contact your healthcare professional for advice.

We would love to know how you are progressing so please take a moment to answer the questions attached to this link.

Lymph Adventure Day

Teenagers and young adults meet for a day of sharing experiences and ideas. Hollie grew up thinking she was one of the only people who had lymphoedema, Ellie didn’t know anyone else either and Ceri-Anne is looking for more group chats. Meet a great bunch willing and able to share their stories. You can connect too via the Lymphoedema Network Wales Facebook page.