NHS Stars Series: Rachel’s Story Rachel describes what led her to set up a support group I love my role as a specialist nurse and feel privileged to be able to help, advise, support and guide my patients living with Lipoedema. It is not uncommon for my patients to have had a bumpy ride navigating […]
Creating a Lipoedema support group Read More »
The Lymphoedema Conference runs at Chester Racecourse from 7th–9th October, with guest speaker Cheryl Brunelle. The annual conference is suitable for all experience levels, and is a brilliant opportunity to learn about lymphoedema, and to network with industry specialists. For further details, visit the website: www.theblsconference.com. This is a Healthcare Professionals Event.
The Lymphoedema Conference – 7th to 9th October Read More »
Throughout the world lipoedema is not rare but it is only rarely diagnosed. As part of our work with the Lipedema World Alliance (LWA) Lipoedema UK have been instrumental in creating a worldwide patient manifesto. This initiative is now supported by twenty-one international lipoedema patient groups and organisations. Please download and share our manifesto and
