Have Your Say on Lipoedema Pain! Participate in Pain Alliance Europe’s Chronic Pain, Mental Health and Self-Management Survey As part of Pain Alliance Europe (PAE), we’re helping raise awareness of what living with lipoedema pain is really like, and we’d love your support. The PAE’s Chronic Pain, Mental Health and Self-Management Survey is open now and is […]
Have Your Say on Lipoedema Pain! Read More »
Do you have lipoedema? Have you ever been pregnant? We want to hear from you… You are invited to participate in an international research study exploring the experiences of lipoedema before and during pregnancy, and in the first year after childbirth. Participation involves completing an anonymous online questionnaire, which takes around 60 minutes and can
Do you have lipoedema? Have you ever been pregnant? We want to hear from you… Read More »
Liposuction for Lipoedema Update Lipoedema UK welcome an update to the National Institute for Health and Care Excellence NICE’s Liposuction for chronic lipoedema Guidance, IPG721. See the update from NICE below: “NICE is aware of the LIPLEG trial taking place in Germany and the July 2025 Federal Joint Committee press release about this trial. NICE will review this guidance
Great News from the National Institute for Health and Care Excellence Read More »
Lipoedema UK is proud to share a new blog article written by our Director of Strategic Partnerships, Mary Warrilow, published on the Royal College of Nursing website and shared with the Women’s Health Forum members. Educating healthcare professionals and working in partnership with respected associations is crucial to raising the profile of this under-recognised condition.
Surgical treatment of lipedema: G-BA includes liposuction in the regular catalogue of services after positive benefit assessment German Joint Federal Committee for Healthcare Services (G-BA) met on Thursday 17th July 2025, and recommended that liposuction for lipedema should be funded by the health insurance system in Germany for people with lipedema. This decision recognises
Welcome to our 2024 Year-End Review An Event-full Year… At the Primary Care Show in Birmingham, our stand was of great interest to hundreds of GPs and Health Care Professionals. Our team shared our resources and knowledge, including diagnosing some visitors on the day! Lipoedema UK volunteer and GP Nicki Mazey delivered a packed-out lecture
Highlights of 2024 Read More »
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
