Treatments
Lipoedema
Lipoedema (Lipedema non UK, (Lipalgia-Wales)) is a long-term condition in which fat builds up abnormally, usually in the legs, hips, bottom and sometimes the arms. It mainly affects women and is often mistaken for obesity or lymphoedema.
Common signs and symptoms
- Symmetrical swelling of both legs (and sometimes arms)
- Feet and hands are usually not affected
- Legs may feel heavy, painful, tender and bruise easily
- Fat tissue may feel soft, nodular or lumpy
- Swelling may get worse over time, especially after standing a lot
- Diet and exercise will improve general health but may not reduce the affected fat in the same way
Despite significant research the exact cause isn’t fully understood, but it is thought to be linked to:
- Hormones (it often appears or worsens during puberty, pregnancy or menopause)
- Family history / genetics
Treatment and management
There is currently no simple cure, but symptoms can often be managed with:
- Compression garments
- Strengthening exercises
- Weight management support
- Manual lymphatic drainage in some cases
- Deep Oscillation therapy
- Pain management
- GLP1’s in some cases
- In selected cases, liposuction specifically for lipoedema may be considered by specialists
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Phone Number
02035 404553
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About Us
The Association of Lymphoedema Practitioners (ALP) is a not‑for‑profit professional body dedicated to supporting, representing and advancing all aspects of lymphoedema practice across the UK. We bring together practitioners working in both private practice and NHS settings, creating a central hub for education, professional development and connection. Our aim is to strengthen the profession and support practitioners in delivering safe, effective and high‑quality lymphoedema care.
We provide access to training, CPD, clinical guidance and practical resources. Through our confidential professional network members can share knowledge, connect with colleagues and feel supported throughout their professional journey. We also offer a patient‑facing directory to help individuals find qualified practitioners in their area, ensuring access to skilled care while championing best practice across all lymphoedema services.
As a company limited by guarantee all income is reinvested into education, resources and activities that benefit both practitioners and the public.
