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If you've found this page, then you may already be aware of Lymphoedema, it's risks, symptoms and complications, but if you are new to the 'lymph-life', then we are here to try and speak frankly and help explain things in 'laymans terms' so everyone can understand and be aware of this condition.
Lymphoedema is a chronic condition and there is no cure for it, but it can be managed, and like most life-long conditions, the earlier the detection, the quicker it can be controlled. Most commonly, it is when the Arms and Legs are subject to persistent swelling, although it can be found in other parts of the body. The affected area or limb can then be susceptible to skin/tissue changes such as appearing folds, dry skin and 'leaky legs', infections, cellulitis, pain, difficulty moving the limb, heaviness or aching and of course, depression due to lack of self-esteem (it's not surprising).
Of course Lymphoedema symptoms can be found at varying degrees, to a mild swelling to 'elephantiasis', as shown in the pictures below.
If you worried about Lymphoedema or need extra advice or support, then please see your GP or contact one of these websites.
The British Lymphology Society (the BLS) - www.thebls.com
Lymphoedema Support Network (LSN) - www.lymphoedema.org