Living with Kaposi's sarcoma
Most people feel overwhelmed when they are told that they have KS. You’re likely to experience many different emotions. These are part of the process many people go through in trying to come to terms with their illness. Reactions differ from one person to another. There’s no right or wrong way to feel.
Partners, family and friends often have similar feelings and may also need support.
For some people, KS may be the first sign that they have HIV/AIDS, and coming to terms with this can be very difficult. There are many organisations that offer help and support to people with HIV/AIDS and we’ve listed some of these below.
Coping with skin lesions can be difficult, especially if they’re very visible. It may be possible to use skin camouflage to cover small flat skin lesions and make them less noticeable. Some clinical nurse specialists, the British Association of Skin Camouflage and the British Red Cross offer a camouflage make-up service and teach you how to apply it.
If you have lymphoedema as a result of KS this can also be hard to cope with, but there are ways in which it can be treated and improved. There are specialist nurses who treat lymphoedema and run clinics that you can be referred to.