Talk Lipoedema is a very special charity to me. My wife, Wendy, has Lipoedema and the support she has received from the charity since diagnosis in 2014 has been invaluable. Talk Lipoedema operates nationally supporting, advocating and educating. Raising awareness of this poorly understood and often undiagnosed chronic condition is a vital element of the charitie's work towards patients getting the support they need to help them manage their condition.
The charity is run by a small group of dedicated volunteers who rely upon donations to cover costs such as information packs for medical professionals and local support groups.
If you would like to know more about the Lipoedema or the work of the charity please follow the link on this page.
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