An evolving archive centred on lived experience, clinical insight, emerging research & critical discussion.
The Lipoedema Lounge is a new and developing forum for people seeking clear, balanced and carefully considered information about lipoedema (also spelled lipedema). It exists for those who feel overwhelmed by the condition itself and by the, often conflicting, information they encounter at every stage from diagnosis onwards.
Through interviews with women sharing their stories in their own words, alongside careful engagement with research and clinical insight, the Lipoedema Lounge explores diagnosis, everyday life, compression, body changes, surgery and longer-term support.
It is a space to slow the conversation down, to learn together and make sense of lipoedema in a new way; that feels informed, grounded and human.
If you would like to be interviewed to share your story, ask a question, or help shape how this forum develops, you are very welcome to get in touch with me, Clare via my contact page
A developing archive of articles and commentary on lipoedema, including discussion of diagnosis, evidence, treatment approaches and the wider debates surrounding the condition.
Expert perspectives, clinical insight & professional commentary on key issues in lipoedema
In-depth conversations
with women living with lipoedema, in their
own words.
Discussion & interpretation of current research, clinical findings and emerging evidence relating to lipoedema.
Key guidance statements, consensus documents and expert recommendations shaping understanding and practice in lipoedema.
Browse all video, audio and visual content in one place including interviews, features and educational material.