I am now 77 and my Lipoedema was diagnosed in 2022. This photo was taken in December 2021. Symptoms like mine are not a family trait, and my problem only started to show post menopause, about 25 years ago. Prior to that I took the contraceptive pill for 23 years without a break, followed by
‘Lucky to develop Lipoedema only in my later years’ Read More »
The Lipedema Foundation Registry (LFR) is an online registry established to help the Lipoedema community, including affected individuals, families, clinicians and researchers. Its goals are to learn more about Lipoedema; understand barriers to diagnosis; better manage symptoms; assess quality of life impact; and develop new treatment approaches. The LFR has developed an ‘Initial Survey’ that
Sharing the load by creating a support group Many of our members describe how they’ve found friendship and support by meeting other women with Lipoedema. This video by the Shuttlewood Clarke Foundation describes one such group of women, who have founded a Lipoedema Support Group in Leicestershire. Watch the video to learn more!
