Patient Stories

‘If there’s one thing I’d like people to take from my experience, it’s that lipoedema doesn’t automatically write your life story for you.’

My experience with lipoedema and exercise I only discovered that I have lipoedema within the last 12 months, so it’s still fairly new information to me. That discovery answered a lot of long-standing questions about my body – particularly the size and shape of my legs, their sensitivity, and the fact that no matter what […]

‘If there’s one thing I’d like people to take from my experience, it’s that lipoedema doesn’t automatically write your life story for you.’ Read More »

‘I hope you don’t mind me saying, but by the shape of your legs and hips, I think you may have Lipoedema’

I didn’t know anything about Lipoedema until 2018, but I noticed my legs were difficult to reduce in size after I had my son, who is now 36. I know some people notice symptoms around puberty, and I may have had it then but because I was unusually tall for a female in the 70s,

‘I hope you don’t mind me saying, but by the shape of your legs and hips, I think you may have Lipoedema’ Read More »

Lisa’s ‘nudey swim’

For Lipoedema UK member Lisa, a sponsored naked swim was a fantastic way to fundraise and raise awareness of Lipoedema. ‘What better way to spread awareness and embrace and accept the way we are than by doing a naked swim?’ she says. ‘Swimming and moving in water generally are great ways to get the lymph

Lisa’s ‘nudey swim’ Read More »

Scroll to Top