24
Jul
Learn how Angelique Charles found her wings through a grueling journey to finally get a proper diagnosis for lipolymphedema.
Published: 24 July, 2020
Interviews
Every person's story is worth telling.
There is no definitive lymphedema or lipedema experience.
From veterans and athletes to college students and parents, life with these conditions is as varied as the people who live with them. Hear from real patients as they share their stories, in their own words.
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30
Jun
Meet Pattie Cornute.
For six years after her lipedema diagnosis in 2007, Pattie avoided exercise because she believed the myth that exercise could worsen her disease.
Until she nearly lost all of her mobility.
Sheer fear and desperation led Pattie to take control of her condition. ...
Published: 30 June, 2020
Contact Us.
We're ready to help.
Looking for more information, or to be connected with your local representative?
We can help. Fill out our contact form to get started.
