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6
Oct
The Lipedema Foundation is a groundbreaking organization devoted to the lipedema community in meaningful ways. Chief Science Officer Guy Eakin talks about the Foundation's history, mission, and registry, which is key to the organization's goal of funding research that can lead to a cure.
Published: 6 October, 2021
22
Aug
To learn that the condition that had plagued her for decades had a name was a relief for Amy Vasquez. For years she heard "calories in, calories out" and was even accused by medical professionals of eating more than she admitted to. She saw similar, big thighs among her family members and thought there wasn't ...
Published: 22 August, 2021
15
Aug
With a host of other medical concerns, Stephanie Roache wasn't focused on managing lymphedema when she was diagnosed. Soon, it became apparent that it could no longer be ignored.
Published: 15 August, 2021
1
Aug
Thanks to a post on Instagram, Amber Grainger realized she had lipedema and was fortunate enough to connect with Dr. Lindy McHutchison of Carolina Vein Center. For the first time, Amber felt validated.
Published: 1 August, 2021
19
Jul
Kelly Maynard offers insights into why lipedema patients should address their full body, how her upper extremities have changed, and that the "constant ache" she used to live with is now gone.
Published: 19 July, 2021
16
Jun
In this insightful interview, Dr. Beidas discusses the particular challenges of lipedema surgery, what to look for when considering surgery, the importance of the newly released Standard of Care, and his plans for a groundbreaking lipedema clinic.
Published: 16 June, 2021

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