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19
Nov
"Thank you for being a friend..." The Lipedema Patient Roundtable was a cornucopia of warmth and gratitude this month in celebration of Friendsgiving. We pulled up some extra chairs to the virtual table as our panelists each brought a special friend along to talk about life, lipedema, and friendship.
Published: 19 November, 2021
27
Oct
"Lip"-or-Treat! Panelists and attendees had a hauntingly good time at the Halloween-themed October Lipedema Patient Roundtable, complete with creative costumes and heartfelt conversations.
Published: 27 October, 2021
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
20
Sep
Does lipedema affect fertility? How about the ability to sweat? And why does lipedema light up on airport scanners? These are just some of the questions that popped up during the September Lipedema Patient Roundtable for our panel of patients and medical professionals.
Published: 20 September, 2021
30
Aug
This article examines cutting-edge insights into the minds of people who have lipedema. We’ll also introduce what’s known as the matrix — the physiological structure lipedema takes within the body, plus its resulting impact on a patient’s thought processes and lifestyle.
Published: 30 August, 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

Let's get social!

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