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19
Apr
Finally receiving a diagnosis of lipedema was a game-changer for Debrena McEwen. Another was connecting with the online community: "They've taught me how to care for myself," she says. "And care is love in action."
Published: 19 April, 2022
14
Apr
Those who follow Sean Mulroney and The Obesity Revolution know his lymphedema journey has been filled with ups and downs. One constant "up" is his use of the Lympha Press LymphaPod to manage his condition.
Published: 14 April, 2022
25
Mar
Mother-daughter duo Sonja and Tayler have a unique bond: they both live with chronic conditions. From the quest for a diagnosis to navigating treatment, going through the process together has allowed lipedema patient Sonja and lymphedema patient Tayler to learn from — and lean on — one another.
Published: 25 March, 2022
15
Mar
Sharon Dodds never stopped reaching out for help, and her message to others with lymphedema and lipedema is "Keep reaching out."
Published: 15 March, 2022
8
Mar
Carol Moody is one determined woman. What's most remarkable about Carol's story is her determination to give this fight "everything she's got" because she is WORTH it. Learn of her Keto diet success and how Lympha Press helps her successfully manage her Stage 3 lipedema and Stage 2 lymphedema.
Published: 8 March, 2022
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

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