22
Jun
Lisa Lugo's interview is inspiring not only because of how well she manages her lipedema and Dercum's disease, but also how she manages her mindset.
Published: 22 June, 2022
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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16
May
Learning that lipedema "was actually a thing" was liberating for Lori Paquette, who lived until her 50s with the question "What was going on with my thighs?"
Published: 16 May, 2022
11
May
Receiving a lipedema diagnosis was a turning point for Molly Gallagher, and understanding that her condition wasn't just cosmetic gave her a sense of purpose: "No stopping lipedema? No…it's not stopping ME."
Published: 11 May, 2022
20
Apr
Fernanda Cooley earned a Doctorate and four Masters degrees, so when this lifelong learner was faced with the one-two punch of breast cancer and then lymphedema, she was relentless in her pursuit of answers.
Published: 20 April, 2022
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
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.
