15
Mar
Dr. Mark Melin wanted to be an astronaut, and now he studies space as part of his groundbreaking work in lymphedema and wounds.
Published: 15 March, 2023
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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Looking for more information, or to be connected with your local representative?
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6
Mar
Before becoming President and CEO of LE&RN, William Repicci "knew nothing about lymphedema." But as he learned 10 million people were affected by a disease that had little recognition in the medical world, he took on the challenge.
Published: 6 March, 2023
15
Feb
In this installment of the Lympha Press Leadership Series, learn more about certified lymphedema therapist Kathleen Lisson. Fueled by curiosity, Lisson says, "I want to wake up every day with the intention of learning something new."
Published: 15 February, 2023
23
Jan
In this fascinating interview with American Vein & Lymphatic Society (AVLS) Executive Director Dean Bender, we learn more about the Foundation and its commitment to advocacy, research, and education.
Published: 23 January, 2023
9
Jan
An interview with Brandy McKeown, CEO of the International Lymphedema and Wound Training Institute.
Published: 9 January, 2023
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
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.
