A conversation with Gaynor Leech and the question that started it all
“I often hear from those that live with lymphedema that nobody listens … Spread the word: Lymphedema exists. We exist.”
Tag: lymphedema awareness day
A conversation with the co-chairs of the LE&RN California Chapter
“This day means ‘we matter,’ ‘I am not alone in this fight,’ ‘my disease is real.’ It’s a day where we can come together and demand that the world hears us.”
A conversation with Emma Detlefsen, the girl in the purple cape
“Maybe at first people are like, ‘Who is this kid?’ But usually after I talk, they realize that I kinda know what I’m talking about.”
A conversation with Heather Ferguson, mother of the Lymphedema Treatment Act
“Lymphedema has become a defining feature of my life precisely because I didn’t want it to define my son’s life.”
“We live in a globalized world”: A conversation with Dr. Epameinondas Gousopoulos
For this year’s World Lymphedema Day, I spoke with Dr. Gousopoulos about the globalization of the lymphedema community, the importance of patient involvement, and his vision as chair of the Europe Chapter of LE&RN.
Lymphedema Awareness Day
Today is a day for us to join together and use our voices not only to spread awareness about lymphedema, but to celebrate our amazing community.