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.”
Author: Alexa Ercolano
Alexa is a writer, book hoarder, and cat enthusiast from Baltimore, MD. By day, she works in the marketing and communications department for a large health system; by night, she runs The Lymphie Life. Learn more about her here!
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.”
Lymphedema Day 2019: Looking at the many faces of advocacy
In honor of Lymphedema Awareness Day, we’ll be spending the month of March getting to know some of the people behind global lymphedema advocacy efforts.
Research Roundup: Examining lymph node clues and fake health news
A summary of lymphedema and lymphatic research news from February 2019.
Research Roundup: From conferences to daytime TV, the spotlight is on lymphatics
A summary of lymphedema and lymphatic research news from January 2019.
Cigarettes and Chronic Swelling: Smoking’s effects on lymphedema
We all know smoking carries health risks, but how does it affect our lymphedema?
Research Roundup: Study reveals treatment gap among patients with cancer-related lymphedema
A summary of lymphedema and lymphatic research news from December 2018.
Product Review: Staying elevated with the Lounge Doctor Leg Rest
I try out the Lounge Doctor Leg Rest for scientific elevation — and serious comfort.
Book Review: “Lipedema Treatment Guide”
A review of Kathleen Lisson’s book, “Lipedema Treatment Guide: A Certified Lymphedema Therapist’s Advice for her Clients with Lipedema.”