Compressed for Success: A conversation with Dr. Sheri Prentiss, Founder and President of the LIVE Today Foundation
“This work is great, and it must go on.”
Stay elevated.
“This work is great, and it must go on.”
Reflections from your local lymphedema blogger, after a decade of writing.
Listen up, lymphies! These engaging podcasts about lymphedema and lipedema are sure to elevate your lymphatic knowledge.
The 2019 NLN Conference was full of amazing information. Here are five of my biggest takeaways.
“I often hear from those that live with lymphedema that nobody listens … Spread the word: Lymphedema exists. We exist.”
“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.”
“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.”
“Lymphedema has become a defining feature of my life precisely because I didn’t want it to define my son’s life.”
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.
Barbara desires to help fellow lymphedema patients by participating in the ULTRA study.