Latest Posts
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Lymphedema Awareness Month 2023: Here’s what’s happening!
From in-person events to virtual webinars, there are plenty of things happening the world over to promote lymphedema awareness throughout the month of March.
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Lymphie Win: After 12-Year Effort, Lymphedema Treatment Act Becomes Law
Like muscles working to pump stubborn lymphatic fluid, advocates of the Lymphedema Treatment Act worked hard to pump the bill along and keep it moving.
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Show Off Your Stems: The Joyful Defiance of Debra Swersky’s Stemwear
For lymphedema patient Debra Swersky, her one-legged legging is more than just an item of clothing: it’s a statement, one she wants others to have the chance to make, too.
Lymphie Stories
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Launched by Alexa Ercolano in 2011, The Lymphie Life features articles detailing patients’ experiences living with lymphedema as well as tips and tricks, research news, product reviews, and interviews with healthcare professionals and community advocates. #StayElevated 💙
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