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Lymphie StrongLymphedema

Flare ups. Pain. Stress.

The life of chronic illness is full of ups and downs. Keep smiling and keep the faith. 💖

lymphedema #lymphiestrong #movethatlymph

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“If you have a rare disease, the search for a diagnosis can often feel like the longest detective investigation - with no clues, lots of blind alleys and, occasionally, disbelieving authorities. It may seem like things are going nowhere, even for years.” Via @rarediseasedayofficial 🦓🦄💞🦋
Lymphedema Awareness is important all year round, and we all do our best to spread the information. March is just a little bit special because it is our month to shine ✨so we go all out with March 6th designated as World Lymphedema Day. This year is a little bit different for me since I’m still in recovery from COVID-19, but we won’t let that stop us!
Thrilled to announce our Lymphie Strong Running & Fitness Club for Lymphedema and new @movethatlymph online partner in 2021 is @lunamedical @absoyogalutely 🤍🧘🏻‍♀️🎈🎉
Congratulations to the awesome team at the Lymphatic Center / Lymphatic Surgery at BIDMC/Harvard Medical School including Anna Rose Johnson, MD MPH, Kathleen Shillue, PT, DPT, OCS, CLT, and Dr. Dhruv Singhal, et al. Published findings highlighting the promise of immediate lymphatic reconstruction for the surgical prevention of #lymphedema. They found a 3.1% rate of #BCRL in patients who received ILR at time of #ALND. Via Twitter http://ow.ly/PVqM50DL3uT
National Lymphedema Network Highlight on COVID-19 Vaccination Injection Site
Kicking off Lymphedema Awareness Month with a webinar with @oasis_pt_and_wellness 🦋💗🦋Are you in pain with lymphedema? Did you realize that there might be movements you can do to help? Join us to hear about Pain Elements of Lymphedema: How to Counteract with Movement and Exercises by Lisa Berman Sylvestri, MSPT, CLT-LANA on 3/1 at 5 PM PST Register via the Events Calendar link in my Bio. 🦋💙

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