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Medicare added a step before some patients can receive pneumatic compression devices. Read about the change and how Lympha Press handles the entire process for you.
The April 2026 Lipedema Patient Roundtable focused on one of the most important—and often overlooked—aspects of living with lipedema: adapting as your needs evolve, without guilt or shame.
The April Lymphedema Patient Roundtable focused on one of the most important (and sometimes most frustrating) parts of managing lymphedema: compression.
The April Research Roundtable explored the complex relationship between lymphedema, peripheral arterial disease, and chronic wound healing.
The March Lipedema Patient Roundtable brought together a dynamic group of experts and advocates to share education, updates, and practical strategies in recognition of Lymphedema Awareness Month.
Influencer AliciaXL discusses her strategies for living with lipo-lymphedema and losing weight — and showing up authentically online.
In recognition of Lymphedema Awareness Month, this Lymphedema Patient Roundtable explored the latest developments in lymphedema and lymphatic research.
In honor of Lymphedema Awareness Month, the March Research Roundtable explored advances in lymphedema care, from the role of advanced imaging in diagnosis to evolving surgical options that help improve patient outcomes.
Read answers to the top questions about Lympha Press, and get tips for talking with your provider about getting your own Lympha Press system for home use.