From President & CEO, William Repicci

Advocacy - Taking AIM

Advocacy - Taking AIM

People can survive the ‘what’ provided they know or have a ‘why’…” – Viktor Frankl

This blog focuses on the “why” for anyone living with lymphedema (LE), to take AIM…and advocate! I offer you heartfelt wishes of courage, encouragement plus perseverance. It’s always about “questions”

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NIH Begins Planning for National Commission on Lymphatic Research

NIH Begins Planning for National Commission on Lymphatic Research

Dear Mr. Repicci,

…We welcome the opportunity to collaborate with LE&RN, the lymphatics research community, and those affected by lymphatics diseases in building a blueprint to further define a structure aligning with the concept of a national commission for lymphatics research. Through a

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The Emotional Price of LDs: Becoming One’s Own Advocate

By William Repicci, President & CEO of LE&RN

At a recent staff meeting, we discussed the emotional impact on those who live with lymphatic diseases (LDs). This includes lymphedema (LE), lipedema, lymphatic malformations (LM) or vascular anomalies. One thing was clear: most doctors know

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The Road to Independence from Lymphedema (LE)

"To be an unwell woman today is to fight against ingrained injustices against women’s bodies, minds, and lives. We no longer have to live in silence and shame." – Elinor Cleghorn, Unwell Women: Misdiagnosis and Myth in a Man-Made World
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