Lymphatic Education
& Research Network

Dear LE&RN Supporting Members and other advocates,

At the recent LE&RN/NAVBO-sponsored Lymphatic Forum in Austin, TX, LE&RN asked researchers to join the fight for expanded research funding. In response, over 100 attending researchers heeded the call to action and signed a

Dear LE&RN Supporting Members and Advocates,

This week, over 140 advocates from across the United States will descend on Washington, D.C., to muster legislative support for increased funding of lymphatic research at NIH and the DoD. We will meet with the Veterans Administration to discuss

Photo Credit: Cpl. Teagan Fredericks, United States Department of Veterans Affairs

Dear LE&RN Supporting Members and Advocates,

LE&RN is fighting to get the Department of Defense and Veteran’s Administration to drastically increase its research and services impacting military personnel. We

Pictured above: NYS Assemblymember Linda B. Rosenthal, LE&RN President and CEO William Repicci, and LE&RN Spokesperson Kathy Bates.

Dear LE&RN Supporting Members and allies,

On October 2, 2018, Governor Andrew Cuomo signed a first-in-the-nation Act, authored by LE&RN. The public health

Bill now includes "lymphatic research" in Committee recommendations

Dear LE&RN Supporting Members and other LE/LD Advocates,

TOGETHER we are making progress. 

The U.S. Senate just passed its second minibus bill, which now goes to the House. Assuming passage there, it will go to the

Dear LE&RN Supporting Members, and Allies in the Fight Against LE and LD,

Along with other LE&RN representatives, I had the honor of meeting with the CEO of the American Medical Association (AMA), Dr. James Madara, in 2016. As we discussed expanding lymphatic disease education among medical

Dear LE&RN Sponsor,

Researcher Sheila Ridner, PhD, RN, called me to say she recently visited a health clinic in rural Kentucky. There on the reception desk was a stack of WebMD magazines with Kathy Bates’ photo on the cover and a headline featuring lymphedema (LE). As she saw visitors leave

Dear World Lymphedema Day Advocates,

As you know, we have been advocating for the World Health Organization to make "Lymphedema Awareness and Cures" its focus in 2018. They have just announced that this year will be dedicated to "Universal Health." Well, that's a step in the right direction,

Dear LE&RN Supporting Members and New York State residents,

If you are a New York State resident with health insurance that is not Medicare, and you have been denied treatment for lymphedema or denied coverage of physician-prescribed compression bandages or garments within the last few