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When it comes to the lymphatic disease agenda, the wheels of change have historically moved slowly. In stark contrast, they are now moving at such a rapid pace that it’s hard to keep up with the momentum. On February 8, the National Heart, Lung, and Blood Institute (NHLBI) at the National Institutes of Health (NIH) shared plans for a National Commission on Lymphatic Diseases during a virtual Open Session. I encourage you to watch this presentation video. On February 28, the Congressionally Directed Medical Research Program (CDMRP) will conduct a special webinar for lymphatic researchers as their $370M medical research budget is opened to lymphedema (LE) and lymphatic diseases (LDs) for the very first time. Over at Centers for Disease Control and Prevention (CDC), LE&RN is executing the second year of a CDC-funded national cancer-related LE awareness campaign. Next up: stay tuned for announcements about the expansion of the LE&RN Resource Center and LE&RN Resource Line.


This is the time of year when LE&RN looks for corporate sponsorships to support the programs so critical to the health and well-being of the lymphatic community. Below, you will find a list of companies that prioritize you first and profits second, by supporting LE&RN. We thank these forward-thinking leaders for investing in our efforts on behalf of all people living with LDs globally.


With great pleasure, I present Lymphatic News Monthly.

Watch NIH VideoCast

Join LE&RN for Congressionally Directed Medical Research Program (CDMRP) Webinar for Lymphedema (LE) and Lymphatic Disease (LD) Researchers presented by Dr. Cecelia Dupecher, Program Manager for the Peer Reviewed Medical Research Program (PRMRP) at CDMRP today at 1:00 pm EST. Dr. Dupecher will summarize the PRMRP program, review the application process for research funding, and answer researcher questions. A recording will be available in the LE&RN Symposium Library a few days after the webinar.

Register on Zoom

Rare Lymphatic Diseases to be Recognized at FDA’s Rare Disease Day Virtual Public Meeting Thanks to Dr. Kimberley Steele and the Medical Students She Advises

Dr. Kimberley Steele, Special Programs & Patient Registry Director at LE&RN, was invited to Spotlighting the Zebras: A Role for Medical Students in Shaping Rare Disease Care at FDA’s Rare Disease Day Virtual Public Meeting. Dr. Steele mentors and supports medical students from across the USA and Canada as they lead Rare Disease Interest Groups with the goal of addressing gaps in medical school curriculum. This initiative is of special significance for Dr. Steele, who has a child living with a rare lymphatic disease - Kaposiform Lymphangiomatosis (KLA).

Join LE&RN Wednesday, March 1 at 3:00 pm EST (12:00 pm PST, 1:00 pm MST, 2:00 pm CST) Thursday, March 2 at 7:00 am Australian Eastern Daylight Time (AEDT) for Implementing Translational Best Practice Models of Care, a free Zoom Symposium presented by Dr. Louise Koelmeyer. Unable to join us live? A recording will be available on the LE&RN Symposium Library within a few days.

Register on Zoom

Did you know that all of LE&RN’s Online Symposiums are available and complimentary in the LE&RN Symposium Library?

Watch in the LE&RN Symposium Library

How Will You Celebrate World Lymphedema Day?

Step 1: Share Your Celebration with LE&RN

Step 2: Upload a Video or Share a Picture for the chance to be featured in upcoming LE&RN spotlights!

Step 3: Celebrate World Lymphedema Day!

On World Lymphedema Day, LE&RN will grant free access to the 2022 Virtual Lymphatic Summit! Sign up to receive a link in your inbox on March 6 to the entire conference.

Sign Up Here for Free Access

Andrea Weinreb to be Honored at New York State Capitol for World Lymphedema Day

Andrea Weinreb, founding member of LE&RN New York State Chapter, will be honored for her outstanding advocacy, education, and fundraising efforts for lymphedema awareness. In 2007, Andrea was diagnosed with lymphedema as a result of cancer treatment. Andrea is a top fundraiser for New York Run/Walk to Fight Lymphedema & Lymphatic Diseases and has lobbied in Washington, D.C., and New York State for all New Yorkers living with LDs.

LE&RN and the North American Vascular Biology Organization (NAVBO) are pleased to sponsor the upcoming Lymphatic Forum 2023 (LF2023), Exploring the Lymphatic Continuum at The Banff Centre, Alberta, Canada, and hosted by the University of Calgary. LF2023 is the fifth iteration of this biennial event that brings together researchers from around the world to present and discuss studies of lymphatics in health and disease. Abstract and Travel Award deadline is March 15. Early bird registration ends April 10. Visit LymphaticForum.org for more information.

Register for Early Bird Rate

Register Today! Live Broadcast on Saturday, April 22

Join dedicated teams and individuals worldwide to fundraise in support of LE&RN’s mission to cure lymphatic diseases. In celebration of LE&RN’s 25th Anniversary, registration is only $25. Every dollar donated fuels lymphatic education. research, and advocacy.

Register Today!

Clinical Trial at Vanderbilt University Institute of Imaging Sciences

Do you have leg lymphedema? If so, and you would like to participate in a non-invasive MRI study, please follow the link below.

Learn More
Learn More

Become a LE&RN Supporting Member

LE&RN’s education, research and advocacy programs are only possible because of Supporting Members and Corporate Sponsors. Please acknowledge the support of these Corporate Sponsors (listed below) and support LE&RN through your membership.

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