Abstract
Double Your Impact: Donate to the $65,000 Match for Hope
LE&RN’s Annual Appeal offers a powerful way to make your donations go further through the $65,000 Match for Hope. Every dollar you donate will have double the impact—fueling LE&RN’s mission to fight lymphatic diseases through education, research, and advocacy. Donate now at CureLymph.org, and your gift will be matched dollar-for-dollar to accelerate LE&RN’s transformative work.
Pioneering Guide Aims to Improve the Early Detection and Treatment of Lymphatic Disease
We are proud to introduce the standardized approach for the diagnosis and management of lymphedema (LE) and lymphatic diseases (LD). Developed by global experts in collaboration with LE&RN, this pioneering guide aims to improve the early detection and treatment of lymphatic diseases, enhancing the quality of life for millions worldwide through knowledge sharing and education. This first-of-its-kind collaboration provides health care professionals with guidelines for preventive measures and delivering consistent and effective care to individuals living with lymphatic diseases. Read the guide at https://lymphaticnetwork.org/groundbreaking-reports
Lymphatic Forum 2025: June 12–14, 2025
LE&RN and the North American Vascular Biology Organization are pleased to sponsor the upcoming Lymphatic Forum 2025 (LF2025), exploring the Lymphatic Continuum, on June 12–14, 2025, in Chicago, IL. LF2025 is the sixth iteration of this biennial event that brings together researchers from around the world to present and discuss studies of lymphatics in health and disease. Register now at https://lymphaticforum.org/
Refer Your Patients to the LE&RN Global Registry for Lymphatic Diseases™
The mission of the upgraded LE&RN Global Registry for lymphatic diseases is to establish the world’s most comprehensive patient-centered registry to inspire ground-breaking research, expedite the development of treatment options, and establish a path leading to the cure for LD. As dedicated lymphatic researchers and health care providers, your patients’ participation in the registry is crucial for accelerating breakthroughs. Encourage them to enroll today at https://lymphaticnetwork.org/ldregistry and be an integral part of pioneering research that holds the promise of transforming the landscape of lymphatics. Everyone living with LDs, including primary and secondary LE, lipedema, and lymphatic anomalies, is welcome to join. Parents or guardians can also grant permission for their children to enroll.
Connect with the LE&RN Resource Center
The LE&RN Resource Center (LRC) is a complimentary global support service to assist the lymphatic community in navigating the complexities of LD, including LE, lipedema, and lymphatic anomalies. We serve people living with LDs and their families, caretakers, and health care providers. The LRC can help find specialized care through the Centers of Excellence network, locate certified LE therapists, and provide educational resources. We encourage you to connect with the LRC and to refer your patients and colleagues. Visit the LRC at https://lymphaticnetwork.org/resource-center. Contact us at 1-855-378-8163 or
Did You Know There Are over 100 Hours of Free Education in the LE&RN Symposium Library?
In 2024, the LE&RN Online Symposium Series featured 13 sessions led by top lymphatic experts, garnering over 10,000 views. With over 100 hours of free educational content now available in LE&RN’s library, the series continues to empower the community with knowledge. Stay informed about upcoming symposiums in 2025 by subscribing to LE&RN’s eNews at https://lymphaticnetwork.org/subscribe and watch all symposium recordings for free at https://lymphaticnetwork.org/symposium-series
William Repicci
President and CEO
Lymphatic Education & Research Network (LE&RN)