On Saturday, May 3rd, I will be one of many speakers at the National Lymphedema Network’s 2025 Patient Lymphedema Summit. This one-day summit is just for people living with lymphedema

We are always looking for ways to improve access to care, and that’s why we’ve recently created an Insurance Coverage Reporting Form.  The information you provide will assist us in

In recognition of World Lymphedema Day, we are excited to share our redesigned information cards! The front continues to feature our popular 6 Things You Should Know About Lymphedema infographic,

To kick off Lymphedema Awareness Month, we are excited to share some big news with you. We are launching a second organization called the Lymphedema Education & Awareness Project!  Just as

15 years ago today, on February 23, 2010, the Lymphedema Treatment Act was introduced into Congress for the very first time. It would take more than 12 years for the

Last year, our group, along with the American Physical Therapy Association (APTA), American Occupational Therapy Association (AOTA), and the Alliance of Wound Care Stakeholders, sent a joint letter to the

If you or someone you care for are being denied coverage for any lymphedema treatment supply or service, or receiving insufficient coverage, please use our new Denial Reporting Form to

Our work frequently involves collaboration with other organizations, which includes long-standing relationships with several different rare disease groups. Primary lymphedema is a rare disease affecting approximately 1 in 100,000 individuals.

In an effort to spread more awareness about lymphedema, and to make sure that all patients know about the new coverage that might be available to them thanks to passage