Save the date for our 2017 Lymphedema Lobby Days in Washington, DC, March 26th-28th! No experience is necessary and everyone is welcome! Last year, over 70 patient advocates from around

On February 14th we’ll be hosting our third annual “Love the Lymphedema Treatment Act Valentines Day Walk.” This is a virtual walk, so anyone, anywhere, can participate or simply support

Our Lymphedema Lobby Days raise critical support for the Lymphedema Treatment Act and we can’t do it without you! I hope you can join us in Washington, DC, March 26th-28th.

The new Congress begins on January 3rd. Many of the most frequently asked questions about what that means and how it affects our efforts are answered here. Is this starting

This was a tremendous year for the LTA! We are so grateful for our incredible grassroots advocates like you, who make their voices heard by writing letters, making phone calls,

We are incredibly proud to be finishing this year with 29 Senate and 260 House cosponsors! Each Congress we have made it further than the last, and we will persist

We are pleased to share with you a new infographic that outlines the many causes of primary and secondary lymphedema in the United States, including incidence rates, entitled “Lymphedema: Not

We are so grateful for the many people who have given of their time and talents to help advance lymphedema care! Today, on Giving Tuesday, we hope you will consider

We know you are eager to know if the LTA will pass this year. A complete summary of just how close we are is below my signature! The current Congress