Today is our annual Valentine’s Day Walk for the LTA! Team members from around the country are walking to raise crucial funds to support our 2017 Lymphedema Lobby Days in

We are thrilled to announce that the Lymphedema Treatment Act was just reintroduced in the House! You can view the bill here and a press release here. We need your

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, with any ability level can

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