We have grassroots advocacy teams in all 50 states! If you haven’t joined your state’s team yet here are a few reasons why we hope you will consider it. No

Last week, the amazing advocates who participated in our 2019 Lymphedema Lobby Days met with 226 Congressional offices from 46 different states! We’ve already gained dozens of more cosponsors as

Today and tomorrow, advocates from around the country will be meeting with hundreds of congressional offices in Washington, DC in support of the Lymphedema Treatment Act! You can support our

This week, The Hill published an op-ed about the LTA written by our two previous House sponsors, Dave Reichert (R-WA-8) and Larry Kissell (D-NC-8). The Hill is an online and

Please contact your Senators this week! The phone numbers with call script and the form to send an email is here. Our new Senate email form now differentiates based on

It is with great sadness that we share the news of the passing of Elaine Eigeman, Board Chair of the Lymphedema Advocacy Group.   Elaine lived with lymphedema for 20

This Congress, the House of Representatives adopted several new rules, one of which could be a game changer for bills like ours. House bills with more than 290 cosponsors are

In a few weeks, advocates from around the country will be meeting with members of Congress for our 2019 Lymphedema Lobby Days. We want to take your stories with us!

This is the final weekend to register for our 2019 Lymphedema Lobby Days, May 5th-7th!   Tomorrow, Sunday, April 14th, is the deadline. No experience is required and everyone, including