Our stories are powerful, and they illustrate to members of Congress why there is an urgent need to pass the Lymphedema Treatment Act! Please share your lymphedema story with us,

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

Thank you so much for helping us reach this huge milestone of support in the House! To see if your Rep is one of our 220 House cosponsors click here.

This week’s 2016 Lymphedema Lobby Days were a huge success! Over 70 patient advocates, hailing from 21 states plus the District of Columbia, met with 214 offices from 38 different

Today and tomorrow, over 70 patient advocates from around the country will be meeting with over 150 congressional offices! Please help increase the impact of our visit by calling your

Thank you to everyone who helped us reach this milestone! You can see the complete list of 201 House cosponsors here, and 13 Senate cosponsors here. If you don’t see

In exactly two weeks from today, patient advocates from around the country will spend two days in Washington, DC, meetings with congressional offices to increase support for the Lymphedema Treatment

Just four days left to register to take part in our 2016 Lymphedema Lobby Days, April 18th-20th in Washington, DC! Monday, April 4th is the registration deadline to join the

Register now for our 2016 Lymphedema Lobby Days, taking place April 18th-20th in Washington, DC! We are just three weeks away from the registration deadline of April 4th, and one