Our trip to Washington, DC was amazing! The Lymphedema Advocacy Group’s 2014 Lymphedema Lobby Days took place on September 8th and 9th. Eighty-five patient advocates participated from the following 24
The Congressional Briefing about lymphedema and the Lymphedema Treatment Act is tomorrow! If you haven’t already done so, using the links below, please call your members of Congress at their
We are proud to share with you a new 5 minute video to help raise awareness about lymphedema and the Lymphedema Treatment Act! Click here to view the video on
A Congressional Briefing about lymphedema and the Lymphedema Treatment Act will be held on September 9th. Please contact your members of Congress, urging them to attend this briefing! Click here
A Congressional Briefing about lymphedema and the Lymphedema Treatment Act will be held on September 9th. We need YOU to urge your House and Senate offices to attend. If you
The August recess is a prime opportunity for you to meet with your Representative in person, share a bit about lymphedema, and urge him or her to cosponsor the Lymphedema
Our 2014 Lymphedema Lobby Days will be taking place September 7th-9th in Washington, DC. We’d love for you to join us – no experience is necessary and everyone is welcome!
Last year we undertook an effort to begin building a grassroots team of advocates in every state. I’m proud to tell you that today we have teams in 47 states!
Lobby Days: Our Lobby Days are fast approaching! If you haven’t signed up yet, we’d love for you to join us September 7th – 9th in Washington, DC. So far
