Thank you for all of your efforts this past year. We finished with an impressive 107 cosponsors – the most support our bill has ever garnered during a cycle of

For the first time in any Congress, our bill has garnered more than 100 cosponsors! To see the complete list click here, nearly 90% of which will be serving in

The Lymphedema Advocacy Group is seeking applicants interested in serving on our Board of Directors for the upcoming term beginning in January of 2015. In particular, we are looking for

I’m pleased to share with you information about the following events taking place in October. Remember that a listing of upcoming lymphedema-related events, and a lot of other information, is

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