Today is the big kick off of our Act Now for the LTA walkathon fundraiser! Every single one of our 19 board members has made a personal donation and pledged

The board members of the Lymphedema Advocacy Group are proud to announce that we have pledged to walk over 600 miles from February 14-28th as part of a fundraiser for

While we wait for the Lymphedema Treatment Act to be reintroduced into the current Congress, this is a great time for you to help us spread awareness. I hope you

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