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

The LTA was recently endorsed by the American Academy of Physical Medicine and Rehabilitation! This is an important milestone for us because it is the first physicians group to join

Last week Louisiana passed a state lymphedema treatment mandate! Like the North Carolina and Virginia mandates already in effect, this law will require that all private insurance policies sold in

Over the last couple of months we’ve talked a lot about how to get your Representative to cosponsor our bill. Do not be frustrated if he or she is not