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

Prior to the introduction of the Lymphedema Treatment Act (LTA), patient advocates including myself and others attempted to obtain coverage for compression supplies by working with the Center for Medicare

A Power Point presentation covering all essential information about the LTA is now available here, and a PDF version of the slides available here. Our information cards and other printable

For the next two weeks Congress is in recess, meaning that members will be at home in their states and districts. This is a perfect opportunity to meet with your

This week, we ask that you contact the following House leadership offices that serve on the two House Committees that have jurisdiction over our bill. A phone script, sample Tweet,

My favorite part of our annual Lymphedema Lobby Days in DC, besides increasing support for the LTA of course, is seeing the impact it has on those attending for the

Our work at this year’s Lymphedema Lobby Days is already paying off in a big way – we’ve gained 10 new cosponsors just this week! They are marked on the

As part of our 2018 Lymphedema Lobby Days, this week 73 advocates from 30 states will meet with over 200 congressional offices, and among them will be four outstanding young

Next week, advocates from around the country will spend two days on Capitol Hill meeting with congressional offices as part of our Lymphedema Lobby Days. For the next few weeks,