Members of the Lymphedema Advocacy Group board travel to DC almost every month to meet with congressional offices and increase support for the Lymphedema Treatment Act. If you live in

In the eleven years since my son Dylan was born with primary lymphedema I’ve seen awareness improve, but we still have a long ways to go. We hope you find

Congress returns to session today. The below list of Representatives and Senators need to hear from you again, because they still haven’t cosponsored the Lymphedema Treatment Act! Want to strengthen

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