Thanks to the great work of our Maryland advocates, while simultaneously working for passage of the LTA they have succeeded in passing a Maryland lymphedema treatment bill! This state law

Thanks to the calls, emails and outreach of many, the LTA has reached the unbelievable milestone of 403 cosponsors! That’s an incredible 75% of Congress, but we can’t let up

In addition to our annual Lymphedema Lobby Days, where scores of advocates from around the country travel to DC to meet with over 200 offices, our board members make small

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