Here are 5 free, quick and easy ways help spread awareness about lymphedema and support for the Lymphedema Treatment Act! Order our free information cards to distribute in your area.

We are pleased to announce four dates for our advocacy training webinar entitled “Advocate for the LTA and Meet Your Members of Congress!” Topics will include: How to become an

We now 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.

Our Washington Post article about lymphedema and the LTA got amazing coverage this week! It ran on the front page of the Health and Science section of the 9/29 print

Lymphedema and the Lymphedema Treatment Act are the topic of the Medical Mysteries column in today’s Washington Post! The article chronicles my family’s experience with primary lymphedema, and our struggle

* Learn to schedule, plan and conduct effective meetings in your local district. * Persuade your Representative in person to cosponsor the LTA. * Get to know your helpful District

Cosponsor Update: Congress is back in session and we are thrilled to report that we have 132 cosponsors! If your Rep’s name isn’t on the list yet please keep writing

We have lots of important news and information to share with you this month! NEW Cost Report Demonstrating Saving This new report from Avalere Health, commissioned by the Lymphedema Advocacy

We are pleased to announce TWO NEW Advocacy Training Webinars from the Lymphedema Advocacy Group (LAG)! We hope you can join us next week, and at future webinars, which we