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

Our Summer Raffle is Underway! Each time you donate $5 or more you will be entered to win prizes donated by CircAid (one custom or standard fit item), Jobst ($100

We have already surpassed the number of cosponsors we had in the last Congress! Thanks to the grassroots advocacy of people just like you, we now have 111 cosponsors. Now,