Giving Tuesday kicks off the charitable season! ‘Tis the season for giving, and we hope you will remember the Lymphedema Advocacy Group when making your end-of-the-year donations. For the first

Save the date! We hope you will be able to join us for our 2016 Lymphedema Lobby Days in Washington, DC, which will be taking place April 18th-20th. No experience

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