Lymphedema Treatment Act Update

MsCjay

In just a few days, on November 2nd-4th, over 30 lymphedema patient advocates from around the country will convene in Washington, DC to increase support for HR 2499!

During this trip, organized by the Lymphedema Advocacy Group, participants will spend two full days on the Hill visiting dozens of Congressional offices and conducting a Staff Briefing to educate members of Congress about lymphedema and this bill.

If you have not already done so in the past week, please go to our website - www.LymphedemaTreatmentAct.org - and visit the Contact Your Representative and Contact Each Of Your Senators pages.

The template letter has been temporarily changed to an invitation asking Congressional staff to attend the HR 2499 Staff Briefing taking place on Thursday, Nov 3rd. Please add a few sentences to the template letter to personalize it then complete your name and address to send this invitation to your Representative and Senators' offices.

Thanks for your support!
Heather Ferguson
Chair, Lymphedema Advocacy Group
www.LymphedemaTreatmentAct.org
info@LymphedemaTreatmentAct.org