In exactly two weeks from today, patient advocates from around the country will spend two days in Washington, DC, meetings with congressional offices to increase support for the Lymphedema Treatment Act. Even if you can’t join us for our Lobby Days on April 19th and 20th, you can make a difference.
The more constituents they hear from in advance of our visit the more likely they will be to say YES when we ask for them to cosponsor our bill. We are making great strides – we have 195 House cosponsors and 12 Senate cosponsors – but the greater the number the greater our chances of reaching our goal of getting the bill passed THIS YEAR!
Heather Ferguson
Founder & Executive Director
Lymphedema Advocacy Group
LymphedemaTreatmentAct.org
