Our Lymphedema Lobby Days raise critical support for the Lymphedema Treatment Act and we can’t do it without you!
I hope you can join us in Washington, DC, March 26th-28th. Additional details, including the links to register and reserve your hotel room, are on the Lymphedema Lobby Days page of our website.
Last year, over 70 patient advocates from around the country, ranging in age from 7 to 80, met with 214 offices from 38 states. Your participation will help us to make this year’s Lymphedema Lobby Days our largest and most impactfull yet. I hope to see you there!
Heather Ferguson
Founder & Executive Director
Lymphedema Advocacy Group
LymphedemaTreatmentAct.org
