Our stories are powerful, and they illustrate to members of Congress why there is an urgent need to pass the Lymphedema Treatment Act!
Anyone whose life has been touched by lymphedema can participate – patients, caregivers, friends or family members, healthcare professionals, etc. Tips on what to include in your story are listed on the submission form.
As of today we have 223 House cosponsors and 16 Senate Cosponsors. Please share your story and help us get the Lymphedema Treatment Act passed this year!
Heather Ferguson
Founder & Executive Director
Lymphedema Advocacy Group
LymphedemaTreatmentAct.org
