Over the last few years we have collected over 600 patient and caregiver stories through our My Lymphedema Story campaign, but we still need more!
Please consider submitting your story if you haven’t already done so.
These stories are shared with members of Congress and their staff. They play a vital role in helping them to understand the challenges their constituents with lymphedema face, and why we must pass the Lymphedema Treatment Act.
Tips on what to include are provided. Our stories are powerful and persuasive, and by sharing your story you’ll be making a difference!
Heather Ferguson
Founder & Executive Director
Lymphedema Advocacy Group
LymphedemaTreatmentAct.org
