We want to share your Lymphedema Story in DC!

by Heather on April 16, 2019

In a few weeks, advocates from around the country will be meeting with members of Congress for our 2019 Lymphedema Lobby Days. We want to take your stories with us!

If you have not already submitted your story to our My Lymphedema Story campaign please do!

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, and stories from anyone whose life has been touched by lymphedema are important – patients, caregivers, friends or family members, healthcare professionals, etc.

Our stories are powerful and persuasive, and by sharing yours you’ll be making a difference. Thank you!
 
Heather Ferguson
Founder & Executive Director
Lymphedema Advocacy Group
LymphedemaTreatmentAct.org
 

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