ACTION ALERT: Email Congress This Week

by Heather on May 23, 2023

Today, more than 100 lymphedema advocates from around the country are on Capitol Hill to thank lawmakers for passing the Lymphedema Treatment Act, and to ask them to support any future legislation and research funding that will benefit lymphedema patients. 

If you are not in DC with us today, please send this email to your members of Congress

All you need to do is fill in your name and address, and personalize the editable template if you wish. When you are done, there will be links for sharing the action alert, so that you can ask friends and family to participate as well, or share it on social media. Thank you for your advocacy! 

Heather Ferguson
Founder & Executive Director
Lymphedema Advocacy Group
LymphedemaTreatmentAct.org

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