Happy New Year!

by Heather on January 1, 2021

January 3rd, 2021 will mark the start of the 117th Congress. We came so close to seeing the Lymphedema Treatment Act signed into law this month and will continue to persevere until the bill is across the finish line!

The Lymphedema Advocacy Group is an all-volunteer organization of patients, caregivers, healthcare professionals and industry partners. We are grateful to have the involvement of stakeholders from all aspects of the lymphedema community. 

A special thank you to our Industry Partners – JOBST, L&R USA, and mediUSA – as well as our Annual Sponsors – ImpediMed, Lymphedema Products, and the Lipedema Foundation – for their support of our work.

We hope you and yours have a safe and happy new year!

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

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