This month, we were thrilled to have our work recognized by the Home Medical Equipment (HME) industry in the article HME’s Road Ahead.
HME industry leaders cited CMS implementation of the Lymphedema Treatment Act as one of the high points for 2024! I was honored that the author also wrote:
“I’d like to give a personal shout out to Heather Ferguson, founder and executive director of the Lymphedema Advocacy Group. Her steadfast commitment and persistence gave birth to the Lymphedema Treatment Act. I believe her journey and her story are inspirational, and it should add fuel to the fire for all of us who are advocating for patients’ access to the appropriate clinical care.”
We’ve come a long way, but there is still more work to do, which is why your continued support is crucial. Please consider helping us reach our 2024 year-end fundraising goal.
You can donate via credit card, debit card, or with PayPal at our Year-End Fundraising Campaign, or by mailing a check to: Lymphedema Advocacy Group, PO Box 1682, Carrboro, NC 27510.
Help us to continue improving care for individuals living with lymphedema!
Heather Ferguson
Founder & Executive Director
Lymphedema Advocacy Group
LymphedemaAdvocacyGroup.org
