Lymphie Win: After 12-Year Effort, Lymphedema Treatment Act Becomes Law
Like muscles working to pump stubborn lymphatic fluid, advocates of the Lymphedema Treatment Act worked hard to pump the bill along and keep it moving.
Tag: LTA
A conversation with Heather Ferguson, mother of the Lymphedema Treatment Act
“Lymphedema has become a defining feature of my life precisely because I didn’t want it to define my son’s life.”
Research Roundup: Axillary Nodes, Advocacy, and the Lymphedema Lobby Days
A summary of lymphedema and lymphatic research news from March 18 – 24, 2017.
Updates on the Lymphedema Treatment Act
Through the tireless work of the Lymphedema Advocacy Group, patient advocates, and politicians like Congressman Dave Reichert championing the bill, there has been a groundswell of support and action.
Recap: Lymphedema Lobby Days 2016
I joined over seventy patient advocates from across the country for an amazing, inspiring, nerve-wracking, exhilarating, and empowering couple of days in Washington, DC.
Lymphedema Awareness Day
Today is a day for us to join together and use our voices not only to spread awareness about lymphedema, but to celebrate our amazing community.