Tag: LAG
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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.”
Filed Under: Lymphie Stories -
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.
Filed Under: Lymphedema news