November 28, 2023
In 2006, my son Dylan was born with primary lymphedema. In 2010, I founded the Lymphedema Advocacy Group, with the mission of making sure that all lymphedema patients would someday have coverage for their compression supplies. Today, thanks to passage of the Lymphedema Treatment Act, we are closer than ever to reaching that goal. But […]
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November 23, 2023
My name is Sarah Bramblette. I’m the Board Chair of the Lymphedema Advocacy Group. This year, I’m thankful that the Lymphedema Treatment Act was passed and that, starting January 1 of 2024, Medicare will cover lymphedema compression garments! I’ve been a Medicare beneficiary since 2013, and during that time my lymphedema has been more difficult […]
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