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

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

One year ago today, we made lymphedema history – the House of Representatives voted on the Lymphedema Treatment Act (LTA) and it was passed with an astounding bipartisan vote of

Last month, I had the privilege of representing the Lymphedema Advocacy Group at Forward Momentum: Future Steps in Lymphedema Management, hosted by the Lymphology Association of North America (LANA) in

Below is a summary of the LTA final rule. You can read the full 65 pages here. We have also inserted notes into our group’s public comment document, which can

We  wanted to send this clarification to assure you that the frequency limitations are based on sets of garments, not individual garments. We apologize that the initial quoted section below

The final rule for implementation of the Lymphedema Treatment Act was just released! The full rule contains a number of different provisions, but you can read the 65 pages related

This is just a reminder that the Lymphedema Treatment Act requires traditional Medicare to begin covering compression garments and supplies starting January 1, 2024. While most other plans follow the

In the coming weeks, the Center for Medicaid and Medicare Services (CMS) will release the final rule for implementation of the Lymphedema Treatment Act. We will alert you as soon