On November 18th, nine organizations, including ours, the Lymphedema Advocacy Group, participated in the National Commission for Lymphatic Disease’s first ever Town Hall. A recording of this seminal event is

We are thrilled to share our new website, LymphedemaAdvocacyGroup.org!  This new site will support our ongoing work to improve insurance coverage for lymphedema treatment and will continue to be developed

We invite you to attend the first ever National Commission for Lymphatic Disease (NCLD) virtual Town Hall taking place on Monday, November 18th, from 9:00am to 12:00pm Eastern time.  The

We are happy to announce that the Centers for Medicare & Medicaid Services (CMS) has retired the Local Coverage Determination (LCD L33829) for Pneumatic Compression Devices (PCDs) effective today, November

Last year, the Lymphology Association of North America and the American Cancer Society hosted a lymphedema summit. The event brought together key experts and stakeholders from across North America to

If you are a Medicare beneficiary, you have until December 7th to choose your health plan for next year. If you are turning 65 in 2025, you may also be

One of our future goals is to gain coverage for prescription shoes for lymphedema patients who are unable to wear standard, commercially available footwear.  If you are a patient who

We have two separate calls to action to share with you this month. First, if you are a patient who can only wear custom-made footwear because your lymphedema swelling prevents

Currently, when a Medicare patient is receiving Home Health services, their compression garments are billed separately through their Part B coverage. That will continue to be the case. Recently, the