Last year, Martha, one of our advocates, contacted us for advice because her private insurance plan had discontinued covering custom compression garments. We were so delighted to get this from

We are pleased to share with you our 2023 Annual Report. Although the Lymphedema Advocacy Group is now in its 14th year of existence, this is the first time we

We were thrilled to share this video about our efforts and accomplishments here in the United States at a recent international conference held in Italy, Lymphedema and Lipedema Across Borders:

Although the majority of the recommendations in our group’s Public Comments were incorporated into the final rule, the issue of therapist reimbursement for fitting and measuring services has yet to be

The link to our new one-pager was incorrect in yesterday’s email, which is copied below. It has been fixed, and we apologize for any inconvenience.  If you are a patient

Today marks two months since the start of Medicare coverage for lymphedema compression supplies. Considering the magnitude of this undertaking – the last time a new Medicare benefit category was

On February 23, 2010, 14 years ago today, the Lymphedema Treatment Act was first introduced in Congress! Click on the image to view a larger online version. If you would

We have a new easy-to-print one-pager outlining key information about the new LTA coverage! Click HERE or on the image at the bottom of this message to view the document

If you are a lymphedema therapist, please consider taking this 10-minute research survey regarding advocacy. The deadline is Friday, February 23rd. A letter from the Doctor of Health Administration student