Tomorrow (Friday, June 28th) is the deadline to submit feedback to the National Institute of Health’s recently launched National Commission on Lymphatic Diseases (NCLD). NCLD’s purpose is to gather input

We are so pleased to share with you these new handouts! As displayed below, there are separate versions for Patients, Providers, and Suppliers.  The front side of each has important

If you or your patients have a Medicare Advantage plan and have been denied coverage, or found that there is no in-network supplier with your/their plan, we need to hear

Dear [CONTACT: first name], We have two opportunities to share with you. The first is an international study about the effects of climate on lymphedema symptoms. All patients are invited to

We know that many people are still adjusting to the new insurance coverage for compression garments and supplies, and unsure about what information must be provided with each order. We

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