Free Lymphedema Learning Session for Primary Care Providers!
On August 1st, the Keck School of Medicine at USC will host a FREE online learning session entitled “Lymphedema: What to Know as a Primary Care Provider.” Please share this
On August 1st, the Keck School of Medicine at USC will host a FREE online learning session entitled “Lymphedema: What to Know as a Primary Care Provider.” Please share this
As promised, we have been working with the Centers for Medicare and Medicaid Services (CMS) to ensure that Medicare Advantage (MA) plans provide the required coverage. We have received some
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