Today is the day to show your support!
Your Giving Tuesday gift will make a difference for those living with lymphedema! For example, a $100 donation allows us to print and ship 500 of our free information cards,
Your Giving Tuesday gift will make a difference for those living with lymphedema! For example, a $100 donation allows us to print and ship 500 of our free information cards,
In honor of Giving Tuesday, we hope you will consider making a tax-deductible donation to our 2025 Year-End Campaign, so that we can continue to expand access, education, and resources
Our 2025 Coverage Report for Lymphedema Compression Treatment Items is now available! We hope that the report aids you in making a more informed decision when choosing your 2026 health
We are grateful to everyone who participated in our 2025 Lymphedema Coverage Survey. A report outlining the results will be released soon. Last week, I had the pleasure and honor
We’ve updated our Provider handout. New information is now included under the “What details and clinical notes must be included with the prescription?” section. Our separate Patient, Provider, and Supplier
We are saddened to share the news that Joan White, founder of the Lighthouse Lymphedema Network (LLN), passed away earlier this week. Joan was a lymphedema patient and true force
The 27th Annual Lymphedema Education and Awareness Conference, hosted by the Lighthouse Lymphedema Network (LLN), is taking place this weekend, on October 17th and 18th in Atlanta, Georgia. This conference
Last week, the Center for Medicare Advocacy presented a webinar to help current and upcoming Medicare beneficiaries understand their different plan options. Click here or on the image below for
Today at 2:00PM Eastern, the Center for Medicare Advocacy is hosting a free webinar to help current and upcoming Medicare beneficiaries understand their different plan options. Click here or on
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