Lymphedema Advocacy Group / Lymphedema Treatment Act

Lymphedema Advocacy Group / Lymphedema Treatment Act The Lymphedema Advocacy Groups works to improve access to care for those suffering from this chronic disease.

Our group led the effort to pass the Lymphedema Treatment Act legislation, which improved insurance coverage for compression supplies. The "Lymphedema Treatment Act” is a federal bill that will amend Medicare statute to provide for coverage of the compression supplies used in the treatment of lymphedema. Although this legislation relates specifically to a change in Medicare law, it would set a precedent for Medicaid and private insurers to follow. Please go to www.LymphedemaTreatmentAct.org to learn more, and to contact your members of Congress and ask them to support this important bill. The Lymphedema Advocacy Group is an all-volunteer, nationwide patient advocacy group leading the effort to pass this important legislation.

We’ve updated our Provider handout. New information is now included under the "What details and clinical notes must be i...
10/25/2025

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. Please visit our website for details (https://lymphedemaadvocacygroup.org/updated-provider-handout/).

We've updated our Provider handout. New information is now included under the "What details and clinical notes must be included with the prescript ...

We are saddened to share the news that Joan White, founder of the Lighthouse Lymphedema Network (LLN), passed away earli...
10/18/2025

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 of nature whose legacy will live on through the LLN and the many members of the lymphedema community whose lives were improved by her efforts.

Joan’s swelling began after a surgical procedure in 1988. After finding no lymphedema treatment centers in the United States, in 1991 she flew to Germany. After she returned and at her own expense, she helped a therapist become trained in Complete Decongestive Therapy. It became her mission to let other patients know that this treatment was available, and in 1993 she started the Lighthouse Lymphedema Network.

As Joan wrote in The Puzzle: An Inside Glimpse of Lymphedema, "Live your life to serve others, and never think you are alone." May Joan rest in peace knowing that the world, and particularly the lymphedema community, has been immeasurably improved through her service.

For details about her memorial services please go to (https://lymphedemaadvocacygroup.org/remembering-joan-white/).

The Lighthouse Lymphedema Network (LLN) conference is taking place this weekend in Atlanta, GA, and the International Ly...
10/15/2025

The Lighthouse Lymphedema Network (LLN) conference is taking place this weekend in Atlanta, GA, and the International Lymphedema Framework (ILF) conference is taking place next weekend in Niagara Falls, Canada. The registration deadline for virtual attendance at LLN is today, 10/15, and the registration deadline for in-person attendance at ILF is Friday, 10/17. Links to register and get more information are in our newsletter at https://lymphedemaadvocacygroup.org/virtual-lln-conference-registration-deadline-is-today/.

Our Lymphedema Supplier Directory now has nearly 300 listings! Please check to see if your supplier is included, and if ...
10/12/2025

Our Lymphedema Supplier Directory now has nearly 300 listings! Please check to see if your supplier is included, and if they are not, ask them to join. Suppliers must add their own businesses. It's completely free, and all they need to do is click on the "Register" button at the top of the page, then follow the prompts to create an account. Together, we can help more patients find the best supplier to meet their needs!

Lymphedema Supplier Directory After entering your location search criteria, click on a business name to view detailed information about each supplier, inclu ...

Do you have insurance-related questions? A great place to start is our FAQ page. You can also find additional informatio...
10/08/2025

Do you have insurance-related questions? A great place to start is our FAQ page. You can also find additional information specific to each type of plan under the Insurance tab on the main navigation menu of our website. (https://lymphedemaadvocacygroup.org/insurance/frequently-asked-questions/)

Lymphedema Treatment Act Questions What is the Lymphedema Treatment Act (LTA) and how does it help patients? The Lymphedema Treatment Act (LTA) is a federal ...

The Center for Medicare Advocacy recently presented a webinar to help current and upcoming Medicare beneficiaries unders...
10/05/2025

The Center for Medicare Advocacy recently presented a webinar to help current and upcoming Medicare beneficiaries understand their different plan options. A recording is now available. (https://medicareadvocacy.org/navigating-open-enrollment-webinar/)

__________ ___________ Description The Center for Medicare Advocacy’s popular yearly webinar is for anyone dealing with Medicare enrollment. Experts cover the basics surrounding Medicare’s Open Enrollment Period, with an emphasis on considerations for people with longer-term and chronic conditio...

Just a few days left to take our 5-minute coverage survey and get 15% off your next pair of Pandere Shoes!
09/29/2025

Just a few days left to take our 5-minute coverage survey and get 15% off your next pair of Pandere Shoes!

Your voice matters—and earns 15% off. Take the 2025 Lymphedema Insurance Coverage Survey (under 5 minutes), open until Sept 30.
How to get your code:
👉 Complete the survey
👉Screenshot the confirmation
👉Email the screenshot to hello@pandereshoes.com
We will reply with your 15% off code
Take the survey now: https://www.surveymonkey.com/r/coverage2025

There’s just a few days left to add your voice! Our 2025 Lymphedema Treatment Coverage Survey only takes 5 minutes to co...
09/25/2025

There’s just a few days left to add your voice! Our 2025 Lymphedema Treatment Coverage Survey only takes 5 minutes to complete and closes at the end of September. Results will be analyzed in October and published in November, in time to assist patients in choosing their plan for next year. If you haven't completed the survey yet, please do!

Please take this 5-minute survey, which will be open until the end of September. Results will be analyzed in October and published in November, just in time to assist patients in choosing their plans for the upcoming open enrollment period.

Come visit Franci at our information table if you are in Nashville for the NLN Conference this weekend!
09/20/2025

Come visit Franci at our information table if you are in Nashville for the NLN Conference this weekend!

We’ve recently added an Insurance Appeal Resources page to our website, which is full of valuable information, advice, a...
09/18/2025

We’ve recently added an Insurance Appeal Resources page to our website, which is full of valuable information, advice, and links. (https://lymphedemaadvocacygroup.org/insurance-appeal-resources/ ) We encourage you to never take no for an answer! Studies estimate that only about 1% of denied health insurance claims are appealed. However, when appeals are pursued, they are often successful, with a win rate of 70–80%!

Insurance Appeal Resources If you have been denied coverage for any lymphedema treatment item or service, we encourage you to appeal! You'll find helpf ...

Get 15% off at Pandere Shoes for completing our 5-minute survey! (https://www.surveymonkey.com/r/coverage2025) These awe...
09/16/2025

Get 15% off at Pandere Shoes for completing our 5-minute survey! (https://www.surveymonkey.com/r/coverage2025) These awesome shoes are designed to fit feet. Just send them a screen shot or photo from the survey confirmation page to get your coupon. Full details are in their blog post (https://pandereshoes.com/blogs/blog/pandere-lymphedema-coverage-survey-2025).

💜 Insurance shouldn’t be a guessing game.
Take 5 minutes ➡️ Make a difference.
Complete the 2025 Lymphedema Insurance Coverage Survey and help shine a light on real insurance coverage for lymphedema patients.
👉 Link here: https://www.surveymonkey.com/r/coverage2025
💡 Open until Sept 30
🎁 Get 15% off your next Pandere order as our thank-you, (Chat with us for details)

Lymphedema Advocacy Group / Lymphedema Treatment Act Lighthouse Lymphedema Network National Lymphedema Network Lymphedema Lymphedema Management Lets Cure Lymphedema

Our 2025 Lymphedema Treatment Coverage Survey takes less than 5 minutes to complete and will be open until the end of Se...
09/16/2025

Our 2025 Lymphedema Treatment Coverage Survey takes less than 5 minutes to complete and will be open until the end of September. If you haven't completed the survey yet, please do! Results will be analyzed in October and published in November, just in time to assist patients in choosing their plans for the upcoming open enrollment period.

Please take this 5-minute survey, which will be open until the end of September. Results will be analyzed in October and published in November, just in time to assist patients in choosing their plans for the upcoming open enrollment period.

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Carrboro, NC
27510

Website

https://lymphedemaadvocacygroup.org/donate/

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