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Lighthouse Lymphedema Network

Shining Light On Lymphedema

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2-21 Survivors Breakfast
3-6 World Lymphedema Day
3-12 Power Symposium
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4-19 FDRS 2024
26th Conference - Save the Date
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Welcome To The Lighthouse

Lymphedema Network

The Lymphedema Treatment Act is a federal bill that will improve insurance coverage for the medically necessary, doctor-prescribed compression supplies that are the cornerstone of lymphedema treatment.

To learn more about this legistation and the ways in which you can support its passage, please visit     This is a patient-driven, grassroots effort and our success depends on people just like you getting involved?

It is very important that your members of Congress hear from you.  The advocacy tools at the Lymphedema Treatment Act website make it quick and easy to contact your legistators via email, letter, phone and social media.

Please take a couple of minutes to ask your members of Congress to support this important bill by taking action today at  

Heather Ferguson
Founder and Executive Director
Lymphedema Advocacy Group
This email address is being protected from spambots. You need JavaScript enabled to view it.

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About Us

The Lighthouse Lymphedema Network is a 501 (C) (3) organization of individuals who are lymphedema patients, or who have an interest in lymphedema.

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