We are thrilled to share our new website, LymphedemaAdvocacyGroup.org!
This new site will support our ongoing work to improve insurance coverage for lymphedema treatment and will continue to be developed with new resources in the coming year.
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Together, We’ve Made History — And the Work Continues!
Thanks to your support, the Lymphedema Treatment Act became law, providing life-changing coverage for compression garments to millions. But there’s still more to do.
That’s why we’re launching our Giving Tuesday & Year-End Fundraising Campaign with the goal of raising $10,000. These funds will allow us to:
- Advocate for fair and expanded coverage for lymphedema treatments.
- Educate patients, providers, and insurers about the new law.
- Address remaining gaps in care and ensure no one faces lymphedema alone.
We can’t do this without you.
Please visit our Giving Tuesday & Year End Fundraising Campaign to learn more about our mission and priorities. Contributions can be made via check, credit card, or PayPal.
Thank you for your unwavering support. Together, we can continue improving care for individuals living with lymphedema.
Heather Ferguson
Founder & Executive Director
Lymphedema Advocacy Group
LymphedemaTreatmentAct.org
