On November 18th, nine organizations, including ours, the Lymphedema Advocacy Group, participated in the National Commission for Lymphatic Disease’s first ever Town Hall.
A recording of this seminal event is now available on the NIH VideoCast website. You can also find it on the commission’s web page, alongside details of past and upcoming meetings.
In addition, we invite you to the second Town Hall Forum, which will focus on rare lymphatic diseases. It is scheduled for Monday, December 2, 2024, from 9:00 am to 12:00 pm EST. You can access the event through this link, where the recording will also be available afterward.
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 recently launched 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
LymphedemaAdvocacyGroup.org
