15 years ago today, on February 23, 2010, the Lymphedema Treatment Act was introduced into Congress for the very first time. It would take more than 12 years for the bill to become law, but we persisted and we prevailed!
We couldn’t have done it without the help of advocates like you, and together, we can continue to improve access to care for the millions of men, women, and children in America who are affected by lymphedema.
In honor of the last 15 years of advocacy, and because there’s more work to be done, we hope you will show your support by donating to our 15th Anniversary Fundraising Campaign.
Every dollar you contribute fuels our mission to close coverage gaps, advocate for fair policies, and empower patients. If you prefer to donate by check, you can do so by mailing your gift to: Lymphedema Advocacy Group, PO Box 1682, Carrboro, NC 27510.
Thank you for your advocacy and support!
Heather Ferguson
Founder & Executive Director
Lymphedema Advocacy Group
LymphedemaAdvocacyGroup.org
As a 501(c)(4) nonprofit organization, the Lymphedema Advocacy Group engages in lobbying activity, in keeping with its mission, to advocate for policy changes that advance lymphedema care. As such, contributions or gifts to the Lymphedema Advocacy Group are not tax deductible.
