Show Your Love for the LTA – Join the Walk or Donate!
2019 was a historic year for the lymphedema community! Passage of the LTA in the House was a huge milestone, and now we need to do everything possible to get the bill through the Senate this year, before the current Congress ends in December.
While the LTA has garnered fantastic bipartisan support, there is much more work to do! Our annual Lymphedema Lobby Days on Capitol Hill garners critical new support for the LTA. While volunteer advocates pay for their own flight and lodging, the event is not without expense. That’s where you come in!
There are two options: you can simply DONATE, or you can JOIN THE FUNDRAISING TEAM! When you join the team you have the option to create a personalized fundraising page. You can then easily share your personalized fundraising links via social media (such as Facebook, Twitter, or email) with friends and family.
Thank you for your support – together, we will pass the LTA!
Heather Ferguson
Founder & Executive Director
Lymphedema Advocacy Group
LymphedemaTreatmentAct.org
As a 501(c)(4) nonprofit organization, the Lymphedema Advocacy Group
engages in lobbying activity, in keeping with its mission, for passage of the
Lymphedema Treatment Act.
