Save the date for our 2017 Lymphedema Lobby Days in Washington, DC, March 26th-28th!
No experience is necessary and everyone is welcome! Last year, over 70 patient advocates from around the country, ranging in age from 7 to 80, met with 214 offices from 38 different states to raise support for the LTA. We hope to have even more participation this year.
This is the first time we have planned a Lobby Days so early in a new Congress.We thank you for your understanding and patience while we finalize the hotel and other details. As soon as plans are finalized, which should be next week, we will let you know so that you can make your travel arrangements. You can read what past participants have had to say about their experience on the Lobby Days page of our website.
Join the team for our Love the Lymphedema Treatment Act Valentine’s Day Walk on February 14th!
This is a virtual event, so anyone, anywhere, with any ability level can participate. As a team member you can set your own goal for walking (or whatever activity is most appropriate for you) and set up a personalized fundraising page to share with family and friends.
More details are available on our CrowdRise page. We also have a brief how-to video about joining the team and setting up your personal page.
Thank you for your support and participation in these events!
Heather Ferguson
Founder & Executive Director
Lymphedema Advocacy Group
LymphedemaTreatmentAct.org
