Our House bill just surpassed 200 cosponsors & we are on Capitol Hill again this week!
For the next three days, members of our board and our State Teamswill be on Capitol Hill meeting with offices about the LTA. You can increase the impact of our
For the next three days, members of our board and our State Teamswill be on Capitol Hill meeting with offices about the LTA. You can increase the impact of our
You can increase support for the Lymphedema Treatment Act by meeting with your members of Congress at a nearby district office! In-person meetings are the single most effective way to
Over the last few years we have collected over 500 patient and caregiver stories through our My Lymphedema Story campaign. Thanks to the efforts of those who attended our Lymphedema
We have grassroots advocacy teams in all 50 states! If you haven’t joined your state’s team yet here are a few reasons why we hope you will consider it. No
In the last few weeks our bill has gained dozens of new cosponsors! Check to see if your members of Congress are included: House bill, Senate bill. Remember, cosponsors do
Even if you are unable to join fellow lymphedema patients and caregivers from around the country at our Lymphedema Lobby Days, March 26th-28th, you can still ensure that Members of
Our 2017 Lymphedema Lobby Days were a tremendous success! The grand totals are: 71 participants from 26 states, with ages ranging from 8 to 81 275 scheduled meetings with offices
The Lymphedema Treatment Act has been reintroduced in the Senate! Lead sponsor Senator Cantwell and co-lead Senator Grassley were joined by nine other bipartisan members of the Senate to reintroduce
Our Lymphedema Lobby Days raise critical support for the Lymphedema Treatment Act and we can’t do it without you! This year’s event dates are March 26th-28th. The deadline to reserve
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