Your Stories were part of last week’s LTA Committee Hearing!
Last week, the Lymphedema Treatment Act took another big step forward when it was included in the “Legislation to Improve and Sustain the Medicare Program” hearing. If you’ve watched the
Last week, the Lymphedema Treatment Act took another big step forward when it was included in the “Legislation to Improve and Sustain the Medicare Program” hearing. If you’ve watched the
This week we cleared another hurdle on the way to passing the Lymphedema Treatment Act! On Wednesday, June 8th, the Ways and Means Heath Subcommittee conducted a hearing entitled “Legislation
Our wildly popular “6 Things You May Not Know About Lymphedema” infographic is now available in Spanish too! To download the English or Spanish version of our infographic flyer, or
We are thrilled to announce that the American Medical Association has endorsed the Lymphedema Treatment Act! They join a long list of supporting groups, which can be seen here. We
In the 27 days since our Lymphedema Lobby Days we’ve gained 27 more cosponsors! That’s incredible progress, but we still need your help to reach our goal of having a
Our stories are powerful, and they illustrate to members of Congress why there is an urgent need to pass the Lymphedema Treatment Act! Please share your lymphedema story with us,
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
Thank you so much for helping us reach this huge milestone of support in the House! To see if your Rep is one of our 220 House cosponsors click here.
This week’s 2016 Lymphedema Lobby Days were a huge success! Over 70 patient advocates, hailing from 21 states plus the District of Columbia, met with 214 offices from 38 different
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