Next week, on September 12th, two individuals working hard to pass the Lymphedema Treatment Act will be recognized at the Rare Voice Awards in Washington, D.C. Fourteen-year-old Sarah Meyer, who

Attention Facebook and Twitter users: please share these posts on social media and tag the members of Congress listed at the bottom who haven’t cosponsored the LTA yet! Twitter: Please

The Lymphedema Treatment Act has cosponsors from every state except for Idaho and Wyoming. If you or someone you know live in one of these states we need your help!

Did you know that animals can get lymphedema too, particularly horses? This short video created by HEALequine encourages kids living with lymphedema to be the best they can be. Several

We’ve finally reached our long-sought 60 Senate cosponsors – sort of. According to Congress.gov, the official government website for tracking legislative information, we have 60. However, three of the Senators

As we approach the final months of the 115th Congressional Session, our lead House sponsor Congressman Reichert is doing everything possible to secure coverage for lymphedema compression supplies and garments.

With the upcoming August recess and midterm elections in November, many members of Congress will be hosting Town Hall meetings and other public events in the coming weeks and months.

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

This week, we ask that you contact the following six Senate leadership offices. A phone script, sample Tweet, and fax forms are below. Choose your method of contact or feel