We were thrilled to recently participate in the Canadian Lymphedema Framework international conference, at which we premiered this poster chronicling our work. The abstract for the poster can be read

Our work to pass the Lymphedema Treatment Act and ensure that all patients have insurance coverage for their vital compression supplies would not be possible without your support!  Your contributions provide the critical resources that enable

Thanks to our advocates, members of Congress from 49 states, three territories, and the District of Columbia are cosponsoring the Lymphedema Treatment Act!  We are grateful to all those who

Patient stories are powerful.  We can give members of Congress and their staff facts and statistics, but it’s hearing how lymphedema and the lack of insurance coverage for compression garments

Our Information cards, available in two sizes and pictured below, are perfect for handing out at holiday gatherings, or tucking into gifts and cards.  Click HERE to order your lymphedema

A huge thank-you to all those who headed our recent calls to action. We achieved our goal of reaching 290 cosponsors in the House, meaning we now have super majority

Although most are still virtual, members of Congress are beginning to hold Town Hall meetings again. The Town Hall Project is a great site for finding out about these events.

We recently reached a super majority level of support in the Senate, and are close to doing so in the House as well! Below I explain why a super majority

Please complete this form, if you have not already done so, if you are interested in attending a virtual meeting with one or more of your Congressional offices in support