Cosponsor Update: Congress is back in session and we are thrilled to report that we have 132 cosponsors! If your Rep’s name isn’t on the list yet please keep writing

We have lots of important news and information to share with you this month! NEW Cost Report Demonstrating Saving This new report from Avalere Health, commissioned by the Lymphedema Advocacy

We are pleased to announce TWO NEW Advocacy Training Webinars from the Lymphedema Advocacy Group (LAG)! We hope you can join us next week, and at future webinars, which we

Our Summer Raffle is Underway! Each time you donate $5 or more you will be entered to win prizes donated by CircAid (one custom or standard fit item), Jobst ($100

We have already surpassed the number of cosponsors we had in the last Congress! Thanks to the grassroots advocacy of people just like you, we now have 111 cosponsors. Now,

The Lymphedema Treatment Act is off to a strong start this session with 102 members of the House already signed on. All of these cosponsors were the result of constituent

Last week, Primary Lymphedema was one of 10 rare diseases highlighted at the National Organization of Rare Diseases’ annual gala in Washington, DC! Each year NORD honors 10 rare disease

It’s been less than six week since our bill was reintroduced and we already have 62 cosponsors! That’s amazing progress, but we still need many more. If you’ve received a

It is with great pleasure that I present to you this new 13-minute documentary – Lymphedema Treatment Act Public Service Announcement. Please share it far and wide to help us