Can you contribute $20, or whatever is right for your budget, so that we can wrap up our Match 2020campaign this week? The amount doesn’t matter, but your support does, and

Regardless of the outcome of today’s election, the current Congress continues through the end of the year. Meaning, the next two month are critically important to us! It’s no secret that

The Lymphedema Advocacy Group is proud to be a finalist for a 2020 RareVoice Award. We are thrilled and honored that our work to improve insurance coverage for lymphedema compression supplies is being showcased! 

As a resource to the lymphedema community, this year anyone can attend the virtual exhibit hall at the National Lymphedema Network’s online conference!The Lymphedma Advocacy Group is one of dozens

We are in the final months of this Congress and need your support to be able to do everything possible to get the Lymphedema Treatment Act signed into law this year! 

In recognition of October’s Breast Cancer Awareness Month, the Lymphedema Advocacy Group issued the following press release about the importance of passing the Lymphedema Treatment Act. If you have any contacts

Our amazing grassroots advocates are the reason the Lymphedema Treatment Act is the most supported healthcare bill in Congress!  Although we have teams of advocates in every state, there are

Five year ago today, which coincidentally fell on my twin sons’ 9th birthday, an article was published in the Washington Post about our family’s struggle to get Dylan properly diagnosed with congenital primary

Congratulations to the following 19 states that have every member of their congressional delegation cosponsoring the LTA: AK, AR, CT, DE, FL, HI, MN, MO, MS, MT, ND, NH, NM, NV, OK,