Thank you to everyone who helped us reach this milestone! You can see the complete list of 201 House cosponsors here, and 13 Senate cosponsors here. If you don’t see

In exactly two weeks from today, patient advocates from around the country will spend two days in Washington, DC, meetings with congressional offices to increase support for the Lymphedema Treatment

Just four days left to register to take part in our 2016 Lymphedema Lobby Days, April 18th-20th in Washington, DC! Monday, April 4th is the registration deadline to join the

Register now for our 2016 Lymphedema Lobby Days, taking place April 18th-20th in Washington, DC! We are just three weeks away from the registration deadline of April 4th, and one

Happy Lymphedema Awareness Day! Today marks the 22nd annual Lymphedema Awareness Day, a tradition started by Saskia Thiadens, founder of the National Lymphedema Network (NLN). Each year, on this day,

We now have 189 Representatives cosponsoring our House bill, HR 1608, and 11 Senators cosponsoring our recently introduced Senate companion bill, S 2373. Click here for the House list, and

March is Lymphedema Awareness Month, and March 6th is Lymphedema Awareness Day! If you are hosting or attending an event, or just want to increase awareness in your area, we

Today, lymphedema advocates around the country will be walking to raise funds to support passage of the Lymphedema Treatment Act! This is our big fundraiser for 2016 and we hope

On Wednesday of this week, LTA lead sponsor, Congressman Dave Reichert, made a passionate statement calling on HHS Secretary Burwell to help improve lymphedema treatment for patients! You can watch