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Newsletter Archives

Sign this Letter to Congress! (Call to Action Item #1)

November 16, 2020

It’s crunch time! The next few weeks will determine if the Lymphedema Treatment Act is passed during this Congress.  Each week we will be issuing at least one call to action, and your participation in each action is critically important.  This week, please use our email form to send a letter to your members of Congress! This […]

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80% of the way to our Match 2020 goal!

November 9, 2020

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 every donation will be matched by our Angel Donor until we reach our goal! Next week Congress will return to work. Our bill has tremendous […]

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Meet “The Team” (and VOTE!)

November 4, 2020

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 Congress has gotten next to nothing passed the last six or so months, as they were deadlocked over the next COVID-19 relief package. In part […]

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We are a Finalist for a RareVoice Award!

October 28, 2020

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!    The winner will be announced live at the RareVoice Awards taking place virtually on December 10th, 2020 at 7:00pm EST. For more information and to […]

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FREE Virtual Education Opportunity

October 24, 2020

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 of exhibitors, so if you’ve ever want to chat with a member of our board this is a chance to do so. Other exhibitors include […]

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Double Your Impact for Helping Lymphedema Patients with our Match 2020 Campaign!

October 16, 2020

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!  Thanks to an incredibly generous Angel Donor, every donation will be matched up to $10,000! That means any amount you donate will be doubled! To […]

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October is an Opportunity to Shine a Light on Lymphedema!

October 12, 2020

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 in the media, please pass this along. We’ve also updated the template letter on our Letter to the Editor form to reflect this information, if […]

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We Need Advocates in These Areas

October 5, 2020

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 some individual Congressional districts where we do not have any members. If you reside in one of the districts named below we hope you will consider joining […]

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A Birthday Wish to Pass the LTA!

September 29, 2020

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 lymphedema, and my shock to learn that the compression garments he would need to wear for the rest of his life would not be covered by […]

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Do you live in one of these states?

September 21, 2020

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, RI, VT, WA, and WI. This is an awesome accomplishment!  If you do not live in one of these 19 states please see the list below. […]

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Announcing 3 New Cosponsors – Only 87 Members Remain!

September 14, 2020

In recent weeks we have gained three House cosponsors – Rep Horsford (NV), Rep Veasey (TX), and Rep Tiffany (WI). Every additional cosponsor helps increase our chances of getting into the next legislative package so let’s add to that list! Only 29 Senators and 58 House members have yet to cosponsor the Lymphedema Treatment Act. They are listed […]

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More Ways to Raise Awareness about Lymphedema & the LTA

September 5, 2020

We are grateful for everyone who recently sent a Letter to the Editor in support of the LTA! If you haven’t had a chance to send yours yet you can still do so by clicking here. A template is provided, so it only takes a moment.  Educational and awareness materials are always available for free download […]

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THANK YOU for Sending a Letter to the Editor about the LTA!

August 30, 2020

Thank you to all those who sent a Letter to the Editor last week in support of the LTA! If your letter was published, please send us a link by replying to this email.  We have contacted the authors of all letters we are aware of that have been published to date, but it’s very […]

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Send a Letter to the Editor about the LTA!

August 23, 2020

Members of Congress pay attention to what their constituents speak out about – especially if it makes it into the paper, and especially in an election year! Using our new Action Alert you can submit a Letter to the Editor to all media publications within a 50 mile radius of your location in one easy […]

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Your Lymphedema Story

August 17, 2020

Stories from patients, family members, and clinicians are critically important. These first-hand accounts illustrate for members of Congress and their staff why passage of the Lymphedema Treatment Act is so important. For most patients, the pandemic has made it even more challenging to manage their lymphedema, and the need for insurance coverage for compression garments and supplies is […]

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The Next Package is in Limbo, but Our Advocacy is Not!

August 10, 2020

Although deliberations over the next relief package have stumbled, our push to pass the LTA cannot let up! Now, more than ever, patients need insurance coverage for their doctor prescribed, medically necessary compression garments. With the recent executive actions, it is unclear what the nature of the next legislative package will be, so we have updated the template language on the call […]

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Three Ways You Can Help Get the LTA into the Next Legislative Package

August 3, 2020

We are so grateful for the advocates who have responded to our calls to action in recent weeks – keep up the great work!  As you’ve probably seen in the news, deliberations over the next legislative package have begun. As our bill sponsor Senator Cantwell continues to push leadership to include the Lymphedema Treatment Act, it’s […]

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Please Keep Calling Your Senators!

July 28, 2020

Now that the initial draft of the next legislative package has been released by the Senate majority party, lawmakers will negotiate to get additional smaller provisions like the LTA added. Senator Cantwell, our bill sponsor, is pushing to get the LTA in, but she can’t do it alone. It will take multiple Senators going to leadership, asking for the LTA […]

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Update: Getting the LTA into the Next Legislative Package

July 19, 2020

Your calls and emails are working!  But we have to keep them coming, here’s why… The Senate majority party is expected to release a bare bones first draft for the next legislative package this week, after which lawmakers will negotiate to get addition provisions like the LTA added. There will be stiff competition, and Senator Cantwell, our […]

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Urgent Action Alert – Contact Your Senators Now!

July 15, 2020

Senator Cantwell, our bill sponsor, has informed us she is pushing hard to have the LTA included in the next legislative package, and has asked that our advocates contact their Senators again now!  The most important action you can take is calling your Senators’ DC offices! The phone numbers and call script are below. Please also write to […]

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