Next Monday, advocates from around the country will be on Capitol Hill to take part in our annual Lymphedema Lobby Days.
We will be urging the Senate to pass the bill, just as the House did in December, so that the LTA can be signed into law this year!
We will be delivering over 1,000 pages of patient stories, from every state, to each Senator, to bring the voices of those who cannot travel to D.C.
And we will also be sending you a special Action Alert next week, so that you can make a difference from home.
None of this would be possible without your support!
If you haven’t yet made a donation to our 2020 Love the Lymphedema Treatment Act fundraiser please consider contributing this week. The amount doesn’t matter, but your support does.
Help us continue to make your voice heard in Washington.
Together, we will pass the Lymphedema Treatment Act!
Heather Ferguson
Founder & Executive Director
Lymphedema Advocacy Group
LymphedemaTreatmentAct.org
As a 501(c)(4) nonprofit organization, the Lymphedema Advocacy Group
engages in lobbying activity, in keeping with its mission, for passage of the
Lymphedema Treatment Act.
