Support the LTA this Giving Tuesday
Our work would not be possible without you! There are four ways you can support lymphedema patients and passage of the Lymphedema Treatment Act on this Giving Tuesday:
Our work would not be possible without you! There are four ways you can support lymphedema patients and passage of the Lymphedema Treatment Act on this Giving Tuesday:
This is a call to action – please use the information on this page to contact Congressional leaders in the House and Senate, urging them to bring the LTA to
Contact your members of Congress on social media and urge them to pass the LTA this year! SAMPLE TWEET or FACEBOOK POST: “With nearly 450 cosponsors, the #LymphedemaTreatmentAct (H.R.930/S.497) is
Regardless of the outcome of tomorrow’s election, current members will stay in office through the end of this Congress in early January. There two things you can do right now
Last week, I proudly delivered a letter from 27 stakeholder groups to House and Senate leadership, urging them to pass the Lymphedema Treatment Act before the current Congress adjourns.
Last month, two individuals working hard to pass the Lymphedema Treatment Act were recognized at the Rare Voice Awards in Washington, D.C. Fourteen-year-old Sarah Meyer was a finalist in the
We are cautiously optimistic that the Lymphedema Treatment Act will be voted on during the lame duck session after the election! Although we will continue to work on adding to
We’ve reached a new milestone, and something few bills ever accomplish – cosponsors from all 50 states! This would not have been possible without the hard work and dedication of
You can help raise awareness about lymphedema and the Lymphedema Treatment Act! All of our educational materials are available for order, or free download, via the Increasing Awareness page on
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