Meet some of our patient advocate heroes!
We have over 1,000 team members in all 50 states. This week, we’d like to introduce you to just a few of these phenomenal advocates. The pictures and profiles of
We have over 1,000 team members in all 50 states. This week, we’d like to introduce you to just a few of these phenomenal advocates. The pictures and profiles of
Congressman Dave Reichert (WA-08) has been the champion of the LTA for many years. He is always looking for ways to educate and raise awareness amongst his colleagues about the
This is amazing, and really speaks to the importance of this issue and the power of our grassroots advocacy! As of the official cosponsor counts yesterday, 9/12/17, here are some
Help raise awareness about lymphedema and the Lymphedema Treatment Act! Our FREE cards are available in two sizes, as seen here. To order yours, and find links to other
Congress is back in session and the members who have not yet cosponsored the LTA need to hear from you until they get on board! Even if you’ve called before,
To date, 311 members (34 Senators and 277 Representatives) have cosponsored the LTA! The list of those who have not yet signed on, along with a call script and phone
Make sure to visit our booth in the exhibit hall if you are attending the National Lymphedema Network’s 2017 International Conference in Orlando, FL! The Patient Summit is October 11th-12th
In our last few newsletters we’ve encouraged you to attend a district meeting with your members of Congress. I know that may sound intimidating, which is why I wanted to
We have reached another incredible milestone – over 300 House and Senate cosponsors! To see if your members of Congress are included check the House and Senate cosponsor lists. With
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