Advocates around the country are showing their LOVE for the Lymphedema Treatment Act!
Valentine’s Day is at the heart of our annual fundraiser. Today, advocates around the country will be showing their love for the LTA by walking in their own communities. And in a few weeks, they will be walking again, but in the halls of Congress!
Your donation will support our annual Lymphedema Lobby Days on Capitol Hill, March 1st and 2nd, and our work throughout the year. We are already 25% of the way to our fundraising goal, so if you’ve already donated, thank you! If you haven’t yet, we hope you will. The amount doesn’t matter, but your support does!
There are two options: you can simply DONATE, or you can JOIN THE FUNDRAISING TEAM! When you join the team you have the option to create a personalized fundraising page. You can then easily share your personalized fundraising links via social media (such as Facebook, Twitter, or email) with friends and family.
Whether you are walking today or simply donating, feel free to download and print the sign below, take a selfie, and share it on social media. Or, you can email it to us by responding to this message and we’ll share it on our Facebook page.
Thank you for your support – together, we will pass the LTA!
Heather Ferguson
Founder & Executive Director
Lymphedema Advocacy Group
LymphedemaTreatmentAct.org
