We hope you can join us in DC for Lymphedema Lobby Days, but if you can’t, please send us your Lymphedema Story and we will hand deliver it to your members of Congress!
Personal letters from constituents are powerful, so if you are unable to attend, please consider sharing your Lymphedema Story.
To ensure that we have time to print and organize all stories, please submit yours by February 1st. Tips on what information to include can be found on the submission form.
If you have previously shared yours you do not need to do so again, unless you wish to send an updated version. If you’d like us to verify if we have a past submission from you simply reply to this email.
As a reminder, discounted hotels rooms are available for only 5 more days, until January 29th or until sold out, and event registration closes on February 16th. Links to register, book your hotel room if you need one, and all details are on our Lymphedema Lobby Days page.
Thank you for your advocacy and hope to see you March 1st and 2nd at Lymphedema Lobby Days 2020!
Heather Ferguson
Founder & Executive Director
Lymphedema Advocacy Group
LymphedemaTreatmentAct.org
