It is with great pleasure that I present to you this new 13-minute documentary – Lymphedema Treatment Act Public Service Announcement. Please share it far and wide to help us increase awareness about lymphedema and support for the LTA!
I was extremely honored when Catherine Seo approached me with the idea for this film. My heartfelt thanks to her and Dr. Mark Smith, Director of The Friedman Center for Lymphedema Research & Treatment, for making this a reality, and to the many others who took part in the filming and production.
We hope that this public service announcement will inspire viewers to take action and make their voices heard!
As of today we have 45 cosponsors. That’s an amazing number considering our bill was introduced only one month and three days ago! If your Rep isn’t a cosponsor yet YOU have the power to change that. Use the advocacy tools on our website under the “How You Can Help” menu and follow the advice in our Advocacy Handbook.
Be persistent and you will get results! Don’t hesitate to contact us if you have any questions or need assistance. We are here to help and would love to hear from you. Thank you in advance for sharing this film with everyone you know.
Together, we can pass the Lymphedema Treatment Act!
Heather Ferguson
Founder and Executive Director
Lymphedema Advocacy Group
www.LymphedemaTreatmentAct.org
info@LymphedemaTreatmentAct.org
