The Lymphedema Advocacy Group is an all-volunteer organization. Each board member has a deep personal connection to this disease and spends countless hours advancing our mission. Our work means a great deal to us, and so does your support.
If you are able to include the Lymphedema Advocacy Group during this season of giving we would be extremely grateful. Every dollar really does make a difference to us! Secure donations can me made through PayPal, or sent by mail to: Lymphedema Advocacy Group, PO Box 1682, Carrboro, NC 27510.
In case you missed our November Newsletter, we’d like to mention that you can request free information cards to distribute in your area using our new Information Card Request Form. Through you, we have already distributed almost 90,000 information cards to raise awareness about lymphedema and the Lymphedema Treatment Act! Your support makes this, and all our work, possible.
The entire Lymphedema Advocacy Group board joins me in sending you our gratitude and sincere wishes for a joyous holiday season!
Heather Ferguson
Founder and Executive Director
Lymphedema Advocacy Group
www.LymphedemaTreatmentAct.org
info@LymphedemaTreatmentAct.org
