This has been a challenging and isolating period for many of us. If you would enjoy connecting with other lymphedema patient advocates in your area, we encourage you to join your state’s team if you have not already done so.
There is no cost involved and no required time commitment. After completing this simple sign-up form you will be introduced to the other members in your state via email.
As a team member you will also receive additional materials and guidance to contact your members of Congress in support of the Lymphedema Treatment Act. If your Representative and Senators are already cosponsors you can assist others in reaching that goal.
While I wish that my son Dylan (pictured to the right with his twin brother Devdan) didn’t have to deal with lymphedema, this condition has brought so many wonderful people into our lives, many of whom have become my dearest friends. I hope you too have found this to be true, and that through joining your state team you will be able to make even more of these invaluable connections.
Together, we can support one another, work toward our common goal of passing the LTA, and make living with lymphedema a little easier!
Heather Ferguson
Founder & Executive Director
Lymphedema Advocacy Group
LymphedemaTreatmentAct.org
