The Lymphedema Lifeline Foundation is focused on providing a Bi-annual educational conference that provides information about local and national medical resources with up-to-date practical educational information.
Our commitment is to Lymphedema patients and their families who live with this chronic disease. To nationally improve Lymphedema awareness and to provide education to healthcare professionals, patients, and caregivers.
If you have any questions about Lymphedema and awareness, just send us a message. We would be honored to help direct you to educational resources pertaining to Lymphedema and awareness.Contact Us
In 2007, Denise Geddes, a Primary LE Lymphedema Patient CMT, CLT decided it was time to create a foundation that educates medical professionals, patients, and their caregivers on the up to date treatment options and to create awareness of this chronic debilitating disease. The Lymphedema Lifeline Foundation was born, since that day the foundation has evolved to having a Bi Annual Education-Awareness Day, a new up to date website and an ever growing Facebook group.
Thank you for your considerable contribution. We are a non profit that strives to help all those affected by Lymphedema, your donation is helping us achieve our mission!