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Community Networks
Introduction
Lymphedema Awareness Foundation (LAF) Community Networks continue to be a very important avenue to share information with Lymphatic Therapists, physicians, patients and their families, about living with lymphedema. LAF Support groups provide speakers and events that assist patients with education, products for lymphedema, legislative and insurance help, and the knowledge that they are not going through this difficult time alone. Since lymphedema is a lifetime affliction, it is important to maintain treatment, self-treatment, and have a group who understands the hardships.
Currently are new groups forming in the FL and PR area. If you are interested in being a part of our awareness team contact: lafinfo@elymphnotes.org ~ Candace Bridgewater
Current Community Networks
Abstract: Information on how to contact your local Community Network
Procedures and Benefits for Establishing a LAF Community Network
Abstract: To establish local assistance, we welcome dedicated and sincere activists to join our LAF Community Network team. Those who have a proven desire to promote awareness and support in their community, are eligible to come on board, either as a support group
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