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9th NLN International Conference - Sept. 22-26 2010 - Breaking through the Barriers: Research, Education, and Practice

NLN Position Papers: Risk Reduction, Treatment, Exercise, Air Travel, Training

Financial Assistance for Compression Garments:

New Books: Lymphedema Caregiver's Guide

Mourning Has Broken

Updated NLN Online Patient Questionnaire

For Professionals: NLN Research Survey

The National Lymphedema Network

The National Lymphedema Network (NLN) is an internationally recognized non-profit organization founded in 1988 to provide education and guidance to lymphedema patients, health care professionals and the general public by disseminating information on the prevention and management of primary and secondary lymphedema.

The NLN is supported by tax-deductible donations and is a driving force behind the movement in the U.S. to standardize quality treatment for lymphedema patients nationwide. In addition, the NLN supports research into the causes and possible alternative treatments for this often incapacitating, long-neglected condition.

 

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Become an NLN member: Join now to receive quarterly issues of LymphLink, the official NLN newsletter, discounts on educational materials and conferences, online access to LymphLink article reprints, and more!

Protect Yourself, Educate Your Community: Lymphedema Alert Bracelets & Necklaces

Become Knowledgeable about Lymphedema: Read the NLN Position Papers, which are drafted by the NLN Medical Advisory Committee to reflect professional positions on key issues including: Training, Air Travel, Exercise, Risk Reduction, and Treatment. Also visit the Lymphedema Q&A Corner and find the answers to frequently asked questions.

Find a Certified Lymphedema Therapist in your area: Resource Guide lists Lymphedema Treatment Centers, Therapists, Suppliers and Training Programs across the country. Join the NLN Affiliate Membership and be listed in the Resource Guide online and in LymphLink.

Find professional and patient educational materials: Visit the NLN Online Store for textbooks, videos, reprints and specialty items, such as Lymphedema wristbands, alert bracelets and necklaces, etc.

Create Awareness: Lymphedema can no longer be ignored. Make sure to wear the NLN Wristband: "Lymphedema We Are HERE!"

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