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H.R. 4662 - Medicare Lymphedema Treatment Bill Officially Introduced

9th NLN International Conference Sept 22 - 26, 2010

Conference Registration

Abstract Submissions

Weight Lifting and LE: Clearing Up Misconceptions

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

Financial Assistance for Garments:

New Books:
100 Questions and Answers About Lymphedema

Lymphedema Management: A Comprehensive Guide for Practitioners

Updated NLN Online Patient Questionnaire

Patient Participation in Clinical Trials

National Lymphedema Network

Who is the NLN?

The National Lymphedema Network (NLN) is an internationally recognized non-profit organization founded in 1988 by Saskia R.J. Thiadens, R.N. to provide education and guidance to lymphedema patients, health care professionals and the general public by disseminating information on the risk reduction 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.

The NLN Mission Statement

The mission of the NLN is to create awareness of lymphedema through education and to promote and support the availability of quality medical treatment for all individuals at risk for or affected by lymphedema.

The NLN is dedicated to:

promoting research into the causes, prevention and treatment of lymphedema;

securing adequate insurance coverage for medically necessary, safe and effective treatment;

expanding the number and geographical distribution of lymphedema treatment facilities and certified therapists.

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