The Wilson Disease Association is dedicated to providing the leadership and resources that will result in increased research, improved health, worldwide detection, and a cure for Wilson disease.
Our website is designed to give patients, family members, and healthcare professionals the most up-to-date information on treatment, legislation, support groups, research, fundraising, and patient stories. We hope you will consider joining us. The WDA does not accept advertising for this website.
This website is not intended to provide advice on personal medical matters or to substitute for consultation with a physician.
|
A WDA Gathering
at
Northwestern University in Chicago, Illinois
Friday, August 28, 2009
12:00 - 3:00
For more information click here
|
|
New WDA Patient Education Publication Available
Wilson Disease: Maintaining a Successful Treatment Plan
Published in March, 2008, this 8 1/2" x 11", 32 page publication includes the topics: Medical Care, Medications, Diet and Nutrition, Special Circumstances, and Family Concerns and Genetics. Also included is a glossary of medical terms, a glossary of genetic terms, and a printed copy of the "Wilson Disease Patient Lab Tracker". If you would like a copy, please contact the WDA office at: wda@sssnet.com or 888-264-1450
|
|
