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.
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NEWS & EVENTS
Scientific Workshop Planning in Final Stages
We are pleased to post the preliminary program for this very important meeting that will be held in Baltimore, April 8 - 9 2013
WDA Meeting - September 30, 2012, San Diego, CA
Canadian Wilson Disease Family Symposium - September 29, 2012, Toronto, Ontario
WDA Meeting - September 16, 2012, New York City, NY
Successful Fundraiser Spurs Planning of Scientific Workshop
NEW! Official WDA Awareness ribbon now available. NOW! Order securely online in the WDA marketplace with PayPal.
All NEW WDA merchandise available now at CafePress.
Information about our tissue banking program.
Your WDA membership is important. There is power in numbers, and we would like to see our membership, currently over 3000, grow to encompass all those who are afflicted with Wilson Disease, in all countries, so that when we speak to the legislature, the pharmaceutical companies, & medical associations, our voice is strong and our message is clear.
Membership Information >>