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.
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.
This website is not intended to provide advice on personal medical matters or to substitute for consultation with a physician. The WDA does not accept advertising for this website.