The Wilson Disease Association is a nonprofit organization dedicated to providing support and hope to individuals worldwide affected by Wilson disease, an inherited disorder that leads to excessive copper accumulation in the body. Through educational materials, research support, and community meetings, the WDA aims to improve the quality of life for those living with this condition.
With a focus on raising awareness and funding for research, the WDA offers resources on signs, symptoms, diagnosis, treatment, and patient assistance for Wilson disease. By organizing events, clinical trials, and support groups, the association strives to unmask the challenges of the disease and work towards finding a cure.
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