Behind The Mystery

Behind the Mystery of Wilson Disease – an inherited condition impacting the liver, brain, and other organs.

Wilson Disease is a rare genetic disorder caused by a malfunction of the ATP7B gene that hampers the body's ability to eliminate copper, leading to.

This special edition of The Balancing Act presents Behind the Mystery of Wilson Disease features insightful discussions with a dedicated physician, an advocacy leader, and a CEO whose company has pioneered the first advancement in treatment for Wilson Disease since 1997. Mandy was diagnosed with Wilson Disease at a young age and shares her journey living with the condition. Her experience highlights the challenges faced by patients in managing their treatment regimens and the need for more convenient options. Hepatologist Dr. Cheung further explains the complexities of Wilson Disease, including its genetic origins, symptoms, and the critical importance of early diagnosis, management, and adherence to treatment. Olga & Montel spotlight the Wilson Disease Association's (WDA) efforts to support patients, improve awareness, and facilitate access to new developments. Rhonda Rowland, VP of the WDA discusses the evolution of treatment options and the organization's role in fostering partnersh

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