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I'm curious to know who else in my area has been affected by Wilson's. My little brother died at 21 and was not diagnosed until the autopsy, so we're still learning about this, and want to connect. I'm hoping to maybe start something out here to get the word out about this disease, since so many are clueless. I've had several medical professionals ask me, "Wilson's? What's that?"
please help me, just by letting me know you're out there, and sharing your story. Thanks!
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