Has anyone ever sued or ever thought of suing your doctors for not diagnosing (or misdiagnosing) your Wegener's sooner? I've been told by my GP and my gyno that I should have sued. How they explained it to me that 4 antibiotic was way too much and that after 1 round of AB that they should have referred my son to a specialist. Another thing is that Josh had chronic fatigue, low-grade fever and bloody nose for 3 months. What are your thoughts. Is it worth it? I've never sued anyone in my life so I don't know if even I have a case. I know WG is tricky to diagnose especially because it's rare, but I get very angry thinking about those three months of undiagnosis and my persistence for the doctors to find something.
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