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Mysterious and challenging life experience. Living with NMSOD
My journey began with a non definitive diagnosed illness, I have learned NMSOD mimics other illnesses from lupus to MS. I stayed at many hospitals with the Hope I would be cured. Had tried all types of medications, from morphine to calm me (mind though at ER everyone thought I lost my mind due to…
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Rare disease has taught me to live one day at a time
My life changed a few months ago when I heard doctors tell me they had a diagnosis for every weird and unexplained symptom I’ve had in the last 6 months. At some point I felt like I went crazy, because I felt so exhausted, constant headaches, unexplained nausea, some skin rash that was really bothersome,…
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I’ve had NMO 12 years
I was diagnosed with NMO August 2nd, 2009. It all started in my opinion nerve in my left eye. Every time I had a flare up I would have IV prednisone and that would help. I Hasan MRI of my brain to see if I had MS. That came back negative. This all started in…