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Okay, some of you will understand
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I got my yearly MRI last week. My neurologist calls yesterday, says 'its better, lesions are smaller ' and she's happy with the results. My major problem is, I'm still disabled, I'm still feeling awful. I still have urinary incontinence. I still have horrible fatigue. My mobility still requires assistance from devices. Yes. I'm grateful I'm 'better ' on an MRI, but so much of MS is 'invisible ' and its so frustrating to be told its 'better ' when everything in your body doesn't feel that way.

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Posted
4 years ago