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#5 | |||
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I had the CFS dx for about a year and a half, didn`t seem to fit real well, but not really enough differences to question it too much. The dx from my pcp and an infectious disease specialist.
It wasn`t until I started walking really bad that my pcp started thinking something else, and ordered a mri, further mris confirmed MS. Have you had MRIs? Fatigue for me was non stop, and got progressively worse.
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ditched the witch . |
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