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At the first time I was diagnosed with MS I was in a fog.

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By madhatter40

1 min read

My neurologist said he was going to run a series of tests to get baseline of my symptoms to start.

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He did the Ocular test looking for problems in my eyes, then we switched over to device that checked the electrical impulse in hand and if I contradicted when he gave me the right impulse(not Fun).This was back in 2003 in NYC, after showing signs motor controls was off and I would partially vision in my left eye just a grayish haze.

After my initial diagnosis I didn't have those types of problem happening right then so I did't worry about.

1 year later I moved from NYC to Charlotte NC and found an excellent young Neurologist I brought all medical records that he worked on in NY and she looked at and quickly after her test to confirm. This has been uphill

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