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My doctor has referred me to a neurologist to be evaluated for MS or any other neurological diseases. She is mostly concerned about MS though due to unsteady gait, left arm weakness, blurry vision and muscle spasms. I was wondering if anyone has been sent to a neurologist for possible MS and if you would be willing to give me an idea of what to expect. I've never been to a neurologist before and I am feeling a bit nervous, would be so thankful for any helpful words. ~♡
I was sent to a Neurologist in Ft Worth, TX at Cooks Chrildrens Hospital for MS Eval. They did physical test, blood work and MRIs. But I'm so use to it, it was nothing. Nothing to stress about friend.
Thank you all for your helpful comments, it has really set my mind at ease. I am so glad I found this site, everyone is so nice and caring here and it's good to know there's somewhere where everyone understands what I am going through. ~ Gentle hugs to all my fibro friends, you all mean the world to me ~ ♡
Yes I go to a Neurologist for loss of balance, but I have a Chari Malformation. He want to do a spinal tap to check for MS, but he said that is not conclusive. I also have Carpel Tunnel. I just pray and go on and try to find natural alternative.
My neurologist did an
MRI.
I always looked forward to my neurologist appts. The rheumo physical exam would have me in much more pain at times. Don't be nervous! Gently hugs!
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