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Senior Member
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Saw the neuro today. Our first meeting since moving to Kentucky.
I liked him with our first handshake. He was very nice and had me go all the way back to when I was first dx. That was in 1984. Asked a lot I mean a lot of questions. Then he tested me with the usual tests that are given on the first visit. My balance and walking was awful. Joking he asked what was I drinking. I didn't do very good on his memory testing. I am going to have an MRI of brain MRI of spine EVP Visual test Neuropsych testing My last MRI was in 2007. I was able to get a copy of it from the hospital I had it done in before I moved. After all tests are done, we will talk about results and where I go from there. He also asked if I would sign up for a clinical research that they are doing. It is for the JC Virus. I never heard of it. I was told it is a research study to analysis and determine precisely where the JCvirus is hiding. It does effect the immune systerm. It is a benign virus, since it produces no symptoms. But the virus can be reactivated in the setting of decreased immune function. He asked me to participate because I have never taken any of the MS drugs. So far it has been with people that have taken one or the other of the drugs. ![]() Took 3 blood vials and urine specimen. I will only have to do it this one time. ![]() Now to wait till all the tests are taken and then see where it leads. ![]() Jappy ![]() |
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"Thanks for this!" says: | 4boysmom (03-25-2009), Blessings2You (03-24-2009), Dejibo (03-24-2009), DM (03-24-2009), Kitty (03-24-2009), NurseNancy (03-24-2009), Riverwild (03-23-2009), SallyC (03-24-2009), SandyC (03-25-2009), Twinkletoes (03-25-2009) |
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