Oh, I have been where you are more than once! Yes, "hysterical conversion reaction" when the myocolonic jerks started. I felt the same as you. I called the MS support group leader that I was supposed to meet for the first time that night and she said, "Oh, I think you need to come and talk w us." It was the best move.

I don't know what you have but see if you can see this guy or the other neuro again in 3 to 6 months so they can see any changes over time.

So many have gone through this. And the Chronic Fatigue/Fibro myalgia sufferers, too.

I'll be thinking about you today and don't you dare be embarrassed for 1 second. They just don't know YET what is wrong.

ANN

Dear :you still are not crazy
 

I am sorry that the results left no conclusions. Sally had a good post also. Please don't give up or give in. We know inside when something is wrong. doctors don't always find out what is wrong. Keep going until you find the answers. I will keep you in my thoughts. ginnie:hug:

It took me 20 years for my diagnosis. And my brain MRI is perfectly normal. It was lesions on my spine and a positive spinal tap that finally got me diagnosed.

Don't give up, and don't let them tell you that you're crazy.