I am in the 'just drop me in the tub' club for dx.

LP was negative at the time ( but I was not in an attack at the time either). My MRI's were either not read right or they are 'normal'; I was never told.

HOWEVER: I have had clinical signs, that led to my dx. If I had gone to different Drs., most likely everything would have be taken as only isoloated incidents, not related. With continiuing with the same Dr, that was, and still is, to not give up everything taken into consideration helped I think. He found signs that I did not know about, clonus, and a couple of others that I can't remember at this time, that makes it MS.

That is my (very long) story in a nut shell. I am on LDN, for 5 months now, and am doing wonderful! I can use my hand and arm again! I am not totally exhausted every day, and I have even stayed up till 4 am talking to friends recently!

Am I perfect? NO WAY! But I feel the best I have felt in more years than I can remember.