I have been going to doctor's for over three years. My primary doctor has finally referred me to a Neurologist. I have been reading and reading about MS and I have many, many symptoms of it and am almost positive that it's what I have. I am just wondering what is going to happen at the Neurologist? What kind of testing is going to be done? And how long does it take to determine if I have it or not? My doctor has insisted for all this time that I have Fibromyalgia but I am missing some key symptoms of that, like absolutely none of the tender points. I have Trigeminal Neuralgia and I just read it usually occurs in people over 50 (I am 36 now, symptoms started for the TN 7-8 years ago, I just found out what it was last year) and if someone as young as I was when it first showed up has TN then there is a really good chance they have MS as well. I have numbness in my feet and hands and arms, I feel like my legs are being electrocuted and stung by bees, I have what feels like RLS from my chin to my toes 24/7, I lose strength and use of my hands and legs all the time. I have vertigo often to the point that I can't walk, I get UTI's all the time and have kidney pain all the time, I lose my words and can't remember what normal everyday things are called…..like yesterday I tried to ask my husband to please hand me the spatula but I could only get out "that flippy thing" because I couldn't remember what it is called. The list of symptoms go on and on. I am so frustrated and just want a diagnosis already. So any insight and information would be greatly appreciated. And any advice as to how to get the Neurologist to act kind of quickly and not make me go another 2 years before we find out what the *%^$ is going on. Thanks and if you read the whole (long) question double thanks and sorry it was so long 🙂