As I was afraid of, my LP results were normal. Now I am so frustrated. It's not that I "want" something wrong with me, I was just hoping it would show SOMETHING so that I could at least get some kind of diagnosis which would lead to some kind of treatment. I feel like I'm gonna be stuck on limbo island forever.![Frown](https://www.msworld.org/forum/core/images/smilies/frown.gif)
During my neurologist appt, I asked him if there was anything I could take to help with all this tingling nonsense, to which he replied "no", then asked me where I was getting all the tingling (it starts in my hands and feet and works its way up), then he said "why, is it bothering you?".
Ummm duhh? I couldn't resist replying "Well if it wasn't, do you think I'd ask you if there was something I could take for it?" He gave me Neurontin (Hmmm, I thought there was nothing you could take for it).
I saw my PCP today and he gave me a referral to a new Neurologist, one that will actually take the time to figure out what is going on.
Just wondering, did it take a long time for most of you to finally get a diagnosis, even if it was something other than MS? Did a lot of you have to go to many different doctors before you found answers?
![Frown](https://www.msworld.org/forum/core/images/smilies/frown.gif)
During my neurologist appt, I asked him if there was anything I could take to help with all this tingling nonsense, to which he replied "no", then asked me where I was getting all the tingling (it starts in my hands and feet and works its way up), then he said "why, is it bothering you?".
![Roll Eyes (Sarcastic)](https://www.msworld.org/forum/core/images/smilies/rolleyes.gif)
I saw my PCP today and he gave me a referral to a new Neurologist, one that will actually take the time to figure out what is going on.
Just wondering, did it take a long time for most of you to finally get a diagnosis, even if it was something other than MS? Did a lot of you have to go to many different doctors before you found answers?
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