I was just diagnosed with POTS. It is a relief to know that I am not CRAZY and that there are other people that have the exact same symptoms and aches that I have been having. I have had so many tests and seen so many Dr's and no one has found anything until this one tilt table test. Then reading this website and the symptoms was like reading a journal from myself! haha Well, I have had that base of the head/upper neck ache and was told I had migraines from my neurologist (ok????) and he put me on Topamax. I still take it cause it seems to work, I dont have that pain. It does nothing for my dizziness, but it does work for that pain. Im on Metoprolol (?) for my POTS, seems to make me worse ..... any suggestions anyone? Laura