What is the first tests you were given when you went to a real FM doctor to get diagnosed. my famiily dr. had only ever found myofacial pain syndrome which she had to send me to a neurologist to be confirmed. but, I would like to go to a real FM Dr. in my area which is -southeast Iowa-, anyway, I was wanting to know what tests I may have to pay for and if anyone knows of an awsome doctor in my area and share a good experience, it would be appreciated. I am kind of scared of doctors right now. Also, what is the best insuance to get? I am also sufferind with TMJ which I used to have splints and pain med for, that I do not have now.also, neuralgia. Where can I find a good Dr. I am afraid to get turned away. they either dont understand my conditions or, they wont treat me without insurance. I have $300.00 saved up right now to get started with a good Dr.