A big thank you for the quick replies.
The feeling of support and knowing that you are not alone really helps. My daughter has said many times I feel like people think I am making this up that the pain isn't real. I will follow up on things mentioned here. It is such a slow go to search hunt find make appointments try meds try more meds try this try that. It is such a needle in the haystack process.

To top it off my daughter is on my insurance plan (a really good awesome old fashioned plan) for about another year then she goes to her employers plan that has a huge 5K deductible with very no coverage until the deductible is met. We feel like a clock is on us. She is fearful of paying for meds each month. The pain patch alone is a chunk of change. She is going to try Cymbalta now and is also on Tegretol she has no headache pain(big surprise its a migraine med) but her MP is still raging. Thank you for your suggestions and advice. We do not feel so alone. Thanks again,Debbie K