I recently got copies of my records from my neuro doc, and they state in the records that I have intractable headaches and significant neuropathic pain issues. I also have my hospital records that show my fibromyalgia history.
Given these things in black and white why am I having problems getting in to a pain clinic? They know I don't have insurance but I told them I would pay for the visits. I've been waiting two weeks and frankly I'm ready to kill something.
My family doc used to be so helpful before my MS diagnosis, but it seems that now that I finally have a diagnosis hes doing nothing. The only reason I have a headache med is because someone else filled in for my neuro doc on that day.
I just don't understand why I can't get any help. It's almost like they are suspicious that I'm wanting pain meds when I never did before. I'm used to being stubborn and toughing it out but it's to the point where I just can't.
I realize that being a self referral is probably weird to the pain clinic docs too but what else am I supposed to do with no insurance and reluctant doctors?
Given these things in black and white why am I having problems getting in to a pain clinic? They know I don't have insurance but I told them I would pay for the visits. I've been waiting two weeks and frankly I'm ready to kill something.
My family doc used to be so helpful before my MS diagnosis, but it seems that now that I finally have a diagnosis hes doing nothing. The only reason I have a headache med is because someone else filled in for my neuro doc on that day.
I just don't understand why I can't get any help. It's almost like they are suspicious that I'm wanting pain meds when I never did before. I'm used to being stubborn and toughing it out but it's to the point where I just can't.
I realize that being a self referral is probably weird to the pain clinic docs too but what else am I supposed to do with no insurance and reluctant doctors?
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