I don't know where to begin, but for two years I've had about terrible joint pain at about 3-7 range, chest pain occasion pain level (5 ), and for about six year horrible stomach pain after eating . All my blood test came back normal for rheumatologist Issues like RA and lupus. The only thing that showed was a potassium deficiency.
So because my joint pain at the time was one sided at the time and I experienced slurred speech, I went to a neurologist. The neurologist did tests which made me get an MRI, but nothing came up. I did have a vitiam D shortage. At the end I was given a sheet of paper directing me to the nerosymptoms site and a horrible antidepressant that I stopped (Which gave me the awareness drinking gives). The site has everything on it, it's so vague it could be applicable to a lot of illnesses. So vagueI raise my eyebrows at the 5% misdiagnosis rate.
I went to a physical therapist and was than refereed to a pain clinic. I went, but wondered why I'm not being tested for illness like gastrointestinal illnesses like chrons or how they don't know I'm not one of the 30% of people with RA that don't test positive.
At the pain clinic I'm treated like someone who can't accept their illness. I don't think there isn't enough concrete proof (In my mind) whatever this is possesses a neurological nature. I feel like I'm being shut out of the conversation for any other cause. I'm wondering what to do.