So went back to see my neurologist, waited 3 months, he did not say much, just said “I can’t help you”, no diagnosis, no suggested treatments. He blamed my autoimmune diseases for the pain and I think neuropathy, he was a little unclear. Said it was due to my PsA being poorly managed.
I am getting concerned about my worsening paresthesia (prickly feeling) in my legs, torso and arms, when I get up in the morning, he seemed to be implying that it was due to PsA? Is that true? Seems more like small fiber neuropathy to me. That is why I went in to see him, still have no answers. He did order a MRA to check out the Pulsatile tinnitus I get at night, that will look for blockages in the blood vessels in the brain.
Also said I have pernicious anemia, so am taking 3000 mcg sublingual of B12, used to inject it a few years ago, but he said they have gotten away from that. Maybe it will help with the fatigue? I wonder if MTX is contributing to the large blood cells?