Active Survey: How Were You Diagnosed

I was finally diagnosed in 2017 because I went to my PCP and told him about symptoms I was having. Told him How I felt like I was leaning to the right even though I was not and I kept felling because of it. He sent me for an MRI asap. He was thinking I may have a tumor. However it back stating I had widespread T2/FAIR abnormalities in the supratentorial and infratentorial white matter in a pattern and distribution with Multiple Sclerosis . Multiple lesions exhibit enhancement and some exhibit mildly restricted diffusion with active inflammation. Then in 2018 my MRI stated I had the a Flair and T2 lesion of Periventricular lesions have the typical elliptical radiating of "Dawson's fingers." MRI in 2020 redemonstration chronic, bilateral, multilobe T2 Flair hyperintensities consistent with multiple Sclerosis. Stable appearance of Multiple demyelinating plaques. No definite associated abnormal enhancements or diffusion restriction to suggest active inflammation. There was no acute intracranial abnormality. MRI 2021 Stable Appearance of multiple demyelinating plaques. Not Showing abnormal enhancement or diffusion restrictions to support active demyelinating plaques. So it seems to me that my medication is doing its job.

Morning, I was diagnosed after a major surgery and my health started to turn for the worse. I lost my kidneys while figuring out what was wrong with me. 19 days in the hospital, not knowing what was wrong, my kidney doctor did a urine check on me and that was when my protein levels were way too high, she talked with me, stating she thought I had cancer, but she wasn't a cancer doctor. So she contacted an oncologist to come and talk with me about my results. Sure enough, I was diagnosed with Multiple Myeloma which had been undeted by my family doctor, even though I had been complaining about my health for over a year.