As a newbie to the World of Blogging, please bare with me. I'm on my second cup of coffee and I still feel groggy. My thought process is all out of sorts. But since this is my first post, I figure I have nothing to lose. Why not get the show on the road? I have both APS and Lupus, Systemic Lupus Erythematosus to be exact. I was diagnosed with both in late Summer/early Fall of 2012. Long before the diagnosis, I had three blood clots (Two in April of 2000), three seizures (one is open to interpretation), MS-like symptoms, dizziness, and plenty of nausea. Didn't get the proper diagnosis throughout those years in between. The only specialist I was seeing was a Neurologist. A true asshole and an embarrassment to those in the medical field. My six month appointments went like clockwork. His eyes constantly in the computer, reading my notes. As if he had no idea who I was. Eventually, he would ask one question concer...
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