Hospital Stay - Part 4 - Sat. Eve / Visitors
The day did not slow down much. I had not slept but for a few minutes of dozing in my 2 different trips in the MRI machine since I got up Friday morning! Jenny spent a few hours with me, she put oils on my feet and just tried to keep me company and comfortable. Ma came back to spend the night with me. We were still waiting to hear results from the 2nd MRI, confirming for SURE that there was no new stroke, and they also began a myriad of tests to exclude all kinds of other things that I dared not even think about, including one I DID want to know about: Lupus.
They have said I am borderline Lupus most of my life. I have many of the symptoms. (hives for one, strange rashes, unexplained low grade fevers for weeks at a time, and unexplained to-the-bone fatigue, bouts of extreme muscle pain, sensitivity to sunlight, heat and cold, just to name a few). I was hopeful maybe my phantom symptoms that make me feel like a hypochondriac would finally have a name.
The physical therapist came in and helped me take some steps. I could take 6. Only six! I was frustrated! The good part was that as the day went on, I could make more words work. And that gave me hope!
I spent the day working my hand as often as I could, as well as trying to flex my foot. It was infuriating to be strapped to the bed and not be able to do much more. Both legs had a little attachment that inflated every 20 seconds or so and then deflated. One arm had an IV, and the other had a blood pressure cuff and O2 sensor. Added to all the heart monitors, I was not going anywhere without a large amount of unhooking and alarm making. LOL
Earlier in the evening, I had sent a message to one of my FLYSistahs (a group of my dearest friends) and she spread the word. After 9:00 there was a knock at my door...
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