| Re: one year after ACDF c5-c6
HTF,
Thank you for the update; I appreciate the perspective and encouragement. I am at 3 months post-op ACDF, C6-7, cord compression. I deal with lots of neuro issues every day. Some are slightly, slightly improved, most are just about the same. I am trying to look a week or more at a time for comparison, if I compare day to day I get VERY discouraged. My symptoms really move around; I just wish my nervous system would calm down a bit. I still twitch and buzz a lot, though some of my tremoring is a bit improved. Also, my balance and dizziness are a bit better - much of this waxes and wanes. I get facial nerve symptoms as well...I don't know if it's related, but I had no neuro problems until the cord compression hit. At this point, I am done investigating; I just want to live and hopefully have gradual improvement. Unless I start falling down, I am done with doctors for the time being.
I am glad to hear you are out doing things that you enjoy. I used to be a runner and have not lost hope that one day I might partake again. But for now...I had a nice lap swim this AM. It's hard to get used to limitations, yet at the same time, one doesn't have to look very far to feel thankful for the blessings they have. Take care - wishing you continued recovery.
Mona
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