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scottm

Stroke Survivor - male
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    784
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    United States

About scottm

  • Rank
    Mentor
  • Birthday 06/05/1958

Contact Methods

  • Stroke Network Email
    Yes

Shared Information

  • Stroke Anniversary (first stroke)
    10-14-2014
  • Facebook URL
    https://www.facebook.com/scott.morris.7140497
  • How did you find us?
    Google Search

Registration Information

  • First Name
    Scott
  • State
    fl
  • Country
    United States

Recent Profile Visitors

4,588 profile views
  1. scottm

    Looks nice, I would have expected girly pink on the bed covers.
  2. scottm

    I got selected for one of those studies but rejected at the final review when imaging showed that my stroke was diffuse with no single point for them to try. So watershed type strokes are not viable.
  3. scottm

    I had right hand shakes for the first year but I kept forcing myself to use it and it slowly settled down. I still have moments but it did get much better with use.
  4. scottm

    Looks nice. My wife collects red viking glass, we have a room full.
  5. Nice looking place and you'll be all settled in no time I'm sure. Congratulations.
  6. So far it seems the Carbamazepine is working without all the side effects. No fog most of the time, no sleepiness or lethargy, fully intact cognitive function. The pain is mostly reduced to a sensation not unlike that produced by the neuros tuning fork when he places it against my body, sort of a buzzing sensation. A little annoying at times but compared to the ice/fire it is a blessing. Only place it isn't really working is my face for some reason. I do have moments where the pain reasserts itself to remind me it is there, but I have practice coping with it. Clothes still sometimes a challenge but overall it feels better. I'll take this as a win. The doc wants an update in 2 weeks after this has reached a stable concentration in my system to see if it needs adjustment. The dose is so low that the pharmacy had to special order it twice as the manufacturer sent the wrong dose the first time thinking the pharmacy made a mistake and nobody takes it at this low of a dose.
  7. scottm

    I prefer to refer to us as dedicated.
  8. scottm

    When I first struggled to open my hand and move my arm it was a long fight. Now that I can ,mostly, several times a day I take time to stretch them and always go out of my way, even if it hurts to use them. They would love to go back to a fist over my stomach but I'm not going there.
  9. That is my approach. I know I don't want them to say something to 'make me feel better' I just want them to be quiet and listen for a minute. More people should do tht.
  10. scottm

    Thanks ladies, first stumble is they have to order the drug at the pharmacy. Apparently they never get requests below 200mg and usually 300+. When I told them he wasn't sure how it would work and wanted to titrate me up they understood. Maybe I should change my sig to be the penguin...🐧
  11. scottm

    I'm in west central FL.
  12. scottm

    One step at a time and don't let someone who hasn't been there talk downhill to you, they just display their ignorance. I started with just concentrating on getting my hand to open, took about a month but one day the fingers moved a little, I celebrated that small act with the nurses in rehab and it set the ground work for what came later. 4+ years later I have a lot of function back in my arm and hand, can walk and mostly think and talk. Still a work in progress. Set yourself a goal and strive for, if it doesn't work today there is tomorrows efforts that may do it but just never surrender. I know people who surrendered and there is nothing good down that road.
  13. scottm

    FWIW, if you like fantasy and characters with a droll sense of humor I can recommend the Belgariad and Malloreon trilogies. These are by David and Leigh Eddings and both the wife and I have read them more than once. They move right along and once you start they have you. I used to read nonstop, now a lot less and not for extended periods because my eyes aren't still, they bounce.
  14. scottm

    I don't know what test for plavix, but the neuro will but they are typically concerned with the actual neurological effects and how to treat that. They will perform a series of tests that test your ability process sensations like touch, vibration, temperature, gait, movement, etc. which help them determine how your brain is working. From all the tests they determine what medications you may need and they may suggest PT or other therapies they think will help.
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