one day it'll all make sense.

Small victories

Played an hour of ball hockey last night after 3 weeks of a very minimal amount of physical activity whatsoever. Thankfully, despite my team having ZERO subs, it actually went better than I had expected. Plus after the game I felt somewhat rejuvenated 🙂 Maybe a result of the exercise I got last night, or maybe a result of actually getting a good night’s sleep once being prescribed Zopiclone to help me fight the bedtime jitters, today I can actually say I feel a bit better than I have been. Still having the problems with right side numbness and lack of sense of taste, but not as foggy headed. I’ll take it, one step at a time.

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Comments on: "Small victories" (2)

  1. Does my heart better to know that you are getting back to Kate.
    It’s never more important than to remain yourself during treatment…because the stupid steroids make us insane. Like shit house bat crazy. God bless Angie and Jeff for dealing with our crazy asses.
    The exercise will help too, though I find it really triggers RLS for me at night..and when I’m on treatment I find it hard to walk around period (lack of energy).
    You’ll be back to kicking ass and eating 5* meals in no time.
    Love ya!

  2. Thanks 🙂 support really does make all the difference, doesn’t it? OMG I used to get RLS so bad! Worst I can remember was on a flight home from Cuba. It was a late flight that ended up being delayed more than an hour… When they finally got us on the plane and taxied out to the runway, a storm hit and we had to taxi back to our gate only to sit in our seats for another hour. My RLS was sooooo bad I thought I may go crazy :-p Ange kinda wanted to knock me out just to settle me down, and I have to say, it wouldn’t have been a bad idea! Haha! That 60 minutes felt like an eternity….
    I’m sooo grateful I haven’t suffered from that since switching off Copaxone. Did you get it before you started the stuff?

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