I had a bit of a relapse in 2010 when I had
a positive L’Hermitte’s sign. My doctor made arrangements for me to be seen at
the Kingston MS Clinic. I am afraid to drive into the city and after all the
time that’s passed since my last appointment in Toronto , it seemed a logical decision. I
didn’t see the neurologist until spring in 2011, and had a new set of MRI’s
done, this time including the neck and spine. Even though there were
significant changes, it was back to no treatment, see us again next year, and call
if you need anything.
I went back in 2012 and nothing much
changed. I don’t qualify for any of these new drugs, and I’m just as glad not
to be into daily injections and more frequent trips out of town. Fatigue was
still an issue, and I was walking with the cane. The other symptoms came and
went.
That summer was terribly hot, right into
the fall. I didn’t go anywhere and was almost house bound. Any energy exerted
required a day of rest, or more. I was glad to see winter come, something new
for me. I figured I’d bounce back after the change of season, but I never
really did. It was a good thing I have so many hobbies that I could keep myself
amused, and I had my family, and my friends.
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