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Saturday 19th
January 2002:
Nothing much happened today, I don't
have to go to the hospital during the
weekend. I feel no changes, this is
great!
Called the hospital at around 1500 hrs
about my samples (blood, spinal fluid,
stools) - no reply yet, but they should
be back on monday.
Alone for a couple of hours, as Lisbeth
needs some time to herself!! :-))
20th january: Just as quiet as
yesterday. No hospital visit. Tried
to sleep in, but I still have problems
sleeping more than 3-4 hours at a time
because of my d...... headache! It's
with me all the time, and I'd like to
know why, as other GBS patients don't
complain about that symptom?? It moves
around depending on how my head is positioned
when I sleep, and is pretty uncomfortable.
Monday 21th
january: At the hospital 09.00,
Lisbeth came with me to listen in to
what treatment the doctors suggest,
based on the results of the samples.
Waited for only 10 minutes, WOW, before
an occupational therapist, Marianne,
was available. 20 minutes later I was
trying to do exercises for my paralysed
facial muscles.
It's a good thing I couldn't see how
funny I must have looked, well, probably
not, as I could not move my face very
much!! :-))
We were there for about
½ hour, after which Marianne
told me that I probably wouldn't be
able to do the exercises alone at home.
So I'm going to be an out-patient from
now on, as regards the therapy. She
took my phone number, and will call
me about my first session, luckily there
doesn't seem to be a waiting list.
After that, we went
back and waited for a doctor. One came
rapidly. This is the 7th new doctor
I've met since I got the syndrome, do
all medicine students specialise in
Neurology?? :-)
He told me about the results of some
of the samples - stools show nothing
abnormal, and there is no sign of Borrelia!
Hmmmmm. Still waiting for the results
of the other samples plus the SSEP examination,
should get the reply to the SSEP tomorrow.
The doctor also mentioned that they
would be looking for signs of a virus
in the other blood samples. Guess the
elimination method is a great thing,
as opposed to jabbing me again and again!!
:-)
My feet have begun troubling
me. The underside of my feet feel worse,
more sensitive and tender, and they
feel like great big lumps when I walk.
I've also begun feeling pain in my face,
especially in the jaw muscles and in
the cheekbone area.
Well, that was today.
I'll be back tomorrow with more information
on the samples, cross your fingers for
me please!! :-)
22nd january 2002:
Woke up today with a great deal of pain
in my feet, so I decided to stay home
instead of going to the hospital - all
I was going to do there was to get the
results of my tests.
I called the hospital
about this during the morning and was
told I should try again around noon.
Tried then and got a nurse who'd just
returned after several months away,
and she couldn't help me at all.
Told her I wanted an
appointment with the consultant neurologist
at the Neuro dept., as I felt I wasn't
going anyway with the current treatment,
which is basically physio. Got an appointment
for the 25th, which was unexpectedly
soon, so I'm looking forward to that.
I have a number of questions to ask
him.
Called again during
the afternoon for the results, but .....
still no reply! Strange!
I am to come in tomorrow in time for
the doctors' rounds. Will try to get
hold of a doctor then, and see if I
can get some answers to my questions,
shouldn't take more than a few minutes.
My feet are feeling
much better this evening, as compared
to yesterday evening and this morning.
I've also relaxed completely all day
long. :-) That is to say, I've been
lying down all day, wonderful, the only
problem is that I wish I could sleep
properly soon. My headache is still
a major problem.
Let's see what wednesday brings.
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