Eventually, I achieved my goal and was moved into the Rehabilitation Ward
where I met some lovely older women who had also had strokes. They were
more independent than I was,
and they were able to move about in wheelchairs, using their arms to
propel themselves to the gym, the shower and to the dining room without needing
a nurse, or one of the ward assistants. I was
determined to learn this new skill as I had never before propelled a wheelchair. I was also anxious that I might fail; the steering was confusing for me
at first, and on a number of attempts I met with the wall. Oops!
I managed to follow others down a corridor to the dining room, where I learned to guide the
wheelchair up to the table and to park between the white linen table napkins that had been set out before the evening meal.
At last I was able to have more solid food. This proved a huge disappointment, as what
sounded appetizing on the order sheet, filled out the previous day,
was often tasteless and too salty, especially for people who were stroke
victims. I was also challenged by having to use knives and forks, by
myself. My left hand ached when I tried
to cut the tough chicken or roast, lamb or beef.
One of the women, whose name was Shirley, was
an artist with works, she said, hung in the National Gallery here in Canberra. Her daughter
had brought in one of Shirley’s superb works to decorate the dull walls of the
ward. Now that I had moved, I hoped that the singing could continue. But one of
the sisters in charge was worried that it might disturb the other
patients. The other women were very
happy to have the singing and would ask if the “choir” was coming today when
they saw me at meal times in the dining room.
Once I had moved to the new ward, Mark transferred the vibrant posters made by
the children. Soon, there was a complaint from the sister in charge, about
hanging things on the wall. I was distressed as the posters were my guide for
the location of my bed. They were a happy reminder of my former life at
school. One of the girls who came to
sing, helped solve the problem by making a hanging out of bright fabric on
which cards and messages could be pinned.
It was a delight to have community singing. Once the singing was
accepted, with certain restrictions, it became a regular part of my gym therapy. A group of parents of
the girls organised to bring them to the hospital on a regular basis. At one
time when my speech had sufficiently improved, Mark brought in my mobile phone
and I was able to make calls and to receive them. I had a call from a cousin
who is a physio therapist; she was just about to board a plane and phoned me
from the airport. Her last final words of advice were to “do what the physios
say”.
If I was in the gym, the singing group came into the gym and sang with me
there. Other patients enjoyed the visits and joined in. They would look forward
to these visits and would ask me if the “Choir” was coming today. As my balance
improved, I was able to bob up and down in time with the beat. One day I
noticed one of the other patients doing the same thing too. If I was in the
ward then my visitors were encouraged to sing too. Soon my friend had put
together a book with lyrics on the front of which was typed:
“Carolie’s Visitor’s
Song Book
A collection
of songs that anybody can sing
To help
with Carolie’s music rehab.
Please help
to sing a song. It will do you good as well as Carolie.”
It certainly did me good, as well as being
enjoyed by the other participants. One teacher later shared how much she had
enjoyed singing “Eidelveiss”, from the “Sound of Music”, when visiting me in
hospital. It was a regular request to be sung from one of the other patients,
who enjoyed our singing. Eventually my singing improved and as we continued I
was able to reach higher notes. The singing seemed to improve my speech as well
and I became more confident to speak and more articulate.
One very enjoyable aspect of being on the Rehab. Ward, was the
occasional visit to the Rehab. Kitchen, where I was supervised by occupational therapists making cups of
tea. One of the assistants was a parent of a former pupil from my school. I
greatly enjoyed our frequent conversations about the school and its fabulous
music program and, also, the very supportive parent community.
To be continued....
Thank you for your story. My father died of a brain Aneurysm rupture. I have had several small strokes where I have had loss of vision and now have a stent in one of my carotid arteries. I was scared because I was told I could have a major stroke when they inserted the stent. It all went well but I do worry sometimes about the future. Your blog helped take some of the mystery out of what could happen. I was only in hospital for a short time but while there in intensive care we were served an evening meal of meat pie. I was amazed that the patients who were heart attack or stroke survivors were given this unhealthy food to eat! I wish you and Carolie all the Best.
ReplyDeletehi Helen, sorry for the delay in replying. Thanks for your feedback. The dreadful food served in hospitals is a scandal. Carolie has a permanent shunt and a skull implant, but is doing remarkably well. The human capacity for survival & recovery never ceases to amaze me. I wish you all the best for the future and don't hesitate to get in touch again if you wish.
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