Matt had a busy yesterday. I was thankful I wasn't working so was able to spend most of the day with Matt. Last week he met with the rehab physician and she arranged for an ultrasound on his kidneys and bladder, to see where the stones are and if they could be causing all the bladder spasms. I was going to spend some time with him watching the Scotties on TV but he was off to occupational therapy for writing exercises.
But the most exciting was physiotherapy in the afternoon. I had brought Matt's left leg brace on the chance they would try and stand Matt. The OT Matt had been seeing in outpatients was there so I knew they were going to try (she doesn't normally work with the inpatients, but she had been waiting for this moment). First they started with what looked like a foot massage, but what they were doing is stimulating the brain to remember how big Matt's foot is. Sounds weird but many pt's with strokes or spinal cord injuries, the brain tells the body that the foot is very small and they believe that is the reason many pt's walk on tiptoes or the side of their feet, loss of balance quickly etc. After they put his shoes and brace on, they placed a table with a box besides his right arm and had him place his hand on it for stability. My job was to take pictures so they could see Matt's alignment, Cecilia would lock his brace in place when he was standing, Sonja stood behind him on the mat and Margaret would make sure his knees didn't buckle. They put the mat/bed in the highest position, then got him to stand. The first time he stood for 3 minutes and they were just testing how he would do. He was able to support his own weight with his right leg and arm. Matt felt fine, no drop in blood pressure and only sat down after muscle fatigue. After a short rest where the therapists consulted over the pictures, they got him standing again, this time for about 5 mins. He noticed his left arm became numb from hanging down so Cecilia held it up for him. They also made him reach for the ceiling with his right hand, which is difficult because of lack of muscle tone but he didn't lose balance, which is what they were looking for (he actually did touch the ceiling he is so tall). We were all very excited and felt there should have been balloons coming from the ceiling or something!
Margaret was very optimistic, but told us that Matt may never walk without the brace or some walking aides and still have a long way to go. But she didn't expect Matt to do as well as he has done so quickly.
Must go, have to go back to work. Just had to write the good news!
Wednesday, February 25, 2009
Monday, February 23, 2009
Weekend at Home
Matt was glad to be home for a few days. He is such a trooper but his eyes always give him away. He doesn't enjoy going to the hospital but he knows it is for the best. We picked him up Friday late afternoon and took him back last evening. While at home he played some Wii, since he can't set his game up at the hospital. There is a room that he can go to but he must book a time for it. Matt enjoys Friday night movie night with the girls with often one or both girls are on his lap. Saturday we took Matt for a massage, sine we couldn't get him an appointment for last Wednesday. He really enjoys it and finds it so relaxing.
I think what Matt enjoys the most is he sleeps better when at home. During the week he doesn't get much sleep with all the different sounds and new bed. But he adapts so well to any situation, much better than I would be!
I forgot to mention on Friday I was there to see physio again. Margaret is really working his core muscles and what she made him do was sit up without help, which he finds he can do quite easily if it is a hard surface. Then she makes him lean to the right while holding himself up with his right hand and arm. Next she makes him lean back at the same time, than pulling himself into the upright position again. He tried it on the left but because his arm doesn't work very well, he must just use his oblique muscles, which is hard for anyone. Margaret is hoping to see him standing this week just to see how he does, so want to be there for that. More good news to come, I am sure.
I think what Matt enjoys the most is he sleeps better when at home. During the week he doesn't get much sleep with all the different sounds and new bed. But he adapts so well to any situation, much better than I would be!
I forgot to mention on Friday I was there to see physio again. Margaret is really working his core muscles and what she made him do was sit up without help, which he finds he can do quite easily if it is a hard surface. Then she makes him lean to the right while holding himself up with his right hand and arm. Next she makes him lean back at the same time, than pulling himself into the upright position again. He tried it on the left but because his arm doesn't work very well, he must just use his oblique muscles, which is hard for anyone. Margaret is hoping to see him standing this week just to see how he does, so want to be there for that. More good news to come, I am sure.
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