We are working on renovations to part of the house so that James can have an area to himself. It will have a bedroom, a mini kitchen area, and a sitting area. We picked up flooring a while ago and the bedroom area is now floored and painted, we are now working on the main area. It is turning into a bit of a bigger job that we originally thought. The walls are in rough shape and we just decided to replace some of the gyprock. I am hoping to have the space livable for him in a couple of months. We are just plugging away at it on the weekends.
Wednesday, 12 February 2014
Home again!
James came home again on February 1 st! He had his first physio session since he came home, yesterday. It is nice to be back with the home team! His physiotherapist said that he can see that James is not as good at using the walker as he was when he left ( his team at GF Stronge did not use the walker with him really at all until the last couple of weeks. ). But he did really well standing without holding or touching anything, (2-3 minutes) and he did great with stretching his shoulder to get his right hand up over his head. James has been doing quite a bit of walking with me just on his arm, and being without the wheelchair for periods of time in the house. Monday was a provincial holiday, and it snowed on Sunday night! When James got up in the morning he wanted to go outside in the snow. I pushed him in his chair halfway out the driveway and he decided he wanted to go back inside! When we got inside we saw that his wheels were packed with snow, so it was a good excuses for a chair free day! He was out of his chair for about 12 hours! James is going to his day program 5 days a week again. His aide takes him to his physio appointments, swim therapy, adapted karate, working in the gym, doing his daily speech and physio excercises, as well as anything else they plan! He is also going to a special needs young adults group at the community center once a week! He is at his happiest when he is busy. James was feeling very lonely and bored at the hospital, and his mood has improved drastically since he came home! Next week he will start seeing a speech therapist in Campbell river at the hospital outpatient center. She will see him twice a month to just follow up on his speech and change his home speech program as needed.
Monday, 13 January 2014
2014!
Well James has a room to himself again. His last roommate didn't work out very well. The roommate was still quite confused, and got up during the night, made a mess of the room and sat on the edge of James bed. James was just a bit freaked out! I suggested that James be the one to move rooms, as I knew James would be able to adjust to being in a new room better than the roommate.
James is using a walker from gf Stronge now. He said that he didn't like his walker because he sometimes bumps his knees. The gf Stronge walker has a flip up seat so there is more room for his knees when he walks. He is being much more cooperative about walking with the walker now!
James also started pool therapy this week! Yay! It's about time! He goes twice a week at the GF Stronge pool and once a week at the therapy pool near gf Stronge.
There is a conference meeting next Monday. And there is a discharge date being talked about! The date they gave me is January 29 th. Since that is a Wednesday, I am trying to get it shifted to Saturday, February 1 st. James has done quite well with his speech. I do feel like he is a bit easier to understand. I think it will just take time for his speech to become clear enough for him to be understood by someone who isn't around him all the time. I was hoping he would get more independent with his walking, but I think that is going to take more time. He is getting better at walking with the rail and a cane, but he still needs a spotter when her uses his walker or walks with the rail and a cane. It is just so hard to be patient, but I think it will just take time...
We have found a great place to practice walking on the weekends. There is a hallway In the basement at gf Stronge that has a ramp and railings. I help James practice rail walking with his cane, we practice some walker walking on the flat part of the hallway and then he plays around coming down the long ramp with his wheelchair! James and Sarah both had a blast going down the ramp with the wheelchair last weekend!
I have finally found the courage to use the buses and trains to get to and from the ferry in Vancouver now! We have done a little bit of exploring Vancouver on the transit on the weekends now. A couple of weeks ago we went to Longsdale Quay ( James bought another fedora hat ) and last weekend we went to the anthropology museum at UBC.
Friday, 27 December 2013
Merry Christmas!
James came home for five days over Christmas. He is sure happy to be home. The day that we were leaving to go over and visit with James and bring him home to visit, we had an amazing hamper delivered! What a surprise! Everything for Christmas dinner plus other food items, plus gifts and stockings for us all! Our tree has never been so full! It was the first Christmas since I was a kid that I didn't know what was under the tree! We brought James' girlfriend with us to Vancouver and she also spent Christmas Day with us. James was so excited to see her! The hotel that we stayed in while we visited with James had an IHOP restaurant attached to it. The food was fabulous! I think I have a new favorite restaurant! Too bad we don't have one near home. We visited with Grampa Cam and Cindy and Paige while in Vancouver. We had lunch and dinner with them, went to a movie and visited at their home. It was a great day. We saw the movie, Frozen. It was great. James saw it once already, but he was super excited to see it with the family! We travelled home on Christmas Eve with James. We saw a pod of small dark colored whales on the ferry trip. We stopped in Nanaimo and had dinner and a visit with gramma Ann, then drove home. We spent Christmas Day with James girlfriend, Rae Ann, and Nana came for dinner. We also went over the Nana's house to see her mini Christmas village that she puts up every year. We ended the day by driving along candy cane lane to see all the Christmas lights! James also spent almost the whole day without his chair! He was 11 hours out of his chair! He even used his walker to go In and out of Nana's house. That was quite a bit of walking! We all got super spoiled for Christmas! We are so blessed to have such awesome friends and family!
James got a new roommate on Christmas Eve at the hospital. He is a man in about his 50s. I hope he is as nice as the last roommate. I am a little nervous about it. The experience with the first roommate James had was so horrible! James' usual doctor is back from hollidays and I look forward to meeting with her next week. James has been trialling a power chair lately. He has practiced with it 3 or 4 times now. He is doing very well with it. He is very careful, and I suspect it won't be long before he is able to use it on his own inside the building. He really enjoys the independence it gives him. I have been very concerned that he hasn't been using his walker much while he has been there. It sounds like both his physiotherapist and his occupational therapist will be spending time walking with him with his walker now though. James had a scope of his throat done again recientely. They were wanting to see how his naso-pharyngeal port ( a flap that opens and closes between the mouth and nose). Is working and how he is handling eating and drinking. The port did close nicely a couple of times while he was making an "A" sound, but it wasn't consistent. I am hoping that it is a sign that it is starting to work. That port being able to open and close when he speaks is very important to the intelligablility of his speech. He was able to also swallow a teaspoon of regular fluid as well as he swallows a teaspoon of thickened fluid. So that is also promising. He is still a choking risk though, and still needs to be monitored when eating.
James and I will be going back over to Vancouver on Sunday. I will stay there until the following Sunday. It will give me a chance to catch up with his therapists and his doctor.
Monday, 16 December 2013
Calmer waters
James has been doing much better the last couple of weeks. I still think that hie schedule should be busier though. He does have a couple of new things added to his week. He has hand class on Tuesday morning and on Tuesday evening and Sunday afternoons he has a speech volunteer working with him. James usual doctor is back this week too. I will meet with her after Christmas. She is familiar with James and his goals, and I am hoping that she can kick James rehab up a notch!
James iPad will be replaced this week too! He will be getting a new speech app on it to try out as well as his old touch chat app. His replacement iPad is a mini and he is pretty excited about that. It will be easier to pack around and keep safe! The occupational therapist is making a pouch for it to go in that will attach to his chair.
James will be getting another throat scope done tomorrow. They are going to watch what happens when he eats, as well as when he talks. His speech therapist wants to also discuss with the doctor if there are any intervention options to help with his speech.
James now has a the social worker for his program checking in with him almost daily too. Just to make sure that he is doing okay and that no one is giving him a rough time. James is becoming more known by other patients and nurses though. There are quite a few patients who talk to James now and keep an eye out for him!
James is very excited about coming home for 5 days around Christmas! His girlfriend has taken time off around that time too, so he is super excited to spend some time with her too!
Saturday, 7 December 2013
Tough few weeks
It has been a tough start for James at gf Stronge. During the first week, he got a roommate who was very verbally abusive and intimidating to James. The roommate then stole James iPad with his communication program on it. The iPad was retrieved from under the roommates mattress, and a couple of days later they moved James to a new room (across the hall) because James was refusing to go in the room and was sitting in the hallway. the day after the move his iPad went missing again, and this time they found the charger in the old roommates drawer, but were not able to find the iPad. So poor James has been the last few weeks without his communication program. I am noticing that he is often just giving up trying to communicate more complex ideas to the nurses. If it takes too much effort to get his point across he will just give up. James' new roommate is a sweetheart though. He is in his 40s and is from Columbia. He speaks Spanish and now James wants to learn Spanish! His new roommate was telling me that he is discharging in by couple of weeks though. I am nervous about who will be rooming with James next!
I spent last weekends visit meeting with police about the iPad, and generally trying to get a clearer picture of the story of the iPad theft. The hospital won't consider it stolen though, only missing. Security says that since no one actually saw the guy steal the iPad it is deflamitory to say it was stolen. He says that even though it was found the first time under the guys mattress, that doesn't mean he put it there. The argument would be, what if the guy was framed. Good grief ! Not sure what the police have been able to do, and if I wanted a copy of the police report I would have to apply for freedom of information act, which is a lengthy and expensive process. It does look like the company that supplied the iPad will replace it for him, but there are lots of hoops to jump through to make that happen. I spent this weekend working on paperwork to get the iPad replaced. I am hoping to have it replaced before Christmas.
There was a meeting on Thursday to discuss James progress so far. I caught wind earlier in the week that the talk was to discharge James because James was wanting to go home. I talked to James' physiotherapist from Courtenay, who wrote an awesome e mail to the new physiotherapist as well as the physio and occupational therapists who worked with James during the summer. Well, I think he sufficiently stirred the pot! When I arrived they were all hopping, and the doctor filling in for James' usual doctor had given James his cell number, and was communicating with him via texting! He convinced James to give it a good try and stick around. A review meeting is now set for January 20th. At that meeting either a discharge date will be discussed or another review meeting set. Basically what we heard is that James is working hard and cooperating despite being homesick. He is using his right hand a lot more, and I have seen a significant change in the function of his right hand. His speech is coming along, he is quite a bit clearer if he plugs his nose. He is scheduled to have another scope done on the 17 th of this month. He is also sitting a bit straighter in the last week or so too. I told them that James needs to be busier too. When he is bored, he gets very homesick.
I took James to a follow appointment with the Neuro Opthomologist yesterday. He saw some positive changes in James eye function in just under 2 months since he saw him last. He said that on their own each of James' eyes works quite well, they just don't work perfectly together. He wants to follow up with more testing in 6 months. He felt that patching one eye or the other might assist James in some activities where there is still some double vision. He also suggested tinting the lense of his glasses on his right eye. That eye is light sensitive since the pupil stays a bit more dialated than the other. He does not feel that James is a good candidate for surgery since his right eye has multiple issues.
Wednesday, 27 November 2013
Gf Stronge
James has been at gf Stronge for almost two weeks now. It has been a tough couple of weeks though. On day 5 he got a roommate. His roommate was walking and talking, and very nasty to James. When James came into the room he would swear at him and started calling him names. He also stole James iPad with his communication program on it. They found it under the roommates mattress . It got to the point where James wouldn't go in the room while the roommate was there. He would just sit in the hallway. They moved James to a new room last Thursday. His new roommate seems to be a really sweet guy. He is in a wheelchair too, and he also has some communication issues. He is able to speak better than James can though, and often let's the nurses know what James is trying to say! James iPad went missing again after they moved him though. The charging cord was discovered in the old roommates possession, but they haven't been able to find the iPad. So poor James is trying to get along without it for now. The society that provided the iPad has said that they will provide James with another iPad, as long as the hospital staff can figure out ways to increase the security around the iPad. James has been having a hard time with the fact that they won't let him go to bathroom on his own either. He has to call a nurse to go to the bathroom. While his transfers are supposed to be just supervised, when he gets a new nurse, they seem to feel the need to actually transfer him themselves, which is very frustrating to James because it is difficult to communicate with them. I did get an email today from his OT that she is going to let him get in and out of bed unsupervised though. She still wants to work on the bathroom transfers.
I also got a call from a fella who works on the recreational therapy team last night. He is going to start taking James out a couple of days a week ! Today they are going to go and get chocolate cake at white spot. They are also planning on going to the movies on another day.
James has an appointment with the Neuro Opthomologist next Friday, and I am going to go over early to Vancouver, so I can go with him. It is to go over the results of some field of vision tests that they did almost two weeks ago.
Tuesday, 19 November 2013
Back at GF Stronge!
James went back to GF Stronge last Thursday! It was hard leaving him there to come home. I am sure he will do fine, but it is hard not to worry about him! He got his schedule yesterday. I am glad that it looks like they will keep him busy! He has Occupational therapy at 9 am, Physio at 10 am, and two half hour speech sessions at 11 am and 2 pm. They are also talking about putting him in pool therapy twice a week and one session a day with a rehab assistant to work on his walking. As well as getting him involved in music therapy and art therapy. He will be going to the recreational pool session on Wednesday nights too. There is also wii games nights on Mondays and Thursdays. Monday night games night is on the spinal injury floor, and I understand that there are a couple of young guys there. I will be going back over to visit James on the weekend. I will probably go over on Friday night, and come home again on Sunday night.
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