Well we made it home. That was an amazingly long trip. We were so excited to get home. When we got home there was a welcoming party, with atleast 50 or more people. It was great.
Since being home we have many things going on. P.T. appointments,my mom had back surgery and Tasha has had surgery on her esophogus. We are very tired and ready for things to slow down.
We miss all of our dear friend from U OF U hospital. We are coming back on the 18th for checkups. We will stop in to see all of you then.
Thursday, October 14, 2010
Saturday, October 2, 2010
October 2, 2010
Well today is the last day here at the hospital. They have done all the prep work so we can leave between 7:30 and 8:00. We have signed the discharge papers today, got most of the scripts that we need and got all of Nick's stuff packed up and in the car. Needless to say this day has really dragged on forever. Waiting to leave is the worst. Everyone here has been so wonderful.
Todays therapy consisted of playing a game of scrabble and then they had him do some weight lifting this afternoon. That is a normal Saturday, but where we are just waiting for time to go by, we would of welcomed a normal therapy day.
We have been watching General Conference today, it has been very good.
Todays therapy consisted of playing a game of scrabble and then they had him do some weight lifting this afternoon. That is a normal Saturday, but where we are just waiting for time to go by, we would of welcomed a normal therapy day.
We have been watching General Conference today, it has been very good.
Friday, October 1, 2010
October 1, 2010
Well it is October. I can't hardly believe it. The weather down here in Salt Lake is beautiful. Nick has been very busy with therapy today, along with tying up all the loose ends to come home.
We have been trying to figure out what we were doing about the Lovenox shots. We finally got it all figured out between myself, the hospital pharmacy and the Insurance company. I was able to get it from a pharmacy here in town, who had the generic formula for it. Thank goodness. It only cost me $85.00 instead of $1400.00. That is unreal. It took alot of work, but it was worth it. I feel like I have been on the phone all day trying to work it all out.
Nick had a rematch of his race with his recreational therapist, and of course Nick won. It was getting pretty wicked at the end, but Nick pulled through. Nick your the man!!!
We have been trying to figure out what we were doing about the Lovenox shots. We finally got it all figured out between myself, the hospital pharmacy and the Insurance company. I was able to get it from a pharmacy here in town, who had the generic formula for it. Thank goodness. It only cost me $85.00 instead of $1400.00. That is unreal. It took alot of work, but it was worth it. I feel like I have been on the phone all day trying to work it all out.
Nick had a rematch of his race with his recreational therapist, and of course Nick won. It was getting pretty wicked at the end, but Nick pulled through. Nick your the man!!!
Thursday, September 30, 2010
September 30, 2010
Today for one of Nicks therapies they took him to Emmigration Canyon and their is a pond up there and let him go fishing. It was really funny because his 2 therapist that was with us said the fish looked really big. They put fish in this pond, but they aren't very big in comparison to what he usually gets when he goes fishing with his Grandpa. Nick and I got a real good laugh out of it. Atleast Nick had a lot of fun doing it.
We also worked alot on curbs. Getting up on them and down them. I think I only had about 4 heart attacks during the process. He has to do wheelies and move himself up or down. One time one of his wheels went off of the curb before the other and he started tipping to one side. Scarry for me, he was all in control. I guess it's just called being a mom.
In O.T. he was lifting weights and a guy saw him and came over and visited with him for a while. This guy was injured about 7 years ago and is living the life that Nick will be living. It was very interesting to listen to some of the things that work for him and what doesn't. I am sure it is different for every individual.
We had to say goodbye to our regular P.T. today. She is leaving for vacation. That was not fun. You get really close to these people that you work with several times a day. There is a certain trust you gain in them. It is amazing. We love you Jenny
We also worked alot on curbs. Getting up on them and down them. I think I only had about 4 heart attacks during the process. He has to do wheelies and move himself up or down. One time one of his wheels went off of the curb before the other and he started tipping to one side. Scarry for me, he was all in control. I guess it's just called being a mom.
In O.T. he was lifting weights and a guy saw him and came over and visited with him for a while. This guy was injured about 7 years ago and is living the life that Nick will be living. It was very interesting to listen to some of the things that work for him and what doesn't. I am sure it is different for every individual.
We had to say goodbye to our regular P.T. today. She is leaving for vacation. That was not fun. You get really close to these people that you work with several times a day. There is a certain trust you gain in them. It is amazing. We love you Jenny
Wednesday, September 29, 2010
September 29, 2010
Well our week is half over, but not without lots of hard work. We have been working some more on transfering from wheel chair to half way to the floor. Nick also did lots of weight lifting. He really enjoys that.
In one of his sessions of O.T. he played with the Wii. They say it helps with his balance. All I can say is OKAY!!!
Nick got his loaner wheel chair today. It isn't as nice as the one he is use to but it will do till he gets his permanent one in about a month.
We did get good news today. We get to go home a day earlier. We are so excited. We will be discharged about 7:30 Sunday morning, then we will go to General Conference and then we get to head for home. The Dr. told Nick to wipe that grin off of his face, but I don't think anything could take the smile off of his face. We are both so very excited.
In one of his sessions of O.T. he played with the Wii. They say it helps with his balance. All I can say is OKAY!!!
Nick got his loaner wheel chair today. It isn't as nice as the one he is use to but it will do till he gets his permanent one in about a month.
We did get good news today. We get to go home a day earlier. We are so excited. We will be discharged about 7:30 Sunday morning, then we will go to General Conference and then we get to head for home. The Dr. told Nick to wipe that grin off of his face, but I don't think anything could take the smile off of his face. We are both so very excited.
Tuesday, September 28, 2010
September 28, 2010
Can you believe September is almost gone. That just makes it that much sooner till we get to go home. Today in therapy we started learning how to bump up on stairs, just in case we need to go somewhere, where there are a few stairs. Much harder than it seems. Lots of muscle power and none of it is Nicks. We also started learning how to lift Nick from the floor to his chair, just in case he falls out of his chair. Nick is starting to learn how to lift himself from the floor to his chair, thank goodness we got to start with a half way mark down. He had a wooden box to go down to that was half way from his chair to the floor.
Nick also worked on the EFS bike. It has electrodes that are connected to his legs and his hips, it has a motor in it, and it forces his legs to peddle the bike. We found that with Nick doing this excercise, it forces his body to do disreflexia. Meaning one side of his body starts sweating from the top of his head down to his injury site, and forces his blood pressure to rise quite significant, but the other side just stays normal. It is really strange.Since then Nick has been very tired.
Nick also worked on the EFS bike. It has electrodes that are connected to his legs and his hips, it has a motor in it, and it forces his legs to peddle the bike. We found that with Nick doing this excercise, it forces his body to do disreflexia. Meaning one side of his body starts sweating from the top of his head down to his injury site, and forces his blood pressure to rise quite significant, but the other side just stays normal. It is really strange.Since then Nick has been very tired.
Monday, September 27, 2010
September 27, 2010
Well we are down to only 7 more days here at the hospital. Can't wait to get home.
Today we worked on car transfers, with just Nick and I doing the transfers, without the therapist helping. We did really good. We make a good team.
Nick also had some more wheel chair races. He won the first race and lost the second one. Where he does the races he has corners he has to go around, ramps to climb, carpet to move on. It can get very difficult at times, but he does really well. It is good practice for him when he gets home.
There are special stretches we have to do with his legs, so we did more practicing on them today also. From here on out they are going to really be vocusing on things we have already learned, but just making sure that Nick and I are knowledgable in them and comfortable.
Tonight we learned about the lovenox shots he has to have for the next couple of weeks. The best part about the shot is it has to go in the belly and he doesn't feel it at all, but he is getting to have little polka dots on his belly from having shots in the morning and the evening.
Nicks legs have gotten really skinny. I tell him he now officially has chicken legs. He is not able to keep the ted hose up on his legs because they are so tiny. He is wearing the smallest they have.
Someone asked Nick the other day what the first thing he was going to do when he got home. His response was "tease my sisters" I guess that won't change.
Today we worked on car transfers, with just Nick and I doing the transfers, without the therapist helping. We did really good. We make a good team.
Nick also had some more wheel chair races. He won the first race and lost the second one. Where he does the races he has corners he has to go around, ramps to climb, carpet to move on. It can get very difficult at times, but he does really well. It is good practice for him when he gets home.
There are special stretches we have to do with his legs, so we did more practicing on them today also. From here on out they are going to really be vocusing on things we have already learned, but just making sure that Nick and I are knowledgable in them and comfortable.
Tonight we learned about the lovenox shots he has to have for the next couple of weeks. The best part about the shot is it has to go in the belly and he doesn't feel it at all, but he is getting to have little polka dots on his belly from having shots in the morning and the evening.
Nicks legs have gotten really skinny. I tell him he now officially has chicken legs. He is not able to keep the ted hose up on his legs because they are so tiny. He is wearing the smallest they have.
Someone asked Nick the other day what the first thing he was going to do when he got home. His response was "tease my sisters" I guess that won't change.
Saturday, September 25, 2010
September 25, 2010
Today has been a long day. Nick and I have a bit tired today, not sure why. There hasn't been but only 1 p.t. and this morning he had an o.t. that a group of them met in the kitchen and make pizza with a banana pudding dessert.
I tried to get Nick to let me watch R.S. general conference but his Utes were playing to I was out voted. I guess I will have to read it next month. Thats the breaks.
I tried to get Nick to let me watch R.S. general conference but his Utes were playing to I was out voted. I guess I will have to read it next month. Thats the breaks.
Friday, September 24, 2010
September 24, 2010
Nick has been very busy today with therapy and all. It is good for him to be busy, it takes his mind off of going home. He is so excited to go home that sometimes thats all he thinks about. But then who can blame him.
Nick has had lots of time to think about his life since he has been here. He is very determined to serve a mission, like a service mission. He has such a strong testimony, and I think it has gotten stronger since he has been here in Salt Lake.
Nick has had lots of time to think about his life since he has been here. He is very determined to serve a mission, like a service mission. He has such a strong testimony, and I think it has gotten stronger since he has been here in Salt Lake.
Thursday, September 23, 2010
September 23, 2010
Today we went hand cycling down to Liberty Park again. They have a cement pathway that goes all around the perimiter of it. Nick loves getting out and getting the fresh air and having new scenery. Plus he really enjoys and hand cycling.
This morning was very crazy. They needed Nicks room for a different patient that needs a lift to get him out of bed. Nick doesn't need the lift. He is to strong. I can't believe all the stuff we had to move. We have accumilated alot of stuff. All seems to be necessary.
We also found out that Nick, I, and a therapist get to go to a session of general conference. We are so excited. The tickets are being sent to us by the first presidency, and we get special seating. We are so stoked.
This morning was very crazy. They needed Nicks room for a different patient that needs a lift to get him out of bed. Nick doesn't need the lift. He is to strong. I can't believe all the stuff we had to move. We have accumilated alot of stuff. All seems to be necessary.
We also found out that Nick, I, and a therapist get to go to a session of general conference. We are so excited. The tickets are being sent to us by the first presidency, and we get special seating. We are so stoked.
Wednesday, September 22, 2010
September 22, 2010
Well we only have 12 days left. Nick is doing very well. His progression has been great. We have gained more friends. It is amazing.
Nick had a race in his wheel chair with his recreational therapist. It started off really good, until Nick's foot slid off of the foot rest. He had to stop and reposition, and get his momentum back up. So needless to say Nick did not win. But he put up a good fight. Nick did rig the therapist chair before hand though. He let some of the air out of the tires and then Nick and his occupational therapist tied on a 5 pound weight under the seat where she couldn't see it. It was all Nick could do not to giggle about it before the race. There will be a rematch before we leave. Nick is determined to win.
We have been working on car transfers. That is more difficult than you could imagine. Right now it is a three man job, but it won't before it will be 2 man and evantually Nick will be able to do it on his own. When he is done with the transfer Nick is really tired.
In one of his O.T.'s today Nick transfered from his wheel chair to a couch, then he had to do lifts to get himself to the opposite end of the couch. Then his therapist decided I needed a challenge. I had to sit at one end of another couch and without using my legs, and doing lifts work myself down to the other end of the couch. They said I cheated because I used my feet to anchor me to the floor. Nicks life without legs is something I don't think the rest of us can comprehend.
Nick had a race in his wheel chair with his recreational therapist. It started off really good, until Nick's foot slid off of the foot rest. He had to stop and reposition, and get his momentum back up. So needless to say Nick did not win. But he put up a good fight. Nick did rig the therapist chair before hand though. He let some of the air out of the tires and then Nick and his occupational therapist tied on a 5 pound weight under the seat where she couldn't see it. It was all Nick could do not to giggle about it before the race. There will be a rematch before we leave. Nick is determined to win.
We have been working on car transfers. That is more difficult than you could imagine. Right now it is a three man job, but it won't before it will be 2 man and evantually Nick will be able to do it on his own. When he is done with the transfer Nick is really tired.
In one of his O.T.'s today Nick transfered from his wheel chair to a couch, then he had to do lifts to get himself to the opposite end of the couch. Then his therapist decided I needed a challenge. I had to sit at one end of another couch and without using my legs, and doing lifts work myself down to the other end of the couch. They said I cheated because I used my feet to anchor me to the floor. Nicks life without legs is something I don't think the rest of us can comprehend.
Tuesday, September 21, 2010
September 21, 2010
It has been a very busy day. Therapy, Therapy, Therapy. All to get us home. Nick really surprised me lots this morning. He did a transfer from his bed to his wheel chair with no assist. All I did was sit in front of him to make sure nothing happened. He did awesome. He has gotten so strong since we first got here. We also worked on car transfers. It is very difficult, but Nick approached it like the pro that he is. Just like he has every other step along the way. As long as he is given time to trouble shoot what he needs to do he does great, they have learned that they cannot just throw him into something. He has to process it in his head.
Nick also played basketball today for his recreational therapy. It is hard to keep the basketball under control, so he has to take it a little slow to keep control.
I told Nick today that he will soon not even need me, and I am not sure what I think about that. Of course Nick put his own comment into it. He said; Mom I will always need you. Nick is such a wonderful kid and I love him so much. I am so greatful to be able to be here with him, and to be his mother.
Nick also played basketball today for his recreational therapy. It is hard to keep the basketball under control, so he has to take it a little slow to keep control.
I told Nick today that he will soon not even need me, and I am not sure what I think about that. Of course Nick put his own comment into it. He said; Mom I will always need you. Nick is such a wonderful kid and I love him so much. I am so greatful to be able to be here with him, and to be his mother.
Monday, September 20, 2010
September 20, 2010
Well the Dr's. came in today and said they are keeping us until October 4. Nick was really hoping that they would let him out early. But Nick is counting down the days till we go home. Today it was 14 days. He still has a good attitude, and loves to tease his nurses and aids.
Today he went up to one of the nurses without her knowing and shook her chair. Scared her to death. He did this twice today. He thinks he is so funny. This nurse keeps threatening Nick that she is going to call security on him. I do have to say that he has come out of his shell. When we first got here he was so solemn, with no expression what so ever. Now he smiles alot and teases alot. They always know he is up to something. It is actually fun to watch.
Nick really wants to go to one of the sessions of general conference. His occupational therapist is working on getting some tickets for atleast Nick and I and the therapist. He is hoping to get more tickets so the family could go with us. That would be great.
Nick has had a very busy afternoon with therapy. He has had 2 sessions of p.t. and then also wellness class. Which is weight lifting. This morning he had 2 sessions of occupational therapy. Which he does alot of muscle toning. Very busy days around here.
Today he went up to one of the nurses without her knowing and shook her chair. Scared her to death. He did this twice today. He thinks he is so funny. This nurse keeps threatening Nick that she is going to call security on him. I do have to say that he has come out of his shell. When we first got here he was so solemn, with no expression what so ever. Now he smiles alot and teases alot. They always know he is up to something. It is actually fun to watch.
Nick really wants to go to one of the sessions of general conference. His occupational therapist is working on getting some tickets for atleast Nick and I and the therapist. He is hoping to get more tickets so the family could go with us. That would be great.
Nick has had a very busy afternoon with therapy. He has had 2 sessions of p.t. and then also wellness class. Which is weight lifting. This morning he had 2 sessions of occupational therapy. Which he does alot of muscle toning. Very busy days around here.
Sunday, September 19, 2010
September 19, 2010
Today has been really quiet. Just what we need after the busy week. We went to Sacrament services and invited our neighbor to go with us. She accepted. It was really a nice meeting.
Bro. and Sis. Stanger from our ward stopped in to see us. It is always nice to see familiar faces from home.
Bro. and Sis. Stanger from our ward stopped in to see us. It is always nice to see familiar faces from home.
Saturday, September 18, 2010
September 18, 2010
Nick is getting to be pretty buff. Big muscles in his biceps. He lifts weights everyday. He is getting up to lifting about 70 pounds with his arms. He uses several different kinds of machines for his weight lifting.
Nick is also getting into watching football, as long as it is the Utah Utes.
We had a lady come visit us. Her son is a patient here. She wanted to know how we are able to accept what has happened and how she could deal with it better. She is the only one in her family who is a member of the church, and she is not real active. We had the opportunity to ask if she or her son had received a blessing. They had received a blessing but I think she is really lacking faith, just through things she has said. Nick was able to talk to her and tell her some of his thoughts. She was very impressed with Nick. Maybe this will be Nicks mission, to bear his testomony to her. Hopefully Nick and I can help her.
Nick is so amazing.
Nick is also getting into watching football, as long as it is the Utah Utes.
We had a lady come visit us. Her son is a patient here. She wanted to know how we are able to accept what has happened and how she could deal with it better. She is the only one in her family who is a member of the church, and she is not real active. We had the opportunity to ask if she or her son had received a blessing. They had received a blessing but I think she is really lacking faith, just through things she has said. Nick was able to talk to her and tell her some of his thoughts. She was very impressed with Nick. Maybe this will be Nicks mission, to bear his testomony to her. Hopefully Nick and I can help her.
Nick is so amazing.
Friday, September 17, 2010
September 17, 2010
Not much different today. Just kept busy with therapies. By the end of the day Nick is really tired. After all his therapies are finished his shoulders really hurt him. He is using his arms and shoulders tons and so the muscles get really tight. Really hot blankets really helps the pain, and loosens up the muscles.
Today Doyle and Keisha left to go home. Nick had lots of fun teasing Keisha, and it was really nice to have them here. Keisha and I went and spent some time together before she had to leave. It was really nice.
Today Doyle and Keisha left to go home. Nick had lots of fun teasing Keisha, and it was really nice to have them here. Keisha and I went and spent some time together before she had to leave. It was really nice.
Thursday, September 16, 2010
September 16, 2010
Today has been a bit slower. Nick had Occupational therapy starting at 8:15 and went till 9:45. Then he didn't have anything until 2:30. At that time we went down to Liberty Park and he rode a hand cyle around the park. 3 rounds. He had lots of fun with that. When ever he has an outing like that he has to accomplish certain goals they set for him. Today he had to initiate talking to someone he has never seen before, that was hard for Nick, but he did it. He also had to come up with 2 positive things about his experience. He loved being out in the fresh air. It was lots of fun. We met lots of new people.
Wednesday, September 15, 2010
September 15, 2010
Well it has been quite the day. I didn't get up to the hospital until around noon. We had the eventful day of doing laundry. Not that much fun when you have to do go to the laundry mat. UGH!!!!
Today happened to be my birthday. Nick happened to tell a few people here, well then it really spread. In one of his p.t. sessions made me a pan of rice crispies, drizzled with chocalate and sprinkles.
My family also suprised me by coming. I was so suprised. They made dutch oven chicken, potatoes and cheesy vegetables. It was so yummy. Keisha also made me a cake. It turned out to be a very nice day.
Today in recreational therapy they put Nick on a hand cyle. Nick was very nervous at first, but got more use to it. He caught on real fast. They had him outside on the sidewalks on campus. Lots of new things have been learned down here. Nicks p.t. had him working on turning onto his stomach and trying to sit up. That takes alot of energy out of Nick. It is amazing to watch.
Today happened to be my birthday. Nick happened to tell a few people here, well then it really spread. In one of his p.t. sessions made me a pan of rice crispies, drizzled with chocalate and sprinkles.
My family also suprised me by coming. I was so suprised. They made dutch oven chicken, potatoes and cheesy vegetables. It was so yummy. Keisha also made me a cake. It turned out to be a very nice day.
Today in recreational therapy they put Nick on a hand cyle. Nick was very nervous at first, but got more use to it. He caught on real fast. They had him outside on the sidewalks on campus. Lots of new things have been learned down here. Nicks p.t. had him working on turning onto his stomach and trying to sit up. That takes alot of energy out of Nick. It is amazing to watch.
Tuesday, September 14, 2010
September 14, 2010
Today has been a pretty good day. When I got here at 8:00 Nick was all dressed and eating his breakfast. He knew he had company coming and he was very excited.
Dan, MaryAnn and Chuck is heading to California and stopped on their way thru to see Nick. They were here for a couple of hours. It was so great to see them. Nick got lucky and got to skip one of his p.t.'s because they were here. He was not upset at that at all.
Nick is still counting down the days till we get to go home. 20 more days and we are on our way. We are both very excited for that day. Life will never be normal again but it can be more normal than being here in the hospital. But we can't complain to much because everyone here has been so wonderful. Every new direction we have had to take, there has been someone here to help in the journey. I am so grateful to them, and for everyone at home that has helped so much. We love you all.
Dan, MaryAnn and Chuck is heading to California and stopped on their way thru to see Nick. They were here for a couple of hours. It was so great to see them. Nick got lucky and got to skip one of his p.t.'s because they were here. He was not upset at that at all.
Nick is still counting down the days till we get to go home. 20 more days and we are on our way. We are both very excited for that day. Life will never be normal again but it can be more normal than being here in the hospital. But we can't complain to much because everyone here has been so wonderful. Every new direction we have had to take, there has been someone here to help in the journey. I am so grateful to them, and for everyone at home that has helped so much. We love you all.
Monday, September 13, 2010
September 13,2010
Well today has been a very busy day. Lots of therapies.We started at 9:00 a.m. had a 45 minute break for lunch and then we were back at it again at 1:00 and went until 4:45. Days like this wear both of us out, but Nick never complains.
He watches others do there p.t. and sometimes gets a bit of a sad look on his face. I know excactly what he is thinking. Nicks heart goes out to them. He is a very tender guy.
Today in one of his p.t. sessions he got to teasing his therapist so much that he couldn't stop giggling. It was so fun to see. He also goes down the hall in the rehab unit trying to run some of the nurses down. They tease them as much as he teases them.
At first they couldn't hardly get him to talk, now I wonder what they think! He is really progressing. Both physically and mentally, maybe even coming out of his shell a bit.
A BIT. That is his new saying and he has some of the nurses even talking that way. It is quite funny.
He watches others do there p.t. and sometimes gets a bit of a sad look on his face. I know excactly what he is thinking. Nicks heart goes out to them. He is a very tender guy.
Today in one of his p.t. sessions he got to teasing his therapist so much that he couldn't stop giggling. It was so fun to see. He also goes down the hall in the rehab unit trying to run some of the nurses down. They tease them as much as he teases them.
At first they couldn't hardly get him to talk, now I wonder what they think! He is really progressing. Both physically and mentally, maybe even coming out of his shell a bit.
A BIT. That is his new saying and he has some of the nurses even talking that way. It is quite funny.
Sunday, September 12, 2010
September 12, 2010
Well we have been here for 4 weeks now. Nick is totally ready to go home. He is counting down the days. We have until October 4th. I think we are both ready for our own beds.
Today we made it to Sacrament Services. They have a small chapel here on the 2nd floor, where they have a small branch. It was really nice. Partaking of the sacrament is such a blessing. Sometimes you don't realize what you miss until you don't have it. We are so greatful for all that the Lord has given us. Being in a place like this, we see situations all around us and can be greatful for all our blessings and for the gospel in our lives.
Today, where it is Sunday, Nick has no therapy. What a nice break.
We have met some other people who are here, both patients and families. We hear there stories. We get to converse with these people everyday. We have aquired some new friends from all over the states. They are amazing. Several of them are from Wyoming. One of the families went to school with Doyle and Carlene. What a small world.
Today we made it to Sacrament Services. They have a small chapel here on the 2nd floor, where they have a small branch. It was really nice. Partaking of the sacrament is such a blessing. Sometimes you don't realize what you miss until you don't have it. We are so greatful for all that the Lord has given us. Being in a place like this, we see situations all around us and can be greatful for all our blessings and for the gospel in our lives.
Today, where it is Sunday, Nick has no therapy. What a nice break.
We have met some other people who are here, both patients and families. We hear there stories. We get to converse with these people everyday. We have aquired some new friends from all over the states. They are amazing. Several of them are from Wyoming. One of the families went to school with Doyle and Carlene. What a small world.
Friday, September 10, 2010
September 10, 2010
Today we went to Temple square for recreational therapy. We had lots of fun. We wondered around the grounds and then went to the conference center, did a mini tour. We didn't have time to do the whole tour they usually do. We were able to see quite abit though. It was a new experience to do sidewalks, and road entries from sidewalks in the wheel chair.
In p.t. we were learning and practicing car transfers. That is not an easy task. One of the times Nick did a head dive into the door. For a little while he had to good sized red marks on his forhead, and his neck popped. We had to come upstairs and have the Dr. check him out and make sure everything was ok. He passed that test, so back to the car we went to practice the transfers some more. Nick was a bit nervous, but did just fine.
While we were downstairs some people came and introduced themselves to us. It was Doyle's cousins, Scott and Paula Heiner. They now live in Green River Wy. There are two other patients here from Green River that they were here to see and one of them we have come to get to know a little. What a small world.
In p.t. we were learning and practicing car transfers. That is not an easy task. One of the times Nick did a head dive into the door. For a little while he had to good sized red marks on his forhead, and his neck popped. We had to come upstairs and have the Dr. check him out and make sure everything was ok. He passed that test, so back to the car we went to practice the transfers some more. Nick was a bit nervous, but did just fine.
While we were downstairs some people came and introduced themselves to us. It was Doyle's cousins, Scott and Paula Heiner. They now live in Green River Wy. There are two other patients here from Green River that they were here to see and one of them we have come to get to know a little. What a small world.
Thursday, September 9, 2010
September 9, 2010
We have had another busy day with therapies. Nick had a lot of fun with a couple different therapies. In his recreational therapy they took a fishing pole outside, tide a screw to the end of it and practiced casting the fishing pole. He got so good that the line and screw went over the fence and caught onto a bush. They want to try to take Nick up Emigration Canyon and take him fishing. He would love that. He wishes he had his fishing buddy with him for that, Grandpa.
In one of his p.t. sessions today we worked on balance. That is a real big issue right now. Oh how we take so many things for granted. He had to toss a ball back and forth to me, then they added in a stick. I would throw the ball to him and he would have to his it with the stick and still regain balance. Harder than what it sounds. Take all the muscles out of your abdomin and middle of your back down and just try to sit. That is where Nick is.
They always have to find things to challenge him with because he is so determined. When they ask him if he is ready to stop an activity he always tells them "a couple more times please".
They are removing his catheter tonight because he has developed a urinary track infection. Thank goodness he doesn't feel anything. I was able to alert the Drs about it because of the color of his urine.
I am learning so much. I have decided I should recieve my nursing degree just from experience. HAHAHA
In one of his p.t. sessions today we worked on balance. That is a real big issue right now. Oh how we take so many things for granted. He had to toss a ball back and forth to me, then they added in a stick. I would throw the ball to him and he would have to his it with the stick and still regain balance. Harder than what it sounds. Take all the muscles out of your abdomin and middle of your back down and just try to sit. That is where Nick is.
They always have to find things to challenge him with because he is so determined. When they ask him if he is ready to stop an activity he always tells them "a couple more times please".
They are removing his catheter tonight because he has developed a urinary track infection. Thank goodness he doesn't feel anything. I was able to alert the Drs about it because of the color of his urine.
I am learning so much. I have decided I should recieve my nursing degree just from experience. HAHAHA
Wednesday, September 8, 2010
September 8, 2010
Well today has been pretty uneventful. Nick has done the usual therapies. He has been doing laps around certain parts of the hospital so he can do some more racing. He loves that. That would be the competitive part of Nick.
They are having Nick drink more water so he can have his catheter removed. He is doing real well with that.
We are so greatful for all the love and support we have recieved from everyone. We love you all.
They are having Nick drink more water so he can have his catheter removed. He is doing real well with that.
We are so greatful for all the love and support we have recieved from everyone. We love you all.
Tuesday, September 7, 2010
September 7, 2010
Well we got right back into the busy routine. I guess our weekend is over. That is the way we progress.
Today in recreational therapy they made a obstacle course. Nicks therapist Isaac and Nick had races in the wheel chair. Nick won most of the races. Then they had to make is a little harder. At the end of the obstacle they had to pick up a frisbee and return to the start, do the frisbee again and then go and pick up a basketball and return to the start. That was a little harder because Nick needs both hands to maneuver his wheel chair. He sat there and did some trouble shooting, decided to loosen his gait belt and put it under his belt. The next time he was able to put the ball between his knees, but that is a trial also. But Nick being Nick, that didn't stop him.
Later this week we will be going to temple square. Nick just has to decide what he wants to do there. Decisions are not his strong suit, but he will figure it out.
Today in recreational therapy they made a obstacle course. Nicks therapist Isaac and Nick had races in the wheel chair. Nick won most of the races. Then they had to make is a little harder. At the end of the obstacle they had to pick up a frisbee and return to the start, do the frisbee again and then go and pick up a basketball and return to the start. That was a little harder because Nick needs both hands to maneuver his wheel chair. He sat there and did some trouble shooting, decided to loosen his gait belt and put it under his belt. The next time he was able to put the ball between his knees, but that is a trial also. But Nick being Nick, that didn't stop him.
Later this week we will be going to temple square. Nick just has to decide what he wants to do there. Decisions are not his strong suit, but he will figure it out.
Monday, September 6, 2010
September 6, 2010
Well, It is labor day. Today has been a little lax. Nick has had one p.t. and one o.t. They had games for all the patients outside, golf, horseshoes, volleyball with a beach ball. Then they had a barbeque for all of us. It was so yummy. Hamburgers, hot dogs, fresh fruit salad, chips, some other kind of salad, it looked a little strange, chocolate chip cookies and lemonade. It was so good to have a change of scenery.
One of Nicks nurses he had the other day really likes Nick and brought him in some homeade zucchini muffins. Haven't tried them yet, still too full from the barbeque.
Nick is counting down the days till he gets to go home. He is very excited to go home, but also a little nervous.
We took some pictures of Nick doing the games, so we thought we would share them.
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| Beach Volleyball, but we are not at the beach!!!!!! |
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| I'm suppose to do what??? |
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| Nick playing golf. He got a whole in one first shot |
This is what I think of you and that camera Alison!!!!!
This is what happens when Nick has an eventful day!!!!!
ZZZZZZZZZZZZZZZZZZ
ZZZZZZZZZZZZZZZZZZSunday, September 5, 2010
September 5, 2010
Well today is Sunday. Nick really looks forward to Sunday. There is no therapy at all. Time to catch up on his rest, and do absolutely nothing. We did get the opportunity to partake of the sacrament. What a blessing.
I think Nick is dealing with a little depression even though he won't admit it. Which would be really normal for what he has been through.
Doyle brought down some potatoes, a roast and the slow cooker. So I went to the trailer and made us a Sunday dinner. Roast, potatoes and gravy, watermelon and corn on the cob, plus I made a chocolate cake. Thank goodness for box cake. It seemed so good to sit down together and eat the same thing. Nick was so excited to have real food. He said my cooking ranked a 10. WOW!!!
Tomorrow will also be a slower day, where it is a holiday. We have heard there will be a barbeque. I guess we will just wait and see.
I think Nick is dealing with a little depression even though he won't admit it. Which would be really normal for what he has been through.
Doyle brought down some potatoes, a roast and the slow cooker. So I went to the trailer and made us a Sunday dinner. Roast, potatoes and gravy, watermelon and corn on the cob, plus I made a chocolate cake. Thank goodness for box cake. It seemed so good to sit down together and eat the same thing. Nick was so excited to have real food. He said my cooking ranked a 10. WOW!!!
Tomorrow will also be a slower day, where it is a holiday. We have heard there will be a barbeque. I guess we will just wait and see.
Saturday, September 4, 2010
September 4, 2010
Well today Nick has only had 2 sessions of therapy. He is okay with that because today he is really tired today. He is getting use to the schedule around here.
Nick has had some really good nurses. He has a few that are able to get him to laugh and smile. Which is good. He has a hard time with some of the nurses and aids and the way they try to transfer him from place to place. We have been taught one way and he is comfortable doing it that way and then someone comes and tries to do it another way. He has said he would just prefer me to assist in his transfers but some nurses and aids take the upper hand. GGGRRRRR!
Nick has had some really good nurses. He has a few that are able to get him to laugh and smile. Which is good. He has a hard time with some of the nurses and aids and the way they try to transfer him from place to place. We have been taught one way and he is comfortable doing it that way and then someone comes and tries to do it another way. He has said he would just prefer me to assist in his transfers but some nurses and aids take the upper hand. GGGRRRRR!
Friday, September 3, 2010
September 3, 2010
This has been another busy day. Lots of p.t. that really works him hard. By the time his last session of p.t. comes along, Nick is really tired and just kind of just goes thru the actions. Poor kid. But still doing really good.
Today he had a really big surprise. We were down in the gym doing the first session of p.t. and someone came behind me and hugged me, I looked around me thinking who knows me well enough down here to hug me. I turned around and there stood my mother and Doyle. We were so suprised, and Nick was so excited.
Then later in the morning his uncle Chris came to see him. What a full but fun day. We got permission to take him over to the Huntsman Cancer Institute. He really likes it over there. Anything but hospital food.
We are so greatful for all the love and support we are recieving from family and friends. Thank you everyone.
Today he had a really big surprise. We were down in the gym doing the first session of p.t. and someone came behind me and hugged me, I looked around me thinking who knows me well enough down here to hug me. I turned around and there stood my mother and Doyle. We were so suprised, and Nick was so excited.
Then later in the morning his uncle Chris came to see him. What a full but fun day. We got permission to take him over to the Huntsman Cancer Institute. He really likes it over there. Anything but hospital food.
We are so greatful for all the love and support we are recieving from family and friends. Thank you everyone.
Thursday, September 2, 2010
September 2, 2010
So Nick just told me that I can't forget to update his blog.
Today has been a crazy day. All we have done today is go go go.
We started with occupational therapy at 9 then had p.t. then recreational therapy then occupational again. This was all before 12. Then he had lunch then we had p.t. again then our educational class then at 4 we have another p.t. At 5 he will have dinner. It has been a very exhausting day, and Nick is really feeling it. He is very tired and his shoulder blades really hurt tonight.
Nick hasn't had any pain meds for 4 days now, besides tylenol. That is so great. He doesn't feel like he always needs to sleep now.
The nurses are really worried about his nutrition. He really doesn't like the hospital food and so he doesn't always eat very much. We try to bring things in for him to eat, sometimes he will eat them and sometimes he won't. Unless it is watermelon, then he will tons of it. One of the guys in the cafeteria found out that Nick likes Dr. Pepper so he will sent one up to Nick every once in a while. I told him I don't mind if he does that as long as he brings me the mint truffle that they usually send with his lunch and dinner. They are really good.
The people have been so good to us here at the hospital. It has really helped alot.
Today has been a crazy day. All we have done today is go go go.
We started with occupational therapy at 9 then had p.t. then recreational therapy then occupational again. This was all before 12. Then he had lunch then we had p.t. again then our educational class then at 4 we have another p.t. At 5 he will have dinner. It has been a very exhausting day, and Nick is really feeling it. He is very tired and his shoulder blades really hurt tonight.
Nick hasn't had any pain meds for 4 days now, besides tylenol. That is so great. He doesn't feel like he always needs to sleep now.
The nurses are really worried about his nutrition. He really doesn't like the hospital food and so he doesn't always eat very much. We try to bring things in for him to eat, sometimes he will eat them and sometimes he won't. Unless it is watermelon, then he will tons of it. One of the guys in the cafeteria found out that Nick likes Dr. Pepper so he will sent one up to Nick every once in a while. I told him I don't mind if he does that as long as he brings me the mint truffle that they usually send with his lunch and dinner. They are really good.
The people have been so good to us here at the hospital. It has really helped alot.
Wednesday, September 1, 2010
September 1, 2010
I came in today and Nick was still trying to sleep. That didn't last long. He seemed to sleep a little bit better last night. They gave him an ambien. We got him up and he was able to dress himself almost by himself. He then was able to shave and brush his teeth. Shaving entails me holding his head perfectly still because he has to take his c-collar off. Hopefully he will be able to get rid of the neck collar next week.
He then started all of his therapy sessions. That really keeps us very busy. He started therapy at 9 and went till 12. He had lunch and then another p.t. at 1.
In p.t. this afternoon he was measured for his own wheelchair. It is quite the process. After they do all the measuring, his therapist has to write a letter to the insurance company. It will be a long process. He will probably come home with a loaner chair at first, until his comes.
After his therapy sessions we have a class on spinal cord injuries. That includes a little knowledge of the spinal column, nutrition, bowel and bladder control, plus so much more. Nick gets really board in these classes.
Yesterday Nick learned to transfer from his bed to his wheel chair without a transfer board. He also had an outing. We got to go over to the Huntsman Cancer Institute, where they have a restaurant. AAAHHH real food for him. He really does not like the hospital food. Next week they are trying for another outing. He wants to go to temple square, so they are working on that one. The doctor has to write an order for it, so we shall see.
Nick has seemed to be a little down today. He is also a bit tired also.
He then started all of his therapy sessions. That really keeps us very busy. He started therapy at 9 and went till 12. He had lunch and then another p.t. at 1.
In p.t. this afternoon he was measured for his own wheelchair. It is quite the process. After they do all the measuring, his therapist has to write a letter to the insurance company. It will be a long process. He will probably come home with a loaner chair at first, until his comes.
After his therapy sessions we have a class on spinal cord injuries. That includes a little knowledge of the spinal column, nutrition, bowel and bladder control, plus so much more. Nick gets really board in these classes.
Yesterday Nick learned to transfer from his bed to his wheel chair without a transfer board. He also had an outing. We got to go over to the Huntsman Cancer Institute, where they have a restaurant. AAAHHH real food for him. He really does not like the hospital food. Next week they are trying for another outing. He wants to go to temple square, so they are working on that one. The doctor has to write an order for it, so we shall see.
Nick has seemed to be a little down today. He is also a bit tired also.
Monday, August 30, 2010
August 30,2010
Well since I have been slacking on the weekend with the blog I guess I'd better get with it.
Not much happens here on the weekends. We did get the opportunity to partake of the sacrament on Sunday. That is a real blessing in our lives.
Today Nick had 3 therapy sessions. In his occupational therapy he learned how to go in and out of doors by opening the door by himself. Almost every door he would come up to people would want to open the doors for him. We would tell them he was in training and they would say, thats ok we still want to open the door for him. People are so helpful.
In his p.t. he is learning all different kinds of balancing. He is getting to strong. He is so determined.
In recreational therapy he worked on a model car. They know what he likes.
While Nick was at therapy Alison and I went and did laundry. I am so thankful to have a washer and dryer in my home. Going to a laundry mat is a pain, but you do what you have to do.
It rained most of the night here, and when we woke up it was pretty chilly.
Yesterday Nick had company. His aunt Carlene and Uncle Blair came to see him and bring us their trailer for us to stay in. THANK YOU SO MUCH!!!! It really is helpful and appreciated. Love ya.
Not much happens here on the weekends. We did get the opportunity to partake of the sacrament on Sunday. That is a real blessing in our lives.
Today Nick had 3 therapy sessions. In his occupational therapy he learned how to go in and out of doors by opening the door by himself. Almost every door he would come up to people would want to open the doors for him. We would tell them he was in training and they would say, thats ok we still want to open the door for him. People are so helpful.
In his p.t. he is learning all different kinds of balancing. He is getting to strong. He is so determined.
In recreational therapy he worked on a model car. They know what he likes.
While Nick was at therapy Alison and I went and did laundry. I am so thankful to have a washer and dryer in my home. Going to a laundry mat is a pain, but you do what you have to do.
It rained most of the night here, and when we woke up it was pretty chilly.
Yesterday Nick had company. His aunt Carlene and Uncle Blair came to see him and bring us their trailer for us to stay in. THANK YOU SO MUCH!!!! It really is helpful and appreciated. Love ya.
Friday, August 27, 2010
August 27, 2010
Today we had a family meeting with all the staff that is helping Nick. We talked about his rehab progress and what he can expect when he is finished with rehab. His expected date to be coming home is October 4th. His recreational therapist has figured out Nick's love of trains and fishing. At some point they want to take him out to go fishing. They said that we could probably take him to temple square also. We discussed some of the items he will need when we get home.
He is still impressing everyone. Dad got to come and see Nick with how much he has improved. We are all so proud of Nick and his progression. They had Nick start doing weight lifting with his upper body to build more muscle strength. His second session of P.T. they was teaching how to to pop wheelies in his wheel chair. I asked them if that was safe. They chuckled at me. The purpose in this is so if his wheel chair tips backwards he would know how to prevent himself of tipping over. He was able to meet a couple of guys who have been in hand bike marathons and learn about there accidents. It has really been helpful for Nick to talk to them.
When he is all done we will have to learn how to jog to keep up with speedy Nick!!! He gets around in his wheel chair so well.
Today Matt and Lindsey Williams stop by to see Nick and also my cousin Shirley and Bill Johns. It is so great to have such great people in our lives to support us. Thank You everyone.
He is still impressing everyone. Dad got to come and see Nick with how much he has improved. We are all so proud of Nick and his progression. They had Nick start doing weight lifting with his upper body to build more muscle strength. His second session of P.T. they was teaching how to to pop wheelies in his wheel chair. I asked them if that was safe. They chuckled at me. The purpose in this is so if his wheel chair tips backwards he would know how to prevent himself of tipping over. He was able to meet a couple of guys who have been in hand bike marathons and learn about there accidents. It has really been helpful for Nick to talk to them.
When he is all done we will have to learn how to jog to keep up with speedy Nick!!! He gets around in his wheel chair so well.
Today Matt and Lindsey Williams stop by to see Nick and also my cousin Shirley and Bill Johns. It is so great to have such great people in our lives to support us. Thank You everyone.
Thursday, August 26, 2010
August 26, 2010
Nick is known as Nick the superstar in the hospital. Nick has done so well today. He got up and dressed with help from occupational therapy. He shaved today and he feels so much better. Physical therapy went really well today. After his first physical therapy session he decided he wanted to go outside and we played two rounds of skipbo. We got back to his room just in time to put things away and then for him to head back down for his second physical therapy session. He is doing alot better with drinking his water with help from his nurse and mom nagging at him. The nurse got him to laugh today. He is smiling alot more everyday.
Uncle Blake stopped in today to see him and brought him some chocolate and a magazine, Popular Mechanics to read and look at. He stayed and visited with us and teased us all. It really boosts his spirit when family comes and sees him.
Uncle Blake stopped in today to see him and brought him some chocolate and a magazine, Popular Mechanics to read and look at. He stayed and visited with us and teased us all. It really boosts his spirit when family comes and sees him.
Wednesday, August 25, 2010
August 25, 2010
Nick has done so well today!!! Nick got a better wheelchair today. It makes it easier for him to wheel himself around. He is getting better and better to get himself out of bed to his wheelchair. His physical therapist got him up twice today. He went outside and learned how to manuver on cement. His occupational therapist got him up and took him to therapy and played some wii today. He gets pretty worn out by the end of the day, but he is doing so well.
The social worker from this floor brought him gloves and hydro pack for him to use when he is in his therapy in his wheelchair. The hydro pack hangs right on his wheelchair.
The social worker from this floor brought him gloves and hydro pack for him to use when he is in his therapy in his wheelchair. The hydro pack hangs right on his wheelchair.
Tuesday, August 24, 2010
August 24, 2010
Nick has had a very busy day today!! He did some occupational therapy and physical therapy today. The physical therapy got Nick up in a wheelchair and did some balance work on him. He now has to work on keeping his body balanced and getting his body used to being balanced. He is starting to move himself a little better everyday. He had a pic line in and it was removed today. That is one more cord remove from his body and one more step closer to being able to come home to his family and daily living. Here is a picture of his back and him in real close. They put Nick back on the cough assist, so they can get all the fluids running thru him. He is doing good today.
The Ronnow's came and visited Nick today and he loved the company. Grandma and Grandpa Heiner came and saw him today, and brought him some goodies to eat. Nick has smiled alot today with all the visitors.
The Ronnow's came and visited Nick today and he loved the company. Grandma and Grandpa Heiner came and saw him today, and brought him some goodies to eat. Nick has smiled alot today with all the visitors.
Monday, August 23, 2010
August 23, 2010
Nick has graduated from orthopedic floor to the rehabilitation floor. He was moved down to the rehab floor at 3pm today. He is all set up and is doing really well today. He starts hospital boot camp first thing tomorrow morning. They have a family room for the families to be in when he is in therapy, we can warm up our food in there. We can get ice in the family room too!! They have a padio just for the rehab patients to have a picnic or bbq with their family. He is still not keen with the hospital food, but I don't blame him.
Nick's incision from his back is looking really good. They took to bandages off and they said they won't need to go back on. They rebandaged the spot where the chest tube was and it is looking really good.
Nick's incision from his back is looking really good. They took to bandages off and they said they won't need to go back on. They rebandaged the spot where the chest tube was and it is looking really good.
Sunday, August 22, 2010
August 22, 2010 (Evening)
This morning the physical therapy got Nick up out of bed and in a wheelchair. Today was the first time he has been out of bed since he's been here. He did really well for being the first time. Nick got a little dizzy when he was up, but he handled it really well. He moved himself over to the wheelchair really well for the first time. They taught him how to wheel himself around the hospital floor and how to turn around corners. He is going to get really good at wheeling himself around by himself.
They released him from Respitory Therapy today. He will still need to use his coughing machine but the respirtory therapy staff won't be coming to his room and make him use his coughing machine in front of them. We just need to get him to laugh, that will be tricky.
Nick will be moving to the rehab floor tomorrow morning and then it will be hospital boot camp. He will do well and probably suprise us all on his improvements.
They released him from Respitory Therapy today. He will still need to use his coughing machine but the respirtory therapy staff won't be coming to his room and make him use his coughing machine in front of them. We just need to get him to laugh, that will be tricky.
Nick will be moving to the rehab floor tomorrow morning and then it will be hospital boot camp. He will do well and probably suprise us all on his improvements.
Nick's uncle Kevin and aunt Trina came and visited him today. They came from Blackfoot. Kevin brought him Grandma Heiner's applesauce and saurkraut. Kevin also brought him a binder with paper and some pictures. They also ran to the gift shop and got Nick his m&ms, so he got his chocolate fix for a while. Kevin almost got Nick laughing today with his jokes.
August 22, 2010
Yesterday was quit the eventful day. Nick has had a lot of company today. Alison brought all of Nick's sisters to see him along with Grandma Smith. After they were here for about 1/2 hour Bp. Campbell and the priest quorum came to see him. He was very suprised. They brought him lots of different gifts. This will give him some things to do while he is down here. Not that he will be board with all the different therapies, especially physical therapy.
We were able to bring him in some pizza, which he really enjoyed. He says it is so much better than hospital food. Which I will have to agree with.
He sat up yesterday about 10-12 times. He is so determined. He was also able to have his chest tube removed. YEAH!!!
We were able to bring him in some pizza, which he really enjoyed. He says it is so much better than hospital food. Which I will have to agree with.
He sat up yesterday about 10-12 times. He is so determined. He was also able to have his chest tube removed. YEAH!!!
Friday, August 20, 2010
August 20, 2010
Well Nick still has his chest tube, he is still putting out to much fluid into his chest cavity. He will probably have it thru the weekend. They will have to evaluate it each day. He has a x-ray every day, that helps to see what is going on in his chest and lungs. Each day he gets stronger and stronger.
He has physical therapy 2 times a day at this point. They put his bed in a chair position, with his feet touching the floor. Then the therapist and either Doyle or myself assist him to sit straight up with back away from bed. He has to help by grabbing ahold of his bed rails and pull himself forward.
This morning when p.t. came in they got him all situated, he grabbed ahold of the bed rails and pulled himself up by himself. That is a great accomplishment. His therapist said wait, wait for me. We were all so suprised.
Like I have always said, Nick one tough kid.We are so proud of him.
Nick does not like hospital food. He says it is not his mothers cooking. I guess I am good for something. The food here is to dry and bland.
They told us today that we can bring any of his favorite foods in that he would like. He was very excited.
We have lots of Dr's and therapist that come in lots, just when he thinks he might get some rest someone comes in. They have taken all the IV's out of his arms, all the monitors off, so it is easier to move him around. They have to come in every couple of hours and turn him so he doesn't get bed sores.
We really appreciate everything everyone is doing at home for us. Prayers we feel them bouncing off the ceiling. Plus everything else.
He has physical therapy 2 times a day at this point. They put his bed in a chair position, with his feet touching the floor. Then the therapist and either Doyle or myself assist him to sit straight up with back away from bed. He has to help by grabbing ahold of his bed rails and pull himself forward.
This morning when p.t. came in they got him all situated, he grabbed ahold of the bed rails and pulled himself up by himself. That is a great accomplishment. His therapist said wait, wait for me. We were all so suprised.
Like I have always said, Nick one tough kid.We are so proud of him.
Nick does not like hospital food. He says it is not his mothers cooking. I guess I am good for something. The food here is to dry and bland.
They told us today that we can bring any of his favorite foods in that he would like. He was very excited.
We have lots of Dr's and therapist that come in lots, just when he thinks he might get some rest someone comes in. They have taken all the IV's out of his arms, all the monitors off, so it is easier to move him around. They have to come in every couple of hours and turn him so he doesn't get bed sores.
We really appreciate everything everyone is doing at home for us. Prayers we feel them bouncing off the ceiling. Plus everything else.
Thursday, August 19, 2010
August 19, 2010
Nick is in a little bit more pain today, But still doing good. First thing this morning around 9:00 physical therapy came to work on him. That is very difficult, and painful. They have him just sitting up and using his arm muscles.They have to support his legs so he doesn't slide out of the bed. It is so hard to watch, but he is a tough kid.
Just when he thought he was going to be able to rest the respitory therapist came in to work on his coughing. They have to use a cough assist machine on him that forces him to cough. We have to keep those lungs a moving so he doesn't end up with pnemonia.
He will be getting the chest tube removed today. YEAH!
The room he is in has a big window so he is able to get lots of sunshine. It also looks out over the Salt Lake Valley, and over Primary Childrens Hospital. So I guess Doyle and I are enjoying the view more than Nick is.
We are so greatful for everything everyone is doing at home. We love you all. Thank you.
Just when he thought he was going to be able to rest the respitory therapist came in to work on his coughing. They have to use a cough assist machine on him that forces him to cough. We have to keep those lungs a moving so he doesn't end up with pnemonia.
He will be getting the chest tube removed today. YEAH!
The room he is in has a big window so he is able to get lots of sunshine. It also looks out over the Salt Lake Valley, and over Primary Childrens Hospital. So I guess Doyle and I are enjoying the view more than Nick is.
We are so greatful for everything everyone is doing at home. We love you all. Thank you.
Wednesday, August 18, 2010
August 18, 2010
Nick Heiner was 4 wheeling on August 14 with elders quorum. He was in an accident, he went over the handle bars of the 4 wheeler and broke his back. He was air lifted to EIRMC. They did a CT scan from the top of his head to the bottom of his pelvis. Things were bad. The Dr. came in and told us he would be a parapalegic for the rest of his life. That was a hard pill to swallow.
The Dr. came in and told us he would need to be air lifted to University of Utah Hospital. Wow Nick's first airplane ride and couldn't even look out the windows. He said it was weird.
We got here to Uof U and they immediately took him in for a MRI of his back, then took him to surgery. He was in surgery for 5 hrs. After surgery he was sent to ICU and has been there for 4 days. Yesterday on 08/17/2010 he had to have a chest tube interted into his chest cavity to drain fluid out of his lungs. They drew out 770 cc's of blood out of his lungs and chest. It was old blood from the injury. He is now breathing lots better.
Today 08/18/2010 he was moved moved out of ICU to the 6th floor. He got the largest room in the whole hospital. It is nice.
He will be here in the hospital for atleast one month.
The Dr. came in and told us he would need to be air lifted to University of Utah Hospital. Wow Nick's first airplane ride and couldn't even look out the windows. He said it was weird.
We got here to Uof U and they immediately took him in for a MRI of his back, then took him to surgery. He was in surgery for 5 hrs. After surgery he was sent to ICU and has been there for 4 days. Yesterday on 08/17/2010 he had to have a chest tube interted into his chest cavity to drain fluid out of his lungs. They drew out 770 cc's of blood out of his lungs and chest. It was old blood from the injury. He is now breathing lots better.
Today 08/18/2010 he was moved moved out of ICU to the 6th floor. He got the largest room in the whole hospital. It is nice.
He will be here in the hospital for atleast one month.
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