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Archive for July, 2002

Karlton communicates

Karlton was able to write to us last night. He indicated that he wanted to write, and the RN picked up on that. She put a blank sheet of paper on a clipboard and gave him a felt-tip marker. He was lying down with his head raised, so it must have been awkward writing in the air. We had to adjust positions so that he could see with his left eye what he was writing with his right hand. The RN asked him, “What’s your name?” and he wrote, “Karlton”. Then she asked, “Do you know where you are?” and he wrote “USA.”

Later he tried writing again. His sentence stated with a T and had “you” in it, but we just couldn’t make it out. He became frustrated and gave the pen a toss.

This morning we arrived after the night shift had left, so we missed out on stories of communication attempts. Yet we saw papers by the side of the bed that had

– 2002 Queenstown
– 1982 Dunedin
– 1996 Christchurch

written on them in someone else’s hand, one sheet for each list. So it looked as if someone had been trying to communicate with him.

Besides the excitement of knowing that he’s able to express a few ideas is the knowledge that he can see fairly clearly out of his left eye. That’s such a relief. The swelling in his face has gone down markedly. We noticed it already yesterday, and it’s even better today (Sunday). The purple in the eyelids too is receding. He looks so much better now.

Yesterday (Saturday) he spent most of the day back in the Intensive Care Unit. We feel very comfortable with the staff there, so we were almost glad for his return. They take such good care of him there. A second set of X-rays that day showed marked improvements in his left lung. The doctor told us that they’d gotten a lot of phlegm out of his left lung with their suctioning.

He was so alert and cooperative while in the ICU that his nurse freed his right hand. Ever since he came out of the drug-induced coma his first three fingers of the right hand have been tethered with long strips of tape. Each strip was folded back upon itself so no adhesive was exposed except where it covered a finger. The three strips were then tied to the bed rail so he couldn’t pull at his tubes and wires. But last night he was given more freedom to explore those tubes and wires, and he didn’t pull them out. So the RN cut off the tape and freed his fingers. I think he was really pleased to have his mobility back again. He gave us a thumbs up sign.

Karlton moved back to the High Dependency Unit (HDU) about 6:30p. It was while he was there and his hand was untethered that he wrote to us.

This morning when we returned to his room, his hand was tethered by the wrist to the bed rail. He’d managed to take the TEDS (tight stockings to prevent blood clots) off his right leg. So that’s probably why he had to go back to being restrained.

He’s breathing really well. The surgeon in charge of his case decided to lower his oxygen level. So he continues to make really good progress.

Yesterday we read to him messages that people have sent to the website. Besides messages from individuals, he had a number from OMBAC, the rugby team he played on in San Diego.

That’s it for today. Mom’s here at the library with me today so that she can answer her emails and she can see the website that Jason constructed. Hope you have a great day!

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A phone call

I called the hospital last night, and while I was talking to my dad, he said that Karlton was trying to write something. My mom later told me that the nurse had asked him what his name was, and he had written “Karlton.” She then asked if he knew where he was, and he wrote “USA.” Well, he can’t get *all* the answers right immediately, but I find it really impressive that he is able to write.

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Conference calling

Alexa and I just got off the phone with Mom, and she had more encouraging news. Karlton has been moved out of the ICU and into the “High Dependency Unit,” which is a level down in terms of seriousness.

He is continuing to breathe on his own. He spends a lot of time sleeping, which anyone who ever lived with him will know. Because of the tracheotomy (which will be reversed when he recovers more) he no longer keeps the whole building rattling with his snores.

The nurses and my parents make sure to hold the phone up to his ear when we call. We have been doing a little “conference calling,” with Alexa and me, and sometimes Alec, on the phone all at once. Alec updated him on the Red Sox last night.

He will need some surgery to fix the bones around his right eye; that will probably happen some time next week. The swelling around his eye continues to improve.

Today some friends from Queenstown drove over 3 hours each way to come see him. We are so impressed with all of his friends!

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Good news! Karlton “graduated” out of the ICU yesterday. His breathing stabilized enough for him to go to the High Dependency Unit (HDU). They moved him about 2:00p in the afternoon.

Yesterday morning, while I was emailing updates, Choy (his mom) and the nurse washed his hair. The staff have been great about shaving him too. He looked really spiffy.

We’ve made friends with another couple whose 40+ year old son is also in the unit . . . for the 2nd time! 20 years ago he was in an accident and fully recovered. But recently he was mugged, and he’s back again. The point of telling you this is that we compare notes from time to time about our sons’ progress. They said that from across the room in ICU they can detect Karlton’s nodding his head as we speak to him. That’s really encouraging!

After the move yesterday afternoon, three friends from Queenstown stopped in and stayed quite a while. Later, Sam, a Dunedin friend, came too. Two of the friends from Queenstown were going to stay at his place for the night. He’d been out shopping for blankets at a thrift shop. When he mentioned that he needed the blankets because of his friend’s snowboarding accident, the people in the shop insisted that he take the blankets without paying for them. They wanted to give him some money too. People over here are so good!

Talked to the people in charge of Karlton’s health insurance. They will pay for our lodging. They will also pay for a round-trip ticket for one of us. Thank goodness he subscribed to a generous health plan!

Things have been a wee bit less comforting this morning. Karlton seemed to have rested well over the night, but he got into breathing distress about 8:00a. Fluid had accumulated in his left lung. Though the nursing staff suction his trach and get him to cough at intervals, they’re less able to clear the left side, and he has less control there too. The machines indicated that he was getting lower percentages of oxygen, and his heart rate kept climbing. The final decision was to return him to ICU for the morning. The nurses assured us that we didn’t have to move all of his things because he’d be returning to HDU in the afternoon. We certainly hope so.

He’s made so many giant strides forward that we shouldn’t be discouraged by a baby step backwards. We’re convinced that he’s in great hands here. We’ll just have to hold on tight. Your continued prayers, positive thoughts, and best wishes are always appreciated. We have also been getting many messages forwarded from the website and promise to read them all to him.

The ICU freely let us use a CD player. The HDU, on the other hand, doesn’t have one. So we plan to buy him a Discman today so that once he returns to HDU he can continue listening to his music.

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Email

My apologies to anyone who tried to use the messages link on the Contact page. It was broken, but has been fixed. Again, if you have messages that you would like to be relayed to Karlton and the rest of the Bontrager family, please use: messages@manifoldreality.org.

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Karlton did really well yesterday sitting up in the Lay-Z-Boy recliner. The changed posture and the new requirements to support his breath exhausted him. He did a lot of sleeping. He was also successful with the new ventilator. The doctors are encouraged, and we’ve been told repeatedly that he’s likely to be moving to another ward where he’ll be more independent.

In the meantime, the hospital is gearing up today for its annual mock crisis. We’re told that the police and fire brigades will have the hospital cordoned off, and no one will get in–not even hospital administrators or high fallutin doctors–without a valid hospital ID. We’ll grab a bite to eat before noon, when it all starts, and then hunker down to see what happens. It’ll be interesting to see how they balance intensive care for the actual patients with readiness exercises with mock ones.

The woman who was snowboarding with Karlton on Friday stopped by yesterday. It was so good to talk with her and learn more details of the accident. According to her, the snow conditions were good, they stayed on intermediate-level trails, and he was not taking any undue risks. She snowboards with a helmet, and he’d been asking about it, apparently considering the possibility of buying one for himself. She works on the slopes, and he’d often catch up with her over her lunch break. They’d do a couple of runs together until she had to go back to work.

Friday was her day off, and they’d been snowboarding together all day, having done about 8 runs. It was their last run for the day. Toward the bottom of the run, she would always ski toward the right and he toward the left, their vision of each other blocked by some rocks. But they’d meet at the bottom to catch the lift up again together. This time his friend was in the lead and so she wasn’t able to see Karlton as they came down the hill. When she got to the bottom and he didn’t join her, she assumed that he’d stopped to help somebody out.

Somebody from the ski resort asked her to help do the final sweep for the day, ensuring that everybody was down from the mountain. So she got to go up one more time. She rode the life with someone from the ski patrol, and she noticed that he got a call just as they got off the lift. She found out later that the call was about Karlton. But she’d already begun the final sweep.

Towards the bottom, she noticed a collection of people from the Ski Patrol. She caught up with them and saw it was Karlton who had been hurt. That was really surprising to her, she said. Even though he was a rank beginner this year, he had worked really hard at learning to snowboard well. She’s much more experienced than he, but he would often give her tips about improving her form. She thinks it was just a random accident. . . a rock in the wrong place at the wrong time. For us as parents, it was a relief to learn these details and know that Karlton had been taking adequate safety precautions.

The Ski Patrol must have assumed that Karlton was Japanese. They called in a Japanese interpreter for him. His friend told the Ski Patrol that he was American, but in all the confusion, somehow the word didn’t get to the interpreter. That poor person stayed around for the longest time hoping to be helpful.

This morning Karlton got a beautiful bouquet from Heather, his housemate at Hamilton. It had orchids, Dutch iris, and many more beautiful flowers. Ethan, from the rubgy team at Hamilton, sent flowers yesterday. The florist sent up a card, saying we could”cash it in” for real flowers whenever Karlton was ready. The same happened with the bouquet sent from Zentropy (Jennifer’s work).

Hope all is well with you. We’re doing well. It’s always a delight to hear from everyone.

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Tracheostomy

Yesterday afternoon KS had the tracheostomy (Kiwi for tracheotomy, I guess). Before, he had the ventilator tube down his mouth. It had to be tied onto his head, and they tied it so tightly that he looked really uncomfortable, with his lips sqeezed b/w the ties. Also, he’d yawn and use his tongue to try to push the mouthpiece out. But now he doesn’t have to do that. His face looks more relaxed w/out any tubes in it.

The plan is to move him to another unit, one with slightly less intensive care. It’s a neurosugical unit with a dependency ward. That means that instead of a 1:1 RN to patient unit, he’ll be in a 1:3 setting. He’ll still be heavily monitored, but they don’t want to have him on any kind of ventilator. The major obstacle at the moment is his breathing. He is breathing on his own, but he’s not fully inflating (or is it deflating?) the alveoli with each breath. This morning the RN put him on a different ventilor for 30 mins. to encourage him to fill and empty his lungs completely. He did well at that, and later she’ll put him on it again for 60 mins. and then keep increasing the time according to his success.

She also plans to sit him up in a Lay-Z-Boy recliner today. That will encourage his diaphragm to support his breathing more.

He continues to be active in the bed. The RN reported that his sheets were in good order when she arrived at 7:00a, but by 7:20 when we arrived, they were pulled out again. He’s taken to using his right hand to grab the railing on the left side and pull himself over on the left. In fact, Mom started massaging his back, and he did just that to give her more space to work with. He also uses his fingers to play with us, catching our fingers in his or tapping us on the hand. Such activities are alternated with periods of sleep.

Maree, the RN today, said that he tried to move his left leg a bit last night. Wow!

His gang of friends stopped by again last evening. They are such really nice people with lots of good energy. They really keep us going.

When we got back to the hotel room last night, there was a beautiful bouquet of flowers from Bunac, the group that sponsored Karlton’s stay in NZ. Another article appeared in yesterday’s newspaper. Unfortunately, we didn’t bring it with us to the University to send it along to you. They’ve got all the facts right, now, so we feel less urgency to respond to the media’s request for interviews.

We sneaked over to the University while the crew was X-raying KS. They should be done by now, so we’ll head back. Thanks again for being so wonderful.

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Making some progress

It sounds as if Karlton is making progress each day.

I called the hospital last night, and my mother seems to think that Karlton is able to see, at least to some degree, through his left eye. She said that as he was sitting in his chair, she was doing something else nearby (not touching him), and he kicked her to get her attention.

Also yesterday, Jennifer called the hospital while my parents were out, but was able to talk to Karlton a bit. The nurse told her that his eyelids were fluttering as he listened to her on the phone. Later, my mother returned and asked him if Jenn had called; he nodded his head a little. Mom claims that while I was talking to him, his heart rate slowed a bit and that he was moving his mouth as if to try to answer me.

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Lots going on

We’re so excited. So many good things have happened. Last night when I returned from emailing at the university, a Chinese energy healer was there. Mom seemed to be comfortable with his work, and we could see marked changes in KS’s behavior. KS had been so restless before, reaching out with his right leg as if trying to explore the space around him, but sometimes nearly kicking anyone who was nearby. After the energy session, he settled into peaceful rest.

Again, people have been so wonderful. One of his friends stopped by yesterday morning about 7:15a on her way to work. As we were leaving the hospital at 9:00p, we ran into another friend on her way in to visit him. She’d been working all day and stopped by on her way home. Another friend brought in bags of pastries from the supermarket where she works. That covered what we needed to eat last night with enough for this morning and still more left over! Rest assured that we are in loving hands.

All of KS’s movements so far have been with his right arm and leg. That’s because the damage is to the right side of his brain. The only thing he was able to do on his left side yesterday was open his eye occasionally. This morning, however, we detected a small movement with his left arm. When asked to repeat it, however, he moved his right instead. It looks as if he’s having to use a different part of his brain to do the tasks he used to with his left.

He’s scheduled for a tracheostomy this morning. That is, they’re going to open an airway in his throat so he won’t have to have the air tube in his mouth. The fear in removing the airway is that his tongue will fall back and block his throat. The trachostomy will allow air to flow even if that should happen. It sounds scarey, but hospital staff assure is that it’s standard procedure and can be reversed when he’s healthier.

The press keeps trying to get an interview with us. Haven’t quite decided how we’ll handle that. Want to bring that up with the hospital social worker.

One of Karlton’s friends went back to Queenstown to start a campaign encouraging people to wear helmets when they snowboard. Great idea, huh?

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Information

This website has been established to help better distribute information about Karlton Bontrager and his condition as he recovers from his snowboarding accident in New Zealand.

Below is an archive of some of the email traffic that has gone out over the past weekend regarding Karlton and his status. Look to this page and this site for more information as it becomes available.

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