Trepidation, anxiety and excitement. That's what fills our thoughts tonight as we go to bed. Tomorrow (Tuesday) morning we have an appointment to see Kevin's pulmonologist when she is supposed to remove his trach. Tonight he went to bed with it and tomorrow he will not have it barring any unforeseen circumstances.
I supposed these are the kind of thoughts that anyone has whenever something you have waited for has finally come. In fact, I remember the feeling distinctly as we found out each time that things were in order for us to leave to Italy. I remember the very first time it took one year and ten months for us to raise enoug monthly support and get our legal permission in order to leave for Italy. I remember having mixed emotions of being excited for the next leg of the journey, but wondering if we were really ready for it. God was always there even if we felt unprepared. We were heading into the unknown with nothing more than faith that God would do what he had said in his word he would do.
Kevin has had his trach for exactly one year and nine months and three days. We have had to learn how to take care of his trach, knowing when to use the suction catheters and when not to, how to clean the inner canula (twice daily) and care for his skin around it all. We have become experts in something in which we didn't care to know. And now it's changing.
We are excited for sure though. Cautiously excited. Having the trach out means we hear more of his natural sounds. The past several days that Kevin has been capped we have heard his natural clearing of his throat more, snoring at night and other sounds that we don't normally hear coming from him. How will this change future speech therapy? There will be more focus on swallowing. He may be able to produce sounds easier or new ones altogether. At some point, we may starting feeding him by mouth. He may have less chance of feeling gagged, less sucretions, less potential for sickness.
All that doesn't take away the hurdles he faces. But we’ve been here before. Standing in the face of the unknown. Tomorrow I hope to write that everyting went great. The procedure painless and smooth. But we don't know what tomorrow looks like. It's unknown. What we do know is that God will be there for us tomorrow, like he has been for every step of our lives. He is greater than any temporary momentary troubles we face on this earth and there is a much larger message that needs to get out to the world.
Thanks for indulging me as I work through my thoughts before heading to bed. He's sleeping now, but I'll give Kevin a kiss on the forehead for you.
Thanks for reading and praying,
Matt, Angie and family
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
Tuesday, June 7, 2011
Friday, June 3, 2011
Update #138 on Kevin - Trach Coming Out!
Okay, I last posted a note on February 19, 2011. I have had more smaller updates on Twitter since then, mainly because their shorter and easier to get out. We had a few things go on since Kevin came home from the hospital on February 18. Here's the short version...
...two days after returning home we had a circuit breaker fire that displaced us for three weeks. Greg gladly opened up his home to the five of us (Matt, Angie, Jacob, Kohl and Kevin!) plus nurses round the clock. The house had to be restored due to smoke and odor damage.
...I had bronchitis and shingles for a few weeks; meanwhile Kevin never seemed to get over whatever he had that took him to the hospital.
...came back home for two weeks and Kevin got bad again. It wasn't as bad as when we took him to the hospital in February, but bad enough to go again. So we took him once more to St. John's ER. They admitted him for a week. They were never fully sure what was going on, maybe pneumonia, but weren't sure. Brought him home on April Fools' Day.
...April was a great month for Kevin at therapy. He was more alert and doing things he hadn't done since December. But the previous few months hadn't been good due to sickness so his charts looked bad. You can really chart that the reason he's not doing good was due to sickness. So the outpatient therapy we were taking him to had to discharge for now.
...May 2, Kevin seemed to be showing similar signs to when we took him to him to the ER, so we headed that way. They ended up treating him in the ER that day and sending us home with meds for bronchitis. That seemed to do the trick.
...In the May, Kevin had an eye infection, but with some antibiotics it's already cleared up.
...Since around the middle of February, we have had approval for twenty-four around the clock nursing. However, we haven't but maybe one week where we had that fully staffed. There have been many different reasons why, some were nurses getting sick or in car wrecks. But suffice it to say, we still need competent and dependably committed nurses to fill shifts. It means constant training and reworking of our schedules. Most of the empty shifts fall to Angie, which is incredibly hard at times.
...of course during all this, we have continued therapy at home. Now that the weather is nice we can take Kevin outside on the deck which was graciously built by United Way volunteers and some of Kevin's friends. It and the other developments they made have been a great benefit going into the outdoor season.
...Kevin's trach has been being capped throughout the day. On our last visit with the pulmonologist (lung doctor) she wanted us to be more aggressive with capping him throughout the day. We had slowly been working him back up to where he was before he started getting sick around the beginning of the year. She said let's aggressively add time each day that he does well. Because she believed he could do it, and so did we.
...This week we have been adding more and more time every day working toward a full twenty-four hour period of capping. His pulmonologist said if he got to twenty-four hours then we could take the trach out. He just did that! In fact, he has had it on for more than twenty-four hours now and still doing great. This morning Angie heard him naturally snoring, because his airway is totally through his nose and mouth when capped.
...We called the doctor and left a message. She called back soon and said let's take the trach out! We can either do it with a nurse or bring him in on Monday. We are discussing it and determining which way is best. Either way, his trach is coming out!
...We'll note something, for sure on twitter, when it comes out. You can read the tweets at http://twitter.com/pray4kevin.
...Remember you can fill out a letter online and send it to Kevin at http://bit.ly/note2kevin. It will be printed off and read to Kevin.
Thanks for your thoughts and prayers. This is a big step for Kevin's recovery. We give God all the glory for getting Kevin to this point.
Thanks for praying and reading,
Matt, Angie and family
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
...two days after returning home we had a circuit breaker fire that displaced us for three weeks. Greg gladly opened up his home to the five of us (Matt, Angie, Jacob, Kohl and Kevin!) plus nurses round the clock. The house had to be restored due to smoke and odor damage.
...I had bronchitis and shingles for a few weeks; meanwhile Kevin never seemed to get over whatever he had that took him to the hospital.
...came back home for two weeks and Kevin got bad again. It wasn't as bad as when we took him to the hospital in February, but bad enough to go again. So we took him once more to St. John's ER. They admitted him for a week. They were never fully sure what was going on, maybe pneumonia, but weren't sure. Brought him home on April Fools' Day.
...April was a great month for Kevin at therapy. He was more alert and doing things he hadn't done since December. But the previous few months hadn't been good due to sickness so his charts looked bad. You can really chart that the reason he's not doing good was due to sickness. So the outpatient therapy we were taking him to had to discharge for now.
...May 2, Kevin seemed to be showing similar signs to when we took him to him to the ER, so we headed that way. They ended up treating him in the ER that day and sending us home with meds for bronchitis. That seemed to do the trick.
...In the May, Kevin had an eye infection, but with some antibiotics it's already cleared up.
...Since around the middle of February, we have had approval for twenty-four around the clock nursing. However, we haven't but maybe one week where we had that fully staffed. There have been many different reasons why, some were nurses getting sick or in car wrecks. But suffice it to say, we still need competent and dependably committed nurses to fill shifts. It means constant training and reworking of our schedules. Most of the empty shifts fall to Angie, which is incredibly hard at times.
...of course during all this, we have continued therapy at home. Now that the weather is nice we can take Kevin outside on the deck which was graciously built by United Way volunteers and some of Kevin's friends. It and the other developments they made have been a great benefit going into the outdoor season.
...Kevin's trach has been being capped throughout the day. On our last visit with the pulmonologist (lung doctor) she wanted us to be more aggressive with capping him throughout the day. We had slowly been working him back up to where he was before he started getting sick around the beginning of the year. She said let's aggressively add time each day that he does well. Because she believed he could do it, and so did we.
...This week we have been adding more and more time every day working toward a full twenty-four hour period of capping. His pulmonologist said if he got to twenty-four hours then we could take the trach out. He just did that! In fact, he has had it on for more than twenty-four hours now and still doing great. This morning Angie heard him naturally snoring, because his airway is totally through his nose and mouth when capped.
...We called the doctor and left a message. She called back soon and said let's take the trach out! We can either do it with a nurse or bring him in on Monday. We are discussing it and determining which way is best. Either way, his trach is coming out!
...We'll note something, for sure on twitter, when it comes out. You can read the tweets at http://twitter.com/pray4kevin.
...Remember you can fill out a letter online and send it to Kevin at http://bit.ly/note2kevin. It will be printed off and read to Kevin.
Thanks for your thoughts and prayers. This is a big step for Kevin's recovery. We give God all the glory for getting Kevin to this point.
Thanks for praying and reading,
Matt, Angie and family
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
Saturday, February 19, 2011
Update #137 on Kevin - Back at Home!
We were able to bring Kevin home last night. He stills needs to rest and continue to recuperate but he's doing so much better. He also got some redness and a slight sore while at the hospital so we are taking great strains to heal that through application of medication and consistent turns every couple hours. At this point he can't stay in his wheelchair for more than a couple hours so that he isn't stressing the already tender skin.
Our home health care agency has been trying to staff the house with 24 hour nursing. We are hoping that this can continue for the unforeseeable future since it has been difficult to give the best of care with only 8 hours of nursing. We won't know about approval for how much nursing we will get for a week or so, but right now they are trying to staff us with as close to 24 hours as possible. For instance, tonight from 10PM -8AM we don't have anyone and tomorrow from 4PM - 8PM we don't either, but the nursing agency is doing their very best to fill all those slots.
Part of the process, for whatever amount of nursing we get is having new nurses. That means lots of training and teaching for how things work at this house and what Kevin needs. Also, right now everything Kevin is getting (medicine, food, care) is spread out over the entire 24 hours to ease him back into things. That means the few breaks we worked into his schedule are gone. Every two hours he is turned (takes about fifteen -twenty minutes), food is every four hours, breathing treatments are every four hours, eye ointment is every two hours, etc…….. Little rest in between and it makes a big difference that we have more nursing right now. We pray it will continue.
If you want to send a message to Kevin, I took an idea from the hospital and added it to his website (http://www.prayforkevin.com/). All you have to do is click this link to send a note to Kevin http://bit.ly/note2kevin. We'll print it off and read it to him. This way Kevin can hear from you even if you can't come by and see him. And if you would like to come by and see Kevin, please try. We know he would love it.
Thanks for all the love and messages at the hospital. Outside of all the emails, facebook messages, and comments we had over thirty St John's "Well Wishes" emails hanging on his wall before we left! It meant so much to us and him.
Thanks so much for your prayers during this difficult time during Kevin's already difficult recovery. Your prayers are heard.
Thanks,
Matt, Angie and family
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
Our home health care agency has been trying to staff the house with 24 hour nursing. We are hoping that this can continue for the unforeseeable future since it has been difficult to give the best of care with only 8 hours of nursing. We won't know about approval for how much nursing we will get for a week or so, but right now they are trying to staff us with as close to 24 hours as possible. For instance, tonight from 10PM -8AM we don't have anyone and tomorrow from 4PM - 8PM we don't either, but the nursing agency is doing their very best to fill all those slots.
Part of the process, for whatever amount of nursing we get is having new nurses. That means lots of training and teaching for how things work at this house and what Kevin needs. Also, right now everything Kevin is getting (medicine, food, care) is spread out over the entire 24 hours to ease him back into things. That means the few breaks we worked into his schedule are gone. Every two hours he is turned (takes about fifteen -twenty minutes), food is every four hours, breathing treatments are every four hours, eye ointment is every two hours, etc…….. Little rest in between and it makes a big difference that we have more nursing right now. We pray it will continue.
If you want to send a message to Kevin, I took an idea from the hospital and added it to his website (http://www.prayforkevin.com/). All you have to do is click this link to send a note to Kevin http://bit.ly/note2kevin. We'll print it off and read it to him. This way Kevin can hear from you even if you can't come by and see him. And if you would like to come by and see Kevin, please try. We know he would love it.
Thanks for all the love and messages at the hospital. Outside of all the emails, facebook messages, and comments we had over thirty St John's "Well Wishes" emails hanging on his wall before we left! It meant so much to us and him.
Thanks so much for your prayers during this difficult time during Kevin's already difficult recovery. Your prayers are heard.
Thanks,
Matt, Angie and family
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
Friday, February 18, 2011
Update #136 on Kevin - Prepping for Home
So, here I sit in Kevin's room listening to Jazz and waiting for the doctor to come in with news that we can take Kevin home today. It's 11:15 AM and she has usually come in around 9:30 AM, therefore anticipation is building.
Kevin has remained great on room air for two days. He's been off antibiotics for a couple days. All his testings have come back with good results. He does have a small sore that is right on top of a scar from one of his old ones. I have the nurses doing "extreme" side turns so that he does not put any more pressure or moisture on the spot. They've pulled unneccessary catheters from Kevin and he's doing good and regulating things on his own. All that's left is a picc line which they will remove towards the last minute.
As far as the pressure spot goes, I will argue that for fourteen months he has had none at home. When he first came home, there were two pressure sores that were healed within about two weeks. At home we only have one "patient" to monitor. So, even if he goes home with it, the hope is between good care, the circulating air mattress and meds he will bounce back from that too.
The pulmonologist came in earlier, commented on my Coltrane playing and stated that he didn't see any reason why Kevin's main doctor in this unit wouldn't let him go home today.
Angie stayed at the house last night and has cleaned like a banshee in order for it to be ready if we bring him home today. I stayed with him at the hospital and helped the nurses get him far on his side for pressure relief.
We have thirty well wishing emails that you all have sent and after being read to Kevin are hanging on the wall in his room. When I read him some yesterday, he opened his eyes bigger, turned towards me and listened. Thanks for encouraging Kevin and us. Many staff have commented that they didn't even know they had this on the St John's website and they thought it was so cool that we have them hanging in his room.
As soon as we get the discharge info, we can get it to our home health care agency, Maxim, and they can request approval for nursing. Because he needs round the clock care we are requesting twenty-four hours per day nursing. Insurance has only paid for eight hours per day so far, but then again, many of you are praying. Our God is bigger than any insurance company's policy!
It's 11:45 AM and still no doc. The Jazz relaxes and calms me. A couple other nurses came in and loved the Ella Fitzgerald and Nina Simone that was playing. Now, hopefully we can listen at home tonight. Now one of my favorites, the Girl from Ipanema (Stan Getz version).
If you still want to send an email message to Kevin, just go to http://www.sjmc.org/ and click "contact a patient" on the right side, the form will pop up. Do it soon, in case we get to go home this afternoon.
Thanks for reading and praying,
Matt, Angie and family
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
Kevin has remained great on room air for two days. He's been off antibiotics for a couple days. All his testings have come back with good results. He does have a small sore that is right on top of a scar from one of his old ones. I have the nurses doing "extreme" side turns so that he does not put any more pressure or moisture on the spot. They've pulled unneccessary catheters from Kevin and he's doing good and regulating things on his own. All that's left is a picc line which they will remove towards the last minute.
As far as the pressure spot goes, I will argue that for fourteen months he has had none at home. When he first came home, there were two pressure sores that were healed within about two weeks. At home we only have one "patient" to monitor. So, even if he goes home with it, the hope is between good care, the circulating air mattress and meds he will bounce back from that too.
The pulmonologist came in earlier, commented on my Coltrane playing and stated that he didn't see any reason why Kevin's main doctor in this unit wouldn't let him go home today.
Angie stayed at the house last night and has cleaned like a banshee in order for it to be ready if we bring him home today. I stayed with him at the hospital and helped the nurses get him far on his side for pressure relief.
We have thirty well wishing emails that you all have sent and after being read to Kevin are hanging on the wall in his room. When I read him some yesterday, he opened his eyes bigger, turned towards me and listened. Thanks for encouraging Kevin and us. Many staff have commented that they didn't even know they had this on the St John's website and they thought it was so cool that we have them hanging in his room.
As soon as we get the discharge info, we can get it to our home health care agency, Maxim, and they can request approval for nursing. Because he needs round the clock care we are requesting twenty-four hours per day nursing. Insurance has only paid for eight hours per day so far, but then again, many of you are praying. Our God is bigger than any insurance company's policy!
It's 11:45 AM and still no doc. The Jazz relaxes and calms me. A couple other nurses came in and loved the Ella Fitzgerald and Nina Simone that was playing. Now, hopefully we can listen at home tonight. Now one of my favorites, the Girl from Ipanema (Stan Getz version).
If you still want to send an email message to Kevin, just go to http://www.sjmc.org/ and click "contact a patient" on the right side, the form will pop up. Do it soon, in case we get to go home this afternoon.
Thanks for reading and praying,
Matt, Angie and family
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
Wednesday, February 16, 2011
Update #135 on Kevin - Out of ICU!
So, more good stuff to report.
After waiting all day, Kevin finally got his MRI's late last night. The hospital is really full here, so he kept getting bumped for more urgent cases.
Then around midnight, Kevin got moved to a new room out of ICU. He is on the same floor in room 845. It's a private room with great nurses and aides so far. Today they pulled him off oxygen because he was doing so well and has been on humidified room air ever since.
I spent the night here with him (the nurses encourage it in this wing) and Angie went home to sleep. Tonight we are tagging out. I'll go home and Angie will stay in the room.
When Angie came up today she brought Kevin's wheelchair. This afternoon the nurses put Kevin in his chair. We wanted to start it out slow, so it was only for 2 1/2 hours but Kevin did great.
We are making arrangements with home health care because they are still looking at Kevin going home later this week, probably Friday. We hope to have more nursing in place so please pray for more than eight hours to be approved.
Feel free to keep sending messages to Kevin through the St John's website. We have read every one to him and hung them on the wall in his room. The link is http://www.sjmc.org/general.asp?id=322&siteuse=11.
Thanks for praying and reading,
Matt, Angie and family
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
After waiting all day, Kevin finally got his MRI's late last night. The hospital is really full here, so he kept getting bumped for more urgent cases.
Then around midnight, Kevin got moved to a new room out of ICU. He is on the same floor in room 845. It's a private room with great nurses and aides so far. Today they pulled him off oxygen because he was doing so well and has been on humidified room air ever since.
I spent the night here with him (the nurses encourage it in this wing) and Angie went home to sleep. Tonight we are tagging out. I'll go home and Angie will stay in the room.
When Angie came up today she brought Kevin's wheelchair. This afternoon the nurses put Kevin in his chair. We wanted to start it out slow, so it was only for 2 1/2 hours but Kevin did great.
We are making arrangements with home health care because they are still looking at Kevin going home later this week, probably Friday. We hope to have more nursing in place so please pray for more than eight hours to be approved.
Feel free to keep sending messages to Kevin through the St John's website. We have read every one to him and hung them on the wall in his room. The link is http://www.sjmc.org/general.asp?id=322&siteuse=11.
Thanks for praying and reading,
Matt, Angie and family
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
Monday, February 14, 2011
Update #134 on Kevin - ICU
Okay, much to update. Good stuff too.
Kevin has been off any breathing machines for over twenty-four hours. He's on flowby or wallflow air. It's basically just room air with adjustable oxygen (right now he's on 50% oxygen).
They stopped irrigating his bladder about 30 hours or so ago and he has had very little blood showing up, just occassional spots. That should continue to clear up over time.
He's only got one antibiotic left out of the three he was on for the pneumonia/infection. It is scheduled to end on Wednesday.
Gastro doctors scheduled a peg tube replacement this morning and it was done before we got here. We were pleasantly surprised when we got here and found out about it. Kevin's Critical Care doctor was surprised that the gastro docs could fit it in so quick and do the procedure in Kevin's room.
Kevin has MRI's scheduled for tomorrow (which again were ordered by his neurologist before Kevin came to the ER). These MRI's are for the regular recovery process and are of his brain and brain stem specifically.
The CC Doctor told us that Kevin has transfer orders ready for him to be moved into a step down unit on the other side of the hospital. However, there has been a waiting list, so we aren't sure when or if he will get moved there before being discharged later in the week.
Now, we are actively looking at post discharge stuff like reopening his home care nursing, alerting his doctors, etc… We are going to be requesting more daily nursing hours from insurance. In fact, we were already looking to do that before this sudden experience and had to put it off. Kevin requires more care than the eight hours of nursing he has been getting. Please pray for this need.
Kevin will also be getting a short break from physical, occupational and speech therapy. We haven't yet decided when in March he will start back up, but we will also be discussing this with his doctors as we make the decision.
Prior to this hospitlization, Kevin has continued to do new things in therapy and his therapists have so great and creative as they stimulate and improve Kevin's functions. His body control continues to get better. He has stood assisted by therapists, and increased neck control to where he can hold his neck up to 17 minutes long once. Back in June, his record for neck control was only a few minutes. He still needs to do this more consistently, but the increase is exciting. In August, we took Kevin for a swallow study which tracked different thickness of liquids as an Xray showed which of his muscles were/weren't working. This study gave Kevin's speech therapist the information needed to know which muscles in the back of his neck needed stimulated to improve swallowing. She has wanted to schedule a new swallow study so that we have a benchmark for comparison.
This ICU stay may give Kevin a little bit of a setback, but as you can probably tell (or already know) Kevin is a fighter. Two steps forward, one step back is still progress.
Thanks for all the notes that were sent through the hospital website, we read them to him today. The ones from February 9 & 10 just got here. Feel free to keep sending them and we'll keep reading them to him. The link is http://www.sjmc.org/general.asp?id=322&siteuse=11 and you can fill out the form. There are fifteen of them taped to Kevin's wall.
Thanks so much for your prayers and encouragement,
Matt, Angie and family
Quicklinks to Recent posts -
Update #133 - http://bit.ly/update133
Update #132 - http://bit.ly/update132
Update #131 - http://bit.ly/update131
Update #130 - http://bit.ly/update130
Update #129 - http://bit.ly/update129
Update #128 - http://bit.ly/update128
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
Kevin has been off any breathing machines for over twenty-four hours. He's on flowby or wallflow air. It's basically just room air with adjustable oxygen (right now he's on 50% oxygen).
They stopped irrigating his bladder about 30 hours or so ago and he has had very little blood showing up, just occassional spots. That should continue to clear up over time.
He's only got one antibiotic left out of the three he was on for the pneumonia/infection. It is scheduled to end on Wednesday.
Gastro doctors scheduled a peg tube replacement this morning and it was done before we got here. We were pleasantly surprised when we got here and found out about it. Kevin's Critical Care doctor was surprised that the gastro docs could fit it in so quick and do the procedure in Kevin's room.
Kevin has MRI's scheduled for tomorrow (which again were ordered by his neurologist before Kevin came to the ER). These MRI's are for the regular recovery process and are of his brain and brain stem specifically.
The CC Doctor told us that Kevin has transfer orders ready for him to be moved into a step down unit on the other side of the hospital. However, there has been a waiting list, so we aren't sure when or if he will get moved there before being discharged later in the week.
Now, we are actively looking at post discharge stuff like reopening his home care nursing, alerting his doctors, etc… We are going to be requesting more daily nursing hours from insurance. In fact, we were already looking to do that before this sudden experience and had to put it off. Kevin requires more care than the eight hours of nursing he has been getting. Please pray for this need.
Kevin will also be getting a short break from physical, occupational and speech therapy. We haven't yet decided when in March he will start back up, but we will also be discussing this with his doctors as we make the decision.
Prior to this hospitlization, Kevin has continued to do new things in therapy and his therapists have so great and creative as they stimulate and improve Kevin's functions. His body control continues to get better. He has stood assisted by therapists, and increased neck control to where he can hold his neck up to 17 minutes long once. Back in June, his record for neck control was only a few minutes. He still needs to do this more consistently, but the increase is exciting. In August, we took Kevin for a swallow study which tracked different thickness of liquids as an Xray showed which of his muscles were/weren't working. This study gave Kevin's speech therapist the information needed to know which muscles in the back of his neck needed stimulated to improve swallowing. She has wanted to schedule a new swallow study so that we have a benchmark for comparison.
This ICU stay may give Kevin a little bit of a setback, but as you can probably tell (or already know) Kevin is a fighter. Two steps forward, one step back is still progress.
Thanks for all the notes that were sent through the hospital website, we read them to him today. The ones from February 9 & 10 just got here. Feel free to keep sending them and we'll keep reading them to him. The link is http://www.sjmc.org/general.asp?id=322&siteuse=11 and you can fill out the form. There are fifteen of them taped to Kevin's wall.
Thanks so much for your prayers and encouragement,
Matt, Angie and family
Quicklinks to Recent posts -
Update #133 - http://bit.ly/update133
Update #132 - http://bit.ly/update132
Update #131 - http://bit.ly/update131
Update #130 - http://bit.ly/update130
Update #129 - http://bit.ly/update129
Update #128 - http://bit.ly/update128
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
Saturday, February 12, 2011
Update #133 on Kevin - ICU
Just finished meeting with Kevin's Critical Care Doctor. Both of Kevin's Critical Care Doctors have been great. We have appreciated their patience and teaching as we went through a difficult situation. We have been able to relax due to the entire staff in the CC unit.
His doctor said that Kevin is doing well and definitely making progress. He is not septic anymore, and now we are just basically finishing up the treatment for his pneumonia. Earlier in the week he had told us about Kevin's X-rays which showed a lot of fluid in his left lung. Today's X-rays were great. They are absolutely clear. It shows too, because Kevin has not been coughing near as much the last few days.
Kevin's progress off the CPAP machine is going well too. With the low settings that I told you about in the previous update (8 Pressure and 30% O2), he is now just needing to tolerate this well. What that means for prayer terms is that he is breathing around 30-37 times per minute now, and he needs to slow down to the 20's. His doctor thinks by tomorrow (Sunday) or Monday that Kevin will be able to switch to flowby.
No real concern left on the light amount of blood in his urine, hopefully that continues to resolve itself. The doctor is thinking Kevin will stay in ICU until Monday. Then maybe between Monday and Tuesday, he will be switched to a step down unit that is outside of Critical Care. Please be praying for the doctors that Kevin will have in that department.
We had asked the doctor earlier in the week to take a look at Kevin's peg tube and see what he thought about replacing it. That should be something that can be done Monday or after next week. Also, I mentioned to him that Kevin is overdue on some MRI's that Kevin's neurologist is wanting. The CC Doctor thinks that can be done around Wednesday next week. We started trying to schedule an MRI back in early December so this will be a great help to get it done now too.
Quicklinks to Recent posts -
Update #132 - http://bit.ly/update132
Update #131 - http://bit.ly/update131
Update #130 - http://bit.ly/update130
Update #129 - http://bit.ly/update129
Update #128 - http://bit.ly/update128
Thanks for reading and praying,
Matt, Angie and family
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
His doctor said that Kevin is doing well and definitely making progress. He is not septic anymore, and now we are just basically finishing up the treatment for his pneumonia. Earlier in the week he had told us about Kevin's X-rays which showed a lot of fluid in his left lung. Today's X-rays were great. They are absolutely clear. It shows too, because Kevin has not been coughing near as much the last few days.
Kevin's progress off the CPAP machine is going well too. With the low settings that I told you about in the previous update (8 Pressure and 30% O2), he is now just needing to tolerate this well. What that means for prayer terms is that he is breathing around 30-37 times per minute now, and he needs to slow down to the 20's. His doctor thinks by tomorrow (Sunday) or Monday that Kevin will be able to switch to flowby.
No real concern left on the light amount of blood in his urine, hopefully that continues to resolve itself. The doctor is thinking Kevin will stay in ICU until Monday. Then maybe between Monday and Tuesday, he will be switched to a step down unit that is outside of Critical Care. Please be praying for the doctors that Kevin will have in that department.
We had asked the doctor earlier in the week to take a look at Kevin's peg tube and see what he thought about replacing it. That should be something that can be done Monday or after next week. Also, I mentioned to him that Kevin is overdue on some MRI's that Kevin's neurologist is wanting. The CC Doctor thinks that can be done around Wednesday next week. We started trying to schedule an MRI back in early December so this will be a great help to get it done now too.
Quicklinks to Recent posts -
Update #132 - http://bit.ly/update132
Update #131 - http://bit.ly/update131
Update #130 - http://bit.ly/update130
Update #129 - http://bit.ly/update129
Update #128 - http://bit.ly/update128
Thanks for reading and praying,
Matt, Angie and family
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
Update #132 on Kevin - ICU
Today continues to bring good news for praise. After trying a little last night, to wean the pressure support (I misadvertently said previously they were reducing the PEEP setting, but I meant the pressure support), Kevin has made great strides today. They reduced the pressure support settings on the CPAP machine from 14 to 8.
They've also lowered the oxygen amount to 30%. Once Kevin is tolerating these levels well, they can switch him to flowby getting him closer to regular breathing.
This morning also brought the news that Kevin does not have Cdiff. He is still having a little blood in his urine, but overall that has improved tremendously since they replaced his catheter and started irrigating his bladder.
We talked to his doctor about changing his feeding tube. If you'll remember, we went in to change it back in September and the doctor said it just needed cleaned out. It has deteriorated more since then and we hoped they might be able to change it. His critical care doctor didn't think this would be a problem, once he got stabilized.
Taylor, Kevin's daughter, arrived from Midwest City yesterday afternoon. We spent the evening together as a family and went back to visit Kevin once the visiting hours started again. Today, she went up to the hospital in order to give Angie and I a break. Thanks Tay!
Thanks so much for your prayers on behalf of Kevin and our family! It means so much.
Quicklings to Recent posts -
Update #131 - http://bit.ly/update131
Update #130 - http://bit.ly/update130
Update #129 - http://bit.ly/update129
Update #128 - http://bit.ly/update128
Thanks for reading and praying!!!!
Matt, Angie and family
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
They've also lowered the oxygen amount to 30%. Once Kevin is tolerating these levels well, they can switch him to flowby getting him closer to regular breathing.
This morning also brought the news that Kevin does not have Cdiff. He is still having a little blood in his urine, but overall that has improved tremendously since they replaced his catheter and started irrigating his bladder.
We talked to his doctor about changing his feeding tube. If you'll remember, we went in to change it back in September and the doctor said it just needed cleaned out. It has deteriorated more since then and we hoped they might be able to change it. His critical care doctor didn't think this would be a problem, once he got stabilized.
Taylor, Kevin's daughter, arrived from Midwest City yesterday afternoon. We spent the evening together as a family and went back to visit Kevin once the visiting hours started again. Today, she went up to the hospital in order to give Angie and I a break. Thanks Tay!
Thanks so much for your prayers on behalf of Kevin and our family! It means so much.
Quicklings to Recent posts -
Update #131 - http://bit.ly/update131
Update #130 - http://bit.ly/update130
Update #129 - http://bit.ly/update129
Update #128 - http://bit.ly/update128
Thanks for reading and praying!!!!
Matt, Angie and family
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
Friday, February 11, 2011
Update #131 on Kevin - ICU
Kevin is continuing to improve. We spoke with his doctor this afternoon and feel really good about Kevin's progress. He has been on CPAP settings on the vent for about 33 hours now with no problems. An hour or so ago, the doctor started lowering the pressure from 14 to 12 (PEEP) on the vent. After a couple hours, if he seems to tolerate it, they'll lower it again. They'll keep doing that and when he is tolerating an 8, they can switch him over to flowby.
For the past couple days, Kevin has been getting food through his feeding tube. It is the same formula that he gets at home, that is jevity 1.2.
For the infection in his body and pneumonia, Kevin has been getting three different antibiotics. Vancomyacin, piperacyllin and another more generic antiobiotic. While these are helping with his infection, there is a side effect too. There is potential for C-Diff in his colon. He had it at Saint Francis and Meadowbrook a year and a half ago, which makes him more likely to get it again. They tested him for it, and we should find out tomorrow.
The doctors' focus had shifted onto the blood in Kevin's urine. Last night they took three steps towards diagnosing it. First they changed his catheter. Next they tried irrigating his bladder. Then they took him for a Ctscan. When they changed the catheter, they found that it had been put in incorrectly when he arrived in the ER. The urologist said just that could have caused the bleeding that we have been seeing since arriving (especially since his blood was too thin). The irrigation has been flushing any blood out of his bladder, and right now the blood is very faint. The ctscan showed nothing of importance and therefore would not need to do a scope based on the ctscan.
We are starting to have more routine with Kevin again. Physical therapy has been coming by each day to work out his muscles and keep him from getting rigid. When they bathed him last night they also shaved him. He was starting to get scratchy barbs on his face so it was definitely time for a change.
For about 36 hours Kevin has been completely off of dopamine. That was the medicine used to raise his blood pressure to regular levels. His blood pressure has stabilized and is doing good. Right now, it is 100/65 with a map of 78. Looking good.
If you've missed the previous updates here are some quick links:
Recent posts -
Update #130 - http://bit.ly/update130
Update #129 - http://bit.ly/update129
Update #128 - http://bit.ly/update128
Thanks for reading and praying!!!!
Matt, Angie and family
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
For the past couple days, Kevin has been getting food through his feeding tube. It is the same formula that he gets at home, that is jevity 1.2.
For the infection in his body and pneumonia, Kevin has been getting three different antibiotics. Vancomyacin, piperacyllin and another more generic antiobiotic. While these are helping with his infection, there is a side effect too. There is potential for C-Diff in his colon. He had it at Saint Francis and Meadowbrook a year and a half ago, which makes him more likely to get it again. They tested him for it, and we should find out tomorrow.
The doctors' focus had shifted onto the blood in Kevin's urine. Last night they took three steps towards diagnosing it. First they changed his catheter. Next they tried irrigating his bladder. Then they took him for a Ctscan. When they changed the catheter, they found that it had been put in incorrectly when he arrived in the ER. The urologist said just that could have caused the bleeding that we have been seeing since arriving (especially since his blood was too thin). The irrigation has been flushing any blood out of his bladder, and right now the blood is very faint. The ctscan showed nothing of importance and therefore would not need to do a scope based on the ctscan.
We are starting to have more routine with Kevin again. Physical therapy has been coming by each day to work out his muscles and keep him from getting rigid. When they bathed him last night they also shaved him. He was starting to get scratchy barbs on his face so it was definitely time for a change.
For about 36 hours Kevin has been completely off of dopamine. That was the medicine used to raise his blood pressure to regular levels. His blood pressure has stabilized and is doing good. Right now, it is 100/65 with a map of 78. Looking good.
If you've missed the previous updates here are some quick links:
Recent posts -
Update #130 - http://bit.ly/update130
Update #129 - http://bit.ly/update129
Update #128 - http://bit.ly/update128
Thanks for reading and praying!!!!
Matt, Angie and family
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
Wednesday, February 9, 2011
Update #130 on Kevin - ICU
Of course, we didn't know what to expect from the weather and we ended up getting 5.5 inches more snow. It seems to be more driveable than the sleet driven snow last week. Glad we weren't 40 minutes to the Northeast, they got 25 inches!!! So, Kevin and I have been fairly isolated today as far as external visitors go. There have been several staff that have stopped by.
The chaplain, a little elderly nun, came by and introduced herself. She told me that she has seen us the past few days and told us what great condition Kevin is in for Home Health Care. She then proceeded to pray for him silently.
Then the Family Care Specialist came by and introduced herself. She said she only started a couple days ago and was there anything that the family needed. I told her that most everything was great. The biggest hangup we have had is the visiting hours. Visiting hours are closed until 6-9AM; then 6-8 PM and finally 10-midnight. We've had a couple come up and not be able to see him during those hours.
Rene, the nurse manager came in and introduced herself too. While I was out (due to visiting hours being off), she brought by an approved power strip for all my electronics and laptop. Earlier I didn't know who brought it in, the current nurse just told me it was there to use.
Stephanie, Barbara and Norma came in after lunch. They are the physical therapists that will be working on Kevin's range of motion. As he improves, they will try more advanced things, such as he does at therapy twice weekly. Examples might include, sitting up on the side of the bed assisted, more strengh training for neck/legs, etc…
Dopamine/Blood Pressure - As far as getting him off dopamine, we slowed down. Part of the issue is that we got a new nurse today, not a bad one, just new to Kevin. During the night, the night nurse had got Kevin down to 2 mg of dopamine. The day nurse hadn't been on more than an hour or two when she saw his Blood Pressure levels hovering near the low side and she bumped up his dopamine from 2 to 5 mg again. It took me several hours to get her to try to reduce it again. She has now his Blood Pressure is doing well and he is getting 4 mg. Hopefully, we can keep taking ten steps forward and only two steps back.
Not sure where it is at, but Kevin has put on some extra weight. He weighs 205 lbs. Before this trip to the hospital he was around 194. So that means he has picked up ten or eleven pounds, although there is the possibility there is a difference in the bed scale and the therapy scale that we normally use.
Ventilator - Twice now they have switched the ventilator so that Kevin is breathing on his own and the vent is helping him. Twice they have stopped it very close to breathing treatments. This is normal at home and normal for Kevin to have increased breathing rates and coughing after a breathing treatment. The doctor said they will keep working on it and not have the knee jerk precautionary reactions. To do everything he can to at the very least get him on flowby (room air).
Today, Kevin has been awake for several hours. Probably 4 hours so far. I have talked with him and put different shows on TV on for him.
We also found out that they might be some sort of blockage in his urinary tract, but not bad, he is still urinating. The doctor is getting a Urologist on board to come see him tomorrow. His echo came back fairly good for his heart. He just had some pulmonary hypertension on his right side. But its not bad and nothing can really be done about it.
Just finished speaking with one of his critical care doctors. Both of them have been great so far, Dr. Taneja and Dr. Suku. We talked about thirty minutes. At the end he told me that he has done this for a long time and that he has seen many chronically trached patients like Kevin and that he has never seen a family more invested or educated about their family member's situation and what to do to help. Makes ya feel like you are doing things right. The doctor also said that Kevin is winning.
Recent posts -
Update #129 - http://bit.ly/update129
Update #128 - http://bit.ly/update128
Thanks for reading and praying!!!!
Matt, Angie and family
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
The chaplain, a little elderly nun, came by and introduced herself. She told me that she has seen us the past few days and told us what great condition Kevin is in for Home Health Care. She then proceeded to pray for him silently.
Then the Family Care Specialist came by and introduced herself. She said she only started a couple days ago and was there anything that the family needed. I told her that most everything was great. The biggest hangup we have had is the visiting hours. Visiting hours are closed until 6-9AM; then 6-8 PM and finally 10-midnight. We've had a couple come up and not be able to see him during those hours.
Rene, the nurse manager came in and introduced herself too. While I was out (due to visiting hours being off), she brought by an approved power strip for all my electronics and laptop. Earlier I didn't know who brought it in, the current nurse just told me it was there to use.
Stephanie, Barbara and Norma came in after lunch. They are the physical therapists that will be working on Kevin's range of motion. As he improves, they will try more advanced things, such as he does at therapy twice weekly. Examples might include, sitting up on the side of the bed assisted, more strengh training for neck/legs, etc…
Dopamine/Blood Pressure - As far as getting him off dopamine, we slowed down. Part of the issue is that we got a new nurse today, not a bad one, just new to Kevin. During the night, the night nurse had got Kevin down to 2 mg of dopamine. The day nurse hadn't been on more than an hour or two when she saw his Blood Pressure levels hovering near the low side and she bumped up his dopamine from 2 to 5 mg again. It took me several hours to get her to try to reduce it again. She has now his Blood Pressure is doing well and he is getting 4 mg. Hopefully, we can keep taking ten steps forward and only two steps back.
Not sure where it is at, but Kevin has put on some extra weight. He weighs 205 lbs. Before this trip to the hospital he was around 194. So that means he has picked up ten or eleven pounds, although there is the possibility there is a difference in the bed scale and the therapy scale that we normally use.
Ventilator - Twice now they have switched the ventilator so that Kevin is breathing on his own and the vent is helping him. Twice they have stopped it very close to breathing treatments. This is normal at home and normal for Kevin to have increased breathing rates and coughing after a breathing treatment. The doctor said they will keep working on it and not have the knee jerk precautionary reactions. To do everything he can to at the very least get him on flowby (room air).
Today, Kevin has been awake for several hours. Probably 4 hours so far. I have talked with him and put different shows on TV on for him.
We also found out that they might be some sort of blockage in his urinary tract, but not bad, he is still urinating. The doctor is getting a Urologist on board to come see him tomorrow. His echo came back fairly good for his heart. He just had some pulmonary hypertension on his right side. But its not bad and nothing can really be done about it.
Just finished speaking with one of his critical care doctors. Both of them have been great so far, Dr. Taneja and Dr. Suku. We talked about thirty minutes. At the end he told me that he has done this for a long time and that he has seen many chronically trached patients like Kevin and that he has never seen a family more invested or educated about their family member's situation and what to do to help. Makes ya feel like you are doing things right. The doctor also said that Kevin is winning.
Recent posts -
Update #129 - http://bit.ly/update129
Update #128 - http://bit.ly/update128
Thanks for reading and praying!!!!
Matt, Angie and family
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
Update #129 on Kevin - ICU
Tonight, in preparation for the upcoming winter storm/blizzard, we decided that I would stay the night with Kevin at the hospital. That way, in case everyone is snowed in, someone is with him in ICU. They are all very nice here and are allowing me to stay on a couch/bed that is in Kevin's room.
Kevin's fever is still gone, two days in a row. His heartrate has become much more normal , right now it is 79 and he's awake (yeah it's 2 AM - he's still a night owl). The medical staff have been weaning Kevin off the dopamine, which is to combat low blood pressure. They have lowered the dopamine from 15 mg yesterday (Monday) to 3 mg by this evening (Tuesday). His blood pressure is remaining steady and keeping up with the changes in medicine.
Also, this evening they have started weaning him off the ventilator. All evening he has been initiating all his breathing and the machine only helps if he doesn't take a deep enough breath. Because of the pneumonia, his breathing has been more shallow. Yet, even with the changes in the ventilator, his lungs are keeping up, for 9 hours so far. After his most recent breathing treatment, he needed a break so they switched back his vent settings with a plan to start the weaning again in the morning.
His nurse tonight, told me that every nurse that comes in to help her do something with Kevin cannot believe that he has been at home with home health care. They have all said the family is doing an excellent job caring for him. They can see it in his skin and the lack of any pressure sores whatsoever. And this morning when the physical therapist came and did and evaluation on him, she said that he has excellent range. They are now sending techs to come and do range of motion even while in ICU.
Apparently, at first Kevin's kidneys were not functioning good after we arrived here. Now Kevin's kidneys are functioning well, so they started giving him food through his peg tube. We spoke with the doctor about the possibility of changing his peg tube while we were here at the hospital, since his is approximately one year and five months old. Once things get stabilized they will look into that.
He still has blood in his urine that is unaccounted for, however it is lessening. They would still like to know where it is coming from. There is a plan to do an ultra sound to see if he has any kidney stones sometime soon.
Tomorrow they plan to restart provigil (at home we use nuvigil), which is an alert medication. However, throughout the day today it has been more alert than yesterday. And as normal, wide awake about an hour ago in the night.
If you would like to send cards you can get the address at St John's website. However, you can also do this digitally by clicking the following link http://www.sjmc.org/general.asp?id=322&siteuse=11 and filling out the form. Kevin is in room 809. We have a wall that we can tape any cards up, cheering Kevin up in the process.
More later, but for now, thanks for reading and praying,
Matt, Angie and family
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
Kevin's fever is still gone, two days in a row. His heartrate has become much more normal , right now it is 79 and he's awake (yeah it's 2 AM - he's still a night owl). The medical staff have been weaning Kevin off the dopamine, which is to combat low blood pressure. They have lowered the dopamine from 15 mg yesterday (Monday) to 3 mg by this evening (Tuesday). His blood pressure is remaining steady and keeping up with the changes in medicine.
Also, this evening they have started weaning him off the ventilator. All evening he has been initiating all his breathing and the machine only helps if he doesn't take a deep enough breath. Because of the pneumonia, his breathing has been more shallow. Yet, even with the changes in the ventilator, his lungs are keeping up, for 9 hours so far. After his most recent breathing treatment, he needed a break so they switched back his vent settings with a plan to start the weaning again in the morning.
His nurse tonight, told me that every nurse that comes in to help her do something with Kevin cannot believe that he has been at home with home health care. They have all said the family is doing an excellent job caring for him. They can see it in his skin and the lack of any pressure sores whatsoever. And this morning when the physical therapist came and did and evaluation on him, she said that he has excellent range. They are now sending techs to come and do range of motion even while in ICU.
Apparently, at first Kevin's kidneys were not functioning good after we arrived here. Now Kevin's kidneys are functioning well, so they started giving him food through his peg tube. We spoke with the doctor about the possibility of changing his peg tube while we were here at the hospital, since his is approximately one year and five months old. Once things get stabilized they will look into that.
He still has blood in his urine that is unaccounted for, however it is lessening. They would still like to know where it is coming from. There is a plan to do an ultra sound to see if he has any kidney stones sometime soon.
Tomorrow they plan to restart provigil (at home we use nuvigil), which is an alert medication. However, throughout the day today it has been more alert than yesterday. And as normal, wide awake about an hour ago in the night.
If you would like to send cards you can get the address at St John's website. However, you can also do this digitally by clicking the following link http://www.sjmc.org/general.asp?id=322&siteuse=11 and filling out the form. Kevin is in room 809. We have a wall that we can tape any cards up, cheering Kevin up in the process.
More later, but for now, thanks for reading and praying,
Matt, Angie and family
_______________________________
Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
Monday, February 7, 2011
Update #128 on Kevin - ICU
We know it’s been a few months since we've done an update on Kevin. Life has moved forward. Angie and I returned to Italy to pack up our house and close out our aspect of the ministry that's still going on there. We had a great Thanksgiving, Christmas and New Year's at home with Kevin and the rest of the family.
However, I'm writing you from an ICU room at St John's Hospital in Tulsa, Oklahoma. It's been a whirlwind this last week, so I'll try to update you quick and get to the prayer needs for Kevin.
Things started getting tough about a week and a half ago. First Angie, then Jacob,
finally Kohl all got the flu. With the blizzard last week and record-setting snowfall in Tulsa, we didn't have nursing. I found myself caring for a housefull of sickos and Kevin. Fortunately, Brandon was able to come and help some days, because of being out of school due to the snow.
finally Kohl all got the flu. With the blizzard last week and record-setting snowfall in Tulsa, we didn't have nursing. I found myself caring for a housefull of sickos and Kevin. Fortunately, Brandon was able to come and help some days, because of being out of school due to the snow.
We thought we had made it out of the woods but Saturday night things took a turn. Kevin has spells of coughing, but it will eventually be resolved with one of several methods of care. He started coughing at 9PM Saturday night and continued coughing, getting more incessant and worse over the next seven hours. We ran through the checklist of everything we were taught to do in order to relieve his coughing (cough syrup, saline breathing treatment, repositioning, xopenex breathing treatments, etc….). After calling a couple medical professionals, we followed their advice and called 911. On a normal day, we could have just taken Kevin in the van, however, there is still so much snow on the ground and driveway that it was not possible. Firemen and EMSA (ambulance service) arrived and got Kevin ready for transport. Angie rode in the EMSA truck and I met them at the hospital driving in the snow in the early hours between Saturday and Sunday.
After some time in the ER, we found a rapidly rising temperature (at home it was 99) of 102-103. His blood was way too thin. His potassium was very high. Kevin’s blood pressure was dangerously low (at the lowest I saw it was 69/39) and his oxygen levels were dropping. He had blood in his urine and had thrown up some as well. Kevin’s heart rate and breathing rate were very fast.
Yesterday afternoon, they moved Kevin into an Adult ICU room on the 8th floor. A vitamin K shot was given to combat the thin blood, electrolytes for the high potassium, dopamine for the low blood pressure, O2 for the low O2 levels and Tylenol for the fever. They found pneumonia and some sort of infection that made him septic. Septic is an issue where the blood is infected. This made the staff use a Septic protocol of constant testing to insure the various levels of his body’s statistics.
During the night (last night), Kevin’s nurse called to tell us that from a blood gas test, his O2 levels were too low in his lungs and his Carbon Dioxide (CO2) levels were too high. They needed to put Kevin on a ventilator in order to keep the infection from winning in his lungs. Since then his blood gas levels have been good. Kevin’s fever is now gone. His heart rate is much more normal now. With the dopamine his blood pressure is getting back to normal, although to wean him off the dopamine it needs to become stabilized. This morning, after we got here, Kevin cracked open his eyes and even turned toward me when we came over to his bedside. He immediately went back to sleep, but that was good since he hadn’t opened his eyes since getting to the hospital. Several other times today, he has reopened his eyes, twice with visitors and a couple others just with Angie and I in the room. Even though he still has some septic symptoms, he is no longer under the septic protocol.
As things progress, we will update you via email, facebook and the prayforkevin.com website. More up to date info can be gotten by following me on Twitter (username mcrosser or pray4kevin) and my Facebook status. Thanks so much for your prayers and thoughts. No flowers or balloons can be sent to his ICU room, but please feel free to send cards to Kevin Crosser, room 809 at St John’s Hospital in Tulsa, Oklahoma.
Thanks for reading and praying,
Matt, Angie and family
_______________________________Pray For Kevin
http://www.prayforkevin.com/
follow on twitter: pray4kevin
facebook: Pray for Kevin
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