Tuesday, December 29, 2009

Wednesday December 30, 2009

Today was an awesome visit. Tahna was there trying to get the nurse to come help him with something. When she went to leave again, he shouted (whisper shouted), "Tahna! Tahna! never mind." It was great to hear him say her name.

Dad has Dysphagia which is the medical term for difficulty in swallowing. It is a sensation that suggests difficulty in the passage of solids or liquids from the mouth to the stomach. He also has Aphasia which is difficulty in speaking or understanding spoken or written language.

He's been doing awesome on the bike in physical therapy. He's been doing standing crunches on his own and walking with help. He's using his right leg more and more

He asked Tahna how long he's been in the hospital, so he still needs reminding of why he's there.


Sunday, December 27, 2009

Sunday Dec 27, 2009

I was able to visit Dad today. It was fun just to spend time with him and mom alone. Rob and Marvin got him a flip mino camera and I was teaching him out to use it. He would grab it out of my hands and try to turn it on. We would record stuff and then re-play it back to him. He would smile. He always loved gadgets like that. Then I showed him my itouch and the fun things it would do. He tried to play with that too.

Mom got him an electric razor. When she showed it to him, he grabbed the box out of her hands and tried to open it. We opened it for him and he instantly grabbed it, turned it on and started shaving his face. He was pretty clean-cut already, but apparently it was bothering him. He shaved himself right there in the wheel chair, then he turned it off and would just turn it over and over looking at it and turning it on and off.

When I told him I had to go, he grabbed my hand and kissed it. It was sweet.

Susie

Saturday, December 26, 2009

Saturday December 26, 2009

These last couple of days have been very bittersweet. When I asked dad if he remembered Christmas, he said yes. When I asked him if he knew who I was, he didn't say or do anything, but Jordan called in to my mom on her cell phone and he actually carried on a conversation with him; some you could understand, some you could not. President Monson's wife is on his floor, for some reason (we gave them their privacy), but when I asked Dad if he remembered who President Monson was, he said No. Also, Rob called in and he carried on a conversation to him as well.

He asked me where my "brother" was. I said, "you mean Brett, my husband?" He said, "yes". So he recongnized that someone was supposed to be with me who was not there. He also told Tahna he had to go to the "union"; meaning "bathroom". So his words are hit and miss, as well as who he recognizes and who he doesn't.

Still, when all the grandkids came in, he smiled and gave each a hug. He did more baby talk to Kamryn and when I asked if he'd had a chance to watch the video I made for him of the family, he smiled real big and said Yes.

He's doing very will in all his therapies. We'll find out next week if he'll be able to stay at IMC. He keeps pulling his feeding tube out and he hates it when he's buckled in his wheel chair. He tried to undo his buckle and I told him I'd unbuckle him as long as he didn't try to escape. He said, "oh no, I won't" and he never did try :)

Susie

Monday, December 21, 2009

We were able to see dad tonight. I haven't seen him in over a week because my family's been sick, so what a change! He smiled when the kids came in and we were able to show him the slideshow of the grandkids I made him. He smiled a lot. I asked him if he remembered "so-and-so" and he would shake his head yes, but whether or not that was just automatic reaction, I 'm not sure. He smiled at the cute and funny pictures.

Joe said he had to leave and he said, "why?" Joe said because he had to go get the kids and he asked, "where are they?" So he was comprehending a lot, it seemed.

Rob called mom while we were there and she put the phone up to dad. He listened to what Rob was saying then he started "talking" quite a bit. It was just babble, but I believe he knew exactly what he was saying to Rob, it was just coming out very quickly. He stopped then I heard Rob say, "I'll see you tomorrow" and dad said, "OK". It was so good to see!!

We showed him Lily's pierced ears and he made a fun face like, "ooo, pretty!" and then we showed him Tyson's buzz cut and he laughed.

Oh, what a wonderful day to see him, it was so good and fun to see him sitting up. I asked him if he wanted to lay down, he said no. That's good, since he's always wanted to be in his bed.

What a wonderful Christmas present to us all. Hang in there dad!

Susie

December 21, 2009

I was able to visit dad today for just a little bit. Dad did everything that the physical therapist asked him to do. He did awesome today, but still looked sad. The physical therapist asked me to tell her all about dad, that she wanted to know who he was so she could cheer him up a little. I really like her, her name is Rhonda. She was very engaging with dad. He asked me for a drink of water and I asked him if he was in pain, he said no. He was more aware than I've seen him in a while.

Tahna
I was unable to go all last week because of work, so I had not seen him in a week and wow what a difference! He was sitting up in his chair and his face got bright and he said "Hey guys" when we came in. He asked how we were and just said a few things here and there. I gave kisses and hugs when it was time to leave. He also gave some baby talk to Kamryn which she just loved. It was good to see him like this.

Joe

Sunday, December 20, 2009

December 20, 2009

We went up to see Pop today and took the kids.
We passed Uncle Mike in the elevators and he said that Pop had just finished his therapy and was tired. We took the kids up and he was visibly happy to see them. They all said "Hi Grandpa" and the twins told him "Merry Christmas" and then ran around his room probably making him crazy. When we left, he motioned for Preston to come over and he gave him a kiss and gave Jack and Kendy a kiss too. It was awesome. He was tired, so we let him sleep. I did ask him if he wanted us to bring up a Christmas tree and he said, "No". It seems, to Tahna's point, that he was trying to figure out where he was and maybe why. He kept staring at the board on the wall by his bed. I think he was trying to read it and wondering why it didn't make sense. That is just my perception.
I also told him that we are glad he didn't leave us and asked if he wanted to leave us and he shook his head "No".
It sure is good to see him brighten up every once in a while. Let's all pray that he can continue to be there and not get moved to long term care. Mom said that they aren't as aggressive with rehab and therapy in those places. We want him to work.
~Brenda and Tony~
Today was a good day. Dad is really active and quick on his responses.

We showed him the Christmas cards the kids had made and read them to him. He held them in his hand and actually licked his finger/thumb to turn the page.

We told him that Rob and Marvin are coming and he said "good thing".

Out of the blue, he said "where's Tiff?"

He said he wanted a "drink of water"

Joe brought the kids today.

Steve

Saturday, December 19, 2009

Yesterday Steve and I were there while the speech therapist worked with Dad. He did pretty good. She explained a lot to us. He is very impaired but is making progress. She would sing a song to him like jingle bells and leaves out words for him to fill in the blank, like- jingle bells, jingle bells- jingle all the ____. And he would say- way. As far as us goes he remembers things and people and then sometimes he doesn't. He never can remember why he is in the hospital. She said Grandkids seem to be the one thing he remembers and to keep bringing them in. She also said when you visit, challenge him. Ask him yes or no questions. Or have him repeat something you do. They really want to try and keep him there. Today they had him exercising on a leg machine. When his left leg got tired they asked him to use his right leg and he did. That was huge!!

Tahna

Friday, December 18, 2009

Dad doing well!

Dad did so good today, all the therpists were so surprised. He was in a good mood and very cooperative. When the bishop came in he said, "Hi, John" and dad said, "Hi, Bishop!" He doesn't normally call people by their name, and with clear recognition. The hospital is re-evaluating him and will let us know at the beginning of the week whether or not he can stay at IMC for physical therapy. We are hoping he can.

Mom

Wednesday, December 16, 2009

Wednesday December 16

Dad was in a very bad mood today. He had to be in his wheel chair, but wanted to be in his bed. You can tell he just doesn't want to be in this state any more. He was supposed to go to a care facility this week, but mom's had to fix some things with insurance, so in last the couple days, dad has finally been starting to do what he needs to do and now the hospital isn't sure he'll be leaving; they may keep him now. It's just a toss up everyday.

Tahna

Sunday, December 13, 2009

We were able to take the kids and see dad today. When the kids came in, he just lit up and was so, so excited to see the grandkids. He took turns grabbing each one and holding their hand, smiling, talking to them (even though we couldn't understand him). He grabbed Alex and pointed at him, then pointed to Steve, trying to tell us something. He then motioned to Alex to cut his hair; we all laughed :) Then he just took turns looking and reaching out to each grandchild, smiling and making them feel so loved. It made their day.

Mike was there. He started rubbing dad's right foot and we all clearly saw it was very painful for him, so not real fair that he can't move his right side, but can feel the pain. He was very awake and alert.

Later tonight, he spoke to mom. She couldn't understand him, but thought to ask, "do you know why you're here in the hospital?". He shook his head no, so then she told him. He closed his eyes and frowned. He's in and out of remembering what happened. He's too weak for physical therapy so they are moving him to a long term care facility tomorrow or Tuesday.

Tahna

Friday, December 11, 2009

I was able to spend some time with dad tonight, but by the time I got there, they had worked him over pretty good with physical therapy and he was zonked out. When he did wake up, he didn't recognize or know who I was. It was heartbreaking. Mom says he's declining and doesn't even recognize her anymore. Tahna asked him if he knew who she was and he shook his head, no. I miss my dad a lot. I got very emotional. He looks very good, physically, even looks like he's lost some weight.

Susie

Dec 10th 2009

They lifted the ban on kids so LeAnn and I took the kids to see Grandpa. We caught him in the middle of doing some physical therapy. They had him standing and trying to straighten him up. It looked very painful. The therapist asked him to look over at his grand kids and he did. He then smiled at little Kami. After they were done they put him in the wheel chair to wait for the occupational therapist. We sat and talked with him for a bit. I put Kamryn on his lap and he just smiled at her. Then to our surprise Kamryn kept saying "Gampa, Gampa". Super cute...
It is so hard to see him like this. I am used to seeing him smile and interact with his grand kids. Please work hard and get better Pop. We love you.

Joe

Thursday, December 10, 2009

December 10, 2009

Today Dad was having a real hard time even sitting upright in his bed. He was sweaty and clammy and working with the speech therapist though not very well. It was a tough day for him. Mom said he had a rough time in physical therapy and that his heart rate was extremely high. They thought maybe his insulin was out of whack or something. That is due to his feeding tube. She feels like he really could use a lot of encouragement.

Brenda

Wednesday, December 9, 2009

December 9, 2009

They had dad stand today, just for a couple minutes and take a couple steps, with help. He's doing great on the 3 hours of physical therapy. He still wants to pull his feeding tube out and oxygen tube. He's had it, I think, and wants to get out.

He only needs oxygen when he's sleeping because he has sleep apnea. He's still very discouraged, but we also see improvements. Thanks to all for your support and prayers!

Tuesday, December 8, 2009

On the 12 floor

Dad is now on the 12th floor. Rehab was slow yesterday, but I hear he is on the best floor of the hospital now. I hear it's the happiest floor in the building. We still need lots of prayers and encouragements for Dad.

Sunday, December 6, 2009

They are going to transfer him to Rehab tomorrow on the 12th floor, and give
him a week to see if he is ready. If not we'll then take him to a care center. He is still
responsive and they are working him out. He did run a high fever due to a bladder infection.
But is now doing better. We are grateful he is still with us. He is a little down, and could use
prayers for his strength and determination. Thanks to everyone for your love and support and prayers. We couldn't have come this far with out it.

Tahna

November 6th 2009

Dad took a little step back today.
He was being naughty. He has pulled his feeding tube out three times today.
When my mother said why are you being naughty he gave here a mischievous grin.
I had to give him a pep talk. I told him he starts rehab tomorrow and has to work very hard. I know he can do it because he taught me the meaning of hard work so I know he can do it. He gave an "okay" then I had to go. He is being moved to the therapy floor at 10:30 tomorrow morning so lets hope he behaves.

Joe

Saturday, December 5, 2009

November 4th Saturday

I was only able to go over to the hospital for a short time today but it was very encouraging. One of the Nurses was feeding my father ice chips. When she told him to chew the ice he did. He would also swirl the ice around in his mouth and she was doing this to see where he is at as far as potentially eating real food. She said he was doing very well. He was swallowing properly, chewing the ice properly and all around doing great. He was very tired as they had already took him around in the wheel chair. They are going to start doing that twice a day for about two hours a time.
He continues to improve. Go DAD!!!

Joe

Friday, December 4, 2009

Visited Dad today. He looks so good. All the swelling has gone away, but his left arm is so skinny. I wonder if it's because of the staff infection that was there? They had him in a wheel chair for about 1 1/2 hrs today and it wore him out. When I got there at 3:30, he was still sleeping (since 11:30) and I couldn't get him to wake, even by 4:00. They also had to give him oxygen because it took so much out of him, but it's good for him.

He got approved to be in the IMC physical therapy for the next week. He's not quite ready, but the head lady really wants him to try it and we're hoping he can stay there, rather than long term care. He has to do 3 hours a day of physical therapy, but now is bushed after only 1 1/2 hrs, so he still needs everyone's prayers to be strong.

Susie

Wednesday, December 2, 2009

The speech therapist came in and during the course of treatment, asked if he wanted some ice. Yesterday when he asked this, the ST had to put the spoon to his mouth, but today he leaned toward the spoon. The ST said that is a good sign. He wasn't real responsive to any other commands, but it was good to hear him whisper some things and try to talk. He kept frowning and grimacing like "what am I doing here??"

It was good to spend time with him.

Susie
They got Dad up today in a wheel chair and gave him a ride around the halls and put him in front of a window to look out. He did really well. He got really tired and needed oxygen but over all did great. He has been answering people through out the day. The speech therapist worked with him today. He wanted his arm restraint off when me and Mom and Ja'Brael were there. We took it off and he said GOSH in a grouchy way. He hates that thing, so when you visit take it off and watch him. Just let him know as long as he doesn't take his feeding tube out, we'll let him loose. He got upset when Mom told him Ja'Brael was moving to Texas.. He needs lot's of encouragement, he is down about being in this situation.

Tahna

Tuesday, December 1, 2009

December 1st.

Dad is doing really awesome today.
I got there about 9 this morning. They were moving him to replace his feeding tube. He looked up at me and mumbled something I didn't understand.
I came back at 10:30 when they said he would be done and Rob and Marv were there along with my Mother. Tony and Brenda came later.
Dad spoke several times while we where there.
When Rob had to leave to get to the airport he said "no" like, please don't go. He then said Bye.
He called Rob by name a couple times and told me he was in pain on one occurrence. He is very verbal and seems to be getting better.
One of the Physical Therapists came in and said he is actually doing well enough if he improves, we might be able to keep him at the hospital for a few weeks for his therapy instead of moving him into a long term facility. Very good news!
Keep it going Dad, we are so glad you are doing better!
Joe

Moved to the 14th floor

Pop is doing well. Tahna said that he tried to talk to the nurse yesterday and it sounded like he said "Your welcome" after she said thank you. He looks much better with all the tubes removed etc. We still have a very long road ahead and hopefully we see improvement. Yesterday, Mom got a list of care centers that the insurance will cover. Rob and Marv took her to visit one that they liked very much. The insurance only covers three so we will visit the other two as Dad will need to move to one very soon. We want to look for one that has rehab so that he can get his brain repaired and reconnecting and his muscles working again. We want him to have the best chance to improve.
He has been moved to the 14th floor. Hospital visitation is still restricted to family, please.

Monday, November 30, 2009

For He is a God of Miracles!

When the physical therapist asked what his name was, my dad said, "John." When they left, they said, "thank you, John", he said "you're welcome." I guess he isn't ready to leave us for now, thank goodness. He is no longer considered critical and will be moved to the 14th floor today for rehab. Wow, what a turn-a-round. He's not out of the woods yet, but he's at least leaving critical care.

Susie

Sunday, November 29, 2009

Still hangin' in there

Dad is still hangin' in there - which is not what the doctor expected. He is stable right now. He is breathing on his own so far. By the end of the week, they may move him to a long care facility, but he has to be able to breathe on his own and manage his secretions (be able to cough on his own.) He also has to be off the heparin and go on the wayfarin in pill form.

They will do 1 more CT scan in a couple days to see how he's doing. He's still vulnerable to infections. He's still got a staff infection in his elbow and possible blot clot in his neck.

He is off the sodium, which is good; his fever is down, his BP is good, heart and lungs all good. We thank the Lord for 1 more day with him.

The Ventilator is out

After much prayer and fasting, we as a family decided to take the ventilator out and to not trach Dad. He looks so much better now that it's out. He's breathing on his own. If he continues to breathe on his own, they will move him to a long care facility in a couple days.

Saturday, November 28, 2009

Byu vs Utah

Had a great time watching the game with dad. No progress today, but he smiled when his grandkids came to visit.

Susie

Thursday, November 26, 2009

Thanksgiving with Dad

Today was very emotional for me. Dad was given another blessing. Thanksgiving certainly wasn't the same, but I was able to spend it with dad in his room, a lot of the time alone with him. I read to him, talked with him and held him for most of the time. I'm grateful for the time I had to spend with him today.

The doctors are giving him periodic doses of steroids to help the swelling come down. This should last for a couple of days.

He had his eyes open today, but not very responsive. Rob and Marvin came to visit and brought him an Elvis beanie baby. He smiled.

Susie

Wednesday, November 25, 2009

Small Turn Around

Everything is so different each day. The doctor says his breathing tube needs to come out by Friday, he's already had it in for almost 3 weeks. He's not doing well today, he's been sleepy and unresponsive all day.

We have 3 options: 1) take the tube out, see how he does and if he can breathe on his own. He's got to be able to cough things out on his own, and he can't do that yet. If they had to re-intubate, they would most likely not have very good success.

2) take the tube out and if he goes downhill, do a DNR and we lose him.

3) do a tracheostomy, then take the tube out. This is the safest measure, but we would have to move him to a long term facility where they would continue to do physical therapy. Could take years.

He's ready to be moved out of ICU. They know he'll most likely live, but what will his quality of life be with each option? He will have severe disabilities. He can't speak now and may not be able to ever. The Dr. is discouraged that his right side is not responding.

We also need to talk about leaving the feeding tube in. If we take it out, he will have to learn how to swallow on his own.

The clot was big enough, it has damaged the other side of his brain. We know he's in there, we know it, but what to do at this point and what would he want? We need lots of prayers at this time.

Susie

Elder Holland's letter

As you may notice, Dad's picture up top is with him and Elder Jeffrey R. Holland and Elder's Holland's wife. Dad helped him move some things from his storage shed a couple of months ago and Elder Holland bought dad lunch for it.

Someone emailed Elder Holland and told them about dad's stroke. He emailed back his sympathies and sent dad a card. What a wonderful man

Tuesday, November 24, 2009

November 24th

Dad is doing great today. Uncle Mike was in today the same time as me. We had a good time hanging out with Dad. The Cardiologist came in today and looked Dad over. Checked the readings on the breathing machine and was amazed at Dad's progress. He said they will continue to ween him off the machine completely today and if they can get him to cough on his own the breathing tube would be out by tomorrow. (With approval from Mother of course)
He was pretty tired but still responsive. He had his eyes open most of the time Mike was there and also when Mom was there.
The family should be very happy and positive about Dad's progress.

Joe

good day

Monday, November 23, 2009

Dad is having a really good day today very alert, understands some commands, healing finally. They had him sitting up for about 12 minutes towards the end he did it on his own for a minute. They said he did great today with Physical Therapy. He smiled a lot when we talked to him today. Tony and Joe said, "I know you can't see it but you kind of have a goat tee" and he smiled.
I talked to him and asked if he remembers having the stroke. Explained some things about the morning it happended, it seems like he was really trying to remember. They said the goal this week is to wean him off the ventilator. If by Sunday he does great without it they will plan to take it out. If he struggles with weaning then they will trach him. 3 weeks is about all the like them to be on a ventilator. Susie made him a DVD, we think he was able to watch some of it.

Tahna
It was nice to have another good day today with Dad. I arrived the same time as Tony this morning and we found Tahna in the room already. We broke the rules and all stayed in with Dad but the Nurse was okay with it. We had a good time talking to Dad. You can tell he was very alert today and could hear what we were saying. Tony told him he liked is Mustache and he gave us a good smile. I also showed him some pictures of Kamryn playing in the leaves and he smiled once again. These are the days that make you forget about the awful days like Saturday. Today Dad's eyes were like I remembered them even before the stroke. He would look right at you and although you saw some sadness I am sure because he wants to communicate, you also saw DAD. It was good to have him back.

Joe

He reached out to me!

This morning when I saw pop, he smiled and tried to reach his hand out to me. It was awesome!

Brett

Sunday, November 22, 2009

I was with dad today from noon to 4:00. He was very sleepy most of the time. He kept taking the oxygen sensor off his finger so the nurse had to switch it to his right arm. The swelling has gone down considerably in his left arm and the sores on his face are gone. No more gowns! They gave him an extra comfy mattress to make him more comfortable. From the CT scan, the hemorrhage has shrunk considerably and the infections seem to be going away. I made him a slide show of his kids and grandkids and we played it for him but he still wasn't aware enough to watch.

Susie
The Dr. just came in to talk to us and said, things are much better!! CT went great! His swelling is down, his bleeding is down. His infections are now getting better. His lungs are better, and there's talk of maybe this week letting him breath without the ventilator. He is sleepy but he is just resting and getting better. The Dr. said things are looking good, and
are no longer worried about the infections as much. Yeah- for fasting, blessings, and prayers!!

Tahna
This morning he isn't very responsive so they are doing another CT on his head as we speak. This morning the Priesthood and Relief Society came and offered me and Mom and Dad the sacrament. Mom had already taken it at the hospital service, so I was grateful and grateful they could give it to him. They sang a hymn and then blessed the bread and touched his mouth with the bread. Then blessed the water and dipped a sponge/swab in the water and put it in his mouth. It was very touching. I am a little worried today.

As soon as he comes back and they let us know, I will let everyone know. So far it has always come back no change. We'll pray for that or better.

Tahna

Saturday, November 21, 2009

The blood clot he has is in his neck not arm. They're hoping it won't travel to his heart or lungs or brain.Using all the meds they can to help the situation. They said the clots he is getting is probably due to the part of the brain that controls clotting, and it is on overdrive; that the platelets are doing their job in one area and then inviting all the other platelets to join too. Having a party unwanted. So they aren't thinning the blood, they are stopping it from getting bigger. When they get too big then they start to branch off and break apart and we don't want that.

Tahna
His CT came back didn't find anything that would cause all the infections yet. They are looking at other things kind of abnormal but aren't bringing that up now. Their goal is to find what is causing his immune system to be so weak. It will be 3-5 days before they get cultures back that may or may not have anwsers to what infections these are or turned into etc.. Still has a fever, was very sleepy this afternoon. He is swolen all over the place. So still up in the air of why things are the way they are.

Tahna

Update and goal for the day

Mom brought Bear in today. He licked Dads forehead but for the most part was pretty scared and wanted Mom. Dad was aware it was him. Mom said Bear misses him and loves him and he made a sad face and frowned. They did a procedure last night to check his heart with a scope to see if the infections were in or around his heart. It was not. They are going to do a CT scan and an MRI of his body not just the brain today to see if they can find a source for all this.
They did an ultra sound on his arm yesterday and found a blood clot in his left arm where the infection is. He still has a high fever. Still no change from yesterday as far as his progress.

Tahna

Friday, November 20, 2009

A fast for Dad

The doctors called everyone to a meeting that could be there. He said that Pop has some underlying conditions that are complicating his situation. He has had a staph infection in his lungs that has turned to a bit of pneumonia. He also has swelling in his left arm and elbow that they believe is another type of staph infection. They are looking at that today and deciding what to do. Staph in the joints is very serious. He also has a blood infection.
Pop's body is fighting all of these things including the sore outbreak around his mouth which they believe is residual from his system being overloaded from the shingles outbreak he had a couple of months ago and that didn't fully get better. So his immune system is very, very weak. It is serious and the doctor was very direct about what might lie ahead. His physical therapy has been very taxing on him so they are backing that off for a while.
So after that, Tony and Uncle Mike gave Pop a blessing. He looked terrible before the blessing and was not responsive at all except his eyes were open but he was looking right through everyone. During the blessing, he closed his eyes the entire time as he would through a prayer. When it was over, he opened his eyes and then I went to say goodbye and talked to him. I asked him if he was doing okay and his eyes widened and he nodded his head. The best response we had seen. Uncle Mike then went to talk to him and your Dad was trying to talk. Uncle Mike said, "Say what you wanna say, brother! Tell me what you want to say etc." and you could clearly tell that he was trying to make motions with his mouth. It was encouraging given all the bad scenarios we are dealing with. It was amazing to me and the first time in a week or so that I have really felt that he is in there. That doesn't mean that he doesn't want OUT regardless of how that happens.
So, it is still touch and go. Mom wants us to do a family fast tomorrow and ask for the Lord to take care of your Dad however he sees fit. So, if you can, please fast and pray. The doctor today said "Bring it on, all the help he can get, bring it on". They are allowing your mom to bring Bear up to see your Dad tomorrow morning. They are trying everything they can.
Pop is still very, very critical. It is touch and go. So, let's plan for the worst and hope and pray for the best.

Brenda

Worried about Dad

Today was a rough day. The Dr. said he doesn't like where dad's health is going. He has multiple infections that are making him very weak. His body not able to fight the infections are bringing on more infections.

We have permission to bring in Bear, his dog and best friend, tomorrow.

The Dr's are not sure what the underlying issue is that is causing the infections. His good, left arm is swollen 3 times the normal size and is hard and full of infection. His brother Mike gave him a blessing this afternoon. Yesterday the physical therapy was so hard, he cried. His fever is increasing, not decreasing and the number of infections in his body is multiplying.

The Dr. requested a meeting with mom and the kids to go over options today. We are having a fast tomorrow for all those who want to, and can participate.
Yesterday dad did really well in keeping his eyes open through out the day, not as sleepy. I brought some of his Elvis gospel music and played it. He had a tear in his eye. The nurse said he coughed on his own...which is good. He has pneumonia, and has had for a couple of days. Apparently he has 2 different types. 1 has cleared up, but he's fighting another type of pneumonia now, but everything looks good. He was able to sit up and balance for almost 5 minutes, which is really good! Uncle Mike was with him this morning and says he did well in keeping his eyes open.

Mom

Wednesday, November 18, 2009

November 18th

I was with Dad between 1 and 3 today. They worked him out for about 20 minutes. They had him sit up and hold himself that way. He did okay. They then leaned him on his Right elbow and he held himself surprisingly well.
I was joking with Dad about riding the fake bicycle earlier and he gave a smile. Still receptive to some commands and not at all on others, but then you can get him to smile when you say something funny so you know he can hear you.
Frustrating but encouraging.
Joe
I was with Dad this morning for 3 hours he was a wake a lot of that time. I talked with him about why he is in there. What happened, showed pictures. He did some frowning. I said, "Dad it is very important that you do what they ask you to do. So if they ask you to hold up fingers or wiggle your toes you need to,that's how they gage your progress. So if you want these tubes out of your mouth and out of this bed you need to do what they ask." Prior to that, the nurse said, "Does he like to watch t.v.?" I said, "ya, can we turn it on?" She said, "yes, try and put it on something he'll like." So I put it on the Mountain channel (sports) and BYU was on. I talked to him about that, and he smiled. He liked it on for a little bit. So after I went down to grab a bite while he was resting, I came back up and the nurse said he did better today. When she said wiggle your toes he did. So he's in there. Don't assume he can't understand. Mom said a prayer last night that he'd be more aware and receptive today, and he was. Bring things for him to look at when you are talking about something. Sports, grandkids etc.. Bring a picture that relates to what you're telling him. That will help him. I felt he has had a good day so far. He is still sleepy. But if you catch him with his eyes open get his attention and talk about things he likes.

Tahna
Dad's sores around his mouth look much better today!

Brett

No Visitors Please

Dad still can not have visitors besides family. If you feel impressed to visit him, please contact my mom first for permission. Thank you!

More responsive today!

Today dad was "responsive" for about an hour. I talked to him and turned on the TV so he could watch sports. I told him he needed to do what the nurses told him! After lunch, the nurses were very pleased with his reactions. They worked a lot on Physical therapy, that made him crash. The nurses said to bring in cards from grandkids, or whoever. He likes to look at them and hold them.

Tahna

CT scan - no change

Quick update.. Dad was very " sleepy" yesterday. He didn't respond to anything they asked him to. This is the worst phase they were talking about. How ever it still gives us peace that he can still squeeze a little and open his eyes. We have our good days and our bad days. He'll have more good days no worries. There was talk about a tracheostomy but that didn't come from the Dr. and he said he wouldn't consider that for another couple of weeks. They did another CT scan last night. Still no change. Not worse, so that is good.

Tahna

Tuesday, November 17, 2009

November 17th 2009

I was with Dad today. He seemed very tired. Not much of a change from the the previous day. The Physical Therapist came in to work him over and she really couldn't get him to wake up. As soon as she left he woke up for a few minutes and listened to Mom and I. Mom left Aunt Kathleen's cute card she brought in his hand and he was still holding it after we got back from lunch. The Dr's got a chuckle out of it. When we got back from lunch he woke up for a bit and gave Mom and I a little smile.
We are now 10 days into this and we are all hoping he turns around soon.
The boys still ask me every day why they cant come into the hospital to see Grandpa John. We try to explain but they don't understand. It is heart breaking but we know they will be able to see him soon.

Joe

Monday, November 16, 2009

An update on Pop......Tony and I were there tonight and had a nice discussion with his night nurse. He was not responding to her neuro checks, but she said it is expected that he has good days and bad days. He has a staph infection in his lungs. That is causing the fever etc and that is a serious infection it could cause pneumonia etc but he is getting antibiotics for that. He also has water blisters on his neck which they think might be an allergic reaction. Some of you may have heard that they were going to put in a trach, but the Dr. decided against it for now. He is still on the vent. She said they are still looking for him to manage his secretions and that he has quite of bit of gunk in his lungs and throat etc. He isn't doing that currently. His mouth looks better but it isn't healed. They are still treating that. They also stopped his sodium today. If you all remember, they were giving him extra sodium to help the swelling and fluid in his brain. They stopped that and are looking for his levels to come down slowly to a normal level. If so, that would indicate that the fluid is declining and swelling is as well. We'll see. She said she suspects his squeezing is a reflex as he can't let go when she tells him to. Just some random things she was talking about. From Brenda

Hard today for me

Today was really hard for me to be with dad. I was supposed to be there from 1:00 - 4:00, but when I saw him, his sores didn't really look better to me, his hands and feet were very swollen, and I lost it. I had to leave for about an hour and a half, but then I went back and the physical therapist showed me how to massage his hands and joints and to elevate him and make him more comfortable. Not much response today from him, although when I said his name from the right side, he tried for a second to look over. That made me happy. Susie

Sunday, November 15, 2009

So most of us were able to pop in today for those that didn't. Not too much changed. Still not incling the way they want. His blood pressure was too high, had a little bit of a respiratory problem. He has diarrhea and a fever they are going to check for a bacteria growth or something. He did not sit on his own today. But Mike waived goodbye and he winked at him.
Mom read scriptures from a paper and he grabbed the paper to hold and look at. He got a little worked up over it and his blood pressure went up so she gave him a break and left the room, it worried her. He wanted to take the tubes out
of his mouth today almost accomplished that.( not good) He tried to figure out how to get out of bed. There were times he was very uncomfortable but others okay. Still looks at you and squeezes your hand. Frowned when I said Jordan and Crystle are leaving today. Hang in there everyone.. We are doing good! From Tahna

Thursday, November 12, 2009

He knew we were there!

So today the 7 kids were all together for the 1st time in 5 years. It was so good to see Rob and Jordan! We all gathered around Dad's bed, held hands and Rob said a wonderful prayer. As soon as we said "amen", we looked up and his blood pressure was rising fast! It got to 208/98. Monitors were beeping. The nurses wanted us out. As we said goodbye one by one, his BP started declining. We know he could feel the spirit and knew we were there. We love you dad! Love Susie

More Sores :(

Today was hard as he started getting an infection around his mouth where the tubes are; it spread to his nose and ears. He looks so uncomfortable! We now have to wears gown and gloves and masks until the infection clears up. Susie

Monday, November 9, 2009

Brett and Tony gave dad another blessing

Sunday, November 8, 2009

Elders in the hospital gave dad a blessing

Dad's stroke November 9, 2009

My dad had a Hemorrhagic Stroke this morning. It was an intracerebral hemorrhage which means a blood vessel broke inside the brain. It took them about 4 hours to stop the bleeding. The concern for the doctors is the hemorrhage is still in there. They have him on some medication that keeps the swelling down. They said the next 7 to 10 days are critical. Once he is out of the clear they will decide if they need to do some surgery to remove the hemorrhage. From Joe
As I understand it, Sunday Morning, Nov 8, dad had a bad headache. He was being very "tipsy" walking funny and talking funny. He told my mom not to call the ambulance! (typical dad :) She did anyway, and it's a good thing. There was nothing leading up to this day to indicate there were any problems.