Don't know if anyone checks this site anymore since I stopped posting in May. However, we have reached an important juncture and want everyone who was concerned to know. Monday, Nov. 9 Timothy will return to work. He will be traveling to Wyoming to rejoin the undercutting crew that he was on when the accident Mar. 6 occured.
This has been a long journey, and Timothy has fought hard to get healthy. Keep him in your thoughts and prayers as he travels and as he begins his physically demanding work routine.
Friday, November 6, 2009
Thursday, May 28, 2009
May 28 at 8:30
At last the halo came off! Oh happy day! The right leg looks good, and the neck is healing--not healed but healing. Timothy now has a collar which we expected, the right leg has a "boot" to keep the foot from drooping, and the left leg continues to have a brace. His "nursing" care is down to a dressing on the right leg (just for a short time), the bone stimulation treatments each morning, and pills. Therefore, I will not be spending all my time at his house. He is steady enough on his walker that we don't fear that he will fall, and he can take care of his basic needs. He will still need someone to cook food, wash clothes, and clean house--not too much different than before the injury! As for food, we have had some wonderful meals brought to us this week. Thanks neighbors!
We will never be able to thank everyone enough who has supported us through this ordeal, but we do appreciate every act of kindness and every caring deed. Thanks everyone for keeping up with us. This will be my last blog entry. Please come see us, drop us a note at PO Box 376, Oregon, MO, 64473 or e-mail us at cdannar@ofmlive.net.
We have come a long way, and the journey will continue as Timothy mends and surgery is completed on the left knee in the future, but I think in time he will make a full recovery.
I feel that your prayers and mine were answered.
We will never be able to thank everyone enough who has supported us through this ordeal, but we do appreciate every act of kindness and every caring deed. Thanks everyone for keeping up with us. This will be my last blog entry. Please come see us, drop us a note at PO Box 376, Oregon, MO, 64473 or e-mail us at cdannar@ofmlive.net.
We have come a long way, and the journey will continue as Timothy mends and surgery is completed on the left knee in the future, but I think in time he will make a full recovery.
I feel that your prayers and mine were answered.
Saturday, May 23, 2009
May 23 at 11:25 a.m.
Looks like therapy will by twice a week on Tues. and Thurs. mornings at 10:00 for an hour. We are looking at Wednesday as being a big turning point. Hopefully, the halo off and good news about progress of Timothy's right leg. No more IV antibiotics after Mondy. Taking only one pain pill each day now.
Timothy and I seem to be in a routine of getting the medicines down, the IV taken care of, the bone stimulator treatment done, and the exercies accomplished.
I have begun to leave him alone for a few hours now and then. He is o.k. with that and keeps his phone nearby at all times. He is able to do more and more on his own, and that pleases him. He is anxious to be independent, and I don't blame him.
Timothy and I seem to be in a routine of getting the medicines down, the IV taken care of, the bone stimulator treatment done, and the exercies accomplished.
I have begun to leave him alone for a few hours now and then. He is o.k. with that and keeps his phone nearby at all times. He is able to do more and more on his own, and that pleases him. He is anxious to be independent, and I don't blame him.
Wednesday, May 20, 2009
May 20 at 7:30 a.m.
We went to our first out-patient therapy yesterday afternoon. The physical therapist determined that there isn't a lot she can do with Timothy until he can put more weight on his right foot. Also, she thought it best to save some sessions for when he has the surgery on the left knee. Insurance only pays for so many each year. She will give us some exercises that he can do at home on Thursday. I was not surprised. It didn't seem like that the PT was doing very much even at Madonna. The occupational therapist will continue working with Timothy's right arm twice a week. We go back Thursday at 10:30, and hopefully we'll have a definite schedule after that session. There is not a speech therapist on staff at this time so OT will incorporate some memory exercises with their work.
Timothy is gaining strength each day. His appetitie is very good, and he is walking with his walker more every day. We had no trouble transferring from walker to suburban or wheeling through the therapy suite. He enjoyed getting out yesterday to St. Joseph and eating at the Sonic. He just sat quietly and watched the traffic for a long time. Finally he said, "Boy its good to be out of the hospital."
Timothy is gaining strength each day. His appetitie is very good, and he is walking with his walker more every day. We had no trouble transferring from walker to suburban or wheeling through the therapy suite. He enjoyed getting out yesterday to St. Joseph and eating at the Sonic. He just sat quietly and watched the traffic for a long time. Finally he said, "Boy its good to be out of the hospital."
Saturday, May 16, 2009
May 16 Sat. morning
We are home! Paper work, last minute good-byes, pictures, exchange of contact info. with friends, last minute instructions--CPR with a halo vest of all things as we were escaping down the hall. I told Faye, the nurse, a sweetheart by the way, "This just won't happen today. I couldn't deal with it if it did!" She said, "O.K. I just have to tell you about it just in case." And finally at 10:00 on the dot we were driving away! Madonna Good-Bye--Home here we come! We were so excited!
Trip home was cold, wet, and drippy or pouring down rain. First glitch was the pharmacy. I had Timothy's insurance card but not the prescription one (didn't realize there was a difference. Mine is the same one.) They delivered stuff later--lots and lots of pills. Luckily home health arrived around 5:00. She had a pill box and helped me sort everything out. She found a glitch in the mg of one that didn't agree with what Madonna had written down. Got that straightened out with about four phone calls.
And then came the IV. It is so simple that the home health person couldn't believe it. And to be fair, Faye couldn't picture the concept of no pole, no pump, etc. either. So she had sent some tubing and extra tubing just in case. Home health person kept questioning and calling to make sure we were getting it right. We were; it worked--nothing to it.
Then came supper--I was determined it would be home-cooked. I had brought sacks and sacks of stuff in preparation. First thing I needed--a potato peeler or even a paring knife--not to be found in Timothy's bachelor dwelling. He did have steak knives. About to lose it, I sent husband home for some essentials for cooking a meal. Luckily, we live about a mile away. Finally around 8:00 we sat down to a meal at home. Not too bad, the potatoes got a little scorced as I was making the gravy, but they were eatable.
We had some visitors in the midst of all these goings-on which I loved. Made Timothy's return special.
Everyting is better today. I'm rested. I've done all the things for him that I am supposed to do at least twice, and I feel more at ease with being a "nurse."
I do not know therapy schedule yet. We go Tuesday at 1:00 for our first visit. It may be just paper work and evaluation.
Trip home was cold, wet, and drippy or pouring down rain. First glitch was the pharmacy. I had Timothy's insurance card but not the prescription one (didn't realize there was a difference. Mine is the same one.) They delivered stuff later--lots and lots of pills. Luckily home health arrived around 5:00. She had a pill box and helped me sort everything out. She found a glitch in the mg of one that didn't agree with what Madonna had written down. Got that straightened out with about four phone calls.
And then came the IV. It is so simple that the home health person couldn't believe it. And to be fair, Faye couldn't picture the concept of no pole, no pump, etc. either. So she had sent some tubing and extra tubing just in case. Home health person kept questioning and calling to make sure we were getting it right. We were; it worked--nothing to it.
Then came supper--I was determined it would be home-cooked. I had brought sacks and sacks of stuff in preparation. First thing I needed--a potato peeler or even a paring knife--not to be found in Timothy's bachelor dwelling. He did have steak knives. About to lose it, I sent husband home for some essentials for cooking a meal. Luckily, we live about a mile away. Finally around 8:00 we sat down to a meal at home. Not too bad, the potatoes got a little scorced as I was making the gravy, but they were eatable.
We had some visitors in the midst of all these goings-on which I loved. Made Timothy's return special.
Everyting is better today. I'm rested. I've done all the things for him that I am supposed to do at least twice, and I feel more at ease with being a "nurse."
I do not know therapy schedule yet. We go Tuesday at 1:00 for our first visit. It may be just paper work and evaluation.
Thursday, May 14, 2009
May 14 at 5:30
Timothy had the last of his therapies and consultations today. Social workers are still trying to co-ordinate our follow-up visit to Madonna. It will probably be sometime in August.
We took a four-block wheelchair walk today. I was talking and pointing out different things. When we left the Madonna grounds, the sidewalk had two or three rough places along the way. When I ran into the first one, Timothy said, "Mom, quit talking and pay attention to where we're going." After the third rough ridge he said, "This wasn't a very good place to go." Finally, I replied, "We aren't always going to have smooth Madonna sidewalks. We've got to learn to deal with all kinds of rough patches." As we reached the Madonna turn-in, Timothy seemed to be holding onto his Halo. I asked him, "Are you shading your eyes from the sun or holding your Halo on?"
"A little of both!", was the wiseacre reply.
So with everything we've been through, Timothy still has his sense of humor. I think I'm ready for the next chapter titled "Back Home Again!"
We took a four-block wheelchair walk today. I was talking and pointing out different things. When we left the Madonna grounds, the sidewalk had two or three rough places along the way. When I ran into the first one, Timothy said, "Mom, quit talking and pay attention to where we're going." After the third rough ridge he said, "This wasn't a very good place to go." Finally, I replied, "We aren't always going to have smooth Madonna sidewalks. We've got to learn to deal with all kinds of rough patches." As we reached the Madonna turn-in, Timothy seemed to be holding onto his Halo. I asked him, "Are you shading your eyes from the sun or holding your Halo on?"
"A little of both!", was the wiseacre reply.
So with everything we've been through, Timothy still has his sense of humor. I think I'm ready for the next chapter titled "Back Home Again!"
Wednesday, May 13, 2009
May 13 at 4:30
Not much happening today. I am trying to tie up loose ends; Timothy continued with his therapies. We went on a long walk this afternoon. Timothy is wheeling his wheelchair more and more by himself and getting stronger all the time. We are saying our good-byes to the staff and the patients and their families who we have become acquainted with while here.
I had instruction on the IV procedure. Think I can handle that.
Just counting down the days and now the hours!
I had instruction on the IV procedure. Think I can handle that.
Just counting down the days and now the hours!
Tuesday, May 12, 2009
May 12 at 2:30
The highlight of Timothy's day was to go to WalMart with Brooke (OT) and shop for a hand-held shower hose and suction cup soap and shampoo holders. Then we bought take-out from a McDonald's in WalMart. Timothy finally got his French fries.
Making all kinds of arrangements to go home. I will learn about IV procedure tomorrow. Therapy sessions and home health care are being scheduled through Heartland in St. Joseph.
Timothy is "walking" more and more with his walker. Arms and legs are all getting stronger each day. Next step is to get rid of the Halo--maybe May 27.
Some of you following this blog have asked for some contact info. for later.--You can send notes to PO Box 376, Oregon, MO 64473. That's Timothy's mailing address. My e-mail is cdannar@ofmlive.net.
Making all kinds of arrangements to go home. I will learn about IV procedure tomorrow. Therapy sessions and home health care are being scheduled through Heartland in St. Joseph.
Timothy is "walking" more and more with his walker. Arms and legs are all getting stronger each day. Next step is to get rid of the Halo--maybe May 27.
Some of you following this blog have asked for some contact info. for later.--You can send notes to PO Box 376, Oregon, MO 64473. That's Timothy's mailing address. My e-mail is cdannar@ofmlive.net.
Monday, May 11, 2009
May 11 at 5:00
Timothy and I just returned from seeing the orthopedic surgeon at St. Elizabeth's. He said everything looked good; that Timothy was a quick healer. The bones are beginning to close together, and the alignment is acceptable. We had absolutely no trouble transferring from walker to suburban and back. When we finally left the Dr.'s office, we took off looking for fast food. Timothy said, "This is my first meal away from Madonna." The Taco Inn was a satisfying change. We will continue our search for Burger King and French fries, however, another time.
We are still scheduled to leave Madonna this Friday around 10:00 a.m. Yahoo!
We are still scheduled to leave Madonna this Friday around 10:00 a.m. Yahoo!
Thursday, May 7, 2009
May 7 at 4:30
Timothy had his first bad experience at Madonna today. His community outing centered around a trip across town to a museum. It took 20 min. to get everything organized and Timothy and the one other participant hooked down safely in the van. It took another 20 min. to get to the museum. When we arrived, it was very chaotic with hundreds of noisey school children on a field trip. The two attendents had not brought enough money for them all to get in (they didn't seem to know it would cost). Jessica was with Timothy and offered to pay his way, but they decided to just take the other gentleman on a "tour of the grounds." Brandi, Courtney Jean, and I came in another vehicle so we paid our way in. Then we were told we had only 30 min. to look around before we had to meet and start back. We could hardly find a path to take the wheelchair with all the kids, parents, and supervisors. Besides all of that the two women in charge cannot drive a van very well or competently operate the equipment!
Timothy and I talked and decided he could be using all of this time to better use--lifting weights, practicing walking with his walker, almost anything. Next week we won't be going on group community outings.
Other than that everything is going smoothly.
Timothy and I talked and decided he could be using all of this time to better use--lifting weights, practicing walking with his walker, almost anything. Next week we won't be going on group community outings.
Other than that everything is going smoothly.
Wednesday, May 6, 2009
May 6 at 3:30
Today we practiced getting Timothy in the suburban again--just he and I with no help. We did all right. On Monday, Madonna is planning on me taking Timothy across town to see Dr. Swanson (leg surgeon) by myself. As I am the one who will be carting him back and forth to therapy sessions in St. Joe, I need to be knowledgeable and confident in how to manage Timothy, the wheelchair, the walker, and the ins and outs of the vehicle. Please wish me luck as we will both be a little nervous.
The highlight of our day was an outing to a local grocery store. We were transported by a Madonna van. Timothy wheeled himself across the parking lot, through the store doors, and down the aisles. He was to locate four items by himself by reading the aisle signs and reading the shelves. He had to make the most economical choices for all items. When we returned, he and the other patient were to date the food items and store them away properly in the "kitchen."
Timothy was excited. He kept saying, "This is the first time I have been "out" since coming here".
The highlight of our day was an outing to a local grocery store. We were transported by a Madonna van. Timothy wheeled himself across the parking lot, through the store doors, and down the aisles. He was to locate four items by himself by reading the aisle signs and reading the shelves. He had to make the most economical choices for all items. When we returned, he and the other patient were to date the food items and store them away properly in the "kitchen."
Timothy was excited. He kept saying, "This is the first time I have been "out" since coming here".
Tuesday, May 5, 2009
March 5 at 5:30
Great news--we'll be coming home May 15! Today the PT took him to my vehicle, and he helped Timothy in the first time, and then I helped him in by myself a second time. I went to Penneys and bought him a pair of sneakers (he has had no shoes this entire time). We are ready to roll.
Goals are for him to walk 15 feet with a walker by then, and be able to navigate his wheelchair by himself before we leave. Tomorrow they are going to start him on what they call "re-entering the community." He and another patient will be taken to places of their choice here in Lincoln. It can be the Harley Davison shop, Wal Mart, park, etc. They will be expected to navigate curbs, sidewalks, doorways, etc. by themselves with maybe a little help at first. They will also be "cooking" one day a week.
The infection doctor arranged for his IV antibiotics to be given only twice a day for 1 1/2 hours each instead of three times for an hour.
Out-patient therapy will be arranged at Heartland in St. Joseph, Missouri and will begin May 18.
I'll post therapy schedules when I know them because we sure want visitors when we get home. We'll be setting up camp at Timothy's house. Thanks again for all the prayers and caring acts of kindness. We couldn't have come this far without you.
Goals are for him to walk 15 feet with a walker by then, and be able to navigate his wheelchair by himself before we leave. Tomorrow they are going to start him on what they call "re-entering the community." He and another patient will be taken to places of their choice here in Lincoln. It can be the Harley Davison shop, Wal Mart, park, etc. They will be expected to navigate curbs, sidewalks, doorways, etc. by themselves with maybe a little help at first. They will also be "cooking" one day a week.
The infection doctor arranged for his IV antibiotics to be given only twice a day for 1 1/2 hours each instead of three times for an hour.
Out-patient therapy will be arranged at Heartland in St. Joseph, Missouri and will begin May 18.
I'll post therapy schedules when I know them because we sure want visitors when we get home. We'll be setting up camp at Timothy's house. Thanks again for all the prayers and caring acts of kindness. We couldn't have come this far without you.
Monday, May 4, 2009
May 4 at 6:00
Timothy had a great day. When I arrived Butch and Jennifer Prussman were visiting with him, and before they arrived, the doctor had taken his trach out. His voice is a little breathy again, but that should end in a day or two. Therapies went well, and the psychologist visited with him a little. He had answers for all her questions. He is telling everyone who visits to be sure and wear their seatbelts. So he did learn something from this experience. He is really enjoying visits from friends.
So now Timothy just has the Halo, the pick line for the IV antibiotic, and a brace on the left leg. Yeah! Yeah!
He and I went to visit with Carl today. He was able to wave and make eye contact. He is starting to come around. Hurrah! Hurrah! Good news all around.
If anyone from home is coming this way by Thursday, we need a favor. Timothy has the UP laptop at his house, and UP has his. Mike can make the exchange Thursday if I have it by then. So if you're coming this way, just call father Tim at home. If this doesn't work no worry, we'll take care of it the next half. If I had known just a little sooner, I would have brought it up with me.
We will learn the new exit date tomorrow!
So now Timothy just has the Halo, the pick line for the IV antibiotic, and a brace on the left leg. Yeah! Yeah!
He and I went to visit with Carl today. He was able to wave and make eye contact. He is starting to come around. Hurrah! Hurrah! Good news all around.
If anyone from home is coming this way by Thursday, we need a favor. Timothy has the UP laptop at his house, and UP has his. Mike can make the exchange Thursday if I have it by then. So if you're coming this way, just call father Tim at home. If this doesn't work no worry, we'll take care of it the next half. If I had known just a little sooner, I would have brought it up with me.
We will learn the new exit date tomorrow!
Saturday, May 2, 2009
May 2nd at 7:00pm
Today Timothy was re-evaluated by all three therapies. Zach, Jeremy and Lisa are spending the weekend in Lincoln with Timothy. Jason Vavara (a railroad buddy) and family came by to visit and brought several magazines for Timothy to enjoy. Otherwise, it has been a pretty quiet day. Timothy's right leg continues to hurt some but otherwise he is pretty comfortable.
Friday, May 1, 2009
May 1 at 3:30
Timothy is back at Madonna. He is in great spirtis, ready to get back to work and to get home. This morning a woman came and brought an ultra sound device that is to promote bone healing. It is to be attached to the site of the bone fracture once a day for 20 min. for several weeks.
To Timothy's railroad friends and others: Timothy has a cell phone now, but not his old cell numbers. So if you haven't heard from him and think you should have its because he doesn't know your number. Give him a call.
Madonna is great but we are all anxious to get home and back to a semi-normal life.
To Timothy's railroad friends and others: Timothy has a cell phone now, but not his old cell numbers. So if you haven't heard from him and think you should have its because he doesn't know your number. Give him a call.
Madonna is great but we are all anxious to get home and back to a semi-normal life.
Thursday, April 30, 2009
April 30 at 4:00
First we were told that the Halo brace was going to come off today between 12:00 and 12:30. The men came who were to supply the new brace. The Dr. was detained. A new time of 2:00 was set. The Dr. arrived and told us that his colleagues had convinced him that the Halo should stay in place for another 4 weeks. The older, wiser doctors say it is healing as it, better not change things just yet.
Timothy, Tim, and I were quite disappointed. However, the neurosurgeton at Mercy had cautioned us just before we left there to not be in a hurry to take it off. He said, "If it is healing, leave it alone."
We are still supposed to return to Madonna tomorrow.
Leg doctor changed dressing on right leg. It looks good. He will look at it again in two weeks.
Timothy, Tim, and I were quite disappointed. However, the neurosurgeton at Mercy had cautioned us just before we left there to not be in a hurry to take it off. He said, "If it is healing, leave it alone."
We are still supposed to return to Madonna tomorrow.
Leg doctor changed dressing on right leg. It looks good. He will look at it again in two weeks.
Wednesday, April 29, 2009
April 29 at 5:45
I stayed the night with Timothy, and Tim was over here by 5:00 so I could go home (our Madonna duplex) and shower. We have been waiting the entire day for the Halo doctor to come by, and we still haven't seen him. Maybe tomorrow.
Timothy has been up on his legs twice today with the aid of a walker, and two assistants. He was able to hop/walk around his bed about 15 feet. The right leg that had the surgery is, of course, very painful, and he can only put toe-tap weight on it for now. He has not had any light-headedness or nausa since the surgery and is eating everything in sight.
While I was blogging yesterday afternoon, they took out what I call the peg tube (it was used at Mercy to give Timothy nutrients, meds, etc). It has been an irritation for weeks becuase the Halo vest was riding on it, and it hasn't been used, but they hesitated to remove it because of yesteryday's surgery--we might need it. One more thing gone!
Every day is one more step of progress. Timothy is sure looking forward to going home now that it is in sight. Asks each day how much longer we think it will be. Unfortuantely, Tim and I are now sure. We feel that Madonna will change the exit date now that they can work with the legs.
Timothy has been up on his legs twice today with the aid of a walker, and two assistants. He was able to hop/walk around his bed about 15 feet. The right leg that had the surgery is, of course, very painful, and he can only put toe-tap weight on it for now. He has not had any light-headedness or nausa since the surgery and is eating everything in sight.
While I was blogging yesterday afternoon, they took out what I call the peg tube (it was used at Mercy to give Timothy nutrients, meds, etc). It has been an irritation for weeks becuase the Halo vest was riding on it, and it hasn't been used, but they hesitated to remove it because of yesteryday's surgery--we might need it. One more thing gone!
Every day is one more step of progress. Timothy is sure looking forward to going home now that it is in sight. Asks each day how much longer we think it will be. Unfortuantely, Tim and I are now sure. We feel that Madonna will change the exit date now that they can work with the legs.
Tuesday, April 28, 2009
April 28 at 5:30
We are at St. Elizabeth Hospital as we planned. The orthopedic surgeon told us the surgery on the right leg went very well. The surgery took 3 and a half hours. Then we had to wait for the Dr. to talk to us. Then we had to wait at least another 2 hours for Timothy to get back from recovery. As the nurse in Timothy's room was hooking up monitors and IV stuff, she gave Timothy a hand-held gizmo. She said he could press the button on it, and it would give him pain medicine. He replied, "Push the button and hold it down." Later his father was trying to explain about the x-rays the Dr. showed us with all his rods, screws, and plates in his leg. Timothy said, "rebar?" Father replied "Yes, with a few hose clamps." Its a good thing they both still have their sense of humor.
They told us the scan on his neck was put off til tomorrow. But just a short time ago they changed that, and said it would take place tonight, but not be read til tomorrow.
We think we will be here until Friday.
I was to be at Madonna by 7:15 this morning so I could ride over in the van with Timothy to the hospital. I don't know if I was nervous about not over sleeping or just plain nervous, but I think I saw every hour go by during the night. Consequently, I have been really tired today.
Thanks again everyone for your prayers and concerns. I know this whole deal has gone on and on. I appreciate anyone who is still hanging in there with us, and keeping up-to-date.
They told us the scan on his neck was put off til tomorrow. But just a short time ago they changed that, and said it would take place tonight, but not be read til tomorrow.
We think we will be here until Friday.
I was to be at Madonna by 7:15 this morning so I could ride over in the van with Timothy to the hospital. I don't know if I was nervous about not over sleeping or just plain nervous, but I think I saw every hour go by during the night. Consequently, I have been really tired today.
Thanks again everyone for your prayers and concerns. I know this whole deal has gone on and on. I appreciate anyone who is still hanging in there with us, and keeping up-to-date.
Monday, April 27, 2009
April 27 at 5:00
I had the weekend at home, and Jeremy was here with Timothy. Sunday he had my sister and two of her sons as visitors. Also, Jessica, Courtney Jean, and Brandi were here.
Timothy did very well on his final driving skills test today. Brooke said that on one part he is her first patient to score 100%. Kevin Markt has spent the day with us, and he agreed that some of those tests were pretty complicated.
Tomorrow Timothy goes again to St. Elizabeth Hospital here in Lincoln for surgery on his right leg. They plan to put in the rod, scan the neck and maybe remove the Halo and trach. We do not know how long he will be there, but he will return to Madonna until at least May 6. When he returns, they will re-evaluate and probably give us a new exit date.
Timothy is still having a fit because I ate one of his Reese's peanut butter cup candy bars. Luckily, Kevin brought him a whole bag full. I never even knew he liked them so much.
This is for Ciara: I visited Carl today. He is doing much better. The PT therapist was asking him to look L and R and up and down, and he was responding.
Timothy did very well on his final driving skills test today. Brooke said that on one part he is her first patient to score 100%. Kevin Markt has spent the day with us, and he agreed that some of those tests were pretty complicated.
Tomorrow Timothy goes again to St. Elizabeth Hospital here in Lincoln for surgery on his right leg. They plan to put in the rod, scan the neck and maybe remove the Halo and trach. We do not know how long he will be there, but he will return to Madonna until at least May 6. When he returns, they will re-evaluate and probably give us a new exit date.
Timothy is still having a fit because I ate one of his Reese's peanut butter cup candy bars. Luckily, Kevin brought him a whole bag full. I never even knew he liked them so much.
This is for Ciara: I visited Carl today. He is doing much better. The PT therapist was asking him to look L and R and up and down, and he was responding.
Thursday, April 23, 2009
April 23 at 4:00
Timothy just finished his last therapy session of the day and is resting. The highlight of our day was a big box from cousin Corey and his friend, Jessica. It contains all kinds of items to keep him entertained and working--3-D puzzles, slinky, airplane models, card games, rubber chicken that hatches an egg (to be squeezed with the right hand), a UP train engine plus home-baked cookies, and some other good stuff. Timothy was quite impressed.
This week he has really taken an interest in his greeting cards and e-mails. He often says, "Why even such and such knows about me and sent a card. Isn't that somethin'?"
Last night for the first time Timothy wanted to read this blog because so many people refer to it in their cards and messages. He didn't understand what they were talking about. He just read the last three entries. He was very touched by the comments his Aunt Susie and Erin had made. Said he would read more later. All of the caring from everyone is just overwhelming.
There is a sixteen year-old boy here with brain injuries, and we have become acquainted with his family. The step-mother came to Timothy's room this week, and was so amazed at his progress. She said, "Timothy is an inspiration for our family." Their son is still in that stage of kinda staring but not yet quite awake. I so hope for the best for them. I know just how they feel.
If I had my life to live over again, I would become an occupational therapist. I have the deepest respect for Brooke and her work.
Well, I may be rambling...Thanks for reading!
This week he has really taken an interest in his greeting cards and e-mails. He often says, "Why even such and such knows about me and sent a card. Isn't that somethin'?"
Last night for the first time Timothy wanted to read this blog because so many people refer to it in their cards and messages. He didn't understand what they were talking about. He just read the last three entries. He was very touched by the comments his Aunt Susie and Erin had made. Said he would read more later. All of the caring from everyone is just overwhelming.
There is a sixteen year-old boy here with brain injuries, and we have become acquainted with his family. The step-mother came to Timothy's room this week, and was so amazed at his progress. She said, "Timothy is an inspiration for our family." Their son is still in that stage of kinda staring but not yet quite awake. I so hope for the best for them. I know just how they feel.
If I had my life to live over again, I would become an occupational therapist. I have the deepest respect for Brooke and her work.
Well, I may be rambling...Thanks for reading!
Wednesday, April 22, 2009
April 22 at 4:30
Timothy had a great day. He started using his right arm a lot more--ate most of his lunch with it. He kept saying, "I wish Brooke could see me. This is all because of her." He is so very pleased that it is not paining him very much, and he is able to use it. The PT therapist found a better wheelchair match for him so it is more comfortable. I went to Alltel and got him a cell phone. Luckily he had insurance which I didn't know so it is just like his old phone the same number and everything. I did block text messaging for now. He can add that later. Didn't think he could deal with that yet. He is just like a kid with a new toy. Another great thing--a guy came with a saw and cut a slot out of his Halo vest so it doesn't ride on his stomach peg line. I wish I'd known they could do that. He is so much more comfortable now. The peg line can't come out until the leg surgery is completed next Tuesday.
After his last therapy, he and I took a stroll around the building outdoors. He has been taken out before, but this is the first time that I felt he really enjoyed it.
He is talking about , when I get the leg fixed, when I get home, and when I get back to work. He is definitely looking forward.
After his last therapy, he and I took a stroll around the building outdoors. He has been taken out before, but this is the first time that I felt he really enjoyed it.
He is talking about , when I get the leg fixed, when I get home, and when I get back to work. He is definitely looking forward.
Tuesday, April 21, 2009
April 21 at 5:00
Some changes were made today. Timothy will no longer need the one-on-one attendant because he is doing so well. He was not happy about that. He said, "Who am I going to visit with when I wake up in the middle of the night?" They have changed his wheelchair to one that he can wheel himself so that he has more control and will be using his right arm more. The OT therapy went very well. He was able to use his right elbow without pain with the help of Brooke's e-stem therapy. Speech therapy is going great. I feel that he is dealing with the accident facts quite appropriately. He is beginning to think about going home and how we can make changes to his house so we can take care of him and later he can take care of himself. He wants a cell phone. He is amazed at all the cards and e-mails. He says, "I don't even know that many people." "Why do they all care about me?" All good signs.
Thanks everyone for your continuing concern and prayers. He is doing so well because of it.
Thanks everyone for your continuing concern and prayers. He is doing so well because of it.
Monday, April 20, 2009
April 20 at 6:00
Today the psychologist and I told Timothy everything we know about the accident. He has not remembered anything about it. When we told him about James and Kevin, he became quite emotional just as anyone would. He had been asking us and the railroad men what happened so it was time to tell him the truth. I think he will remember what we told him tomorrow. That was one of the concerns--that he would have to be told more than once and have to endure the pain over and over.
The therapists were alerted that he was aware of the facts so they were careful with him but kept him busy. The speech therapist had him use the computer and find the stompers 4x4 website. That helped take his mind of things for awhile.
Right now he is resting. The psychologist will be in from time to time to talk with him this week.
The family has been dreading this moment, but I am glad Timothy knows the truth so we can deal with it honestly.
The therapists were alerted that he was aware of the facts so they were careful with him but kept him busy. The speech therapist had him use the computer and find the stompers 4x4 website. That helped take his mind of things for awhile.
Right now he is resting. The psychologist will be in from time to time to talk with him this week.
The family has been dreading this moment, but I am glad Timothy knows the truth so we can deal with it honestly.
Sunday, April 19, 2009
April 19 at 6:30
Zach and Alethia reported on Timothy awhile ago. They said he had a pretty good weekend with some visitors from Oregon filling up part of his day Saturday. His evaluation therapies were completed Sat. afternoon so Monday he should back to work. Timothy's bigggest complaint right now is his mouth. Either the antibiotics or his breathing through his mouth when sleeping is causing it to be very sore. They are to give him something for that today.
Thanks Mike for visiting us at St. Elizabeth's and for your help. We appreciate your continuing concern. It means a great deal to our family.
Thanks also to Gang 8568 for your card and support. Timothy will enjoy reading all the signatures. You railroad guys are the best!
A big "Thank You" to Jessica who stayed with Timothy during the night while he was at St. Elizabeth's so Tim and I could get some rest. We have learned that we really don't want Timothy alone in the hospitals. He can't talk loud enough to relay his needs.
I'll be back to Lincoln tomorrow and will have first-hand reports on his therapy sessions tomorrow evening.
If those reading this have time, I really appreciate your comments especially when I am at Lincoln.
Thanks Mike for visiting us at St. Elizabeth's and for your help. We appreciate your continuing concern. It means a great deal to our family.
Thanks also to Gang 8568 for your card and support. Timothy will enjoy reading all the signatures. You railroad guys are the best!
A big "Thank You" to Jessica who stayed with Timothy during the night while he was at St. Elizabeth's so Tim and I could get some rest. We have learned that we really don't want Timothy alone in the hospitals. He can't talk loud enough to relay his needs.
I'll be back to Lincoln tomorrow and will have first-hand reports on his therapy sessions tomorrow evening.
If those reading this have time, I really appreciate your comments especially when I am at Lincoln.
Friday, April 17, 2009
Friday, April 17 at 5:30
It was a long day. This morning the infection doctor said we needed to leave Timothy at St. Elizabeth's one more day because his temperature got over 100 degrees last night. Then after lunch, the orthopedic surgeon came in and said he had just talked to the infecton doctor and convinced him that under the circustances, it was normal for his temperature to rise during the night. So finally, around 4:00 we were settled back at Madonna. Timothy seems very glad to be back here.
Thursday, April 16, 2009
April 16 at 3;30
Doctor Swanson said the foot looks good. He cleaned it all out very throughly and closed up the incisions. The rod surgery is still planned in two weeks. He said Timothy should be able to put weight on that right leg almost immediately after that surgery. He is scheduled to return to Madonna tomorrow. Therapists there will re-evaluate him, and he should be back on all his therapies Monday.
I want to mention again, that we think he is ready for company. Everything is looking swell!
I want to mention again, that we think he is ready for company. Everything is looking swell!
Wednesday, April 15, 2009
April 15 at 5:30
We've had several good reports today. The orthopedic surgeon was a lot more positive today. The infection is only in the foot not up the calf. The surgery on that leg for the rod is still scheduled in two weeks. Of course, tommorrow's cleansing of that foot infection will tell us more. The neurologist checked his Halo pins and thinks we can get two more weeks out of them which is good. Hopefully, Timothy will be back at Madonna Friday and back to his therapies by Monday. Madonna is keeping his room for him for now so we don't have to gather up his things, and they are allowing us to stay in their housing although technically we are not a Madonna patient family.
We are feeling better about things after talking with the several doctors involved with Timothy's care at Saint Elizabeth's.
The railroad support has again surprised us with a visit and a beautiful flower arrangement. Thanks Mike and Carter.
While we were visiting Madonna one of Timothy's student therapist who he really likes, Megan, told us that she has completed her training at Madonna and will not be there when Timothy returns. Timothy will really miss her. She is the one that makes him plant gardens, go shopping, arrange his closet, add and subtract, and know the date, time, and place.
We are feeling better about things after talking with the several doctors involved with Timothy's care at Saint Elizabeth's.
The railroad support has again surprised us with a visit and a beautiful flower arrangement. Thanks Mike and Carter.
While we were visiting Madonna one of Timothy's student therapist who he really likes, Megan, told us that she has completed her training at Madonna and will not be there when Timothy returns. Timothy will really miss her. She is the one that makes him plant gardens, go shopping, arrange his closet, add and subtract, and know the date, time, and place.
Tuesday, April 14, 2009
April 14 at 2:00 p.m.
Timothy got the external fixator removed today. Before that surgery another doctor came in and examined his left knee that has the ligament damage. He said that it was developing scar tissue and thus making it stronger. He wants to restart physical therapy with that leg and let him put weight on it. That's the good news.
The surgeon talked to us after the fixator surgery. He is very concerned about the infection in the right foot. He is keeping him at St. Elizabeth's until at least Thursday. They will start antibiotics intravenously immediately and look at it again Thursday. He said it looks bad.
Here is where we are: Saint Elizabeth Regional Medical Center, 555 South 70th Street, Lincoln, NE 68510
Phone: 402-219-8000 (not Timothy's phone yet)
website: www.SaintElizabethOnline.com
I don't know about e-mail services yet. We thought we were only going to be here this morning and then back to Madonna. We're a little rattled right now.
As always, keep Timothy in your prayers.
The surgeon talked to us after the fixator surgery. He is very concerned about the infection in the right foot. He is keeping him at St. Elizabeth's until at least Thursday. They will start antibiotics intravenously immediately and look at it again Thursday. He said it looks bad.
Here is where we are: Saint Elizabeth Regional Medical Center, 555 South 70th Street, Lincoln, NE 68510
Phone: 402-219-8000 (not Timothy's phone yet)
website: www.SaintElizabethOnline.com
I don't know about e-mail services yet. We thought we were only going to be here this morning and then back to Madonna. We're a little rattled right now.
As always, keep Timothy in your prayers.
Monday, April 13, 2009
April 13 at 4:00 p.m.
The family has talked it over, and we think that Timothy would benefit by having visitors, especially on the weekends when he is not occupied with any therapies.
However, that brings us to a discussion that we have been putting off. Timothy's doctors have told us that because of his severe brain injury he absolutely cannot have alcohol for a very long time if ever. It is going to take several years for his brain to heal entirely. The family completely understands and agrees. We realize this is going to be difficult for many friends to deal with as part of their fun times together have included alcohol. If you are a true friend. alcohol will not be talked about around him or brought around him. Our family is taking a very firm stand on this subject.
On a lighter note, Timothy has been teasing the therapists again today. This time he told his pretty P T therapist while she was bending over working with his legs that he thought he was going to throw up. Of course she jumped up and wanted to know if he was o.k., did she need to get some help, etc. Again, he thought he was pretty funny.
He is enjoying visiting with his dad who hasn't been here for awhile. Uncle J.C. and Aunt Julia also paid him a surprise visit today. He will be enjoying the cookies they brought after supper tonight.
However, that brings us to a discussion that we have been putting off. Timothy's doctors have told us that because of his severe brain injury he absolutely cannot have alcohol for a very long time if ever. It is going to take several years for his brain to heal entirely. The family completely understands and agrees. We realize this is going to be difficult for many friends to deal with as part of their fun times together have included alcohol. If you are a true friend. alcohol will not be talked about around him or brought around him. Our family is taking a very firm stand on this subject.
On a lighter note, Timothy has been teasing the therapists again today. This time he told his pretty P T therapist while she was bending over working with his legs that he thought he was going to throw up. Of course she jumped up and wanted to know if he was o.k., did she need to get some help, etc. Again, he thought he was pretty funny.
He is enjoying visiting with his dad who hasn't been here for awhile. Uncle J.C. and Aunt Julia also paid him a surprise visit today. He will be enjoying the cookies they brought after supper tonight.
Sunday, April 12, 2009
April 12 at 10:40 a.m.
Jeremy and Lisa are with Timothy this weekend, and I am home catching up. I would like to share what I have learned about one of Oregon's teenage boys--William Hollis. William's brother was handing him a hand-held radio with an extended antenna out a window. The antenna went through William's eye and hit some cranial nerves in the back of his neck. The brain and eye are o.k., but the nerves are injured. There is some paralysis of the right side of his face, and his eyes won't work together. He is walking with a walker. He is coming home Wed. and will continue therapy. As always no one knows for sure the final outcome. His parents are Steve and Wanda.
The Holt County community has poured their prayers, concern, along with care packages and some money on our family. We are extremely grateful and thankful for the support shown our family since Timothy's accident. Please continue to keep Timothy in your prayers. However, we hope you'll think of the Hollis family now, and help make their lives easier just as you have ours.
The Holt County community has poured their prayers, concern, along with care packages and some money on our family. We are extremely grateful and thankful for the support shown our family since Timothy's accident. Please continue to keep Timothy in your prayers. However, we hope you'll think of the Hollis family now, and help make their lives easier just as you have ours.
Friday, April 10, 2009
April 10 at 3:30
Timothy is getting onery. Today Brooke, the occupational therapist was using e-stem therapy on his right arm (the one that is injured). She was asking him if she could increase the strength, he said yes. Then when she did his eyes got big and he yelled ouch like she had shocked him big time. However, he was just kidding around. Poor Booke is very pregnant, and she and I both were alarmed. Timothy had a big laugh. He really likes Brooke, and tries very hard to do everything she asks. She really makes him work that right arm. Later she was having him put weight on the elbow, toss and reach with his left but lean on the right.
The speech therapist makes him do logic puzzles. At first she tried to use cards, but Timothy told here he didn't like card games. Today he planted a garden with all kinds of clues as to where to put all the vegetables using directions north, south, east, and west. Stuff like the potatoes are planted on the north just to the right of the squash. He does very well. She asks lots of math problems. He is reading and comprehending. Not writing as yet.
With both his legs being hurt, the physical therapists have to pretty much work on balance and with his arms.He is using a slide board excellently to transfer from one place to the other. He uses the strength in his left arm a lot.
As for food, he can have everything pretty much except crunchy like chips or hard like pretzels.
When I ask him about friends coming his reply is "Not yet." I know many friends would like to visit, and I really hate to ask anyone not to come. However, I understand that he would like to be a bit more back to his old self. This is a very hard time for him, but he is working as hard has he can to get back home.
The speech therapist makes him do logic puzzles. At first she tried to use cards, but Timothy told here he didn't like card games. Today he planted a garden with all kinds of clues as to where to put all the vegetables using directions north, south, east, and west. Stuff like the potatoes are planted on the north just to the right of the squash. He does very well. She asks lots of math problems. He is reading and comprehending. Not writing as yet.
With both his legs being hurt, the physical therapists have to pretty much work on balance and with his arms.He is using a slide board excellently to transfer from one place to the other. He uses the strength in his left arm a lot.
As for food, he can have everything pretty much except crunchy like chips or hard like pretzels.
When I ask him about friends coming his reply is "Not yet." I know many friends would like to visit, and I really hate to ask anyone not to come. However, I understand that he would like to be a bit more back to his old self. This is a very hard time for him, but he is working as hard has he can to get back home.
Thursday, April 9, 2009
April 9 at 3:30
Timothy has had a really good day. He has been up in his wheelchair almost the entire day waiting for his therapists, ready to get to work. He is using his right arm a little with each one, and he is very excited about that. I think he realizes that the more and better he works, the sooner he can go home. His reasoning skills are improving by leaps and bounds. He is being promoted from the orientation class to cognitive skills because he has remembered his assignments all week.
I hope it doesn't come to him that this is a little like school!
His fixator is to come off of the right leg next Tuesday. Later he will have surgery on that leg and even further down the road, surgery on the left leg.
I hope it doesn't come to him that this is a little like school!
His fixator is to come off of the right leg next Tuesday. Later he will have surgery on that leg and even further down the road, surgery on the left leg.
Wednesday, April 8, 2009
April 8 at 10:00
Today I would like to tell you about a couple we have met here at Madonna. Their complete story is at caringbridge.org then brantburt (website) and then Journal. Their entry of Mar 25 is below.
Kellie is 33 (Timothy's age) her husband Brant is 35. He is the one with the brain injury through no fault of his own. They have 3 children, the oldest is in kindergarten. They live in Lee's Summit. My heart goes out to them. I hope some of you reading this about Timothy will feel compelled to help with her efforts to contact legislative members.
Wednesday, March 25, 2009 12:25 AM, CDT
Through this experience with B.B. and dealing with brain injury, I have learned alot. First, that Missouri does not take care of it's residents. At least not completely.
In 2005, Governor Blunt cut all funding for gov. assistance for outpatient rehabilitation benefits. They will take mercy on you if you are under the age of 22, blind or pregnant. Otherwise, if you are in need of rehab benefits due to a serious injury, such as brain injuries, than you are a lost cause and deserve to be in a nursing home.
Pretty horrible huh? Well, I just learned yesterday that there is a bill trying to be passed to override this. It is senate bill 77 and is titled, Inclusion of Comprehensive Day Rehabilitation Services in Mo HealthNet. This is exciting!!!
Most people that are dealing with brain injuries are having to turn to Medicaid to help with services that their insurance company will not pay for. Such as medical equipment, medications and extended care in an inpatient facility.
The reason this is so important, is because there is not an insurance plan out there that will provide rehab benefits for a lengthy amount of time. What we have learned is that the brain heals slowly and a month or two isn't enough. A lot of insurance companies, will pay for inpatient/out patient rehab -for a limited amount of time. Then what happens when they are finished with inpatient rehab? According to Matt Blunt they should either be completely functional @ that point or live in a nursing home.
I do not believe that's right. Those people deserve a chance to continue their rehab!! If insurance is not paying for the outpatient rehab, than what are you to do? Pay out of pocket? That is not possible for the average person. Especially, if they do not have an income, due to their injury. This saddens me greatly.
Right now, we do have an opportunity for our voices to be heard.You can contact your local legislator asking them to support this bill. This bill is sponsored by Senator Stouffer and is SB77/HB530. You can go to www.moga.mo.gov and click on legislator look-up. Based on your zipcode, you can find the name and contact information for your state representative and senator. You may also call 573-751-3824, which is the senate communications line.
The "Talking Points" for letters when contacting state reps and senators regarding bill SB 77, are as follows.
1) Following discharge from a hospital, most adults have no options to continue their rehabilitation.
2) These services can help individuals to participate in their communities and return to work.
3) These services bridge people with brain injuries to other services such as vocational, technical, educational, and supported employment.
4) This rehabilitation keeps people out of nursing homes or institutions which cost taxpayers more money (approx. savings of $67,242 per person per year)
5) Many people are able to return to work and become a taxpayer upon completion of rehab.
It is very important to realize, this could be any one of us!!! This could be you, your spouse, your parent, best friend, sibling etc...
I'm sure you would want the best for their future. By supporting this bill, it can provide comfort for your future, should some chance this situation would be yours.
Not only could this benefit my husband, but so many other families that are faced with these challenges. I want to stand up and shout "BRAIN INJURED PEOPLE ARE NOT A LOST CAUSE!"
As you can see, I am very passionate about this issue. Your voice DOES matter. Please contact our legislators to show your support. You will be doing a wonderful thing for B.B. and so many other families!! It gives people opportunities to reclaim their lives. At least, let them have that chance! Please, Please, Please help me support this cause!!!
Love, Kellie
Kellie is 33 (Timothy's age) her husband Brant is 35. He is the one with the brain injury through no fault of his own. They have 3 children, the oldest is in kindergarten. They live in Lee's Summit. My heart goes out to them. I hope some of you reading this about Timothy will feel compelled to help with her efforts to contact legislative members.
Wednesday, March 25, 2009 12:25 AM, CDT
Through this experience with B.B. and dealing with brain injury, I have learned alot. First, that Missouri does not take care of it's residents. At least not completely.
In 2005, Governor Blunt cut all funding for gov. assistance for outpatient rehabilitation benefits. They will take mercy on you if you are under the age of 22, blind or pregnant. Otherwise, if you are in need of rehab benefits due to a serious injury, such as brain injuries, than you are a lost cause and deserve to be in a nursing home.
Pretty horrible huh? Well, I just learned yesterday that there is a bill trying to be passed to override this. It is senate bill 77 and is titled, Inclusion of Comprehensive Day Rehabilitation Services in Mo HealthNet. This is exciting!!!
Most people that are dealing with brain injuries are having to turn to Medicaid to help with services that their insurance company will not pay for. Such as medical equipment, medications and extended care in an inpatient facility.
The reason this is so important, is because there is not an insurance plan out there that will provide rehab benefits for a lengthy amount of time. What we have learned is that the brain heals slowly and a month or two isn't enough. A lot of insurance companies, will pay for inpatient/out patient rehab -for a limited amount of time. Then what happens when they are finished with inpatient rehab? According to Matt Blunt they should either be completely functional @ that point or live in a nursing home.
I do not believe that's right. Those people deserve a chance to continue their rehab!! If insurance is not paying for the outpatient rehab, than what are you to do? Pay out of pocket? That is not possible for the average person. Especially, if they do not have an income, due to their injury. This saddens me greatly.
Right now, we do have an opportunity for our voices to be heard.You can contact your local legislator asking them to support this bill. This bill is sponsored by Senator Stouffer and is SB77/HB530. You can go to www.moga.mo.gov and click on legislator look-up. Based on your zipcode, you can find the name and contact information for your state representative and senator. You may also call 573-751-3824, which is the senate communications line.
The "Talking Points" for letters when contacting state reps and senators regarding bill SB 77, are as follows.
1) Following discharge from a hospital, most adults have no options to continue their rehabilitation.
2) These services can help individuals to participate in their communities and return to work.
3) These services bridge people with brain injuries to other services such as vocational, technical, educational, and supported employment.
4) This rehabilitation keeps people out of nursing homes or institutions which cost taxpayers more money (approx. savings of $67,242 per person per year)
5) Many people are able to return to work and become a taxpayer upon completion of rehab.
It is very important to realize, this could be any one of us!!! This could be you, your spouse, your parent, best friend, sibling etc...
I'm sure you would want the best for their future. By supporting this bill, it can provide comfort for your future, should some chance this situation would be yours.
Not only could this benefit my husband, but so many other families that are faced with these challenges. I want to stand up and shout "BRAIN INJURED PEOPLE ARE NOT A LOST CAUSE!"
As you can see, I am very passionate about this issue. Your voice DOES matter. Please contact our legislators to show your support. You will be doing a wonderful thing for B.B. and so many other families!! It gives people opportunities to reclaim their lives. At least, let them have that chance! Please, Please, Please help me support this cause!!!
Love, Kellie
Tuesday, April 7, 2009
April 7 at 2:30
We have learned several things today. The external fixator on Tim's leg will probably be removed soon. It will be splinted and he will be given antibiotics to get rid of any infections. Then he will have to have a rod put in to straighten. This is all good. The fixator wasn't doing the job properly. The Halo will stay in place for now. They are thinking Timothy has a little nerve damage in the right arm but not a lot. They will be working with it more aggressively now that they are sure there are no broken bones.
This is a fast-paced hospital. They rapidly assess the problems and start fixing them quickly.
Timothy's attitude and behavior with all of the doctors, nurses, therapists, etc. is always very polite, courteous, and patient. I am so proud of him right now. It has got to be aggravating and confusing that different ones ask the same questions over and over and poke, prod, and bend continually.
Zack and Alethia were here today to hear and interpret the results of the scans and x-rays. They are always a welcome support team.
Thanks, Mike and Chris for your visit last night. He seemed glad to see you, and wasn't too emotional.
This is a fast-paced hospital. They rapidly assess the problems and start fixing them quickly.
Timothy's attitude and behavior with all of the doctors, nurses, therapists, etc. is always very polite, courteous, and patient. I am so proud of him right now. It has got to be aggravating and confusing that different ones ask the same questions over and over and poke, prod, and bend continually.
Zack and Alethia were here today to hear and interpret the results of the scans and x-rays. They are always a welcome support team.
Thanks, Mike and Chris for your visit last night. He seemed glad to see you, and wasn't too emotional.
Monday, April 6, 2009
April 6 at 4:30 p.m.
I wrote so much on Saturday that I thought everyone would enjoy a break.
I am back in Lincoln after a brief trip home. Timothy is very alert today and is enjoying his company--Jessica, Brandi and Courtney Jean. He is not nearly as emotional today as over the weekend. He is beginning to understand that the external fixator on his leg and the Halo are not permanent. I think he must have been pretty frigtened when he couldn't voice his concerns. Timothy thought he would being living here from now on. Now that he can voice his fears, we can reassure him.
Everyone here is very pleased with his rapid progress.
I am back in Lincoln after a brief trip home. Timothy is very alert today and is enjoying his company--Jessica, Brandi and Courtney Jean. He is not nearly as emotional today as over the weekend. He is beginning to understand that the external fixator on his leg and the Halo are not permanent. I think he must have been pretty frigtened when he couldn't voice his concerns. Timothy thought he would being living here from now on. Now that he can voice his fears, we can reassure him.
Everyone here is very pleased with his rapid progress.
Saturday, April 4, 2009
April 4 at 8:30 a.m.
Just a quick note. Timothy is going through a very emotional time right now. It might be best if friends remembered him with a card rather than a visit for awhile. Timothy has requested no visitors at this time. Hopefully he will be ready for visitors again soon.
8:30 p.m.
The following note was written by Timothy's dad: To Jean, Jane, Amanda & April. I am so sorry I ruined your day. It's sometimes hard for me to keep things together. But please know your effort was truly appreciated. It won't be long before this phase is over, and you all will be able to laugh and talk of better times with Timothy.
To all who have helped us, from our hometown and Timothy's railroad family--Thank you is not enough, but it is all I can say. Tim Dannar (Dad)
Obviously,it has been quite a day. Timothy was delighted to see his Grandmother Dannar and Aunt Susie, but was reluctant to have other guests. He is beginning to realize where he is and the condition he is in. He is uncomfortable and often in pain. He would rather his friends not see him like this.
With that said. I want everyone to know that he is improving daily. The fact that he can voice his wishes is wonderful. He had a real meal for the first time today. He was able to visit with Zach and Jeremy pretty much like old times. We are just so thankful that we are getting our old Timothy back.
8:30 p.m.
The following note was written by Timothy's dad: To Jean, Jane, Amanda & April. I am so sorry I ruined your day. It's sometimes hard for me to keep things together. But please know your effort was truly appreciated. It won't be long before this phase is over, and you all will be able to laugh and talk of better times with Timothy.
To all who have helped us, from our hometown and Timothy's railroad family--Thank you is not enough, but it is all I can say. Tim Dannar (Dad)
Obviously,it has been quite a day. Timothy was delighted to see his Grandmother Dannar and Aunt Susie, but was reluctant to have other guests. He is beginning to realize where he is and the condition he is in. He is uncomfortable and often in pain. He would rather his friends not see him like this.
With that said. I want everyone to know that he is improving daily. The fact that he can voice his wishes is wonderful. He had a real meal for the first time today. He was able to visit with Zach and Jeremy pretty much like old times. We are just so thankful that we are getting our old Timothy back.
Friday, April 3, 2009
April 3 at 6:00 p.m.
The ocuupational therapist did some more eye testing today. We were concerned that he was having double vision. However, that may not be so. She believes now that he has some eye damage that is causing his left eye to see grey, blurry images. This will probably repair on its own. More testing will be done next week by a more qualified person.
Tests were completed on Timothy's neck, both knees and shoulder. The alignment on the broken tibia is of concern and will be x-rayed further. There might be some nerve damage around the shoulder.
Timothy was given chocolate pudding, a fig newton and juice today. All were swallowed without a problem. He will start a semi-normal diet tomorrow. Everyting will be ground or chopped for awhile.
We can understand almost everything he says now. His voice is still pretty whispery. First words we could understand were, "Take me home." He is developing an attitude part of the time. He loves his ice chips. About an hour ago he said to me, "Ice chips" and then "Right now!" He is also becoming very emotional at times expecially when we mention family and friends, and then other times seemingly for no reason.
He has a lot of pain, and they are trying to reach a balance where he is comfortable but not so sedated that he can't work with his therapists.
We got a care package from Tricia. We will soon learn a lot about New Mexico. Also, had a visit from another railroad friend. Thanks, David for stopping by.
The weekend will be busy--Jeremy, Zach, their girl friends, Aunt Susie, and Grandma Dannar all plan to visit.
Tests were completed on Timothy's neck, both knees and shoulder. The alignment on the broken tibia is of concern and will be x-rayed further. There might be some nerve damage around the shoulder.
Timothy was given chocolate pudding, a fig newton and juice today. All were swallowed without a problem. He will start a semi-normal diet tomorrow. Everyting will be ground or chopped for awhile.
We can understand almost everything he says now. His voice is still pretty whispery. First words we could understand were, "Take me home." He is developing an attitude part of the time. He loves his ice chips. About an hour ago he said to me, "Ice chips" and then "Right now!" He is also becoming very emotional at times expecially when we mention family and friends, and then other times seemingly for no reason.
He has a lot of pain, and they are trying to reach a balance where he is comfortable but not so sedated that he can't work with his therapists.
We got a care package from Tricia. We will soon learn a lot about New Mexico. Also, had a visit from another railroad friend. Thanks, David for stopping by.
The weekend will be busy--Jeremy, Zach, their girl friends, Aunt Susie, and Grandma Dannar all plan to visit.
Thursday, April 2, 2009
April 2 at 4:30 p.m.
This has been another outstanding day. Timothy is hooked up to a machine that monitors his oxygen intake. All other tubes, lines, picks, etc. have been removed. He has a smaller trach with a cap so he is beginning to talk enough that we are beginning to hear and understand. He has been sitting up in a wheelchair all day until just 30 min. ago. We took him outdoors for a walk in his wheelchair. He played shape/color bingo perfectly, responded correctly to simple math problems, responded correctly to where he is and where he lives. He identified his brothers and grandmothers correctly from pictures.
Dad Tim says, "He has come a long way today."
X-rays are ordered for his legs and right arm to see how they are doing.
Dad Tim says, "He has come a long way today."
X-rays are ordered for his legs and right arm to see how they are doing.
Wednesday, April 1, 2009
April 1 at 2:30
We are getiing acquainted with Timothy's care givers. Everything is going very well. Timothy has been up sitting in a wheel chair for 4 hours. All kinds of therapists have worked with him today so they can come up with goals which they will relay to us tomorrow. He has been very co-operative and seems to know everyone is trying to help him get better. The OT took him for a short tour of the building, past an aquarium, and around his part of the facility. She had him work at a machine that he had to turn the wheel using his good left hand. She had him wash his face and brush his teeth. He has tried to mouth words. Today or early tomorrow they will put in a smaller trach and cap it so he should be able to talk some.
Thanks, Bruce, Dana and Hayden for the flowers. They are lovely. I posted all cards and pictures on the wall.
At Madonna' website (www.Madonna.org) people can send messages (Madonna Mail icon)which will be printed out and delivered to Timothy. Messages must include patient's first and last name.
Thanks, Bruce, Dana and Hayden for the flowers. They are lovely. I posted all cards and pictures on the wall.
At Madonna' website (www.Madonna.org) people can send messages (Madonna Mail icon)which will be printed out and delivered to Timothy. Messages must include patient's first and last name.
Tuesday, March 31, 2009
March 31 at 6:00
Yeah! We made it to Madonna. Timothy came by amublance and Tim and I were not far behind. We all reached here about 4:00 p.m. Timothy's Mercy nurse and even the ambulance crew gave him some seditives so he is still asleep. Tim and I are very impressed so far. He will have someone staying in his room at all times. Tomorrow a team of people will do his assessment and then tell us what all he will be doing. We will be allowed to sit in on his therapies and can be here anytime.
Housing is available for the family members at a very reasonable rate. There is a cafeteria and several free drink machines.
Tim noted that the facility is spotless--far cleaner than my house right now.
We are excited to be here and ready for Timothy to get to work.
Here is the address: Madonna Rehabilatation Hospital, 5401 South St., Lincoln NE 68506, Room 138.
Housing is available for the family members at a very reasonable rate. There is a cafeteria and several free drink machines.
Tim noted that the facility is spotless--far cleaner than my house right now.
We are excited to be here and ready for Timothy to get to work.
Here is the address: Madonna Rehabilatation Hospital, 5401 South St., Lincoln NE 68506, Room 138.
Monday, March 30, 2009
March 30 at 9:30
Well, it is has been quite a night and day. Unfortunately, Timothy did fall out of bed. As far as we can tell he did not hit his head and x-rays show no problems. I had barely gotten to the hotel when the nurse called so I came back for the rest of the night. Then this morning the hospital arranged for a "sitter" so I could get some rest.
I left for three hours. when I came back someone came to say that the rehab facility might not take Timothy for awhile because he had to have a "sitter" because he woouldn't stay in bed. I have not cried througout this whole time but I cried then. I was so certain that getting to rehab immediately was the most important next step. When I could think straight I called Zach. Wisely, he told me to call Madonna myself and explain the situation. I did. They immediately said they were communicating with Mercy, knew the situation and that it would not affect his acceptance. They were only waiting on authorization from Timothy's insurance.
So Timothy is scheduled to leave here at noon tomorrow for Lincoln. I so hope it happens.
In the meantime, a friend and mother-in-law of my nephew, Dale came by when Timothy was having one of his restless times. She started rubbing his shoulders and lower back. He settled down and enjoyed it so very, very much. I will have to learn how to do this.
Bryson and Kim were here to spend time today. And thinks to Rich Tim is back up here to drive with me to Lincoln.
Our family has always been ones to take care of ourselves, but we are learning that at this time we need help from our friends. And we are so appreciative.
This is the most awful experience of my life, but it is teaching me about love, friendship and caring.
I left for three hours. when I came back someone came to say that the rehab facility might not take Timothy for awhile because he had to have a "sitter" because he woouldn't stay in bed. I have not cried througout this whole time but I cried then. I was so certain that getting to rehab immediately was the most important next step. When I could think straight I called Zach. Wisely, he told me to call Madonna myself and explain the situation. I did. They immediately said they were communicating with Mercy, knew the situation and that it would not affect his acceptance. They were only waiting on authorization from Timothy's insurance.
So Timothy is scheduled to leave here at noon tomorrow for Lincoln. I so hope it happens.
In the meantime, a friend and mother-in-law of my nephew, Dale came by when Timothy was having one of his restless times. She started rubbing his shoulders and lower back. He settled down and enjoyed it so very, very much. I will have to learn how to do this.
Bryson and Kim were here to spend time today. And thinks to Rich Tim is back up here to drive with me to Lincoln.
Our family has always been ones to take care of ourselves, but we are learning that at this time we need help from our friends. And we are so appreciative.
This is the most awful experience of my life, but it is teaching me about love, friendship and caring.
Sunday, March 29, 2009
March 29 at 4:30 p.m.
Timothy had some visitors from home today plus one of his railroad friends. He had another good day. He flicked Zach with his water sponge a couple of times, responded to his YES and NO paper several times, and even tried to tell me somehing using marker and paper. However, I couldn't understand what he was trying to write.
Just now he was determined to get out of the bed. He had his legs over the bed sides and was pulling himself upright with his good arm. Luckily the weight of the halo brace forced him back down, but he just kept trying. I called in the nurse so she could see what was happening. After a quick moment she went for some Adavan (spelling may not be right). Anyway something to calm him.
I am not staying the night with him so I wanted to make sure they knew what he is doing.
Just now he was determined to get out of the bed. He had his legs over the bed sides and was pulling himself upright with his good arm. Luckily the weight of the halo brace forced him back down, but he just kept trying. I called in the nurse so she could see what was happening. After a quick moment she went for some Adavan (spelling may not be right). Anyway something to calm him.
I am not staying the night with him so I wanted to make sure they knew what he is doing.
Saturday, March 28, 2009
March 28 at 5:00
After yesterday this was a quiet day--just Zach, Alethia and I are here. However, Timothy has accomplished some new things. Early this morning I asked if I could take some ice chips and rub them on his lips and tongue not let him swallow them yet. Timothy seemed to really like that. When Alethia got here,she took the tiny sponges on a stick that they use to "brush" his teeth and filled them with water and let him suck on those. Timothy really, really enjoyed that. Then he started reaching for them and put them in his mouth himself. Later I thought maybe he could handle a washcloth so I held a dampened cloth, and he took it from my hand and wiped his eyes and face.
We also played around with the paper with YES and NO. Zach held it up and asked Timothy if Alethia was a Dum Dum. Timothy looked around and found Alethia and didn't do anything. Then Zach asked him if Alethia was a pretty good girl. Timothy took his fist and punched the yes on the paper. We all had a good laugh.
I really feel he understands quite a bit. For instance when the nurses come to change his dressings, he stays very still, doesn't do his bed swivels or restless leg movements. Almost always he stays quiet whild they all do the things they have to do for him.
As has been his habit from the beginning, when he is tired of us asking him to do stuff he sighs a huge sigh and closes his eyes shut. Then we go away and leave him be for awhile.
We also played around with the paper with YES and NO. Zach held it up and asked Timothy if Alethia was a Dum Dum. Timothy looked around and found Alethia and didn't do anything. Then Zach asked him if Alethia was a pretty good girl. Timothy took his fist and punched the yes on the paper. We all had a good laugh.
I really feel he understands quite a bit. For instance when the nurses come to change his dressings, he stays very still, doesn't do his bed swivels or restless leg movements. Almost always he stays quiet whild they all do the things they have to do for him.
As has been his habit from the beginning, when he is tired of us asking him to do stuff he sighs a huge sigh and closes his eyes shut. Then we go away and leave him be for awhile.
Friday, March 27, 2009
March 27, at 6:00 p.m.
Timothy had lots of company today and responded to everyone, squeezed their hands, followed them with his eyes, and seemed to know who they were. He is following lots of commands and maybe trying to say a few words. Continues to be very restless at times and appears to try to get out of the bed. The nurses got him up in a huge chair, and he was content there for over an hour. We are learning some ways to communicate with him which is a comfort to me. We have a piece of paper with YES on one side and NO on the other. Sometimes he will point to one or the other when we ask very simple questions.
Everyone who came today felt he had improved quite a lot since their last visit.
We are all encouraged.
Everyone who came today felt he had improved quite a lot since their last visit.
We are all encouraged.
Thursday, March 26, 2009
March 26 at 7:00 p.m.
Aunt Susie and I traded shifts. Timothy has been asleep most of the time since I arrived around 4:30. Susie said they had had him sitting on the edge of the bed, and it had really tired him. He did wake long enough for me to say hello, and he squeezed my hand and raised each of his legs for me. Then he got restless for awhile and tore a hole in his air mattress. They are replacing that now. His right leg has a brace with several sharp points on it, and he really gets to moving those legs.
Wednesday, March 25, 2009
March 25 at 8:13 p.m.
The last two days have been very encouraging. Timothy continues to make eye contact, respond more often to commands, stay awake longer, and move about in his bed more. The neurosurgeon said he was encouraged with his recent progress. Aunt Susie is still staying with Timothy, and she is very excited.
We received a surprise in the mail today. The Friends to Friends network sent Timothy a check for a nice amount of money. This network, I understand, is a volunteer effort by the employees of Union Pacific Railroad. We are grateful for their help.
I think I have mentioned before how concerned Timothy's railroad friends of been. They continue to call or visit Timothy almost daily.
Our community has been wonderful as well. Tim and I are home, and everywhere we go people ask about Timothy or tell us they are following this blog. We are very appreciative of all the prayers, care packages, cards, and supportive comments, actually I guess you could say we are overwhelmed with all the love everyone has shown our family.
We received a surprise in the mail today. The Friends to Friends network sent Timothy a check for a nice amount of money. This network, I understand, is a volunteer effort by the employees of Union Pacific Railroad. We are grateful for their help.
I think I have mentioned before how concerned Timothy's railroad friends of been. They continue to call or visit Timothy almost daily.
Our community has been wonderful as well. Tim and I are home, and everywhere we go people ask about Timothy or tell us they are following this blog. We are very appreciative of all the prayers, care packages, cards, and supportive comments, actually I guess you could say we are overwhelmed with all the love everyone has shown our family.
Tuesday, March 24, 2009
March 24 at 9:28
Tim and I did come home. Tim has been coughing a lot and needs to see a doctor. I am going back without him this time. We left Aunt Susie in charge. I talked to her just a bit ago. Timothy was moved to a regular room, and he remained active most of the day. We have both noticed that he really seems to enjoy the time spent with the physical therapists. That just began. We are glad this will be increased. Susie feels he is following her more with his eyes,and he is trying to lift his right leg off the bed a little. That's the leg that has broken bones and is in a metal brace. I had not seen him ever try to do that. I think the therapist's work has influenced this movement. Aunt Susie was very impressed with his progress from last week. It has been a very good day.
Tim's address: Mercy Hospital, Room 658, 1111 6th Ave., Des Moines, IA 50314-2611
Stacie, I did not mean Timothy changed the rules. I meant the doctors changed the rules.
Tim's address: Mercy Hospital, Room 658, 1111 6th Ave., Des Moines, IA 50314-2611
Stacie, I did not mean Timothy changed the rules. I meant the doctors changed the rules.
March 24 at 7:05 a.m.
I'm going to write this quick. When I got here this morning early Timothy gave me a thumbs up with both hands. That is definitely not a reflex said the nurse who was right there. Also, more eye movement seeming to respond to voices.
I would just like to go home now before they tell me something that ruins the day!
We think we understand the game, and then they change the rules.
I would just like to go home now before they tell me something that ruins the day!
We think we understand the game, and then they change the rules.
Monday, March 23, 2009
March 23 at about 5:00 pm
I decided to include the time because the computers at the hospital have the wrong time on them; and I can't change it therefore, the post time is always wrong.
Not a lot of change in Timothy. He was not as responsive as yesterday. Almost didn't write but was afraid readers would think something really bad happened. He has been assigned a physical therapist who began working with him last week.
Jessica and Brandi visited today and brought a delicious homemade meal sent by Cindy. It was much better than McDonalds. I wished Timothy were able to enjoy the green bean casserole as it is a favorite of his.
Not a lot of change in Timothy. He was not as responsive as yesterday. Almost didn't write but was afraid readers would think something really bad happened. He has been assigned a physical therapist who began working with him last week.
Jessica and Brandi visited today and brought a delicious homemade meal sent by Cindy. It was much better than McDonalds. I wished Timothy were able to enjoy the green bean casserole as it is a favorite of his.
Sunday, March 22, 2009
Sunday Evening
This was a pretty good day. When Tim and I came into Timothy's room this morning, we could tell a difference. Timothy seemed to be following us a little with his eyes, and the nurse said later she felt he was following her a little also. He did the hand squeezes on request several times. Once when I said I was leaving, he seemed to reach out,grasp my hand and squeeze hard. Lisa also felt that he reached for her shoulder another time. The nurse said that when she was "brushing" his teeth he opened wide when asked and spit out the cleaner on request. Spitting is good! During Timothy's wakeup times he is making a lot more face expressions not just the stone cold set look from days before.
We know we have a long road ahead. We delight in the alert times but there are a lot of still kinda asleep times. The main things is we feel today that Timothy is making important progress.
We appreciate Calvin and Debbie spending much of the day with us.
Jeremy and Lisa, our support for the weekend, also just left. Tim and I so depend on Jeremy and Zach and their girls to help us through this difficult time.
Everyone is being so supportive and helpful. It is unbelieveable. Thanks!
We know we have a long road ahead. We delight in the alert times but there are a lot of still kinda asleep times. The main things is we feel today that Timothy is making important progress.
We appreciate Calvin and Debbie spending much of the day with us.
Jeremy and Lisa, our support for the weekend, also just left. Tim and I so depend on Jeremy and Zach and their girls to help us through this difficult time.
Everyone is being so supportive and helpful. It is unbelieveable. Thanks!
Saturday, March 21, 2009
Saturday, March 21
Timothy is breathing without the vent and the nurses had him sitting up in a reclining chair for about 45 min. He is still not very responsive. However, the nurses assure us that he is very tired from being in the chair. He had several visitors today which helps make our time at the hospital go faster.
Yesterday Timothy's eyes were open quite a bit and he did squeeze Lisa's (Jeremy's fiancee)hand.
Thanks again for all your prayers and concern.
Yesterday Timothy's eyes were open quite a bit and he did squeeze Lisa's (Jeremy's fiancee)hand.
Thanks again for all your prayers and concern.
Friday, March 20, 2009
Day by Day
Tim and I are home for a day. Aunt Susie, Zach and Alethia (Zach's girlfriend) are with Timothy. Alethia called around 1:00 p.m. to say that Timothy had his eyes open and when she told him she was there, he seemed to know. She also asked him to squeeze her hand, and he did. Then she asked for a "thumbs up." First he tried to hold up two fingers but then changed it to his thumb.
As in the past several days, not too much has developed since then. Zach says Timothy is pretty restless--not sure how much he is aware of his surroundings yet.
This is better than yesterday. We plan to be more aggresive with our presence--talk, laugh, play music, talk of fun times in the past--not tip toe around as much.
Thanks Stacie for your suggestions. We are grateful for all comments.
As in the past several days, not too much has developed since then. Zach says Timothy is pretty restless--not sure how much he is aware of his surroundings yet.
This is better than yesterday. We plan to be more aggresive with our presence--talk, laugh, play music, talk of fun times in the past--not tip toe around as much.
Thanks Stacie for your suggestions. We are grateful for all comments.
Thursday, March 19, 2009
Downhill Again
After yesterday's encouragement, the neurosurgeon had this to say this morning, "Timothy has been off of dipravan (seditive) for 24 hours. By Monday morning it is important that he be showing some better signs of improvement. He should open his eyes with awareness of his surroundings, he should be trying to mouth words, and he should be squeezing our hands on command and with force." So far last night and today that has not happened.
Prayers for Timothy are just important now as two weeks ago. Tim and I are discouraged but not without hope.
Prayers for Timothy are just important now as two weeks ago. Tim and I are discouraged but not without hope.
Wednesday, March 18, 2009
Better news
I talked to the neurosurgeon this morning at 8:00. He insists that Timothy is making remarkable progress. Reminded me that it is amazing that he is in one piece and mending as quickly as he is after all he's been through. I mentioned how discouaraged we become when he moves a finger or toe, but then doesn't respond for hours. The doctor said that I have to understand that for Timothy right now that is a huge effort and takes all of his will and strength. I should be most thankful that he can do it at all. I mentioned he had yawned real big this morning. He said that was marvelous--using his front lobe.
Another doctor (internist I think) said they are taking him off dipravan today and see what happens, also changing settings on vent so Timothy is doing more of the breathing. We'll have to wait and see how this goes.
All in all we are most encouraged this morning.
By the way--Thank you Cindy for the 12' banner in Timothy's room and to everyone who signed it. Doctors, nurses and visitiors have commented and say how great it is for Timothy and us to have so much community support. I apologize for not mentioning the banner sooner. That has been a wonderful boost.
Another doctor (internist I think) said they are taking him off dipravan today and see what happens, also changing settings on vent so Timothy is doing more of the breathing. We'll have to wait and see how this goes.
All in all we are most encouraged this morning.
By the way--Thank you Cindy for the 12' banner in Timothy's room and to everyone who signed it. Doctors, nurses and visitiors have commented and say how great it is for Timothy and us to have so much community support. I apologize for not mentioning the banner sooner. That has been a wonderful boost.
Tuesday, March 17, 2009
March 17, 2009
Not much to report. Tim and I had really hoped Timothy would be very responsive today after the trach and peg surgeries yesterday. However, it was 4:00 before nurses withheld the dipravan (seditive) for 30 min. Timothy opened his eyes but didn't really focus on me, and he would not squeeze my hand.
Hopefully, I'll have some encouraging news tomorrow.
Hopefully, I'll have some encouraging news tomorrow.
Monday, March 16, 2009
Update
This morning Timothy had a tracheostomy and a peg tube put in. The trach is so the breathing tube which is very uncomfortable could be removed. The peg is so he can have nutrients delivered directly to his stomach. It will take at least the rest of the day for the anesthetic to wear off. Tomorrow we will know more about his alertness.
Sunday, March 15, 2009
What Happened
Timothy works for Union Pacific Railroad on a traveling gang. During the last few months he has been working in Marshalltown, Iowa. Tim was riding in a car with two co-workers back to their motel in Marshalltown for the night on March 6th. We do not know the details of the accident but their vehicle left the roadway and rolled down an embankment. Tim and his co-workers were all ejected from the vehicle. Tim was Life Flighted from the Marshalltown hospital to Mercy Medical Hospital in Des Moines, Iowa. Tim suffered a fractured C2 vertebrae, compound fracture to his right leg, and had three small brain bleeds as a result of the accident. His leg has been set back in place using an external fixator. He is in a halo brace to stablize the vertebrae in his neck. Tim remains in the ICU at Mercy Medical on a ventilator and in a coma. He is listed in critical but stable condition. The Dannar family will continue to update Tim's blog.
Tim's mailing address while in the ICU is:
Tim Dannar
Mercy Medical Center
ICU Bed 12
1111 6th Ave
Des Moines, IA 50314
Tim's mailing address while in the ICU is:
Tim Dannar
Mercy Medical Center
ICU Bed 12
1111 6th Ave
Des Moines, IA 50314
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