Tuesday, September 30, 2008

Lisa here...

The family wanted to thank everyone so very much for keeping Brad in your thoughts and prayers. He wouldn't be as far as he is today without your help and support. We especially wanted to thank the following people for their generous donations to the Brad Cochran Recovery Fund:

Barb and Greg Luckey (GA)
Jessica and Shane Russell (GA)
Dave and Vickie Ruddell (FL)
Kim and Rob Anderson (CA)
Katie and Rodger Johnson (KS)


I think it is so amazing that Brad has people thinking of him literally all around the world. From Georgia to China back to California. Thank you everyone. Your continued support is much appreciated. Take care, The Cochran Family

Monday, September 29, 2008

Need your help with something

To those who visit Brad at the hospital, the nurses told us that Brad needs to be out of his bed 90% of the time. He needs to be up walking around or at least sitting in a chair in his room. He's currently spending 90% of his time in bed. SO, please encourage him to get out of bed, take a walk, sit in a chair, anything that will keep him active to build his strength/endurance. Thanks, Zak
Zak here. Brad was finally taken out of ICU this weekend and the 50-60 staples in his scalp were removed too. He had a reaction to being taken off one of his medications that caused him to have the hiccups for 2 days straight -- that annoyed the hell out of him and made it hard to sleep. Finally the nurse gave him some meds that took care of them. A big hurdle for Brad right now is getting himself motivated to make progress and do what it takes to make himself well. Nearly two weeks of morphine and being bed-ridden has sapped his drive -- no surprise there! He's being weaned off the morphine and we're working to encourage him to take ownership of his wellness. This mainly involves listening to the nurses and doing limited PT.

If you're interested in knowing more about brain injuries and how they can affect a patient's behavior and personality, here some fairly straight-forward info http://www.tbiguide.com/

Saturday, September 27, 2008



Hello, this is Zak again. Visited with Brad yesterday and this morning. I think the nurses on the floor have taken to Brad. He gets a good amount of attention from the young nurses in the ICU. He's been standing up and walking short distances (he gets worn out easily). April, Dad, Travis, his nurse Katrina and I took Brad out to a small garden area in the hospital today for about 30 minutes -- he was happy to be outside for the first time in the 10 days since the injury. Hand eye coordination is slowly returning to Brad, he's feeding himself, brushing his teeth and operating the remote with little problem. He's been joking about having the skull pieces is his abdomen and is a little weirded out by the soft-spots in the front of his skull. It sounds like they're going to take the staples out of his heads today and there was talk about him getting out of ICU soon. He has had some bouts of agitation (common with head injuries), mixes up words occasionally and April thinks he's been cussing more than usual. But overall he's making some great progress considering the injury.

Thursday, September 25, 2008

Zak here. Visited Brad this afternoon. His first non-hospital meal request was...blueberry waffles, hah! He ate a couple bites of the waffle dad brought to him from Waffle House. He's not eating much, so his energy level is still very low and he sleeps most of the time (which is good healing time, so that's good). The doc did note some additional brain swelling today, so he's back on Manitol (I think I have that right) to help keep that in check. He showed some signs of confusion during conversations, but is still increasingly more alert and focused each day. I showed him the video I posted on the blog -- he got a good laugh out of that. I left when two nurses came in for the sponge bath, which I'm sure he enjoyed. Brad now knows there's a blog dedicated to him and loves to hear the comments you post, so keep 'em coming. Also please keep in mind the recovery account we've set up to help the family deal with what will be some pretty steep medical bills coming from the long months of care and rehab in Brad's future. Thanks to all for checking in.

Wednesday, September 24, 2008

April and family here. It's unbelieveable how much improvement he has made in 24 hours! Today his speech is even clearer, his sentences are more substantial, his humor is DEFINITELY still in tact! With all this new found glory, it is however, taking a toll on his energy. He gets wiped out quickly.
He got fitted for a helmet,(which we all decided will need some "flair"), he ate a few bites of his first "meal" since last Wednesday (hospital food...not sure if "meal" is what you want to call it); cooked carrots (1), chipped beef (1 bite), didn't touch the mashed potatoes, and a few sips of unsweetened tea!
The PA told us the other day that normally these types of head injuries have a high mortality rate...YOU'RE PRAYERS ARE CLEARLY WORKING ON BRAD!
PLEASE don't forget to check the blog for the information on the Brad Cochran Recovery Fund. Any donations will be greatly appreciated towards Brad's enormous medical bills.

Tuesday, September 23, 2008

Beth here....just got back from seeing Brad, it amazes me how well he is progressing. They are talking about downgrading him from ICU tomorrow. He is smiling and able to recognize people. He is joking around and flipped me off earlier for trying to help him change the channel on the TV. We are all so glad that he is awake.

Incredible: 09/22/08 3:40 pm



Derek and Family here......(Brad giving thumbs up above and smiling to the right)
As you can see from Zak's post below Brad is now breathing on his own!! He just met with the therapist and he was able to sit up with a little assistance but mostly on his own. He sat at the side of his bed and lifted his feet as directed. The most incredible thing is that he is talking. He speaks quietly due to his throat being sore from the tubes but he is cracking jokes, smiling and asking for things like water and to lay down. He is able to chew ice and swallow on his own which is a major achievement. He is still really groggy and sleepy from meds and the fact he has been sleeping for six days straight.

Brad still has a long way to go and will require alot of therapy and future work to ensure he is getting all the care he needs. Brad is young and is not established financially and with his current state and inability to work as well as the unknown about his abilities in the future the financial concerns will come soon (regular bills, medical bills, etc). Brad has health insurance with a very large deductible and the fact that the insurance will cap at some point. With all of this in mind the family has started the Brad Cochran Recovery Fund to help support Brads financial situation as at a minimum he will be out of work for months if not years. There is no minimum and anything is appreciated. If you feel it in your heart to provide a donation please make a check out to the Brad Cochran Recovery Fund and mail to Derek & Lisa Cochran 11023 Sonterra Lane, Frisco TX 75034 or give to a family member. All funds will be used solely towards Brads bills exclusively 100%. Thank you all for your thoughts and prayers....they are working.
Zak here. We've had some good news again today. Brad is now off the ventilator and breathing on his own. A shave and tooth brushing later (thanks to Beth), he's starting to look like his old self. Without the tubes down his throat he manages to speak a little -- his first words, when the nurse pointed to dad as asked "who is that?" were were "my dad". He's giving thumbs up, recongizing people who come to visit him and is, overall much more alert. I haven't been able to get in to the hospital to see him today but will be stopping by to visit tonight.

Monday, September 22, 2008

Here's something to make you smile. A video of Brad from back in tha day

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HE JUST OPENED HIS EYES!!!!!!!
10:06 am
It's April. We just met with the Occupational Therapist. She performed a series of commands on Brad while we watched. It was amazing to witness. She asked him to sqeeze her hand. He did. She wet a paper towel, placed it in his left hand, and asked him to "wash his face"...with a little help from her,bringing his hand to his face, he made a swiping motion around his nose.

She told him to sqeeze her hand once for YES and twice for NO, "Are you a boy?", no response. "Is the sky yellow?", no response. She thought he may have fallen asleep on her. She must have worn him out! It was so touching to see him able to follow a few of her commands now that he's off the sedation medicine.
The OT did tell us that we will need to slowly start focusing on stimulating his hearing and touch senses. She said we can start implementing some of Brad's favorite music into his day and turning on the TV for 20-30 minutes at a time...just to give his brain a chance to work at hearing and interpreting things around him.

One thing she told us to do is for family and friends to start putting together some pictures/collages WITH LABELS of who is in the picture so that when can he finally open and use his eyes, they can start showing him the photos. What a great idea. Nothing over the top, just simple photos. You can send mail them to us and we will bring them here to his room. Please mail your pictures to me:

Cochran
162 Threechop Drive Marietta, Ga 3oo64



9/22 update 9:06 am

Derek Here.......
Encouraging signs this morning. Both the Dr and the PA were in and began the tests to see if Brad could handle being off the sedation medication. They totally turned of the machine that sends the medicine to Brad and within about 15 min the Dr began asking questions. Brad opened his eyes!!!!!!!!!! Although very slightly it was a dramatic step, the Dr would swat at his eyes and Brad would flinch showing a great reaction. The DOC also asked Brad to wiggle his toes on each foot independently and he did, he squeezed both hands on command. The most exciting moment for ME was that the nurse asked if he knew i was there and he moved his head in a slight nodding motion. After about an hour and 1/2 of being off the meds he was then put on a breathing test, he has been breathing on his own for about an hour now!!!! They will leave him off the ventilator a little longer then test his blood to ensure he is receiving enough oxygen, if the blood tests are encouraging he will be taken off the ventilator all together. His eyes are not permanently open due to pain meds but at this writing he is gong through some more verbal command tests and can slowly nod his head yes to questions and still squeezing hands. We are all very encouraged although he still has a long road ahead of him. More to come........

Sunday, September 21, 2008

9/21 10:14 pm edt update


Derek here.......
I arrived at the hospital this morning and was kept out while Brad was having his bandage and drains removed. Dad joined me shortly thereafter and we went in to see Brad. He seemed very peaceful and resting. The nurses cleaned Brad up as best they could and he looked really good without his bandage and freshly cleaned face and body. He seemed to be a little puffy in the face as his swelling sort of moves around his face and neck areas. As we sat and talked with Brad to tell him we were here and to just chit chat on daily events the nurse updated us on his overnight condition and the plan for the remainder of the day and the big day planned for Brad on Monday. As Dad spoke to Brad directly telling him we were there and asking him to open his eyes Brad shed a couple of tears, so we know he is in there, listening and trying hard to show us. We also had planned time to meet with the Neuro Surgeon to discuss Brads CT scans and plans to slowly reduce his medication in an attempt to "wake" him up. Zak and April arrived and we were able to meet with the Dr to discuss Brad and his progress. Dr Chitale said that the swelling looked pretty good and that the portions of his skull that were temporarily removed to allow the brain more space has helped. The Dr spent alot of time with us and was very detailed in his explanation of the CT scans. He showed us scans from the first day, prior to the surgery, right after the surgery, two days later and the most recent scans from yesterday morning. The scan showed swelling that was expected but not overly aggressive. He was very detailed and pointed out all of the parts of his brain and areas of concern as well as areas that reacted well to the surgery (parts of his skull were removed to allow the brain to swell, and relieving the pressure on his brain) we also discussed the plan tomorrow to slowly take him off of the sedative to see if he can handle breathing on his own and swallowing. Basically they will cut the sedative in half in hopes he will wake and respond to commands to squeeze hands and open eyes. We are all being cautiously optimistic while hoping to see progress in his condition. We will know alot more tomorrow morning and hope to report good news to all. Keep praying and thinking of Brad.
This is Beth, I noticed that our Aunt Jann left a comment and wanted to make sure that no one missed it. We appreciate everyones thoughts and prayers.


Jann said...
It's Aunt Jann. I am so thankful to you 'kids' for creating this blog so those of us who can't be with you can be updated regularly. BJ and I have also talked twice since the accident. This will give him a break from the phone so that's another good aspect of the blog as well.As you know I experienced this identical life tragedy with my own brother, Brad, back in 1979. So I can honestly say that I KNOW EXACTLY how all of you are feeling. I am so happy that there are so many of you to give one another love and support.Brad, BJ and family are on two prayer chains and in the prayer petition book at St. Cletus parish in St. Charles, MO. There are hundreds of people you've never met or will never meet who are praying for ALL of you, but especially for Brad.Please tell Brad that I'm sending my love. My thoughts and prayers are with him and all of you every day. xoxo
September 20, 2008 9:38 PM

Sunday September 21, 2008

This is Zak. Some positive news today. They took off his bandages today and removed two of the four drains from his head -- and it sounds like the remaining two will come out tomorrow. Tomorrow's a big day. They're going to reduce Brad's sedation to see how he reacts. Nobody seems sure what tomorrow will hold for him. Hopefully we get some more good news.

I was up at the hospital with Brad until about 12:30 last night. He seemed to have a very restful day -- probably due to the morphine. Although he's in good hands at the hospital, it's really hard to leave him at night. I don't want him to ever feel like he's alone. And judging by the countless family members in his room at any given time of the day I like to think that he knows we're all here supporting him. The nurses have been pretty tolerant of us breaking the "no more than two family members in the room rule". Thanks again for the support and prayers. Z

Saturday, September 20, 2008

A picture of reality


This was taken of Brad today Saturday, September 20th.

Brad the day of the surgery.
Wednesday, September 17th



Brad goofing around last year on the way to the Zoo.




















One of all the siblings and kids, before Luke was born.

Saturday, September 20, 2008




This is April. Zak and I got to the hospital this morning around 11. Bob and Derek were already there. They taught us how to give Brad some PT as he will need it several times daily. Brad's facial swelling has gone down significantly since yesterday! We heard from Bob and Derek about last night's drama. Apparantly, one of the nurses wasn't real confident in herself which created some tension. Brad wasn't doing well due to the fact that his ventilator had a hole in one of the pieces and the tape that holds his tubes in place was drooping into his mouth. He was having difficulty breathing so they had to suction out the "gunk" that accumulated in his mouth. Luckily, they fixed it. I'm just glad Lisa and I weren't there because we would have been a MESS.

We did get some fairly promising new today. On Monday, Dr. Chitale has ordered Brad's sedation medicine to be reduced by half. They are going to evaluate his ability to respond to commands and if he can respond positively, they can further decrease the meds.....alot sooner than we anticipated! YAY! We will all be there to root him on.

I just want to say than you to everyone who has prayed for Brad and put out positive energy! PLEASE keep them coming.

There will be a few people writing on the blog, this is a family effort to inform people about what happened with my youngest brother, Brad. I am Brads sister, Beth and then there are my two older brothers Zak, the oldest and Derek the middle brother and their wives, April, who is married to Zak and Lisa, married to Derek and my Dad, Bob. My family can write about their experience with the phone call on the morning of the accident, I can only relay mine.

My Brother Brad is 22 years old, fun loving, carefree and all heart. He is always trying to make people laugh. He is the baby in the family. He rides mountain bikes, skateboards, likes music and is a "ladies man" He can go anywhere and get a number without even trying. He loves life and lives it to the fullest.

9/17/08 Wednesday 0500
The phone rings, waking my husband and I up, Its 5 am... who would be calling? I look at the caller ID and I see a hospital number. Its my dad on the line. He tells me that Brad is in the hospital, has been out and sustained a head injury. I figure he will be okay, I am not panicked, I ask my dad if he is intubated, he says yes. Now I am worried, I know what this can mean. I have done this before, I have been the nurse in the ER for these patients. I immediately feel that knot move from my stomach to my throat, trying to contain myself until I get off the phone. I have to be strong, I have to process everything, I feel like my whole world has been tilted on its side. I rush to get dressed and brush my teeth, I ask my husband Bill to print me out a map to the hospital, he does, I tell him to make it two in case the outcome is immediately bad and he has to come right away. I tell him I am going to need him to call in to work for the day so that he can stay home with our daughter.

I drive to the hospital and I don’t think it has ever taking me so long to get to the interstate. I get to the hospital at 0602 and walk in to the ER, I am directed to a room where my brother is laying under a warming blanket on a vent, unconscious with sedation. My dad and oldest brother, Zak are at his side. I immediately go into assessment mode, heart rate is normal, normal blood pressure, good reflexes on the left side, purposeful movement on the left, empty bottles of mannitol on the counter. Mannitol is a medication to help decrease the swelling on the brain. Brad is still in c-collar, I ask my dad if they told him about any kind of cervical spine injury, Dad says no, just the head injury. I realize that as much as I hate to throw around title, I need to know what is going on, and it is easier to relay situations in medical jargon. I tell them that I am a nurse and that I would like to see the nurse taking care of him. I know that this does not get me points, in fact it makes people mad, nobody likes it when toes are being stepped on. The nurse comes in, doesn’t make eye contact, begins to package him to go to CT. I ask if he was intubated in the field or at the hospital. She says that they intubated him when he got here, that initial report from the field was that he was talking, though I don’t know his initial GCS. He was riding in the back of the truck and was thrown from the vehicle. He has multiple small subdural hematomas( bleeding in the brain) and a closed skull fracture. They have paged neurosurgery to come, Brad has been at the hospital for about 2 hours and has received appropriate life saving treatment, He is as stable as he can be given the situation.

The neurosurgeon arrives and tells us that he has looked at the CT scan and he feels like with Brads situation he feels like immediate surgery is required. He tells us that he is going to remove 2 pieces of skull from each side of his head to allow room for swelling. He tells us that he will place the bone in my brothers abdomen for storage. More family has arrived, April, my aunts on our mothers side Melinda, Julie, and Teresa, and a cousin Travis and his fiance, Crystal. We are all anxious and upset. He is taken directly to the OR from a repeat CT scan. We are directed to the OR waiting room, where we wait until about 1100 when the doctor comes out to tell us how the surgery went, He says that Brad did well in surgery, there was less bleeding than expected. He tells us that he is going to keep Brad sedated and intubated for 10 days at least to allow the brain to rest and allow plenty of time for the brain to swell and then go back down.

Brad will be in ICU, we are given a room number an hour later after he has been taken up from the recovery room. We go upstairs and wait for the nurse to let us back. When we are allowed to go back to see him, we are taken to his room, we walk in and he is laying in the bed, breathing tube in place, on the monitors, with about 5 IV medications going, they are giving him steroids, tube feedings, blood pressure medication, IV insulin, and antibiotics. He has his head wrapped up in a dressing that looks like a big white turban. He has no other injuries that we are aware of, they have removed his cervical neck collar. We spend some time with him and my dad and Zak go to try to find out where my brother left his truck. Derek and Lisa are on the way from Texas, and should get in through the night. I stay at the hospital, My husband comes to the hospital, the nurse comes in and informs us that Brad has developed a fever, they give him Tylenol through the tube that is going to his stomach.

I realize that I haven't eaten since the day before and it is 4 in the afternoon. My husband takes me to get something to eat, and we come back to the hospital until shift change for the nurses when they have all family members leave for two hours, My husband and I go home to feed our children and I need a shower and I pack a bag to stay at the hospital. I don't have to go back to work until the weekend, I arrange for my daughter to spend the night with a friend. I pack a bag, kiss my husband goodbye and head for the hospital to stay with my brother, I intend to stay for the first 48 hours.

I get back to the hospital about 10 pm. The night shift nurse is there in the room and I ask about his fever and his neurological checks, She informs me of my brothers status, he is stable, no longer has a fever, and asks if I am the family member that is a nurse. I say yes that I am an ER nurse. Brad is getting finger sticks every hour to check his blood sugar, They are good after being on the insulin for a while and the insulin is stopped, the blood pressure medication is stopped too, because it has improved. He has started to move his right side more, we are having to keep his hands tied to keep him from grabbing for the tube when they stop the sedation to check his reflexes. I sit in the chair by my brothers bed, teasing him about various things. Though it is not nearly as entertaining as when he partakes in the banter. I tease him about the tube feedings that he is receiving....umm lunch. I tell him that if he starts to run another fever, they will give him rectal Tylenol. I cope with my fear and anxiety through humor. I try to sleep a little at a time in the room. They come to get him for a repeat of the CT scan to determine the progress of the swelling and bleeding. They let me stay all night until the change of shift in the morning.

9/18/08 Thursday 0630- I go to the waiting room and make a makeshift bed from chairs, I stay until they are done with the change of shift, I wish that I was allowed to be back when the PA came back, I want the results of the CT scan that was done through the night.

My brother, Derek has arrived from Texas and my dad arrives at the hospital, we are in the room, talking to Brad, holding his hands, worrying about his condition. Zak and April arrive around noon and we visit with Brad for a while, we all need to eat, we decide to go to lunch, I go back to the hospital, Brad is running a fever when I get back, he has gotten more Tylenol. He seems to be more agitated, moving his legs in the bed, still his hands are restrained and Derek teases Brad about being tied up by nurses. He occasionally pulls against the restraints and has started to furrow his eyebrows. He gets agitated every time we turn him or when his breathing tube is suctioned. He is needing medication to sedate him and another to help relax him, we have also had to start back on the insulin and blood pressure medication. We have noticed that Brad has new swelling in the right side of his face, mostly his eye. The nurse says that this is to be expected. I am coming to the realization that this is going to be 1 step forward and 2 steps back with his recovery. Derek says that he is going to stay so my dad and I go back to his house and I get a couple of hours of sleep and a shower. We are all back at the hospital that night, my family stays for a while and I call my husband to bring me a few things and some food. It is late and everyone plans on meeting back at the hospital the next morning, Bill arrives and we eat, and I stay in the room again with Brad that night, I have seen some neurological improvement over the last 24 hours, he is using his right side more and when sedation is held for a few minutes he can flutter his eyelashes, we ask him to attempt to put up two fingers, I can see the muscles in his arm working, but he appears unable to control his fingers. I joke with him to just give us the middle finger. His heart rate and blood pressure are stable, he is more calm when someone is in with him. I sleep by the bed again in the fold out chair, the night shift nurse doesn't kick me out at 630 for change of shift, so I am there when the Dr. comes in.

9/19/08 Friday 0715- I ask about Brads progress, inform him of my observations, and his states that he is pleased with his condition, we are still on track to keep him sedated for 10 full days, he states that there is no reason to rush. The doctor asks about the ultrasound that they do to check for blood clots, the nurse informs him that it was negative, the chest xray that was done that morning looks good. I feel a little better about the progress. Dad calls and he asks if there is anything that he can bring me, I ask him just to bring a coffee. We all meet back at the hospital at 1000 and talk about his progress, what the doctor has said. I have a previously scheduled appt for my dog at the vet and I haven't seen my child in two days, I go with my dad to run a few errands and get some lunch, I have to leave after to take care of the appts I have. We plan on meeting at Lisa's Parents house for dinner. I take Jack(the dog) to his appt and sleep for about an hour. We go to dinner, everyone is there except for Brad, We toast to a speedy recovery. I finally allow myself to have a good long cry before going to bed. I pray that my brother will get better, I have to get up in the morning for work, so I try to get to sleep, I will be back at the hospital on Monday.