Brain Injury Support Group
Traumatic brain injury occurs when a sudden trauma causes brain damage. TBI can result from a closed head injury or a penetrating head injury. Symptoms of a TBI can be mild, moderate, or severe, depending on the extent of the damage to the brain. Outcome can be anything from complete recovery to permanent disability or death. A coma can also affect a child's brain.
There are people on this board who have suffered a severe TBI and been in a coma. I'm sure they will respond next time they check in here.
There are also quite a number of caregivers on here. So I think you'll find good support of people who've been where you currently are.
I like your attitude and am glad that you are there for your husband. I would say keep talking to him & being there for him.
Since the beginning I've believed that Roger can hear me. As a matter of fact I have a blog that charts his progess for family and friends and in it I asked them that if they went to visit him they wouldn't talk around him as if he wasn't there because he is. I asked them to please not be afraid to hold his hand and tell him about anything positive (nothing negative, please). I've asked the nurses and the doctors to please not discuss his condition around him, that I would like to be the one to decide what I want him to know and how he hears it.
I read various things to him... The sports page, the comics, the Bible, all the cards that people send, all the things people write in the visitors book I have in his room. I've even been reading the book he was reading, having taken up where he left of.
I download his favorite songs on my MP3 and play those, as well as uplifting Christian music. I've also started downloading sermons by preachers I know he admires and plug those in his ears. :o)
When the Reds play, I put that on TV for him as well as old classic movies, which he loves.
As our children haven't been allowed where he is I record messages from them and play those for him.
I try to keep him current about our lives... Telling him the things that we do and that when we're doing them he's always with us.
I give him body massages and do range-of-motion exercises with him daily.
I stroke his face often. I also can't seem to stop kissing it.
It tell him I love him constantly. I tell him that the children and I are fine, that he was so wonderful to see that we were cared for financially in the event something like this happened. That we love him and miss him but that there's no hurry, we're going to wait for him to wake up no matter how long HE NEEDS for that to happen. I tell him not to be afraid...
I try to stimulate him in various ways. He breaths through a trach so I'm not sure if he can smell but I give that a shot anyway. I stick all kinds of scents under his nose: his favorite herbs like rosemary and basil, various aromatherapy oils, my perfume, his cologne, etc. When he's warm, I rub him down head to toe with cool cloths. When he's cold, I rub him with warm ones. I've thought about bringing his alarm clock in, setting it off, and telling him he's late for work but decided that would be cruel. I may yet resort to that though.
I got a book off of Amazon called, "Coma - A Healing Journey" by Amy Mindell. In it, she basically describes ways to get in tune with a comatose persons and how to establish ways to communicate with them. I just started reading it. He gets transfered to a nursing home on Friday and I'm hoping that environment will be more quiet and conducive to the process.
Roger was the sweetest man ever and always took wonderful care of us. Now it's our turn to take care of him.
Kiki
My son was not in a coma but he was unconscious for 3 weeks. He has a TBI and we are nearing the one year anniversary of when I brought him home. It took him well over a year and 3 weeks of intensive therapy to get him to any condition where that was een possible... but I keep fighting. Send me the link to you blog please. I also have one where I blog about how I (try to) keep faith in the midst of the journey. I wish I had started it earlier! I also have a blog that is a devotional for caregivers...it is not easy - but don' t give up.
Two things - as long as there is breath - there is hope.
And rejoice in every single bit of progress no matter how small - and consider how far he's come not how far he has to go.
This is a great site with lots of encouraging people here - I can't fix your situation (but I wish I could) but I can be here to listen....
jeanie
All of the things that you mentioned, saying he will move a little if you touch him a certain way, my husband did NONE of that. In fact they did an EEG, twice, and it came back that there where no brain waves. Then one day when I was talking to him he squeezed my hand, it was the most awesome feeling. I too, sent him to a nursing facitity. It took 6 men to carry him in, and about two weeks later I walked in and he was walking down the hall (with assistance). They told me that it would take about 6 mo of comma stemulation therapy, and it didn't take but maybe half. Now, he was younger, just turned 30, and of course everyone is different. However, I will say this, just from personal experience and observation I firmly believe that the patients that have constant family support do much better than the ones that dont. People will tell you they can't hear, don't bother talking or turning on the tv, BULL. I would joke with him everyday when I walked in, that was just how we were, and whisper in his ear your wife wants a diamond. When we left that place for good, the first thing he said was he wanted to go to the mall and look at jewlery. He is doing great now, he is a machinist at Ford, so don't give up hope :)
I too, had a TBI a few yrs ago, not as bad, I was a pedestrian and hit by a jeep. I went through a lot of therapy, speech and so forth, but things are going good. Keep your chin up and good luck to you!
The docs have, as I think I mentioned, been nudging me toward hospice. In truth I'm meeting with them tomorrow ONLY because I want to be informed, not because I'm ready to go there.
A friend of mine's mother is a retired hospice nurse. She said that they aren't just about dying but about living and that they might be able to give me ideas on how to carry on under the circumstances.
I'm open to all things at this juncture.
Thanks again. It means a ton.
Kiki
In my own situation.....I will tell you that my husband has a hypoxic brain injury post minor surgery. We are 11 months into therapy and he tells me daily." I heard you, and I understood everything you said , I just could not respond." ( This was while in his coma and the 6 months post coma that he was in decreased level of conscientious )......It is hard. He still never looks at me. He can not focus, has severe speech issues and many many issues from memory, swallowing, seeing, hearing ect. ......but every now and then he surprises me and I understand his speech as he reassures me that HE IS IN THERE. He did hear and understand me.
Try and be strong, we all know how very tough this is. Your husband may or may not come out of his coma. Only our good Lord knows this for sure but, find peace in knowing that he can hear you and feels every bit of the love you have for him.
Wow, I saw you mentioned the Reds earlier, and I can't believe - we were practically neighbors, I'm from Florence, KY. I wish I could come over to visit and talk and support you in person, but my dad just had his second TBI about 2 months ago in a car wreck and I had to suddenly move to Florida to help with him. I will be thinking of you and hope that things will improve for you both. Don't forget to take good care of yourself as well - as my doctor has had to remind me, we can't take care of everyone else if we don't take care of ourselves too.
Sarah
Sarah, wish like crazy you were still in Florence but I'm grateful for the contact from afar. :o)