Hi, I am a caregiver for my hubby who 18months ago had a sca resulting in severe hypoxic brain injury. He has been home a month, he’s doing well , but requires 24 hour care. I am always amazed at the number of members who write their own posts! I can’t visualise my hubby ever being able to do this? Anyone else thought this and how long does it take? Any thoughts would be grateful x
Hypoxic recovery: Hi, I am a caregiver for my hubby... - Headway
Can take few years often to recover that much. I was v lucky. From being told vegatative state would be best outcome for me I went back to school 8 weeks later. Learned to walk again etc.. in that time. Dr advice is best guidance but it's not bullet proof. Best support any care giver can provide in the long-term is to look after themselves too. Best of luck you both.
It really depends on the brain, my boyfriend sustained hypoxic brain injury and we were told the brain damage looked severe and we would be lucky if he came out of a vegetative state.
It took him 6 months to recover and he is able to stay in the house independently and only relies on me for cognitively challenging aspects such as finances and cooking complex meals (he can warm up a mean ready meal!)
The guide is anytime from 6 months to 2 years however there are studies that the brain can continue to develop and rewire years later so don't give up and keep persevering to help him and one day he might write a post on here for you
If you need anyone to talk to about Hypoxic Brain injury recovery do feel free to message me.
He will in some way or another, I found myself doing all sorts of different things with him to supplement from giving his food/sweets in different wrappers (babybel, daryleigh dunkers, etc) anything slightly complex to challenge his motor skills (he is food orientated haha!) and then things like children's homework books to help with the thought process side of things. Just keep doing what you can and he will find some way back, it is remarkable what the brain can do.
my 24 year old daughter had a hypoxic brain injury 6 weeks ago and we've been told that the damage looks so severe that it is unlikely that she will ever make any improvement and will remain in a vegetative state. Apart from remaining hopeful, did you do anything in particular to stimulate recovery and what were some of the first signs of improvement you saw and at what stage. I would love to hear more about your experience if you would be happy to share it.
I know every injury is different but your story had given me something specific to grab onto in that we've both been told the same thing and in your case there was more improvement than the doctors expected.
What tests have they done to "see" the damage? I was told my hubby would be vegetative. Today they called to tell me he will be doing in hospital physical therapy. He's made "miraculous improvements". I noticed improvements when we tried a kiss or head nods just read their body language. My husband couldnt squeeze a hand which the drs rely on but he did other things until it came back. Wiggle a toe, raise your arm, blink twice, smile if you love me, be creative..
Hi, after two weeks, I used to take in his trains/tracks that he would play with constantly with our grandchildren/ I would try and place the train in his hand and encourage him to put the train on the track/ I would do this over and over. Also I would take Lego bricks in. I would constantly try and engage with him. I also used to massage and excercise his limbs daily
They told us my bf had severe damage after a hypoxic brain injury 7 months ago tomorrow and to expect vegetative but he has beaten all the odds and is back with us (apart from some cognitive and balance stuff)
When he was in a coma for the first week I found it really hard to talk to him (I think I told him 3 times what I had bought his family for christmas haha!) Instead I played music and as I got stronger in the situation (I was a wreck too) I started to read to him.
Once he "came round" a bit more I felt I had more to talk to him about and I used the room to help me (ended up pretending to be a tv antenae because the tv wasnt working at one point.
Further down the line when he was a bit more independant I brought him biscuits and snacks in wrappers that would test his fingers to stimulate recovery and motor skills (didnt know if I was helping or not but I did it) I also brought him puzzle books and easy activities.
Our first signs of improvements were that they had managed to bring him off ventilation and he had been able to understand what was asked of him a little, then he moved his hands and opened his eyes, I always felt like you could imagine people running in his brain testing all the circuits etc before he woke up.
Try anything is my advice, sorry for the long post!
I found playing kids games helped when my husband was first ill. We started on basic things like snakes and ladders, snap etc (with help from me of course) and then progressed slowly to things like ludo. Anything that keeps the mind working is good. Even laying the table (and getting it right!) all help with getting the brain involved.
Hi you are doing a good job. I had my tbi in 1998 and still improving. So it will take years. When I came home I was wheelchair bound and lost my temper a lot at first I had 24 hour care we reduced this over the years and for the last few years my husband has been my carer. He cannot put up with my moods any more so he is divorcing me. So it will be hard work for you but as the person with tbi I would of been happier if he has left at the very beginning. I now need to readapt my life not sure how this will go.
I used to be a senior cancer research nurse which I will never return to. I have found this site very useful so if possible encourage participation. You will both find it useful I think. It will be good for your hubby to realise he is not alone. Everyone with tbi is different but we all deep down want to go back to how we were it takes years to accept that will not happen if I had found this site at the beginning of my new life/personality Maybe I would not be getting divorced. It is useful to talk to people who understand.
Hi my husband has been home just over 4months. It’s been 19months post injury! He needs fully 24hour care, he has no memory of his life which is heartbreaking as we have been happily married 39years. But since being home he is making good but slow progress. His Speach and tolerance levels are improved. His fitness is improving and is now able to walk 25mins daily. We just have to take each day and try to keep positive, who knows how far we can go. Good luck