C5 Injury
#1 *kelly*
Posted 01 February 2005 - 02:15 PM
#2
Posted 01 February 2005 - 05:34 PM
Please E mail me at jon-paul.crooks@ntlworld.com
I was in exactly the same situation almost 3 years ago, (C-5) incomplete
I've learned alot and I'm walking.
Hope to speak soon.
C-5 Incomplete, Diving Accident in Mexico. Walking with crutches, In controlled pain !
Big respect to all SCI people !
#3
Posted 01 February 2005 - 07:06 PM
That best of luck,
Glenn
http://www.Iwouldntchangeathing.com
#4
Posted 02 February 2005 - 08:56 AM
I, like your partner also had a fracture of C5, this resulted in a neurological level of C5/6.
As a C5/6, I too have movement in my arms and wrists, but no finger function. A general summary of someone with this level of injury, and their resulting abilities, can be found here:
http://www.apparelyz...onality/c6.html
I too have sensory sparing, in that I can feel touch all over my body. I cannot feel temperature or light pain though. Is your partners sensation normal, ie, can he feel temperature and pinprick sensations all over his body?
If he has normal sensation, I have read that there maybe a possibility of further recovery. This is only what I have read, so don't get your hopes up too high, the best thing is to talk to your surgeon about this.
Swelling of the spinal cord can take upto 2-3 years to go away, and the final recovery will not really be finalised untill then. Having said this, a good indicator of his abilities would be known better after 12 weeks, but it's still very early in his recovery to tell.
Prognosis for Anterior Cord Syndrome is good if recovery is evident & progressive during first 24 hours, after 24 hrs, if no signs of sacral sensibility to pinprick or temp are present, prognosis for further functional recovery are poor. Only 10 to 15% of patients demonstrate functional recovery.
Like I said above, the amount of recovery your partner has, will depend on what type of incomplete injury he has. For my injury, I never regained any motor control below C6, but as I said, I have sensory sparing everywhere.
Regards
Simon
#5 *Ian*
Posted 10 February 2005 - 08:54 AM
Solscher@AOL.com Ian
#7
Posted 02 September 2005 - 09:59 PM
While it is wonderfull that you give out your email addresses to help each other out, I would still hope that you could post your questions and answers on the forums.
We all learn a lot from each other and hopefully there is not anything that we cannot talk about here as adults. If we regulate the discussions to back channels, then the forum people lose out and the questions get covered by less people.....less perspective.
#8
Posted 04 September 2005 - 10:31 AM
I would advise against giving out email addresses publicly, as there are programs out there which harvest email addresses for spam purposes.
If you are a member of this forum, you can click on the members name and send them either a personal message which they can read next time they visit the forum, or you can email them through the email facility which keeps the members email addresses confidential.
Of course the best option would just be to have a conversation on this forum so others can give their perspectives on the subjects.
Regards
Simon.
#9 *IJ34*
Posted 06 October 2005 - 11:37 AM
I am very new to this and still in shock but I would like to try and understand from someone what lies ahead for him and how best can friends support and help. Also what are good/bad signs to look out for.
Please post answers in the forum as I am sure plenty of other people will benefit from your answers.
In anticipation...thankyou!
#10 *Melissa*
Posted 07 October 2005 - 01:34 PM
He also has a really strange reflex. When I stretch his left leg into his chest, the fingers on his left hand extend out straight and when I lay his leg back down, his fingers curl again. It's really weird and the nurses and doctors can't explain it, wondering if any one here might know.
#11
Posted 07 October 2005 - 03:26 PM
There seems to be a strange relationship between the legs and fingers. I read this at another forum:
Quote
Wise is the first name of a doctor specializing in SCI.
The full thread is here.
#13
Posted 08 October 2005 - 12:45 AM
I'm not a C-anything, and I doubt my story will shed any light on things, but I had something similar happen to me with my feet and toes. My cord problems were present at birth, but before my actual paralysis in '03, if I rotated my left ankle or wiggled my toes, my right ankle/toes would mirror the same movements. I think it's probably because I also have a split spinal cord, where the lion's share of my cord ennervates the left leg. In other words, cord nerves that were supposed to ennervate my right leg, went to my left leg instead.
Actually, this anomaly ended up being my saving grace, as most of the cord injury from '03 affected my right leg, leaving my left leg with only neuro deficit.
Anyway, your question reminded me of my own quirky neuro manifestations, and I thought I'd just share them.
Blessings,
~Joed
Female. Incomplete para following a cord stroke in '03. Spina-bifida, severe scoliosis. 18 surgeries total...five spine-related: Three fusions w/hardware, two tethered cord releases.
#14 *IJ34*
Posted 11 October 2005 - 11:20 AM
Have now received news, the doctors have advised him that he will never walk again, he has movement in his shoulders, arms and chest but none in his hands and fingers but they are hopefull that this will improve. He can feel people touching his legs etc but cannot move them, sounds very similar to your husband Melissa, I know these injuries are very individual with regards to outcome but I would really appreciate any info on these boards with regards to how best support and help...I am at a loss as to how to just help out...
#15
Posted 09 February 2009 - 01:24 AM
kelly, on Feb 1 2005, 02:15 PM, said:
im a young girl (14) and broke my C5 this summer, during a diving accident. i could help you out. just ask for my email
#16
Posted 18 February 2009 - 10:18 PM
#17
Posted 19 February 2009 - 06:26 PM
I am really bothered by your post. First of all, not like your partner went out and decided to have a SCI. Don't you know how "LOST" he feels in all of this? What a drastic change HIS life has become? I'm sure all the changes are driving you nuts, but I'm sure if HE were asked, he'd have some ticks with you. I doubt that he likes being dependant on you. Nobody likes being dependant on anyone else. Just human nature. You don't really state how long you two have been together. Whatever time it is, is still time invested in the other. How would YOU feel if it were YOU who had the SCI and HE were contemplating leaving YOU because of something you cannot help. Herbie, life is not fair. We don't always get to choose the path that our life takes. I hope that you give some serious thought to this before you make any decisions to leave. And if you do, you should really communicate fully with your partner BEFORE you start packing.
My 2 cents.
Stella
#18
Posted 19 February 2009 - 08:21 PM
kelly, on Feb 1 2005, 09:15 AM, said:
Hi. I'm 18 and just recently broke c1-c6. When I was first injured that is all the movement I had too. I was told I'd never walk again, but now (7 months later) I am able to take steps with a walker. My only problem is my low blood pressure drops dramatically when I stand preventing me from standing for more than 2 minutes at most so far. My advice to you is to advise him to try things first on his own. I learned the more I try to do things on my own, the more I recovered. Feel free to msg me. Good luck.
- you were only given this life because you're stong enough to live it.
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