Traumatic Brain Injury and Post Concussion Syndrome For traumatic brain injury (TBI) and post concussion syndrome (PCS).


advertisement
Reply
 
Thread Tools Display Modes
Old 05-02-2014, 09:59 PM #11
anon062314
Guest
 
Posts: n/a
anon062314
Guest
 
Posts: n/a
Default

I understand where all of you are coming from.

Hugs back B.
  Reply With QuoteReply With Quote
"Thanks for this!" says:
Hockey (05-03-2014), Living_Dazed (05-02-2014), music-in-me (05-03-2014)

advertisement
Old 05-03-2014, 10:51 AM #12
music-in-me music-in-me is offline
Member
 
Join Date: Aug 2013
Posts: 127
10 yr Member
music-in-me music-in-me is offline
Member
 
Join Date: Aug 2013
Posts: 127
10 yr Member
Default

Hi Everyone,

I just read this post, and I know exactly how you all are feeling. I have improved with my Neuro rehab, and I am so grateful to have been able to participate in a wonderful program. I am a medical professional who had 18 years of practice before the injury. The Neuro rehab team thinks I can eventually return to work (initially thought my former profession), but now that they have done other tests with processing speeds, visual-spatial activities, multi-tasking, and visual motor skills they do not think this is possible at my current status.

I also told them I do not feel capable of direct patient care anymore, and I feel I would be putting them at risk, which they all agreed was true. It is hard to accept giving up a career I really enjoyed, but I know the potential danger in returning if I am no longer capable of helping people.

I also have not returned to my musical outlet because I am not capable of playing guitar or singing for more than 2-3 songs, and I played and sang in 2 bands where we would play up to an hour to 1 1/2 hours ( about 12 songs) with little to no break.
I can't even consistently sing along to songs in the radio as I once loved to, but at least I can sing and play for even a short time.

It is hard to accept the visible and "invisible" changes brought on by a brain injury. I find it especially hard to continue to "press on" when it seems like I have reached a plateau in some areas. This injury is much harder to recover from than others, because there is no set time limit or expectation of recovery period. And I find it particularly frustrating when I seem capable of doing a task one day, then incapable of doing the same thing on another day, like taking down important messages for appointment dates and times. I messed this up so much, I begin not to trust myself.

I am not losing hope, I am simply trying to find a place of internal peace which says I am where I am now, and if it never changes I can live with it. I am always hoping for healing, but I found a journal from last August, and I couldn't believe how much had changed, but also what really hasn't changed for me. Had one of those moments that you all felt when looking at pre-injury pictures.

I am in the process of getting a referral to a Neuro-optometrist to help with my visual-spatial deficit (tested 6% last week out of 100%-yikes!). I don't know what will come of this. Also doing multiple tests to find out about the nature of "spells" which have sent me to the ER by ambulance twice within a month. It's a never-ending doctor's appointment, but I am grateful for the ability to get referral to the doctors and try to figure out everything.

I am mostly grateful for the recovery I have had, but struggling with accepting what might be permanent losses and the new me, too. Such a fine wire to walk across. Please take care, everyone. I am grateful to have you all to commiserate with.
M-i-m
music-in-me is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
anon062314 (05-03-2014), berkeleybrain (05-03-2014), Hockey (05-03-2014), Living_Dazed (05-03-2014), SmilinEyesMs305 (05-03-2014)
Old 05-03-2014, 05:46 PM #13
SmilinEyesMs305 SmilinEyesMs305 is offline
Member
 
Join Date: Jun 2011
Posts: 242
10 yr Member
SmilinEyesMs305 SmilinEyesMs305 is offline
Member
 
Join Date: Jun 2011
Posts: 242
10 yr Member
Default

Quote:
Originally Posted by Hockey View Post
If you don't mind me asking, what's your subject area? I'm married to a professor.

When your whole life in based on your cognitive abilities and, driven by your intellectual curiosity, I am sure that it is exceptionally difficult to come to terms with a TBI. A brain injury is a challenge to every patient's sense of self,but that must be doubly true when your identity is so inextricably entwined with your intellect.

I feel for you.
Hockey-

I totally feel for you. I was working full time and going to grad school full time prior to my accident. Straight A student all my life, over acheiever, etc. That's what's hard for me to reconcile. If I wanted to do well before, I just worked even harder, (although I now realize this wasn't emotionally healthy all the time). Now if I do that, I pay for it for days, even weeks. The end of my fall semester & a term paper resulted in 3 seizures over Christmas break.

I've been able to recover a lot of my academic skills through cognitive therapy with a speech therapist and accommodations via the university's disability resource office. But it's annoying because people in my master's program, (in SPECIAL ED), think there is nothing wrong with me and think I'm "cheating" or getting special help that I don't deserve, because I have extensions for some of my work or take exams in a private area to deter distractions. I HATE that I can't perform at the intellectual level I used to.
__________________
What Happened: On 3/8/11 I was stopped waiting to merge into traffic when I was rear ended by someone doing 45 mph. I walked away from the accident, to fall into the pit of PCS 5 days later... (I have had 2 previous concussions, but neither developed into PCS.)

Symptoms 3 Years Post: Physical: migraines, infrequent vertigo, neck and back pain (from accident), tinnitus, visual field deficits in left eye, problematic light sensitivity, (including visual seizure activity), noise sensitivity, EXTREME fatigue, semi-frequent disrupted sleep cycles,
Cognitive: semi-frequent Brain fog after cognitive strain, limited bouts of impulsivity, unable to concentrate for more than short periods of time without fatigue, word finding problems, slowed processing speeds, impaired visual memory;
Emotional: easily overstimulated, depression, anxiety;

Treatment so far: Vestibular therapy; Physical Therapy; Vision Therapy; Vitamin Schedule; Limited caffeine; Medications; attempting to limit stress and overstimulation; Yoga; Cognitive Therapy
SmilinEyesMs305 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
anon062314 (05-03-2014), berkeleybrain (05-03-2014), Hockey (05-03-2014)
Old 05-03-2014, 08:03 PM #14
Mark in Idaho Mark in Idaho is offline
Legendary
 
Join Date: Feb 2009
Location: Somewhere near here
Posts: 11,417
15 yr Member
Mark in Idaho Mark in Idaho is offline
Legendary
 
Join Date: Feb 2009
Location: Somewhere near here
Posts: 11,417
15 yr Member
Default

SEM,

You may need to create a distinction between your intellectual performance and your academic performance. Intellectual performance may have minor deficits while academic performance suffers greatly. You may have the same intellectual skills but need more time to use them. Academic performance is very comparative within a standard protocol of comparison, such as test taking and time to write a paper.

We often can not maintain the same performance time wise or in a large room with others taking a test and the ambient sounds and sights of such a room. We need the distraction free environment and maybe a bit more time. It does not mean our intellectual skills are less.

I am surprised that others in a special ed program are questioning your needs. They are studying to accommodate the needs of persons with special learning and testing needs. Are they just getting the additional degree to qualify for better pay or do they have a true desire to help those with special needs ?????

Your life experience will give you a very special insight into the needs of others.

My best to you.
__________________
Mark in Idaho

"Be still and know that I am God" Psalm 46:10

Last edited by Mark in Idaho; 05-03-2014 at 09:32 PM.
Mark in Idaho is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
anon062314 (05-03-2014), Hockey (05-03-2014)
Old 05-03-2014, 08:45 PM #15
SmilinEyesMs305 SmilinEyesMs305 is offline
Member
 
Join Date: Jun 2011
Posts: 242
10 yr Member
SmilinEyesMs305 SmilinEyesMs305 is offline
Member
 
Join Date: Jun 2011
Posts: 242
10 yr Member
Default

[QUOTE=Mark in Idaho;1067425]SEM,

You may need to create a distinction between your intellectual performance and your academic performance. Intellectual performance may have minor deficits while academic performance suffers greatly. You may have the same intellectual skills but need more time to use them. Academic performance is very comparative within a standard protocol of comparison, such as test taking and time to write a paper.

We often can not maintain the same performance time wise or in a large room with others taking a test and the ambient sounds and sights of such a room. We need the distraction free environment and maybe a bit more time. It does not mean our intellectual skills are less.

I am surprised that others in a special ed program are questioning your needs. They are studying was to accommodate the needs of persons with special learning and testing needs. Are they just getting the additional degree to qualify for better pay or do they have a desire to help those with special needs ?????

Your life experience will give you a very special insight into the needs of others.

-------------------
Mark-

I agree with you about intellectual versus academic functioning. It was hard in the beginning to accept accommodations, but I know that without them, I can not give my best work.

I think it goes back to this being an "invisible" injury. A lot of people in my life judged me prior to this by my academic/intellectual abilities. Now that I need accommodations to show my best intellectual ability and people can't see how bad I'm suffering on the inside to have the same academic abilities, (via accommodations and the help of a cognitive therapist), I feel like I'm not good enough. (I have always had very low self-esteem and this has really shook me even more).

And yes, it makes me sick that many of the people in my program don't understand my need for accommodations. Our program is mostly full of people who work for nonprofits, so money is not the motivation for completing the program.

My first professor when I started back, said that he didn't really feel my "accommodations were necessary" when I handed him my letter from my disability resources office. A class later, a classmate asked me how I got lucky enough to get out of taking exams, (but I was really taking them in the academic testing center instead of with my class). And this past semester, someone asked me if I visited my Dr. in jail now because they consider me disabled and have provided paperwork saying so.

But the BIGGEST blessing, is that I now understand so much more what my students go through, especially those with autism who have sensory issues. It's going to make me a much more compassionate, understanding therapist when I hopefully can return to the field when I finish my degree.
__________________
What Happened: On 3/8/11 I was stopped waiting to merge into traffic when I was rear ended by someone doing 45 mph. I walked away from the accident, to fall into the pit of PCS 5 days later... (I have had 2 previous concussions, but neither developed into PCS.)

Symptoms 3 Years Post: Physical: migraines, infrequent vertigo, neck and back pain (from accident), tinnitus, visual field deficits in left eye, problematic light sensitivity, (including visual seizure activity), noise sensitivity, EXTREME fatigue, semi-frequent disrupted sleep cycles,
Cognitive: semi-frequent Brain fog after cognitive strain, limited bouts of impulsivity, unable to concentrate for more than short periods of time without fatigue, word finding problems, slowed processing speeds, impaired visual memory;
Emotional: easily overstimulated, depression, anxiety;

Treatment so far: Vestibular therapy; Physical Therapy; Vision Therapy; Vitamin Schedule; Limited caffeine; Medications; attempting to limit stress and overstimulation; Yoga; Cognitive Therapy
SmilinEyesMs305 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
anon062314 (05-03-2014), Hockey (05-03-2014), music-in-me (05-04-2014)
Old 05-04-2014, 09:56 AM #16
Hockey's Avatar
Hockey Hockey is offline
Magnate
 
Join Date: Jun 2009
Location: I know it's somewhere around here...
Posts: 2,032
10 yr Member
Hockey Hockey is offline
Magnate
Hockey's Avatar
 
Join Date: Jun 2009
Location: I know it's somewhere around here...
Posts: 2,032
10 yr Member
Default

Why are the "caring" professions filled with so many uncaring people?
Hockey is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
anon062314 (05-04-2014)
Old 05-04-2014, 01:47 PM #17
MiaVita2012's Avatar
MiaVita2012 MiaVita2012 is offline
Member
 
Join Date: Dec 2012
Location: N/A
Posts: 685
10 yr Member
MiaVita2012 MiaVita2012 is offline
Member
MiaVita2012's Avatar
 
Join Date: Dec 2012
Location: N/A
Posts: 685
10 yr Member
Heart Me Too

I cannot even respond like I want to because I will get upset. I just want you to know I can relate. It is very hard to deal with.I had to let the Higher Power take over and form this new person I am becoming
__________________
What Happened: In 2011 I was in a MVA
.


Symptoms: Physical: I am always cold in any season!!I cannot tolerate anything pressure on my head(sun glasses,hats)longer then a hour,Lock jaw/Displaced TMJ, Dropsey, Hands go numb, Arms go numb, back of head numb (when asleep),Muscle spasms in face & upper body,migraines, concentration headaches, dizziness, nausea, neck and back trauma (from accident), tinnitus, extreme light sensitivity, noise sensitivity, EXTREME fatigue, impaired vestibular system, balance off, Pupils NEVER equal, disrupted sleep cycles,speech problems.

Cognitive: Cognitive Behavior, Brain fog, impulsivity, speech problems, word finding problems, slowed processing speeds, impaired visual memory, impaired complex attention

Emotional: Unable to handle stress or overstimulation without getting extremely irritable or angry, easily overstimulated, MAJOR depression, major anxiety, Panic attacks

Treatment so far: Treatment for PCS,PTSD,Depression & panic,Vestibular therapy, Physical therapy, Vitamin Schedule,Walking,No Dairy, No eggs, No caffeine, No artificial coloring, Sleep with 2 pillows, Very little sugars consumed, Eat healthy,No alcohol, Medications, limit stress and overstimulation.

~*~Learn to treasure yourself and your Divinity. Be willing to accept yourself completely. Be yourself, be graceful, be kind, be wild, be weird ... be true to yourself~*~
MiaVita2012 is offline   Reply With QuoteReply With Quote
Old 05-04-2014, 10:04 PM #18
Puppeteer Puppeteer is offline
Junior Member
 
Join Date: Jan 2014
Posts: 10
10 yr Member
Puppeteer Puppeteer is offline
Junior Member
 
Join Date: Jan 2014
Posts: 10
10 yr Member
Default

Oh gosh yes... though it's a couple steps worse for me, I suppose, because I also feel this way about thoughts and memories. They're still there for me to access, albeit without anywhere near as much ease, but they feel foreign. Formed and stored by a brain so significantly different to the one I have right now that they may as well not be my own. Weird to describe.
Puppeteer is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Hockey (05-05-2014)
Old 05-05-2014, 11:03 AM #19
Hockey's Avatar
Hockey Hockey is offline
Magnate
 
Join Date: Jun 2009
Location: I know it's somewhere around here...
Posts: 2,032
10 yr Member
Hockey Hockey is offline
Magnate
Hockey's Avatar
 
Join Date: Jun 2009
Location: I know it's somewhere around here...
Posts: 2,032
10 yr Member
Default

Quote:
Originally Posted by Puppeteer View Post
Oh gosh yes... though it's a couple steps worse for me, I suppose, because I also feel this way about thoughts and memories. They're still there for me to access, albeit without anywhere near as much ease, but they feel foreign. Formed and stored by a brain so significantly different to the one I have right now that they may as well not be my own. Weird to describe.
Welcome, Puppeteer!

Yes, I know what you mean. The memories are yours, but not yours.

Do any of you feel like you're just going through the motions emotionally and not really connecting, like you used to?

I love my child, but she feels I'm distant - and I think she's right. It never occurs to me to be spontaneously affectionate. I can't seem to describe it. I'm just not a complete, integrated personality. It's like I'm watching my life, rather than living it.
Hockey is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
anon062314 (05-09-2014), goodgrief20 (02-15-2017)
Old 05-05-2014, 12:35 PM #20
"Starr" "Starr" is offline
Member
 
Join Date: Apr 2012
Location: Ottawa, Ontario, Canada
Posts: 312
10 yr Member
"Starr" "Starr" is offline
Member
 
Join Date: Apr 2012
Location: Ottawa, Ontario, Canada
Posts: 312
10 yr Member
Default

Quote:
Originally Posted by Hockey View Post
I love my child, but she feels I'm distant - and I think she's right. It never occurs to me to be spontaneously affectionate.
I can relate to this for sure. I find this with my husband. I have to make an effort to be affectionate and kind of go through the motions, even though I don't feel it, for his sake.

Like remembering to kiss him when he gets home from work or hug him when he's feeling down or hold his hand if we are sitting together on the couch. Those things used to come naturally because I wanted to, not anymore.

And things I used to like, now kind of irritate me. Like he'd put his hand on my back and rub if I was upset, now I can't stand that. Its not comforting, it just makes everything worse. It's ok if he'll just put his hand on me and leave it still, but there's something about the movement that I just can't handle.

I've told him many times about how this now bothers me, but he doesn't seem to get it and continues to do it. I don't know why this changed, but it did.

Same with holding hands, he always wants to move his thumbs around on my hand and I can't stand that either. Just hold still, that I can tolerate!!

Starr
"Starr" is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
anon062314 (05-09-2014), Hockey (05-05-2014)
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
What happened?? Blessings2You Multiple Sclerosis 12 08-15-2009 11:01 AM
What ever happened to ..... Alffe Social Chat 2 03-16-2009 11:00 AM
It's happened to me as well. Koala77 Traumatic Brain Injury and Post Concussion Syndrome 8 03-09-2008 06:53 PM
Help! What Happened? JOE1 The Stumble Inn 13 02-10-2008 11:16 PM
Hi This is what happened to me rsd kitti New Member Introductions 6 02-20-2007 07:20 PM


All times are GMT -5. The time now is 02:49 PM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.