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

Reply
 
Thread Tools Display Modes
Old 02-08-2012, 04:56 PM #1
xanadu00 xanadu00 is offline
Member
 
Join Date: Jan 2012
Location: Minnesota
Posts: 239
10 yr Member
xanadu00 xanadu00 is offline
Member
 
Join Date: Jan 2012
Location: Minnesota
Posts: 239
10 yr Member
Default

1. I am so sorry that you're having to suffer like this. Nobody should have to go through that.

2. I am spending my days pretty much the same day you are spending yours: sitting in the dark by myself, listening to audiobooks, posting on here, "reading" posts via my text-to-voice software, etc. I can't even look at the screen briefly without two pairs of sunglasses and a transparent yellow plastic cover over my screen. I can't read, can't watch TV, shouldn't drive (but do so anyway because I have no choice), can hardly listen to any music, can only have limited conversations with people, etc.

3. Before this happened, I had already been suffering from sometimes crippling OCD for 15 years--and nothing I have dealt with since my brain injury has come close to being as excruciating and agonizing as my severe OCD episodes. I also had chronic fatigue syndrome for 10 years before acquiring my brain injury. I have dealt with both of these conditions primarily by myself; I have been isolated for the majority of the past 12 years.

4. When I got my brain injury (by being rear-ended while sitting at a red light), I was 4 months away from defending my dissertation and getting my Ph.D, which I had been working on in poverty for the past 8 years. Before that, I had already nearly had to drop out twice because of the OCD and CFS. Now I can barely read or write because of the light sensitivity and dizziness, and still haven't defended my dissertation. My career is in pretty serious jeopardy.

5. Despite all that, there are many, many reasons for me to go on living, and there will come a better day in my life. Five years from now, I will be in a better place and will be so glad that I didn't give up. You are younger than me, and have A LOT of life ahead of you. Chances are excellent that you will recover at least most of what you have temporarily lost due to PCS, and will be able to go on leading your life and perhaps accomplish great things. So you absolutely may not give up. You owe it to yourself and all the other people you will help in your life to keep fighting and never give up.

6. I'm going to post soon about James Stockdale, who was a POW in Vietnam for seven years and endured unspeakable suffering, including 2 years of solitary confinement. After the war, he went on to become Ross Perot's vice presidential nomination and wrote several books.
__________________
Male, 39 years old, suffering from PCS as a result of being rear-ended on 1/23/11. Part-time philosophy professor.

Last edited by xanadu00; 02-08-2012 at 05:28 PM.
xanadu00 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Dmom3005 (02-08-2012), SpaceCadet (02-08-2012)
Old 02-08-2012, 05:02 PM #2
xanadu00 xanadu00 is offline
Member
 
Join Date: Jan 2012
Location: Minnesota
Posts: 239
10 yr Member
xanadu00 xanadu00 is offline
Member
 
Join Date: Jan 2012
Location: Minnesota
Posts: 239
10 yr Member
Default

7. Nothing I said in the above post is intended in any way to minimize the awful suffering you are now enduring. Many people will never go through anything as difficult in their entire lives. You will not only survive it, but will come out on the other end a better person than you would have been without it. Many people who never endure suffering end up being selfish and unable to empathize with others--as we discussed in your post yesterday.

8. Be strong, love yourself, and endure your pain with courage and dignity. A better day will come, my friend.
__________________
Male, 39 years old, suffering from PCS as a result of being rear-ended on 1/23/11. Part-time philosophy professor.

Last edited by xanadu00; 02-08-2012 at 05:29 PM.
xanadu00 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Dmom3005 (02-08-2012), SpaceCadet (02-08-2012)
Old 02-08-2012, 06:31 PM #3
Mark in Idaho Mark in Idaho is offline
Legendary
 
Join Date: Feb 2009
Location: Somewhere near here
Posts: 11,427
15 yr Member
Mark in Idaho Mark in Idaho is offline
Legendary
 
Join Date: Feb 2009
Location: Somewhere near here
Posts: 11,427
15 yr Member
Default

Nick said <They say you can't tell if you have high blood pressure though...it has no symptoms. >

All you need to do is take you blood pressure when your symptoms increase. Didn't you order a BP home kit?

Have you asked about getting some blood pressure meds, propanolol, etc.?
__________________
Mark in Idaho

"Be still and know that I am God" Psalm 46:10
Mark in Idaho is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Dmom3005 (02-08-2012)
Old 02-08-2012, 06:59 PM #4
SpaceCadet's Avatar
SpaceCadet SpaceCadet is offline
Member
 
Join Date: Oct 2011
Location: Las Vegas, NV
Posts: 756
10 yr Member
SpaceCadet SpaceCadet is offline
Member
SpaceCadet's Avatar
 
Join Date: Oct 2011
Location: Las Vegas, NV
Posts: 756
10 yr Member
Default

I was ordering one online but the transaction failed....not enough funds. I'm going to get one from Walmart when my Unemployment drops on my card this week.

I missed the appointment on the 31st last month because I couldn't even get out of bed. I haven't felt good enough (long enough) to schedule another appointment and borrow my mom's car. Nobody has time to take me to my appointments.

I'm getting a car hopefully this weekend....then I could take myself next time I have an okay day and feel up to driving.
__________________
What happened: I was randomly assaulted from behind in June of 2011. I was knocked unconscious for an unknown amount of time (less than 30 minutes) and have no memory of the event. CT scan showed contusion and hematoma of the left frontal lobe. I spent 3 days in the hospital. Diagnosed with Post-Concussion Syndrome in September 2011. Currently have Medicaid, Medicare and SSI.

Current symptoms: Brain fog, mild memory issues, problems with spontaneity, occasional spacing out, word finding difficulties, tinnitus in right ear and some other things that I can't explain.

Life after the brain injury: 4 years after the injury, I'm engaged to my beautiful girlfriend of 5 years, I'm the CEO of my own business, Notorious Labs, I've taught myself how to program complex games and apps which is a feat I never thought I'd accomplish and now live a semi-normal life with very mild PCS symptoms.

Slowly but surely regaining my life back.
SpaceCadet is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Dmom3005 (02-08-2012)
Old 02-08-2012, 07:51 PM #5
Dmom3005 Dmom3005 is offline
Legendary
 
Join Date: Aug 2006
Location: Indiana
Posts: 13,019
15 yr Member
Dmom3005 Dmom3005 is offline
Legendary
 
Join Date: Aug 2006
Location: Indiana
Posts: 13,019
15 yr Member
Default

nwsmith

You definately need to take the bp. Its possible that a lot of
the problem has to do with this. I had bp problems, and when
put on a medicine it cleared up that particular part of the problem.

I didn't even know I had a problem. Luckily it showed up almost
immediately. After I almost fainted.

Donna
Dmom3005 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
SpaceCadet (02-08-2012)
Old 02-08-2012, 08:22 PM #6
SpaceCadet's Avatar
SpaceCadet SpaceCadet is offline
Member
 
Join Date: Oct 2011
Location: Las Vegas, NV
Posts: 756
10 yr Member
SpaceCadet SpaceCadet is offline
Member
SpaceCadet's Avatar
 
Join Date: Oct 2011
Location: Las Vegas, NV
Posts: 756
10 yr Member
Default

My fellow hermit (Pete),

I'm sorry to hear your living pretty much the way I am...it's not the business. Thank you for spacing out and numbering your reply, too.

Your light sensitivity sounds pretty vicious. I, too, am struggling with light sensitivity...as you can see in my signature. I'm not sure it's as serious as your's, but it's pretty bad. I have my computer/laptop screen turned all the way down...and when I'm in the dark room, that still doesn't help. My smart phone is on the lowest setting as well. I'm going to have to try that transparent cover over the screen thing. You described it pretty good in a prior post...it's like when your taking a nap and someone comes in and turns the lights on suddenly...lol.

Are you able to work?

What kind of OCD were/are you struggling with? I'm dealing with some extreme OCD myself...I don't even want to talk about it in public, maybe I'll PM you sometime about it?

Thank you so much for the encouraging words...It truly, truly means a lot to me. I'm sorry it took me a minute to respond - I've been screwed up all day and just barely pulled myself free of that uncomfortable, debilitating mind-state.

Dmom3005,

Yeah, I'm working on it...I had an appointment with a NP who was really great to me the last time I seen her. I completely missed the appointment the 31st of last month because I wasn't even well enough to get out of bed. I'm hoping that the majority of these strange feelings and mind-states I'm put in are blood pressure related...and the medicine will do me justice.

Sorry to hear you went through something similar, glad you got it under control.

Thanks...
__________________
What happened: I was randomly assaulted from behind in June of 2011. I was knocked unconscious for an unknown amount of time (less than 30 minutes) and have no memory of the event. CT scan showed contusion and hematoma of the left frontal lobe. I spent 3 days in the hospital. Diagnosed with Post-Concussion Syndrome in September 2011. Currently have Medicaid, Medicare and SSI.

Current symptoms: Brain fog, mild memory issues, problems with spontaneity, occasional spacing out, word finding difficulties, tinnitus in right ear and some other things that I can't explain.

Life after the brain injury: 4 years after the injury, I'm engaged to my beautiful girlfriend of 5 years, I'm the CEO of my own business, Notorious Labs, I've taught myself how to program complex games and apps which is a feat I never thought I'd accomplish and now live a semi-normal life with very mild PCS symptoms.

Slowly but surely regaining my life back.
SpaceCadet is offline   Reply With QuoteReply With Quote
Old 02-08-2012, 08:39 PM #7
Eowyn's Avatar
Eowyn Eowyn is offline
Member
 
Join Date: Jun 2011
Location: Sunset Coast, USA
Posts: 711
10 yr Member
Eowyn Eowyn is offline
Member
Eowyn's Avatar
 
Join Date: Jun 2011
Location: Sunset Coast, USA
Posts: 711
10 yr Member
Default

You sound very much the way I felt through most of November and December and January. I was seriously depressed. I mean, SERIOUSLY. I assume you've seen a psychiatrist? Seeing a counselor on a regular basis to talk to someone? Do you have a friend who can come hang out with you a couple days a week in the dark?

It sucks. It really and truly sucks. I am just starting to come out of it now after a med change and a lot of really horrible days. Hope you see light at the end of the tunnel soon.
__________________
mTBI and PCS after sledding accident 1-17-2011

Was experiencing:
Persistent headaches, fatigue, slowed cognitive functions, depression
Symptoms exacerbated by being in a crowd, watching TV, driving, other miscellaneous stress & sensory overload
Sciatica/piriformis syndrome with numbness & loss of reflex


Largely recovered after participating in Nedley Depression Recovery Program March 2012:

.


Eowyn Rides Again: My Journey Back from Concussion

.
Eowyn is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
SpaceCadet (02-08-2012)
Old 02-08-2012, 09:45 PM #8
xanadu00 xanadu00 is offline
Member
 
Join Date: Jan 2012
Location: Minnesota
Posts: 239
10 yr Member
xanadu00 xanadu00 is offline
Member
 
Join Date: Jan 2012
Location: Minnesota
Posts: 239
10 yr Member
Default

Quote:
Originally Posted by nwsmith1984 View Post
My fellow hermit (Pete),

I'm sorry to hear your living pretty much the way I am...it's not the business. Thank you for spacing out and numbering your reply, too.

Your light sensitivity sounds pretty vicious. I, too, am struggling with light sensitivity...as you can see in my signature. I'm not sure it's as serious as your's, but it's pretty bad. I have my computer/laptop screen turned all the way down...and when I'm in the dark room, that still doesn't help. My smart phone is on the lowest setting as well. I'm going to have to try that transparent cover over the screen thing. You described it pretty good in a prior post...it's like when your taking a nap and someone comes in and turns the lights on suddenly...lol.

Are you able to work?

What kind of OCD were/are you struggling with? I'm dealing with some extreme OCD myself...I don't even want to talk about it in public, maybe I'll PM you sometime about it?

Thank you so much for the encouraging words...It truly, truly means a lot to me. I'm sorry it took me a minute to respond - I've been screwed up all day and just barely pulled myself free of that uncomfortable, debilitating mind-state.

Thanks...
I'm barely able to work. Right now I have an editing assistantship through my department which is only about 5 hours/week. It's mostly proofreading and copyediting hard copies of accepted journal submisssions, which I can manage, but it's just about all the reading I can do. Going through a volume of papers in a period of a few days stresses me out so much that I have to take a break from reading for a week or so afterward, and usually by the time I'm ready to start reading again, it's time for another round of editing. This is contract work that ends at the end of May; as of that time, I will be unemployed and, if I'm lucky, on Medicaid.

My OCD is "pure obsessional," which is a misnomer, since pure obsessionals have mental compulsions. But the gist of it is that I get horrible intrusive thoughts stuck in my head that cause unbearable anxiety. I've been managing it pretty well the past few years, but it still pops up now and then. Feel free to shoot me a private message anytime about your OCD. There is nothing you could tell me that would shock me; I've heard about all the different bizarre subtypes. (Anyone on this forum should feel free to email me with OCD questions.)

It sounds like you're feeling a little better now. If so, I'm very glad. Hang in there, man. When you're sitting there in the dark too messed up to do anything, remember that I'm probably doing the same thing.

Pete
__________________
Male, 39 years old, suffering from PCS as a result of being rear-ended on 1/23/11. Part-time philosophy professor.
xanadu00 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
SpaceCadet (02-08-2012)
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
I give up Iffynah Reflex Sympathetic Dystrophy (RSD and CRPS) 5 08-08-2008 12:21 PM
Give Thanks for.... Corkybird Sanctuary for Spiritual Support 10 11-22-2007 07:51 PM
I give up Bronco4586 Reflex Sympathetic Dystrophy (RSD and CRPS) 51 06-04-2007 09:26 AM
'I can't ever give up' BobbyB ALS 0 01-15-2007 08:00 AM


All times are GMT -5. The time now is 06:25 AM.


Powered by vBulletin • Copyright ©2000 - 2025, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise (Lite) - vBulletin Mods & Addons Copyright © 2025 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.