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


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Old 08-14-2007, 07:23 PM #21
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Default Call it what it is: TBI

Hi Mint

I think the term post-concussive syndrome is really not accurate. You need to think about concussion for what it is: a brain injury. Brain injuries can widely range in severity. What most people call PCS is actually "mild traumatic brain injury." The word mild is misleading, because the effects of MTBI can be debilitating and life-long. I suffered a TBI a little over 2 years ago. There is an excellent book on the subject of MTBI, which I recommend to you. It is called Coping with Mild Traumatic Brain Injury: A Guide to Living with the Challenges Associated with Concussion/Brain Injury, by Diane Roberts Stoler and Barbara Albers Hill. This is a very comprehensive book on all aspects of MTBI, how it affects your life, physical, mental and emotional effects, and recovery. It is an excellent resource.
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Old 08-16-2007, 08:19 PM #22
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Hello, Post concussion syndrome is a new term for me. I have never heard of it before coming here last week. I received a tbi when I was five about 42 years ago when I was hit by a car. Among other injuries, I had to relearn how to talk, and my personality was drastically changed. There has really been no therapy available for me when I was growing up. I just had to learn, relearn and adjust on my own. School was difficult for me, and I was always put in the slow classes. M y moods were always dark afterwards and as a result I have very volatile mood swings. I do talk with a therapist, and take a mood stabilizer which does seem to help. Other than that I just try to learn the best way I know how. I have developed skill as a medieval calligrapher over the past 5 years or so.
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Old 08-25-2007, 05:39 AM #23
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This is interesting PCS McGee... everything you have written I can relate to. I have had PCS since April 2005, with some days waking up like it is day 1 again. It's been harder than anything I know of. Even using the PC makes me very dizzy (anyone know why this is?)
Your message is a ray of hope to my life! I'm sick of being sick...
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Old 09-10-2007, 05:55 PM #24
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Quote:
Originally Posted by Mint View Post
How long have you had PCS symptoms and how bad was your original injury?

Are things getting better for you?
I've had the most recent bout of PCS symptoms since 2004. I also had an shorter bout where most of the symptoms went away where the injury was in 1998 and the symptoms faded dramatically on their own in a few years.

The most recent concussion would probably be termed 'moderate', with only a few seconds of greying or blacking out after impact. However, the symptoms from this concussion are more dramatic, with the following symptoms

*Concentration issues
*Dyslexia when writing or typing
*Issues forming coherent sentences or speaking verbally (loss of vocabulary, etc.)
*Headaches (these are fortunately getting a lot better and are few/far between)
*Feeling of pressure/'congestion' in the back of my head, at the base of the skull/beginning of spinal column (nothing has shown up on any x-rays or MRI about vertebrae being out of alignment or any soft tissue issues. This also tends to occur more with headaches. I also have borderline-to-high blood pressure, which I'm sure ties into this symptom somewhere)
*Inability to deal with being in large groups of people-I'm almost agoraphobic
*Depression and anxiety issues
*Radical mood swings
*Easily irritated/extremely short temper
*Extreme inability to deal with stressful situations-at some point where the stress level reaches a certain point, all sorts of things begin misfiring. Something seems to take over on a fight-or-flight-instinct level and I just physically leave the situation. Naturally, this has caused a lot of problems, and has cost me one job, one relationship, and has repeatedly strained friendships.

Overall, I've had some symptoms improve, but overall things have been steadily declining.

I share a lot of the frustration that the other posters have with the medical community's reaction and treatment- I remember doing a lot of online research and took a bunch of printouts to the doctor when I first got treated, and the doctor actually TOLD me to my face that I was more well informed and knowledgeable about PCS than she was. Her treatment, rather than refer me to a neurologist, was to tell me that I'd have these symptoms for the rest of my life and to prescribe anti-depressants (Xoloft, which did absolutely nothing and I have since stopped taking them).
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Old 10-15-2007, 05:52 PM #25
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Wildcard, your symptons are just about the same as mine other than the dislexia. (spelling?) What interests me the most about yours is what you said about the base of your skull. I have the feeling there that when I am extra tired and not the just tired feeling, my skull feels like it is not attached to the very top of my spine. I have asked and asked about it. Like you, nothing showed up in the MRI. My blood pressure is also high and I have to now take pills for it. 2 years ago I was rushed to hopsital with a hypertensive crisis 230/190 - the pain in my head was absolutely unbearable fortunately I didn't have a stroke as was expected! Pre accident I didn't have any signs of high blood pressure. I don't know if there is any link. I also feel that I know more about PCS than my GP - even though he had it at med school. I note that the insurers psychologist has actually criticised me for studying up PCS - but it we didn't ourselves who would! The accident that caused this for me was in 2001 and was very minor. Since then I have re injured about 4 times, the latest being 3 weeks ago - the last brought back the worst headaches and memory problems. The headaches have got better and are mainly when I let myself get too tired. The key is not to get too tired.
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Old 10-20-2007, 05:08 AM #26
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Quote:
Originally Posted by Lucy View Post
The headaches have got better and are mainly when I let myself get too tired. The key is not to get too tired.
I think that is the key too. My headaches are worst when I am stressed or tired so I always try to get enough sleep.
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Old 10-29-2007, 03:43 AM #27
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Grin

Mint, do you find that if your night's sleep is interrupted it can ruin your next day and in some cases the next few days. I notice that if I am too tired going to bed I can't sleep that night (just like a grizzly todler) and then the next day is a mess and then it takes a couple of days to catch up. I had eye surgery the other day and was given vallium - great sleep that night!!!! I can't control the icons - can't put them where I want to and now I can't get rid of the jolly thing!!! It was a grin to go after the vallium!
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Old 10-30-2007, 02:27 PM #28
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@Lucy

Quote:
Mint, do you find that if your night's sleep is interrupted it can ruin your next day and in some cases the next few days. I notice that if I am too tired going to bed I can't sleep that night (just like a grizzly todler) and then the next day is a mess and then it takes a couple of days to catch up.
Yes, usually if I have had a bad night's sleep then the next day I feel terrible. Very sleepy, headache and generally not alert, although this has happened after a few days of good sleep too.
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Old 11-01-2007, 06:04 PM #29
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Trig

I've had what I believe to be PCS for 22 years now. I haven't been clinically diagnosed with PCS but here are my symptoms after suffering a severe concussion / seizure disorder when I was about 10 years old.

- Headaches (constant dull pain)
- Fuzzy thought (but I get by)
- Memory problems (I'd tell you what they were, but I can't remember. )
- Depression (difficulty being happy at or feeling good, if I am happy it doesn't last longer than an hour.)
- EASILY Irritable (my girlfriend can attest to this)
- Dizzy (well it's kind of dizzy.. It's like I can't see straight/focus)
- Trouble concentrating (I can't even focus on conversations many times)

------

someone here also mentioned difficulty forming sentences or speaking sometimes. I also have that problem that may be related to PCS.

A more complete analysis of my condition is below, which I have pasted from my first post here.

Quote:
Hi,

I'm sure I could give you a lengthy story, but I'm gunna try to summarize for you.

Dave - 33 years old - Chandler, Arizona

I suffered a severe concussion when 9 or 10 years old which gave me a Seizure Disorder (about 23 years ago). I was on Phenobarbital and then Dilantin til puberty set in. I've been seizure free for 20 years.

I'm in good health. I exercise, take vitamins, eat right, don't smoke, drink on the weekends, no drugs. I have suffered from the following since 18 years old.

- Headaches (constant dull pain)
- Fuzzy thought (but I get by)
- Memory problems (I'd tell you what they were, but I can't remember. )
- Depression (difficulty being happy at or feeling good, if I am happy it doesn't last longer than an hour.)
- EASILY Irritable (my girlfriend can attest to this)
- Dizzy (well it's kind of dizzy.. It's like I can't see straight/focus)
- Trouble concentrating (I can't even focus on conversations many times)

Anyhow, I've had CAT Scans and MRI's. Docs say everything looks fine. I've tried anti-depressents which really messed me up bad (I had EVERY side effect possible) and I've also tried therapy, shrinks, books, meditation... I've tried pretty much everything... but,

Then I found some articles talking about Neurotherapy, and I've been looking into this pretty seriously. I'm an Audio Visual technician, so I'm comfortable with computers and technology. I would REALLY like to try this kind of therapy, but the devices and the software are really expensive. So this brings me to my questions.

1.) Could Neurotherapy help me?

2.) How could a regular guy with regular insurance get a device and software

3.) Heck, can I build one and download the software?

4.) There are some clinics here in Arizona, is there some special routine for getting in there and treated?

Thanks so much for reading.

-Dave 33 / Chandler, Arizona

p.s. When I was young I had a CAT scan and was able to alter my brainwaves to make the paper read out go crazy, and then was able to get it very quiet. I guess I was way ahead of my time.



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Old 11-06-2007, 12:20 PM #30
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I wasn't diagnosed that long ago, probably mid-May, early July. But with having 3-4 head injuries in my life, the doctor said I should have probably had it checked earlier. Go figure... lol But, my family is helping me cope with it because I can't seem to get it around my head that I can't be rude to them lol
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