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


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Old 06-25-2013, 07:44 PM #1
fkd5322 fkd5322 is offline
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Default Trying to recover from my PCS after a year and a half.

All I want is to feel Normal, healthy, and happy.

It's been a year and a half since my injury. I use to have headaches that were more noticable but they've gone down a good anount. When I get stressed out i feel like the pains in my head become more noticeable or start up. One other thing I feel dosn't help the headaches/ head pains I'm going through is being on my phone& watching TV. I've had such trouble trying to stop both theae habits, I know that instead of cutting them completely out of the equation I should just cut down the time I'm on the computer,Watching TV, or on my Phone. Will making the change and cutting down the amount of time i spend on eletronic really help my headaches go away completely? Also I've been drinking, a habit I find extremely hard to stop. I'm 21 and all my friends do for fun is drink and because I get very bored I go out with them but i always end up feeling that it can't be good for the recovery I'm still going through.

The last thing that I feel like is not helping the headaches is STRESS. I had a falling out with my first love and it's caused depression, anxiety/ panic attacks. I'm stressing out at times like a mad man. This can't be good for any sort of recovery right?


Another issue that i've been going through is my smell has become distorted. Instead of smelling the actual odor that is present I smell these odd smells that I havn't been able to compare to anything I've ever smelled in my life. It's like Instead of smelling pizza I'll smell soap. Like my nose is playing tricks on me. I work at a restaurant where food is around at all times. I can't say that i've ever smelled anythong even close to the delicious scent of food that I'm sure everyone else smells. I'm going to washington DC in 2 weeks to THE SMELL AND TASTE CLINIC. The doctor there is suppose to be a speacialst in smell disorders. It's very exapensive, about 6,000 dollars. I wonder if I'm making the right decision spending money on this. Getting my smell back to normal is so very important to me.

Please... Advice and help. I'm 21 and my parents arn't beong much help. What should i do to fix this problems I'm still going through with my PCS.
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Old 06-25-2013, 08:29 PM #2
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Hi! Welcome! Thank you for sharing yrour story! Did your headaches go away in their own? Did you do any kinds of therapy or medication?

Others here can help you more than me though.

Thanks

Quote:
Originally Posted by fkd5322 View Post
All I want is to feel Normal, healthy, and happy.

It's been a year and a half since my injury. I use to have headaches that were more noticable but they've gone down a good anount. When I get stressed out i feel like the pains in my head become more noticeable or start up. One other thing I feel dosn't help the headaches/ head pains I'm going through is being on my phone& watching TV. I've had such trouble trying to stop both theae habits, I know that instead of cutting them completely out of the equation I should just cut down the time I'm on the computer,Watching TV, or on my Phone. Will making the change and cutting down the amount of time i spend on eletronic really help my headaches go away completely? Also I've been drinking, a habit I find extremely hard to stop. I'm 21 and all my friends do for fun is drink and because I get very bored I go out with them but i always end up feeling that it can't be good for the recovery I'm still going through.

The last thing that I feel like is not helping the headaches is STRESS. I had a falling out with my first love and it's caused depression, anxiety/ panic attacks. I'm stressing out at times like a mad man. This can't be good for any sort of recovery right?


Another issue that i've been going through is my smell has become distorted. Instead of smelling the actual odor that is present I smell these odd smells that I havn't been able to compare to anything I've ever smelled in my life. It's like Instead of smelling pizza I'll smell soap. Like my nose is playing tricks on me. I work at a restaurant where food is around at all times. I can't say that i've ever smelled anythong even close to the delicious scent of food that I'm sure everyone else smells. I'm going to washington DC in 2 weeks to THE SMELL AND TASTE CLINIC. The doctor there is suppose to be a speacialst in smell disorders. It's very exapensive, about 6,000 dollars. I wonder if I'm making the right decision spending money on this. Getting my smell back to normal is so very important to me.

Please... Advice and help. I'm 21 and my parents arn't beong much help. What should i do to fix this problems I'm still going through with my PCS.
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Old 06-25-2013, 10:58 PM #3
Mark in Idaho Mark in Idaho is offline
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5322,

You have plenty of things you can do before spending $6000 becomes a worthwhile expense. Drinking, carousing, visual stressors and such all need to be ended or reduced to next to nothing. Working in a restaurant is a high stress activity.

Unfortunately, your skateboarding accident may have all but ended a lot of your fun, at least for the time being.

I doubt you will ever return to normal until you are willing to spend an extended period living a very abnormal, quiet and protected existence. There just is no quick fix to brain injuries.
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Old 06-26-2013, 12:37 AM #4
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5322
I, too have a 21 yr old with PCS who is going on 2 yrs. There are loads of things you can do to help yourself.

First try to string the good days together.

My daughter has had luck with acupuncture and an osteopath for her headaches.

Check out if you have florescent lighting and change it to incandescent. You might want to check into different screen tones. (blue works best for her).

Check out the sticky that tells you what has helped others.

PCS can on and on...please reduce your partying. I know it's hard and you feel isolated...one day at a time.

Keep us posted...we care
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Old 06-26-2013, 06:46 PM #5
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Default Feel for you!

If I'd been 21 going through this, I know I would have made some bad decisions! You may be more responsible than i was at your age. i hope that you are!

You need to stop abusing alcohol for the sake of your injured brain. If you have to drink, have one or two and that's it, but it's best to quit until your symptoms resolve. That said, I actually found that having a Guinness helped my headaches sometimes because it's as if the very taste of my favorite beer helped alleviate the stress causing my headache, but I never drink more than two beers or else I feel horrible the next day. My body is just not ready for that! It may never be and I'm okay with that now.

Anyway, I also had a smell issue when I was more symptomatic but nothing as severe as yours. I just would have bouts of super-smelling or smelling bad odors that weren't there. I wouldn't shell out $6000 yet. Proper rest and eliminating alcohol could provide the opportunity for your brain to truly heal. Do that before you throw that much money at the problem.

Good luck to you. Try to eliminate as much stress from your life as you can. Be boring for a little while. Your brain will thank you.
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I have recovered my cognitive function, and I've overcome severe vertigo through sensory integration therapy. Wellbutrin has helped me escape depression. I have recently had a few stress-related migraines, as well as headaches stemming from eye strain. I'm also dealing with tinnitus, lack of stamina, extreme light sensitivity, and eye pain. Diagnosed with 9 different vision issues: convergence insufficiency, pursuit eye movement deficit, egocentric visual midline shift, photophobia, visual information processing delays, accommodative insufficiency, saccadic eye movement deficit, lack of coordination, and central peripheral visual integration deficit.

*First concussion: October 2010. I was pregnant and got rear ended. I associated my mild PCS symptoms with baby brain and blamed my light sensitivity on allergies and dry eyes.
*Second concussion: December 2011. I hit my head on a wooden beam, saw stars but did not lose consciousness, and I had very disturbing PCS symptoms but didn't go to the doctor.
*Third concussion: August 2012. I caused a car accident as a result of PCS symptoms. Thankfully no one was injured but me. My husband confronted me, and I finally sought help and took medical leave from work. My symptoms worsened, and I developed severe vertigo.
*Fourth concussion: November 2012. I was riding in a car with a friend and we were hit head on by a driver who lost control of her car. I didn't have a big increase in PCS symptoms.
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Old 06-26-2013, 06:53 PM #6
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Default P.S.

I forgot to say, stay off your computer/phone as much as humanly possible. Learn from my mistakes. I spent too much time on the computer despite feeling eye pain and had a HUGE setback. The doc I saw said it could take me 1-2 years to recover, if I ever can fully. (I am getting a second opinion!) My situation is different than yours but the lesson still holds--if your head is in pain when you are doing something, that means you should stop what you are doing or else you run the risk of making yourself much much worse. You will find that if you listen to your body and rest, you will be able to gradually up your activity levels.
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I have recovered my cognitive function, and I've overcome severe vertigo through sensory integration therapy. Wellbutrin has helped me escape depression. I have recently had a few stress-related migraines, as well as headaches stemming from eye strain. I'm also dealing with tinnitus, lack of stamina, extreme light sensitivity, and eye pain. Diagnosed with 9 different vision issues: convergence insufficiency, pursuit eye movement deficit, egocentric visual midline shift, photophobia, visual information processing delays, accommodative insufficiency, saccadic eye movement deficit, lack of coordination, and central peripheral visual integration deficit.

*First concussion: October 2010. I was pregnant and got rear ended. I associated my mild PCS symptoms with baby brain and blamed my light sensitivity on allergies and dry eyes.
*Second concussion: December 2011. I hit my head on a wooden beam, saw stars but did not lose consciousness, and I had very disturbing PCS symptoms but didn't go to the doctor.
*Third concussion: August 2012. I caused a car accident as a result of PCS symptoms. Thankfully no one was injured but me. My husband confronted me, and I finally sought help and took medical leave from work. My symptoms worsened, and I developed severe vertigo.
*Fourth concussion: November 2012. I was riding in a car with a friend and we were hit head on by a driver who lost control of her car. I didn't have a big increase in PCS symptoms.
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Old 06-27-2013, 06:20 AM #7
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Default I hope you listen!

Hello and welcome to Neurotalk

Everyone here gave you really good words to live by, and I hope you heed it and take recovery seriously. You only have one brain and you can help it along if you take the strength to do so.

Check out the vitamin stickie at the top. Those vitamins and supplements will help you along with good nutrition -- fruits, veggies, and limit or cut out msg.

Alcohol and brain healing are really just opposites. At this point in my recovery, I can tolerate a little alcohol, but not much and I don't want to set myself back or stay stuck and never go forward. I don't want to relapse either. If you read through these threads, you'll find that people can and do relapse from OVERdoing thing or stress....you name it.

Recovery, for me, meant life changes too. I had to leave my job for a time to let my brain heal. You might not be able to do that, but you can give your brain rest. It needs that, and lots of it, to heal too.

Here's wishing you well in recovery.

Sincerely,

pm
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[SIZE="1"]What happened. I was in a car accident 2-23-2013, and got a mild concussion from it. I had some time off for brain rest, got somewhat better, but slipped into PCS in March 2013.

Symptoms I had: dizziness, light and sound sensitivity, fatigue, tinitis, occasional headaches and migraines,

Symptoms as of 5--2013: poor sleep, tinitis, some confusion /short term memory blanks, balance. The other symptoms are mostly gone, but flare up if I OVERdo something.

Therapy I had: vestibular

3 months in: I could drive more and for longer distances. I felt like a younger, happier version of myself and I feel so blessed to have this feeling.

9 months in and I am working full time. I do get tired, and some sound and light sensitivity from time to time, but mostly I am over most of my symptoms.
I pray every day and I m praying for your recovery.

Over a year in: I can multi task (limited) and have humor in my life. But when I am tired, I am very tired.
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Old 06-27-2013, 11:14 AM #8
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Default Alcohol is bad news for PCS patients

Quote:
Originally Posted by fkd5322 View Post
Also I've been drinking, a habit I find extremely hard to stop. I'm 21 and all my friends do for fun is drink and because I get very bored I go out with them but i always end up feeling that it can't be good for the recovery I'm still going through.
Not to pile on, but to reiterate what poetrymom and others have stated, abstaining from alcohol will be important for you to make progress. I suggest reviewing the following articles.

http://www.msktc.org/tbi/factsheets/...c-Brain-Injury

http://www.tbicommunity.org/resource...Spring2008.pdf

You own your recovery process. I agree with Mark there are a lot of things you can do to improve your symptoms before spending $6k for a smell and taste clinic. Lifestyle changes (more quiet rest, no alcohol, less computer media time) are likely to be much more effective in improving your symptoms.

Best to you as you recover.
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What Happened: On November 29, 2010, I was walking across the street and was hit by a light rail commuter train. Result was a severe traumatic brain injury and multiple fractures (skull, pelvis, ribs). Total hospital stay was two months, one in ICU followed by an additional month in neuro-rehab. Upon hospital discharge, neurological testing revealed deficits in short term memory, executive functioning, and spatial recognition.

Today: Neuropsychological examination five months post-accident indicated a return to normal cognitive functioning, and I returned to work approximately 6 months after the accident. I am grateful to be alive and am looking forward to enjoying the rest of my life.
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