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Traumatic Brain Injury and Post Concussion Syndrome For traumatic brain injury (TBI) and post concussion syndrome (PCS). |
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#1 | ||
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I am a 44 year old woman. In July 2012 I suffered a severe concussion. I don't remember how it happened. I suffered amnesia my speech was impaired motor skills impaired memory issues light and sound sensitivity. All the things you would expect. I missed just over a month of work ( probably should have been more). I never felt completely better. Then the end of December I suffered a blow to the face while shoveling snow. Another concussion, not as bad but all the symptoms seemed to get even worse .That was 5 months ago. A total of 10 months and still not back to normal. Will I ever be right again?
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#2 | ||
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A very good question! So difficult a thing to go through. I hope it helps to know that I am slowly improving, and my life is much better this spring than it was last spring! The brain will continually improve, if you do the things required. Lots of good advice from people here. getting vision assessed (not your eyesight!!) by a neuro opthamologist is very important as many brain injuries affect how the eyes function.
Hang in there!!!!
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What happened: Legs pulled forward by a parent's hockey stick while resting at the side of the rink at a family skate....sent me straight back. I hit the back of my head (with helmet) on the ice, bounced a few times, unconscious for a few minutes. September 11, 2011. Off work since then…I work part-time at home when I can. It has been hell but slowly feeling better (when I am alone☺). Current symptoms: Vision problems (but 20/20 in each eye alone!) – convergence insufficiency – horizontal and vertical (heterophoria), problems with tracking and saccades, peripheral vision problems, eyes see different colour tints; tinnitus 24/7 both ears; hyperacusis (noise filter gone!), labyrinthian (inner ear) concussion, vestibular dysfunction (dizzy, bedspins, need to look down when walking); partial loss of sense of smell; electric shocks through head when doing too much; headaches; emotional lability; memory blanks; difficulty concentrating. I still can’t go into busy, noisy places. Fatigue. Executive functioning was affected – multi-tasking, planning, motivation. Slight aphasia. Shooting pain up neck and limited mobility at neck. Otherwise lucky! Current treatments: Vestibular therapy, Vision therapy, amantadine (100 mg a day), acupuncture and physiotherapy for neck, slow return to exercise, magnesium, resveratrol, omega 3 fish oils, vitamins D, B and multi. Optimism and perserverance. |
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#3 | |||
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Hello Yankees Fan,
This is a good place. First, check out the vitamin stickie on the top. There are nutritional things you can do to start some brain healing from the inside. Diet is important too. I have taken caffeine and alcohol out of my diet in my recovery. I can't remember the rest of your symptoms, but you have had 2 serious head hits close together (I think) Can you get any more time off work for brain rest? (Meaning limiting screens, reading, and other physical activitiy too) Other, very experienced people will weigh in. Take care, 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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#4 | ||
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What are your current activity levels? Do you spend a lot of time on the computer or doing any sort of manual labor? How are you doing emotionally? What treatments, if any, have you tried, and are you on any medications? Knowing this info might help in terms of making any recommendations to hopefully help 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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#5 | ||
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Also, what are your primary symptoms? Headaches? Cognitive fuzziness?
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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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#6 | ||
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New Member
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Thanks everyone
Prior to my concussions my neurologist put me on topirmate to prevent severe migraines and cluster headaches(3+ 1/2 years). Other than multi vitamins, vitamin and fish oil I don't take any meds. Initially he had me take a anti depressant to try and help me rest after the first concussion. At the closest dose it made me very jittery and I would only sleep a few hours. So I asked to come off it. I don't drink alcohol or coffee and I've limited myself to one cup of tea or a soda a day. I'm a waitress. Full time. Not rocket science but I have to focus and it getsloud at times . Probably louder in my head than others if that makes sense. My activity level isnt what it used to be. I used to hit the gym 5-6 days a week. Now I do light exercise at home. I have good days and bad days.....more good days thank God. I get confused at times. My short term memory is horrible I getheadaches that seem to be in the area I suffered the traumas. I can get very agitated, which isn't at all normal for me. At first my Dr said probably 6 months to heal. Then maybe a year. Last time I asked him if I would ever be normal again he said there was still a good chance. He's one of the best drs in my area. I get there is no real timeline. I guess I just need to know how others cope and that I'm not crazy. |
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#7 | |||
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Quote:
Hello again! No, you are NOT crazy at all. I too have problems with my short term memory. I find I have to write important things down or I will completely forget them. And yes, noise can very VERY loud for us. Earlier in my recovery I had to leave the table where my family was eating because the sound of spoons on the bowls was just **too** loud. And it was-- for me. Can you use any ear plugs at work? I know some people here use those to help with noises. I think there are some good ones that you might be able to work with -- but I don't know Being agitated or cranky is part of this whole PCS thing -- for me anyway. Our brains are trying to heal and we keep having to use them for work etc. As for the nutrition, our injured brains need more than the One A Day kind of multivitamins. I hope you'll look over the regime posted in the stickie and really think about adding more of these supplements to your diet. The hurt brain needs more of all that stuff to get beter, All for now, 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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#8 | ||
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Legendary
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Yankees Fan,
Welcome to NeuroTalk. You ask a very common question. It sounds like you have received just medical care. Recovering from a concussion takes more than medical care. Often, what doctors fail to do, we can do for you. Much of recovery comes from learning work-arounds and accommodations. Changes to daily activity levels can be a big help. Please tell us about each and all of your current symptoms and struggles. Don't worry about sounding like a complainer. We have all lived through this. And, help us out by putting a double paragraph space after ever 5 lines. Many of us struggle to visually track from the end of one line to the start of the next. Read the Vitamins sticky at the top. You need extra B's and others for your injured brain. What anti-depressant did you try ? Do you have any idea about the type of force that caused the first concussion ? Knowing the direction of force can help us with ideas for you. Have you been in any previous physical traumas, car accident, etc. ? Often, concussion symptoms get aggravated by untreated injuries to the spine, especially the neck. We are here for you. Let us know how we can help. My best to you.
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Mark in Idaho "Be still and know that I am God" Psalm 46:10 |
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#9 | ||
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Thanks Mark
My current symptoms are headaches, tunnel vision, noise and light sensitivity, whooshing sound in my ears, confusion, memory loss, trouble sleeping. At times I feel off balance. When I'm tired or have had a busy day my speech slurs a little or I can't come up with the right word. I don't have these symptoms everyday and I don't always have them all at the same time. If there is a lot of background noise around me I feel a little dizzy. Or if there is more than 1 conversation going on near me I can't follow along. My doctor had me on nortriptyline hcl. I was home alone at the of the first concussion. About 10 am I had laid down because I wasn't feeling well. Next thing I remember is being in the middle of the living room touching my forehead because it felt like it was bleeding. It wasn't but I had a lump the size of a baseball. Then I started vomiting. As far as previous traumas...I do remember having a couple mild concussions as a child. The doctors didn't seem to concerned. I missed a few days of school and couldn't watch TV for about a week each time. |
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#10 | ||
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Legendary
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Yankees fan,
It sounds like you have a good case of Multiple Impact Syndrome. This is the result of multiple concussions that use up the brain's reserve capacity to overcome injury. I think your biggest problem is the high level of sensory stimulation from your job. All of your symptoms are common to concussion and aggravated by sensory overload. Getting better brain nutrition will help your brain tolerate the stress but not overcome it. The first skill for you to learn is to "Stop to think." This means stopping all activity and maybe even close your eyes so you can focus mentally. Over time, you will do this almost subconsciously. This will greatly help when you get stuck trying to find a word or process a thought or calculation. Multi-tasking is not an option. Even healthy brains are fatigued by multi-tasking. As you learn to switch between tasks rather than try to hold multiple tasks in process at the same time, you will find you can get just as much done. This might mean completing a task completely before moving on to the next task or making written notes of the next step of a task so you can let go of the need to maintain the task in memory. The long held habits of depending on our memory and ability to multi-task are too stressful for the injured brain. At your age, you should think seriously about adapting your life to these new limitations. The brain starts to naturally deteriorate slowly in the mid 40's. The injured brain struggles even more. Planning a less intense and stressful life can greatly enhance your ability to avoid the roller coaster of symptoms. There are more issues for you to consider but this is already a lot to process. My best to you.
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Mark in Idaho "Be still and know that I am God" Psalm 46:10 |
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