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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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Junior Member
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As I have been resting from my concussion over a year ago, I have not exercised regularly at all. I went from an extremely high activity high calorie diet, to an extremely low activity and high calorie diet.
Naturally I put on literally 20 pounds in the first month, then changed my diet. The other day I tried going on an exercise bike (I haven't had any symptoms besides headache and ear ringing in a few months), only for 5 minutes with not too much head movement, and I have a huge headache now. Could just blood flow after a year of not exercising cause a headache? Are there any other low impact exercising regimens that will help me lose some of the weight I put on? I have an alarming family history of heart conditions so this is really quite important. |
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#2 | ||
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Legendary
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I suggest you lower your calorie intake and learn to start back to exercising slowly. Even an exercise bike can be started slowly. Get a blood pressure and pulse monitor and find the BP and pulse that does not cause symptoms.
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Mark in Idaho "Be still and know that I am God" Psalm 46:10 |
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#3 | ||
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Member
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Walking slowly, as tolerated. Try short walks...a few a day. That can help. Hang in there. It gets better (slowly!!!)
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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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#4 | |||
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Member
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Quote:
Now a year and three months after injury I have near enough permanent earache/headache and have been told this is occipital neuralgia. Just be very careful!
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PCS following head injury November 2012. Experienced dizzyness, light and noise sensitivity, hypercusis, fatigue, insomnia, migraines, facial pain, problems concentrating, irritability, sensory overload, exercise intolerance. Symptoms mostly resolved, working full time and I am now mostly better. I wake 6am daily since my injury. Was experiencing daily Neuralgia which was controlled with Cymbalta 30mg, Lyrica 200mg daily. Now only on 30mg Cymbalta. |
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#5 | ||
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Junior Member
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I have never had a neck injury, nor have pretty much any of the symptoms like that.
Currently I have been using quite a bit of screen time due to online school, but now i am printing off all my notes and literally cutting down by screen time by 1000%, which is quite a feat for me. I have also completely reinvented my diet, as well as am now taking some supplements (vitamin d, multivitamin, etc), and my headaches are not as frequent, or as bad. I also have a family history of quite serious migraines, how do I tell apart migraines from headaches? |
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#6 | ||
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Junior Member
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mrsmith--headaches vs migraines are largely different I believe in their intensity/duration and associated pain. Migraines are generally more severe (and can last longer) and are associated with sharp/stabbbing/throbbing pains, whereas headaches are more localized, less severe and more "pressure"-related.
As far as exercising, I echo what Mark said regarding getting a heart rate monitor. I've had one for a while now and it has definitely helped with my ability to ease myself back into working out and measuring my intensity levels. Start at an BP intensity level that you know will not induce symptoms and slowly progress from there to build up your tolerance. If your symptoms return or feel worst, take a couple of days off and try back at a lower level. From everything I've experienced, if you are not pushing yourself at a sub-symptom threshold level to slowly increase that threshold/retrain your brain to take on more on a steadfast basis, you progression will be stunted. Quote:
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#7 | ||
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Junior Member
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Im 9 months in and have been using a heart rate monitor for exercise . I keep my heart rate at about 60 to 70 % of max and also monitoring my head pain and pressure. If the symptoms increase back it down. I also found heavier weights didn't raise my heart rate but really messed me up the following 2 days physically and emotionally.
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