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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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#11 | |||
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Wisest Elder Ever
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I'd also like to suggest that you avoid glutamate. This neurotransmitter is the culprit that causes brain cell death.
Monosodium glutamate is an artificial synthetic form of it that floods the nervous system in an unnatural way and causes nerve problems. People with peripheral nerve damage often get more pain when eating this in food. There are natural forms of glutamate in our foods, like Parmesan Cheese, but it is bound to organic compounds and do not flood our blood stream when eaten like synthetic MSG does. MSG is in alot of things. It is best to avoid soups/stews at restaurants. Chinese food especially contains it and often even when you request no MSG, you will get it. If you feel headache or blurred vision after a restaurant meal, that is a sign there was alot of MSG in it. Some processed food makers like Lays, have lines of "natural" chips (potato or corn) that do not have MSG added. But most of the flavored types like Doritos etc, are filled with MSG.
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All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei ************************************ . Weezie looking at petunias 8.25.2017 **************************** These forums are for mutual support and information sharing only. The forums are 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.
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"Thanks for this!" says: | Hockey (05-30-2014), Living_Dazed (05-30-2014), MomWriterStudent (05-31-2014), SarahSmile0205 (05-30-2014) |
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#12 | |||
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Hockey,
Yep. That wall is frightening in public. I can't function. Plans to complete my list for the day...AND THEN I DONT. I have to give myself a break but I haven't learned how to not over do yet. If I get things done and overdo then I feel bad. If I don't get things done then I feel bad. It's a work in progress. Does help knowing I'm not alone. Plus I like to hear everyone's survival tips, strategies, and work arounds. Tahanks to Mark I set a timer in the kitchen now. I'm easily pulled off task. Oh look, the fan is on...burnt food on stove. Ugh. Timer works. Jace
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. *TBI with mild to severe damage November 2012 from car crash. Stroke with hemorage & 4 clots in veins in brain Feb/Mar 2015. *Vestibular damage, PCS, hypercusis, severe visual processing and tracking issues, short term memory loss, headaches/migraines, occipital neuralgia, cognitive issues, neurological issues, brain fog, brain fatigue when over stimulated, twitching, vertigo, neck issues, nerve issues, PTSD, personality change, Since stroke left side weakness, rage, worsening of vestibular problems, recall, speech, memory. *Can't drive or work. Have done occupational therapy, cognitive therapy, physical therapy. Learning work arounds, and strategies to be competent in daily life. Change your attitude/perspective changes your life. As TBI survivors this is a vital part of our healing and living. *Working on getting to know and accept the new me. |
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#13 | ||
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Hi everyone,
I still experience those "spells", mostly when I am around several people and multiple conversations or activities going on. My Neuropsychologist wants me to follow up at Cleveland Clinic Epilepsy Center, though I have had 3 EEG's which all came back without abnormal electrical activities. I am told I stop and stare, usually with a fixed gaze to the extreme right or left, and when I come around, I cannot say anything but , "well", for the first few minutes. I remember some of these episodes, but not all of them. Is there a test or way to prove what causes these episodes if not a seizure? I thought I was going crazy, since there seems to be no "reason" for these to keep happening to me, since no seizure activity found on EEGs. Hockey, I am afraid of the "big freezes" too, since I have been sent from Neuro Rehab twice in a month to the ER on an ambulance for these kind. I haven't had these bed ones in about 2 months, so I'm crossing my fingers they don't happen again. Are you who are experiencing these episodes finding they happen only in crowded or stressful situations, or even when you are alone? Mine can happen either way, but mostly if I am in a busy, crowded environment. Thanks for you responses. Take care, M-i-m |
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"Thanks for this!" says: | Living_Dazed (05-30-2014), Sitke (06-01-2014) |
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#14 | ||
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Guest
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Quote:
Irlen Specialists find the exact color that fits your specific needs. Some colors work for some people, some don't. The testing process will specify the color need that you have. Vestibular Specialists most likely don't use the process that finds this and also probably don't use prescription lenses. Helen Irlen developed the method, so you have to be trained through her Institution to be able to get the correct lenses. Just putting different colored paper over white paper would have minimal results, but if it did offer some relief it would be wise to look further into the lenses that would allow for you to not have to deal with any lighting no matter the external circumstance. |
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"Thanks for this!" says: | Living_Dazed (05-30-2014) |
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#15 | |||
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Magnate
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Quote:
Last edited by Hockey; 05-30-2014 at 02:24 PM. |
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"Thanks for this!" says: | music-in-me (05-30-2014) |
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#16 | |||
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I do hit these walls mostly when it comes to writing down my thoughts... I can not properly convey what I want to say in a manner that people can understand..
As for the diet... sorry, I do not understand Mark... are you saying a high- protein diet is better? I have read it 3 times and for some reason I am not comprehending...
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The Start: MVA, t-boned, on 1-12-14 (my sons 5th birthday) and did not think anything of it.. my back hurt on site but everything else seemed ok. Lost about 10-12 hours from about 3 hours after the accident to the next day...Experienced terrible brain fog for over a month, plus intense headaches, nausea, dizziness, cognitive difficulties, disorientation, no short term memory, depression and just an overall hangover feeling daily. Current Situation: I'm about 7 months in and my local neurologist has waived her white flag and therefore I am headed to Dallas to be seen (I have family there). The headaches are still daily. I have nausea, dizziness as well. Drugs I have been on- Vicodin (off), Naproxen (off), proanolol (off), topamax (off), cataflam (off), Midrin (off), Flexeril (off) and now Namenda XR (off), Nortrptylin (off), Verapamil (off) Therapy- Osteopath, Vestibular and balance therapy, fuzion/soft tissue massage, acupuncture Drs- ER (no help), GP, Chiropractor, Neurologist and Osteopath |
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"Thanks for this!" says: | Living_Dazed (05-30-2014) |
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#17 | |||
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Member
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MrsD and Sarah,
It's actually mostly fat (but natural, 3 chain I believe), then protein, carbs, sugar. The natural 3 chain fat may provide better brain energy than carbs is what I think I understand. Talking to dr tomorrow about it to see if it will help my brain from hitting the brick wall. I have to take my time and really think about what I'm doing or I'm very messy. Even my posts here I scour for errors. I think that's the teacher in me. MSG...we aren't a chip family or snacks family. I like popcorn or a mister misty slushy every now and then. Those are my guilty pleasures. But I am going to really watch for MSG. Did not know it was that bad. Thanks. Jace
__________________
. *TBI with mild to severe damage November 2012 from car crash. Stroke with hemorage & 4 clots in veins in brain Feb/Mar 2015. *Vestibular damage, PCS, hypercusis, severe visual processing and tracking issues, short term memory loss, headaches/migraines, occipital neuralgia, cognitive issues, neurological issues, brain fog, brain fatigue when over stimulated, twitching, vertigo, neck issues, nerve issues, PTSD, personality change, Since stroke left side weakness, rage, worsening of vestibular problems, recall, speech, memory. *Can't drive or work. Have done occupational therapy, cognitive therapy, physical therapy. Learning work arounds, and strategies to be competent in daily life. Change your attitude/perspective changes your life. As TBI survivors this is a vital part of our healing and living. *Working on getting to know and accept the new me. |
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"Thanks for this!" says: | mrsD (05-30-2014), SarahSmile0205 (05-31-2014) |
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#18 | |||
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Member
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So lots of avocado? Let me know what the doctor says... and what foods are good vs just ok... I would love a diet for when I go back to work (yes, I am still hopeful) that would help with brain function...
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The Start: MVA, t-boned, on 1-12-14 (my sons 5th birthday) and did not think anything of it.. my back hurt on site but everything else seemed ok. Lost about 10-12 hours from about 3 hours after the accident to the next day...Experienced terrible brain fog for over a month, plus intense headaches, nausea, dizziness, cognitive difficulties, disorientation, no short term memory, depression and just an overall hangover feeling daily. Current Situation: I'm about 7 months in and my local neurologist has waived her white flag and therefore I am headed to Dallas to be seen (I have family there). The headaches are still daily. I have nausea, dizziness as well. Drugs I have been on- Vicodin (off), Naproxen (off), proanolol (off), topamax (off), cataflam (off), Midrin (off), Flexeril (off) and now Namenda XR (off), Nortrptylin (off), Verapamil (off) Therapy- Osteopath, Vestibular and balance therapy, fuzion/soft tissue massage, acupuncture Drs- ER (no help), GP, Chiropractor, Neurologist and Osteopath |
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#19 | ||
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Legendary
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Sarah, The diet is high in fats and low in sugars and carbohydrates. Medium Chain Triglycerides (fats) are common to help with this. MCT oils can be used. When the liver processes fats in the absence of carbs, they are processed into ketone bodies. Only the brain and nervous tissues can metabolize ketone bodies.
The wiki link I posted does a good job of explaining it in detail. http://en.wikipedia.org/wiki/Ketogenic_diet
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Mark in Idaho "Be still and know that I am God" Psalm 46:10 |
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"Thanks for this!" says: | SarahSmile0205 (06-01-2014) |
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#20 | |||
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Member
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Doctor rescheduled for next week. Will ask about the diet then. My neurologist is great but extremely vigilant about all of my health care as he feels everything can affect the brain. I do appreciate him.
Jace
__________________
. *TBI with mild to severe damage November 2012 from car crash. Stroke with hemorage & 4 clots in veins in brain Feb/Mar 2015. *Vestibular damage, PCS, hypercusis, severe visual processing and tracking issues, short term memory loss, headaches/migraines, occipital neuralgia, cognitive issues, neurological issues, brain fog, brain fatigue when over stimulated, twitching, vertigo, neck issues, nerve issues, PTSD, personality change, Since stroke left side weakness, rage, worsening of vestibular problems, recall, speech, memory. *Can't drive or work. Have done occupational therapy, cognitive therapy, physical therapy. Learning work arounds, and strategies to be competent in daily life. Change your attitude/perspective changes your life. As TBI survivors this is a vital part of our healing and living. *Working on getting to know and accept the new me. |
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