How long does post concussion head pain and cognitive fatigue last?
Hello and happy new year everyone,
I was rear ended twice in the last three years and I am really struggling the second time with the TBI, post concussion syndrome and the returning to gradual activity. First does anyone have any experience with how long the head pain lasts with activity or cognitive fatigue? I found taking breaks every time the head pain worsens helps but it’s so frustrating as it’s painful and takes forever to do anything. Thank God that all the MRI’s and CT scans were good but I am seven months post accident and just wondering if any has experienced anything similar and has some insights. Still struggling with the memory, brain fog, cognitive fatigue, confusion and multitasking is next to impossible which doesn’t help as my career requires all of those things. My speech pathologist is optimistic and just wanted to know what is everyone else’s experienced opinions.
Thank you so much everyone and I hope you are all doing well and are having a blessed new year so far.
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@emdlewis
yes, has been 5 years ago but was told that i shouldn't still be in pain...
that was 4 months after my initial fall and injuries. They found a ruptured disc. the headaches it came down to ocular migraines . broken floating rib didn't help any. as For the other issues you describe and the doctor not listening, i would be looking for another doctor. My daughter got lucky in that in her 5th try landed a good one and he treats us both. very talented younger man. i can only hope you find one that still cares about every patient that is his and treats them with respect. good luck. Have a rest of the day blessed and Ps, after time some of the symptoms have gotten better and no i did not get the disc repaired would have meant surgery and i am not for that at all after having a tumor removed from my brain.
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2 ReactionsThank You
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1 ReactionI have now gotten smacked in the head with 2 IV pumps during transport of a Patient up to the floor at a Hospital. I had a headache and was nauseated for three days, I had to sit for about 20 min before I could get on my feet. You just never know when something is going to accidently hit you, you need to be prepared for anything. I did call my Neurologist on the second day and he in a Joking manner told me to "Stop Banging Your F-ing Head" we both laughed but it isn't funny, He is right, now I am very cognoscente of my surroundings and I keep my wits about me no matter what. It is a lot more work when you realize that it really doesn't take much anymore to make me feel sick and dizzy .
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1 Reaction@jenniferctbisurvivor keep your head up, keep at it every day. You are the one that has to fight it and wake up every day and do what you have to, we are right here with you doing the same thing every day, it is rough. Being in EMS everybody understands what is going on and some actually help me by not saying anything when I start to lose my train of thought, they just wait until I give up. I may ask the same question again and forget what I was told earlier it bothers me more then it bothers the people I talk to about it. But you have this and dont let anybody make you feel any different. We are all strong individuals and can be stronger together
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1 Reaction@ccmedic5 just an update, I am now on Ajovy, nortriptyline, taking my busbar and my zoloft. I have to get a blood test that is new and see if it shows up as early dementia. I have learned to stop when I feel an outburst coming and I try to direction it and ask myself is there a reason Im this angry, it happened on the 5th, I was sitting alone and became pissed off for absolutely ne reason. I sat for 15 min alone and was just getting angrier. Wife came home and I yelled at her and she aske what was wrong and I told her and she was asking more questions and I answered her and I told her to just give me a bit to figure this out. I did and felt better. The small headache is still there, the hand shaking is stronger then before. I did go see my neurologist and she said we are going to do a sleep study for Sleep Apnea, we are also send me to an ENT to see about the dizziness and the nausea, MRI did show air in the mastoid bone in the ear.So hope everybody is feeling better it takes time. I have to keep my mind open yet till we do these other tests and see if it gets better, Neuro told me that it could still be CTE but no test or cure anyway so we treat symptoms.
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