What Impact Will Moderate or Severe TBI Have on a Person's Life?

Center of Excellence for Medical Multimedia
What Impact Will Moderate or Severe TBI Have on a Person's Life?

The effects of moderate to severe TBI can be long lasting or even permanent. While recovery and rehabilitation are possible, most people with moderate to severe TBI face life challenges that will require them to adapt and adjust to a new reality.

Moderate to severe TBI can cause permanent physical or mental disability. Because polytrauma is common with moderate to severe TBI, many patients face additional disabilities as a result of other injuries. Even patients who appear to recover fully may have some long-term symptoms that never go away.

Challenges with work and completing tasks that were once routine can be much more difficult than before the injury. Some patients find that the skills and abilities that they used before the injury to meet these challenges are not as sharp as they once were.

These ongoing challenges can also affect the patient’s personal life. People who have experienced brain injuries may take longer to do cognitive or “thinking” tasks associated with memory, such as coming up with the correct change in the checkout line at the grocery store or placing an order at a restaurant. Family relationships will almost certainly change, and in some cases the patient will be totally dependent on their caregivers.

Despite the advances in early diagnosis and treatment of moderate to severe TBI, the fact remains that traumatic brain injury will be a life-changing experience for many patients. Helping the patient, family members, and caregivers to cope with these long-term consequences is an important part of TBI rehabilitation.

Motor Deficits and Disabilities

For many patients, the damage to the brain resulting from a moderate to severe TBI may lead to life-long disabilities or motor deficits. The term disability in relationship to TBI means a loss of physical or mental function caused by damage to the brain. Motor deficits refer specifically to the effect of damage on motor skills or movement.

Examples of disabilities and motor deficits caused by moderate to severe TBI include:

  • Paralysis
  • Spasticity (muscle stiffness) or uncontrolled movements
  • Problems walking, talking, or swallowing
  • Difficulty carrying or moving objects
  • Vision problems
  • Loss of fine motor skills, such as buttoning a shirt
  • Inability to recognize something based on touch
  • Difficulty thinking and remembering
  • Difficulty with social relationships

Other challenges that a patient with moderate or severe TBI may experience include:

  • Difficulty making and keeping personal and professional relationships
  • Difficulty being part of social activities
  • Difficulty taking part in recreational or leisure activities
  • The decreased ability or inability to keep a job or go to school

During the rehabilitation and transition phases of TBI treatment, members of the healthcare team will provide information to the patient and their family members about dealing with these issues. Specific tools and coping strategies will be suggested. Examples of coping strategies and tools include:

  • Writing a detailed list of steps needed to complete a task
  • Using prompts or visual aids to help remember things
  • Using assistive devices to move around, such as a walker or a wheelchair

Learning new ways to do things is a very important part of recovery.

Other Potential Effects

The long-term symptoms of TBI can be divided into several categories, including physical changes, cognitive effects, sensory effects, perceptual effects, social-emotional changes, and others. You’ll find a partial list of these symptoms and possible effects below. Keep in mind that the severity and duration of symptoms and effects will vary greatly from one patient to another, depending on the severity of the TBI.

Physical effects

  • Sleep disorders
  • Loss of stamina (easily fatigued)
  • Appetite changes
  • Difficulty swallowing
  • Physical paralysis or spasticity
  • Chronic pain
  • Loss of control of bowel and bladder functions
  • Seizures
  • Difficulty regulating body temperature
  • Hormonal changes

Cognitive effects

  • Difficulty with attention, focus, or concentration
  • Distractibility
  • Memory problems
  • Slow speed of processing
  • Confusion
  • Perseveration, which is the abnormal persistent repetition of a word, gesture, or act
  • Impulsiveness
  • Difficulty with language processing
  • Problems with executive functions, which include planning, cognitive flexibility, abstract thinking, rule acquisition (determining right from wrong), initiating appropriate actions, and inhibiting inappropriate actions

Speech and language effects

  • Aphasia (difficulty with talking or expressing ideas, understanding everyday language, and problems with reading and writing). Types of aphasia can include:
    • Receptive aphasia, which involves difficulty understanding the spoken word, or
    • Expressive aphasia, which means the patient knows what they wish to say but is unable to get the words out. In some cases, the patient is able to perceive and comprehend both spoken and written language, but is unable to repeat what they see or hear.
  • Slurred speech
  • Speaking very fast or very slow
  • Problems with reading comprehension

Sensory and perceptual effects

  • Difficulty recognizing and distinguishing between touch and pressure sensations
  • Difficulty perceiving temperature
  • Difficulty perceiving movement and positions of the arms and legs
  • Difficulty with fine discrimination (for example, distinguishing between small everyday objects, like coins)
  • Difficulty integrating and understanding information gained through the five senses (sight, smell, touch, hearing, and taste)

Effects on vision

  • Partial or total loss of vision
  • Diplopia, which is weakness of eye muscles that causes double vision
  • Blurred vision
  • Problems judging distance
  • Involuntary eye movements, called nystagmus
  • Photophobia, which is intolerance of light

Effects on hearing

  • Decrease or loss of hearing
  • Tinnitus, which is ringing in the ears
  • Increased sensitivity or intolerance to sounds

Effects on smell and taste

  • Anosmia, which is loss of or diminished sense of smell
  • Loss of or diminished sense of taste
  • Bad taste in the mouth

Social-emotional or behavioral effects

  • Dependent behaviors
  • Fluctuating emotions
  • Lack of motivation
  • Irritability
  • Aggression
  • Depression
  • Lack of inhibition
  • Denial or lack of awareness
Posted on BrainLine August 9, 2018. Reviewed March 28, 2019.

About the Author

The Center of Excellence for Medical Multimedia (CEMM) is a dynamic initiative from the Office of the Surgeon General, supplying award-winning interactive multimedia for patient education throughout the Military Health System.

Center of Excellence for Medical Multimedia. (n.d.). Moderate to Severe TBI: Long-Term Effects. Retrieved March 28, 2019, from https://tbi.cemmlibrary.org/Moderate-to-Severe-TBI/Long-Term-Effects

Comments (561)

Please remember, we are not able to give medical or legal advice. If you have medical concerns, please consult your doctor. All posted comments are the views and opinions of the poster only.

I have a sTBI and I'm able to accomplish a lot

last year people attack on me and try to kill me .i have serious brain injury and stay comma in 3 weeks loose my memory as well.i know that attackers but bcz i am illegal in this country police don't do my help still that attacker threat me but police dont want arrest that criminals i dont know what i do .bcz my life not safe here dont know why police dont bother about my life.

Hello there I am a TBI survivor, I was hit by a car crossing the street when I was 12 years old. I am 29 now.

I am writing to ask if there is any correlation between TBI and violent behavior that the aggressor did not realize was from the TBI. At 9, the child was a victim of a violent attack by his dad. They never did any follow-up and the focus became about me and not the abuse the child suffered. I have taken an interest in this as I too believe I am the victim of an undiagnosed TBI that affected my life. The child and I have some of the same rage, mood swings, emotional outbursts etc.. Can it lead to violence and other tendencies that go undiagnosed?

My husband had a TBI over 20yrs ago. We have been married for 18yrs and I am ashamed to say that I have until recently just gone off info related by his family. Never have I read about what "frontal lobe injury " really meant in terms of his behavior and personality. Over the years he has had several impulse control issues, gambling related, drug use, even sexually related issues that have nearly ended our marriage many times over. I've always asked him "why" he did what he did and his answer has always been the same, "he didn't know?" I always deemed that as a "cop out". Most recently he left our home on foot for a trip to the store and was gone for 48 hours! No call or text to me letting me know where he was or that he was ok! I called police reporting him missing and mildly put, I was a nervous wreck thinking the worst had happened! When he came home I was relieved and angry that he could make such a poor decision. He had run into an acquaintance and was asked to help him relocate, he was offered drugs and his cell battery died. Never did it occur to him how worried I would be or what an impact his lack of impulse control would cause. After this incident I decided to read more about all the personality changes and defects his injury has caused and I felt terrible! In all our years together I had never been aware of the numerous effects his frontal lobe injury has had on him. Consequently the overall effects it has had on our relationship, as I had not known him prior to this injury. His moodiness, inability to control his impulses, his temper, etc. Now I feel much more educated but as a result I am even more worried as to how to deal with these personality defects. How to help him control his impulses, his moods and how all this has and will continue to effect me and our relationship???

After reading a lot of these other comments, I am blessed, and feel almost silly now posting. I fell down my stairs and got 13 staples in November 2019. Still having many symptoms, I have gone through physical therapy and am now starting a cognitive therapy but get frustrated that what I can do has become so limited and keep wondering when it’s going to get better. Any advice on the line between pushing yourself and rest? Additionally, does the actual impact spot hurt for a while for others?

I am 10 months post fall and I still have pain and edema where I fell on my left cheek and shoulder.. I was running at the time so had quite a forceful fall on concrete. I also have periods of sleepiness and moodiness. I feel so alone because I am no fun to be around and people have noticed.

I suffered a TBI at the end of August 2019 after falling from a height resulting in two subdural haematoma's and a subarachnoid haemorrhage in the temporal region. I was treated in hospital and now back to getting on with life. I turn 22 next month and forever worrying about the impacts this may have on me in the future or the chances of re-bleeding. Anyone experienced similar?

had same injuries from a fall with skull fracture. when I was 70(now77).plus you can grow whole new pathways in your brain called axons at your young age. this is not a recurring condition but don't take a bunch of blood thinners

Sorry to hear about your accident.

My son had an accident January 21 2020 em had sever brain damage the had to remove half of his skull had a lot of bleeding I the brain he last in the ICU a month an half..the doctors to me my son would need 24/7 care that he would never walk or be normal again. So they gave us some time to about his condition, if we wanted him to keep breathing with ventilator he wouldn’t be able to eat he had a trak and feeding tube on side of his stomach..so the family came to the conclusion to pull the plug, my son was a free spirit person loved to work on bikes, and help people, so we knew he wouldn’t want To live that way, not been able to be himself again, but in my mind i wonder if we did the right thing to transfer him to comfort care...he passed on February 27th 2020 I miss him so much that I still think his alive and just doing his thing in LA where he lived...I have a huge void in my heart,

Dear Josie,
I’m struggling with the same problem right now.

It breaks my heart to hear that you question whether you did the right thing. My mother suffered a traumatic brain injury on June 25. 2020 and I am often told by others not to lose my faith. Life has been hard for me since, but I always remind myself of what everybody has been telling me, “never lose faith.” So please, have faith in your decision. Because if your selfless heart, your son is no longer suffering. Open your heart and look for signs from him. I promise he is all around you, telling you to thank you for loving him enough to set him free. Keep your faith, and always keep searching for him; because he is right there by your side.

i wish you well.

I am so sorry for your loss... A devastating time for you all as a family.
My 27 years old son also had a very severe brain injury November 2018.
He also had his scull removed and his brain swelled... He was In a coma for 2 months maybe longer.
We was told exactly the same.. I often wonder if he forgives me as I fought for him to stay..
I let his body make the decision and it kept going... He does have a tube in his tummy and the trachy was removed some weeks later..
But he can not speak, eat, drink walk.
However he knows who we are, has a sence of humour and astonishingly he can work a motorized wheelchair..
He seems happy and is still in care rehabilitation as they think he has potential... But was it right.. I hope so...
You did what you thought was right but as a parents we always judge ourselves... In any decision.
Bless you and may happy memories feel your aching heart.

God bless you and family. Such a difficult decision. My only grandchild severely abused at 41/2 months. Worse case of shaken baby Drs had seen. Medical induced coma, life support, Drs told my son there was no chance. Son was 26 at time. I couldn’t help him with such a tough decision. Son decided to give his only child a fighting chance. Mother was in jail. Only grandchild still lives on feeding tube, he’s quad, only involuntary movement, infant like state for all his life. In 2012 son committed suicide. I found him with 1/2 his face from shooting self. My husband and I now raise my grandson while trying to hold down our jobs. You made the best decision you could. No one can ever fault you for doing what you felt was best for your son. My grandson is now 11. I have measures in place for no vent, no DNR, so many difficult things to face. God will decide his fate. I will love him and hold him till then. He survives on partial brain stem. Pituitary Gland barely functions. When God wants his angel back, I will hold him tight until they take him. Plans all made to have his brain researched just incase we can learn even one thing about his brain that might help in saving another child. The could have, should haves, questioning your difficult decisions will only make you hurt more. There is no wrong or right. I will pray for you. Losing our children is not the cycle of life. It’s just wrong.

I am so sorry for the loss of your son. I think you know you did the right thing. You just want him back. You want him back whole and healthy. Warm hugs to you and your family.

wow, that's so sad. I'm so sorry for your loss.

its been almost 9 years now since that day, that motorcycleaccident brought me to coma for 10 days, and i don't remember it at all, for 4 months, i dont even remeber what happened they just told me everything, my problem now is this tension headache/everyday/all day rated 5/10 and this dizziness that i get when standing up plus this paresthesia on my right leg. any idea how to slow this down or better, make it disappear.

I also had dizziness when standing up and lying down after my TBI. I was told that your inner ear is effected and seen a chiropractor who made adjustments to correct the vertigo I was experiencing. It helped me alot.

Does anyone have an history with severe DAI traumatic brain injury. My husband got into an car accident and that was the result also with a lot of broken bones. He has endured a lot of surgeries but his body is healing fine. He was answering commands but had coded and now he doesn’t. He just moves around but is aware when someone is there. He has only been in the hospital 20 days. Do anybody knows what to expect?

I know how it is to have your head shattered. 7 years ago I had a motorcycle come through the driver door at my truck. When he came through the window his head hit mine. I was in a coma for a month I kept dying for 2 weeks and they didn't think I was going to make it. Luckily I'm stubborn and I proved them wrong. When I came out of a coma I've been told I was like a little kid again. They put me in a bad caregiving hospital but luckily my mom put me in for a waiting list to get into Craig hospital and thankfully I did get that 3 months after my accident. They helped me learn how to live again. I still have a lot of issues with my memory, like people's names or places I'm on my way to. If people are talking to me and uses the company's given name for a product I won't know what they're talking about. But if they come to me and tell me they're looking for fertilizer for their lawn I can take him right there. But throughout time you get used to it.it's like a joke my mom and I have cuz one day we were talking and I wanted a banana and I couldn't think of the word so I told her it was yellow and showed her how it was shaped and that's when she told me banana so as long as you guys keep a good sense of humor and don't let it kill you inside things will get better.

My son had an car accident November 2018 and suffered a severe DAI TBI with multiple other injuries. He was in ICU for weeks, had ETV surgery which failed and then had a permanent shunt implanted to relieve the excess cerebral spinal fluid. It was tragic. He was in inpatient rehab for 5 weeks and then sent home. I felt completely incapable of caring for him but as a mom, you do what you can do, research everything possible and accept any help that is offered. It was hard, very hard but 20 months later...my son is working part time, taking a class at a community college and is able to care for his personal needs. There is hope. It may not seem like it but the brain is an amazing organ that is capable of healing, however very, very slowly. My son does not remember the accident or being in the hospital for 2 months. His memory has slowly returned but for about 6 months he did not remember even what he ate for breakfast. You can do this. It will challenge you like nothing ever has but you find the strength out of your love for him. Ask God for strength and for people to support you. You arenot in this alone.

I’m not a doctor. My husband had a brain injury about 8 years ago. They’ve given up on helping him & the only thing I can do for you is to offer my heartfelt condolences. It’s a miracle if they remember you in any capacity. After a long time of hope you finally realize that the husband you knew & loved is not there anymore. That’s when the grief sets in. You try to stay positive for everyone, but you’ve lost the man you’ve had so many joys with. But he’s still there & you still love him. I will say this, this has got to be one of the most tragic things I’ve ever been through. I’ve lost my brother & mother, but it was different. I could grieve then heal. Not so with this. Some days you feel ok even cheerful just to have him. Then others it feels like you’ve had your heart & soul ripped from you. It’s especially hard if they’ve lost the will to survive. I pray your pain will not be so hard. Get someone you can talk to & be honest with.


I am so sorry to hear of your husband's accident. My TBI came back in 1981, following a car accident as well, but no broken bones. While I was in a coma(5 weeks), I was also aware when others were in the room. I did start responding to questions by squeezing their hand - one for yes, two for no. It was only my right arm, however. My left side was basically paralyzed, and I had limited to no use of that for about the next year. Every brain injury is unique. I do not know the severity or specifics of your husband's injury, but know that it will not be the same for you or him from now on. Be adaptable, and patience is of utmost concern. Although it has been some 40 years since my injury, there are still times when old deficiencies crop up from the injury, but, with time, I have learned to cope with a good many of them. My thoughts are with you as you embark on this journey. That is how you must think of it - as a long journey, not an overnight stay.

Andy, Thanks for sharing - My son was injured in 1995 and I am really trying to follow others - he was 14 and now 39 and still struggles with learning, memory - not so much physical - but very easily stressed out - prayers for everyone to heal

how many days he spend in comma will determine the outcome

My exhusband had a TBI before we met and had children. Just wondering if they have found that the children are
genetically affected with learning disabilities possibly because of defective genetics. I say no, my son thinks yes

Physical trauma does not affect how the DNA duplicated. An easier way to explain it is if i get my arm cut off. My children will still have both arms. There are a few things that affects sperm for example radiation.

No, i was in a level 3 acoma back in 1996 for 2 months. I got a severe t.b.i. and after I have two daughters. Ones in collage studying to be a nurse and doing very well. The other is doing very good with no assistance in school.

It was really helpful. I used a lot on my project that I am doing in school. Thanks. 5 stars.

I had a fall at work on 10-6-2018, I was unconscious for about 30 minutes and had a brain bleed and was put in a coma for two weeks while they fixed my hip and ribs and other assorted broken bones .I spent two months in hospitals ,now My broken bones have mended but I still have diplopia ,tinnitus, headaches and have trouble with maths and have memory issues,I am so sick of being like this, being irritable is an understatement! I feel bad for my elderly mom taking care of me ,I would be lost without her nagging me to eat or take a bath ..or brush my teeth as I forget to do stuff!

You are not alone I fell like I slip in and out of reality and it takes other people to help steer me and keep me on course. It requires a level of dependence on others that I never wanted. I’m a grown ?!* man and I should remember to eat, shower, and accomplish tasks. The adaptation required to live this new life is enough to drive a man insane. I hear you brother. Hang in there. You have less tools in your toolbox than you did before. But at least you have some tools. Learn to use the ones you do have. I set three alarms to accomplish every task that I need to get done. I never turn the alarm off until the task is accomplished. Keep it together. Focus on sleep and not drinking alcohol. Again you are not alone.

I had a TBI back in 12/21/2014 things had been going ok only grunge was I always had severe head aches and then they turned to sharp needle like pains in my brain at random times and would come more often if I’m stressed but for years now since then I’ve used alarms for many many things not just to wake up in the mornings like normal people do but to even remind me to leave my house for work or get ready for work so many make fun of me at work because I need an alarm as they to even “shower” but what they don’t know is after a TBI it is very difficult to remember many things after that situation, and lately I’m having gaps of moments where I don’t remember at all what I did such as me turning in an order to a customer at work I won’t remember I ever did that and it worries me because I don’t know how much worse this can become

I was 41 when I was catapulted from a 4 wheeler in Mexico. My helmet came off and I bounced down a dry riverbed on my head. I was told I bounced 3 times and was traveling about 45 -60 mph. I was unconscious for nearly an hour. I awoke in a Mexican ambulance and I'm told that for the next 18 hours I only spoke Spanish. This doesn't sound remarkable but before the accident, I had a very rudimentary understanding of the language. I was told that I was having conversations with hospital staff and my English speaking wife. I ended up suffering an anterior sternoclavicular dislocation, I broke the first four ribs on the left side completely displacing the 3rdn and 4th rib. I broke either the spinous or transverse process at C5 & C6, and fractured my skull from around the hairline on right side that seemed to transverse the skull ending behind my left ear. As I was on vacation at the time, I opted on completing the holiday. Oddly enough, I don't really recall too much over the next 7 days.
After returning to the states, my wife made me go to my primary care physician (PCP). I had all x-rays and records from Mexican hospital. As my PCP could not read the Mexican medical records, he ordered his own CAT scan and x-rays. When I returned to work colleagues noted issues with my memory and speech. I was sent home until cleared by neurologists and word from PCP. My PCP noted that by breaking the first 2 ribs and the length of the skull fracture that the trauma was equal to being sent through the front window of a speeding car. The neurologist saw the x-rays and CAT scan and the issues I was having was positively a TBI.
Initially, my short term memory very poor. So much so, as I could tell you a story get distracted and see you again and tell you the same story. I had expressive aphasia that lingers to this day. I was diagnosed with dyskinesia that has resolved. My memory has improved but I still have lingering issues just not as bad. The social-emotion and behavior affects do linger but have improved. Initially, a commercial could send me into tears. It's not nearly that bad anymore but I remain a sensitive fellow. Prior, no one would confuse me with being sensitive. I have anger issues still but not as bad. I continue to get irritated easily. To this day, I can not go into a enclosed space that is crowded without a panic attack ensuing. I learn not to take elevators during busy times of the day or go christmas shopping in a normal hour. After nearly 10 years, I've gotten accustomed to navigating the my world with the remaining symptoms. It's a part of my make-up now. In my case, most of the symptoms remain but they have lessened.
I hope this gives any readers a glimpse into a typical TBI and the issues that accompany some of us. For those that read this and say, "that is exactly like me," know that you can adapt and make it work for you the best you can. A poem by a German poet captures those of us that suffer from TBI's. Let everything happen to you; Beauty and terror; Just keep going; No feeling is final. Best of luck.

I am a 59 yr old vet with moderate TBI issues that include extreme rage ,getting lost ,forgetting things,at times I feel like have to concentrate to make my legs,I don't have friends,I hate being around people,I hear and smell things that aren't real and I cry for no reason. Numerous other things happen that I know aren't right. After 33 years of begging for relief from these problems I was diagnosed with moderate TBI. Treatment was the government mandated handful of drugs the V.A. uses to cure everything. I have continually asked for help for the last 33 years. I have a diagnosis of moderate TBI along with all the symptoms and some things nobody seem to know about. I have no idea what treatments are available. I have no idea if any of these problems are permanent. I have been in prison twice since I started asking for help. I don't believe I should have to beg for help when people get hurt because of me. I shouldn't have to go to prison because these people have decided not to help for the past 40 years

Hi Michael, I am sorry for your trauma and injury - non THC CBD Oil would really be of help to calm your nervous system. Prayers for you to feel God's presence and know his love - you sound like a survivor and I pray you hear God's voice and receive his strength to move ahead with victory of which you deserve!!!!

Dear Sir are you under the VA?

What branch did you serve in? I see an Army Doc that is the best I’ve ever heard of. His name is Dr. Rigg at Eisenhower Army Medical Institute. It’s in Augusta, GA.

I had a biking accident nearly five years ago that resulted in a moderate TBI and an incomplete scalping. Being fifteen years old, I was fortunate enough to only have a skull fracture and moderate brain swelling. The swelling resulted in about three weeks of time I can't recall, but I was able to recover! My parents, both nurses, talk about how fortunate I was to have survived and still be fine - which I am. But, I can't help but feel like something is wrong with my brain. Some days are clear, and other days are cloudy. Some days I wake up happy and chipper and able to play chess (one of my main hobbies) easily and without fault, other days I am irritable and depressed, incable of sitting down to look at the board. I live functionally, working a full time job and in academics full time, working to become a nurse as well. But my brain is worrying me. I have a hard time remembering both my childhood and teenage years before my accident. Recently, I can't seem to recall details within more than a few weeks. My memory seems entirely cloudy. Last year has almost faded from my memory, I only remember key facts like the job I was working and people I was friends with. I've mentioned these things to my parents, who both said to tell my Primary Care Physician; she told me there was nothing to worry about. Maybe this was a predicted result, but if it was, it wasn't prominent within three years following my accident, which concerns me. I can't help but feel anxious about it.

Wow, I've had a very similar experience. 2 1/2 years ago I fell and hit my head on the pavement - long story that resulted in a minor brain bleed (causing a seizure) and a fracture to my temporal lobe. Ever since the accident my memory has been such garbage that it's almost scary sometimes, but I didn't realize this even a year after the accident because my memory was never great to begin with. However, I'm often concerned that I can't find the right words when trying to explain things, or that when I am talking my mind goes blank trying to recall something that I just read or I just completely lose my train of thought. The entire 6 months after the accident were fuzzy, and having two separate neurologists didn't help. I never brought this up because I didn't notice anything drastic at the time, and now I feel like it's too late to contact them. Anyway, I guess it's reassuring that I'm not alone.

Hi, my son at the age of 16 had a fall from a roof, 32feet, his leg caught railings on the way down and this slowed his fall. He had broken ribs, broken wrist, deep wound to his calf, and a compressed fracture of the scull. He was never in a coma but had Bell’s palsy on the left hand side of his face and could not walk. It was rough and go if he would survive. He looked and walked like a 90 year old man. 5 months after the accident a tear ran down his cheek and his beautiful smile came back! He is now approaching 36, drives an articulated lorry for a living and has 3 gorgeous children. I know he’s not 100% but he’s done great. My partner struggles to cope with his behaviour sometimes, and that is a strain as I know he cannot cope with things and does reply on me to help out when he’s stuck but I will always be there fo him. I am blessed that he is good, still works and has given be 3 gorgeous grandchildren. I have no idea if he will suffer any issues as he gets older but the surgeon said all those years ago, just get in with your life! And he has done. His time to go was not then and I thank all the professionals who helped him to recover. It took possible 2 years after the accident to say he had made an almost 100 % recovery. He was young enough for his brain to heal and has a massive scar on his head which reminds us all of the incident. He his his head when snow boarding and took a wise decision to get himself checked out some 6 years ago, ,that was the first time he saw the ex ray and the black mass of dead brain, he was shocked but just accepted it and is enjoying life. I hope this has been helpful to read. Luv him to bits.

I had tbi from domestic violence sent upstate NY broke. Bone in head got plate put in with VP shut drain blood and fluid in 2016 .now I'm having memory issues .diagnosed with MS last yr an Dr now says have early stages of dementia.i don't have trouble doing daily task just people say I repeat my self alot is it possible it from trauma instead of dementia. I cook drive no trouble bath clean pay bills on time so Dr really got me thinking and concern I'm only 48 to young for this .worked in health care 24 yrs prior to tbi .always tired and headaches Neuro Dr call um cluster headaches.energy level low sleep 12 hrs a day some days more and some days don't even sleep so what should I do before anything advances .

I have had several head injuries... Age one, fell down a flight of stairs, knocked unconscious. Age 11, fell off a bike, found unconscious on the road. Age 12, I was riding a new horse who ran away with me and knocked me off on a large tree branch. I had 25 stitches above my right eye … Then at age 17, I had a car accident and rolled down a 25 foot embankment, again, knocked unconscious.

At age 60; I started having hand tremors. An MRI showed I had a rare brain cyst, making me the 40th person ever. In Nov, 2016, I had brain surgery. The cyst was filled with spinal fluid. When the surgeon pierced it, it drained and pulled away from the brain tissue, causing it to bleed. I have learned that is not a good thing. I was in intensive care and a rehab center afterwards. Then 'physical therapy' for a number of months, which consisted of playing games and Journaling. My close friend also helped me so much with the symptoms. She had an aneurism.

I am now retired and on SSI... I had to leave my job. I feel so fortunate to be getting a pension as well.

My husband took care of me. It was (is) a strain on him. Our youngest daughter left her partner and moved in with us in December along with her two daughters and two pit bull dogs. They are all crammed in one bedroom. Since they moved in it has been a challenge for me, as you could imagine. I feel as if I am digressing. After reading your comments it is helpful to admit it could be so much worse.

Thank you for your support. I feel more hopeful.

Some days are just okay and I feel clear enough to think like I used to sometimes. But most days feeling not foggy, it only last a few hours and others not at all. I take naps every day & feeling foggy leaves me sad,impatient, irritable, but I try to not let this control or happen when I know I feel this way. My incident where 2 people hurt me and I was in shock when I woke up bloody. I dont remember much. Just bits here and there. I dont have enough for pieces. Is it normal for ne to feel slow & foggy , & not be able to explain things well if I say them; is it normal to fight with daily functions and hate artificial lighting? I just dont know. I just want it to end.

Thank you for posting. You’re not alone or crazy for what’s going on. I was in a horrific motorcycle accident that broke most the bones in my body and gave me a decent TBI, that was fortunately controlled with drugs, not surgery. This was two years ago. Just lately I have started to come out of what seems like a day dream, things were just foggy, hard to comprehend, words are lost from me, and emotions can be all over the board without the ability to express the way I mean to or want to. I know lots of people that have light sensitivity after a decent blow to the head. I pray time helps with your injuries and the symptoms ease because having a disconnection from your body is terrifying.
Something that helps is a support system. This is harder to find after a little time from your trauma; while the world moves on from what happen to you, you’re stuck putting the pieces together. Still getting up to speed on the traumatic experience. Most people will not understand and it is so maddening. I recommend journaling because it can help sort all of the complex loses you are dealing with. Also know that your pain is unique to you. No one has experienced what you have and you’re stronger for it. Please know there are still kind, wonderful people out there and I am sorry for the hurting you’re experiencing.

Hi Cindy, I have survived multiple brain injuries, and I am still struggling with the effects of them, daily. Yes, your issues are normal, so relax, you are not alone. Talk to your Doctor about them, they need to know. Also there are support groups with people who are going through the same issues. The key is to not worry, you are "normal", okay ?

I am 67, I was unconscious briefly, at age 6, when I hit the left side of my head on pavement after falling off my bike. I had difficulty learning for about a year and was almost held back in school. Stress and/or fatigue can cause me to have TIAs, a migraine, and/or experience scotomas—no headache but central vision loss.

My daughter was 1 when she stopped breathing lack of oxygen she is now turning 6 shes having a hard time learning writing identifying letters speech is delayed, lazy eye slower time tracking... she is in regulat kindergarten but she is struggling to keep up having frustrations then that turns into behaviors . She understands everything just takes longer to process and her right side from tracking issues to slower overall reaction is more noticeable or affected on right side not left. Any advice or things that I can do or know that might help and wish u knew sooner ..or explaining ur experience living with it from start to now of injury

My daughter was 1 when she stopped breathing lack of oxygen she is now turning 6 shes having a hard time learning writing identifying letters speech is delayed, lazy eye slower time tracking... she is in regulat kindergarten but she is struggling to keep up having frustrations then that turns into behaviors . She understands everything just takes longer to process and her right side from tracking issues to slower overall reaction is more noticeable or affected on right side not left. Any advice or things that I can do or know that might help and wish u knew sooner ..or explaining ur experience living with it from start to now of injury