How to explain persistent concussion symptoms to your family
Scripts for every age, a family handout and clear requests that relatives can act on
Safety Behind the Wheel Foundationdrivewithcare.org
Last reviewed:
For survivors and families14 min read
Imagine a 44 year old school bus driver named Dana. Four months ago, a pickup truck rear ended her at a red light. Her bruises healed long ago. She still gets headaches by midafternoon, loses her train of thought, and asks her kids to turn the TV down.
At a family barbecue, her brother asks when she is going back to work, and she does not know what to say. Her family loves her, but nobody can see a headache or feel brain fog.
If your symptoms have lasted weeks or months, you may know that moment. This article gives you plain words to explain them: scripts for adults and children, specific requests, and a one page handout to fill in and share.
Why your family may not see what you feel
Concussion symptoms come in several groups. The CDC lists physical ones, such as headaches, low energy, dizziness, and being bothered by light or noise [1]. It also lists thinking problems, such as feeling slowed down or foggy, along with mood changes like irritability, sadness and nervousness, and changes in sleep [1]. Almost none of these show on your face.
The CDC also points out that a person may not notice or admit to problems after a concussion [1]. Relatives, and even health care providers, can overlook them too [1]. A relative who seems unaware may have had no way to notice.
Expectations that no longer fit
Your relatives may have heard that people bounce back fast, and many do. According to the CDC, most people improve in two weeks or so after a concussion, while others stay symptomatic for months or more [1, 2]. Older adults and people with an earlier concussion may take longer [2].
A Canadian guideline for adult care, the Living Concussion Guidelines, estimates that roughly 20 to 30 percent of people still have symptoms after the first month [3]. The guidelines also note wide differences in recovery, even between people with similar injuries [3]. A relative’s idea of how long it should take is a guess, and it may not fit you.
What families go through
A small study by UK researchers interviewed four relatives of people whose mild TBI symptoms had lasted more than three months [7]. They described many of the struggles that families face after more severe brain injuries, though with less intensity [7]. They found the injury hard to make sense of. Their sense of loss could grow when what they were told did not match what they saw at home [7]. The authors called for information that is steady, open and realistic [7].
A larger New Zealand study tracked 99 family members of adults with a mild TBI, and partners made up about half the group [8]. At six months, their average quality of life was close to population norms, and their mood scores were below clinical cutoffs [8]. Their strain eased between six and twelve months [8]. Still, the authors said even a mild injury touches family members to some degree [8].
Before you talk, decide who needs to know what
You do not owe every relative the same story. The TBI Model Systems are federally funded brain injury research centers. Their factsheet on talking about an injury says you choose whom to tell, and when and how to answer [4]. It favors brief, plain answers, with each person hearing only as much as you are comfortable giving [4].
The same factsheet suggests planning hard conversations before they happen [4]. Write down the questions that trip you up, draft answers, and practice them out loud, so you are not inventing an explanation on a day your head already hurts [4].
Choose a time of day when your symptoms tend to be lowest, in a quiet room with the TV off. One or two people at a time is easier than a full holiday table, and you can always finish another day.
Comparison compiled by Safety Behind the Wheel Foundation
Who needs to hear what
| Person | What they may need | How much detail |
|---|---|---|
| Partner or spouse | Daily effects, triggers, danger signs | The most |
| Children at home | What changed and that it is not their fault | Simple and honest, by age |
| Parents and siblings | What is hard, what helps, how to help | Some |
| Extended family | A short summary and one way to help | Brief |
| Family friends | That you are healing and may cancel | Very brief |
Based on TBI Model Systems advice on sharing information [4] and family guides on talking with children [5, 6].
Words for the adults in your family
Describe effects in daily terms. Instead of naming post concussion syndrome, say what happens: after 20 minutes of reading, your eyes ache and the words swim. After a loud dinner with three conversations at once, you need two hours in a dim room.
Explain that symptoms rise and fall. You might manage a grocery run on Monday and feel wiped out by a phone call on Tuesday. The Living Concussion Guidelines, at their top grade of evidence, tell care teams to explain that a short rise in symptoms after more activity is common [3]. A flare after a busy day does not mean you are sliding backward, and your family can learn to expect it.
Name the hidden emotional ones too. Irritability, sadness and nervousness are on the CDC list of concussion symptoms [1]. Naming them helps your family read a short fuse as part of the injury, while you still take responsibility for how you treat people.
When Dana tried this with her brother, she skipped the medical words. She told him she could drive a bus for eight hours before the crash and now struggles with a 30 minute meeting. Her brother had pictured her resting comfortably at home, and he stopped asking about a date.
If someone keeps doubting you
You cannot force anyone to understand. You can hand a doubter the handout below or invite them to a medical visit. The Ontario guidelines list an information sheet for patients and families among their tools, so ask your care team for something similar [3]. A counselor can also help you plan what to say [4].
Talking with children and teens
Children notice changes in a parent even when nobody explains them [6]. A review of nine studies looked at children whose parent had a stroke or another brain injury, such as a severe TBI [9]. Many children wanted information about the injury, and talking helped them cope [9]. Many also took on new jobs at home, and some effects lasted for years [9]. Headway, a UK brain injury charity, says research suggests children manage better when adults are honest with them at a level they can follow [5].
None of these sources focus on concussion alone. A U.S. military guide used below covers moderate or severe TBI, and the review and other guides cover brain injuries of all kinds [10, 9]. Much of their advice may still fit, because children react to what they see, such as a parent who spends the afternoon in a dark room.
A few points apply at every age:
- Say more than once that nothing they did caused the injury, since young children often blame themselves [11, 6].
- Tell them you love them just as much as before [6].
- Keep meals, bedtime and the school run as steady as you can [5, 10].
- It is fine to say you do not know [6].
- Invite questions again and again. As one guide puts it, “No question is too silly.” [6]
Fatigue needs special care. A guide from Ireland’s National Rehabilitation Hospital warns that children may think a tired parent will be fine after a short rest [11]. It advises explaining how deep the fatigue runs, so children do not push you into plans you cannot manage [11].
Comparison compiled by Safety Behind the Wheel Foundation
What children may understand at different ages
| Age | What they may grasp | What helps |
|---|---|---|
| 2 to 3 | Moods and tension at home | Routines, hugs, simple words |
| 4 to 5 | Simple ideas; may think they caused it | Clear reassurance, play, picture books |
| 6 to 11 | Cause and effect; growing empathy | Real explanations, step by step, small jobs |
| 12 to 17 | The full picture; worry about friends | Facts, honesty, help with what to tell peers |
Sources: Defense and Veterans Brain Injury Center, revised 2019, for moderate or severe TBI [10]; McGill University Health Centre, 2014 [12]; National Rehabilitation Hospital [11]; Headway [5].
Young children, up to about age 5
Children of 2 or 3 can tell anger, sadness and joy apart on a parent’s face [10]. Keep explanations short, and use picture books or play. Guides suggest giving preschoolers a toy doctor kit or dolls to act out what is happening [12, 10]. At 4 and 5, magical thinking is common, and young children often blame themselves for a relative’s injury [10, 11].
Script: My head got hurt in the car crash. It is healing slowly. Sometimes it makes me sleepy or grumpy. That is the hurt talking, and you did not cause it.
School age, about 6 to 11
By about age 8, children understand cause and effect better and can feel for others [10]. Give real explanations instead of magical ones, and walk through what will happen step by step [12]. Some become angry or resentful, or tired from extra chores [12]. Many children of 6 or 7 enjoy having a job of their own [10]. Keep the jobs small, since extra caring duties can cut into a child’s time with friends [5].
Script: The crash shook my brain, a bit like a bruise on the inside. You cannot see it, but it gives me headaches, and loud noise makes them worse. That is why I sometimes leave the room when it gets noisy. It is getting better, and my care team is helping.
Teenagers
Teens can understand how complex a brain injury is [11]. If they sense you are holding back, they may fill the gaps with their own guesses [5]. Give them the facts about your symptoms, treatment and what to expect [12]. Help them rehearse what to say when friends ask [10]. Encourage them to stay busy with school and friends, and try not to lean too hard on older children at home [10, 5].
Script: I want you to have the real picture. I still have concussion symptoms: headaches, trouble concentrating and running out of energy fast. Most people improve, and mine is taking longer. Ask me anything, and you never have to cover for me.
Watch how they are doing
Kids often keep their worries to themselves [5]. Look for sudden, extreme changes in behavior, pulling away, or risky behavior, and ask your child’s doctor or a counselor for help if you see them [12, 10]. Let the school know what is going on so teachers can watch for changes [5, 11]. Some rehabilitation teams will meet with a child to explain brain injury and answer questions, so ask yours [11].
Ask for help your family can give
Relatives often want to help but freeze without a clear task. The CDC notes that support from family and friends can help recovery [2]. One study followed 166 adults with mild TBI seen at a trauma center emergency department [13]. Those whose families had fewer resources before the injury reported more concussion symptoms three months later [13]. That is an association, and the effect was modest, but it fits the idea that practical support matters.
Vague offers tend to fizzle. When someone says to call if you need anything, turn it into a task with a day, a time and an end date. Match the job to the person, too: the cousin who loves to cook may hate driving.
Requests you can borrow
Checklist from Safety Behind the Wheel Foundation
- Drive me to physical therapy on Thursdays at 2:00 for the next four weeks.
- Take the kids to the park on Saturday morning so the house is quiet for two hours.
- Cook a double batch on Sunday and drop half off.
- Come to my next appointment and take notes, if I ask you to.
- Be the one who updates the wider family, so I get fewer texts.
- Lower the TV or move a loud conversation to another room when I give our signal.
- Call before you stop by, so I can rest first.
- Let me keep the jobs I can still do, even if I am slower at them.
The TBI Model Systems factsheet suggests a signal that tells your helpers you need out of a conversation [4]. A tap on the arm or a code word works.
When you ask, keep it short: I have a specific favor. Could you drive me on Thursday at 2:00? It would save my energy for the kids that evening. If you cannot, that is fine.
Make a one page handout for your family
A written page saves you from repeating yourself, and relatives can reread it later. The Living Concussion Guidelines advise care teams to give concussion education in written, spoken or picture form [3]. The authors of the family study above called for consistent information, and one shared page can help everyone hear the same story [7].
Fill in the blanks in your own words, give a copy to whoever helps most, and update it monthly. The CDC encourages you to keep telling family and loved ones how you are feeling, and to tell your provider if you are not improving or symptoms get worse [2].
When my family should call 911
The CDC lists danger signs that call for emergency care right away [1]. Anyone with me should call 911 or take me to an emergency department if I:
- Get a headache that keeps getting stronger instead of fading.
- Have new weakness, numbness or clumsiness, or a seizure.
- Throw up again and again.
- Slur my words or act in a way that is unusual for me.
- Have one pupil noticeably larger than the other one.
- Seem confused, restless or agitated, or do not know people or places.
- Faint, look extremely sleepy, or cannot be roused.
Questions to ask your care team
Question checklist from Safety Behind the Wheel Foundation
- Do you have written information about lasting concussion symptoms that I can give my family?
- Can my partner or another relative join part of my next visit?
- Which symptoms should my family expect to rise and fall, and which changes should they report?
- Can someone on the team talk with my children about my injury?
- Which signs of stress in my children should I raise with their doctor or a counselor?
- Could counseling help me or my family adjust to the changes at home?
- Which tasks at home can I keep doing, and which should I hand off for now?
Frequently asked questions
Should I tell my young children about my concussion?
Family guides say yes, in simple words. Children notice changes anyway, and Headway notes research suggesting they cope better with honest information [5, 6]. Keep it short, say it is not their fault, and come back to it often [6].
What if my family keeps saying I should be better by now?
Share the facts: the CDC notes that some people stay symptomatic for many months [2]. Give them your handout and ask your care team for written information for families [3]. If someone still doubts you, put your limited energy into the relatives who do listen.
Is it a problem if my teenager is doing much more at home?
Some extra help is normal, and children in the review often took on new jobs [9]. Headway cautions against relying too heavily on older children, because it can cut into their time with friends [5]. Share the load with other adults and protect time for school and friends.
The bottom line
Recommendation from Safety Behind the Wheel Foundation
Your family cannot see headaches, fatigue or brain fog, so they need you to describe them in terms of daily life. A planned talk and a filled in handout can do much of that work for you. Children do better with honest, simple words and steady routines, and young ones need to hear often that the injury is not their fault.
Ask for help as specific tasks, and keep talking as things change. If your family still struggles, your care team or a counselor can help. Call 911 for any danger sign.
Sources and further reading
- 1Centers for Disease Control and Prevention. Symptoms of mild TBI and concussion. Updated September 15, 2025. cdc.gov/…/signs-symptoms/index.html
- 2Centers for Disease Control and Prevention. What to do after a mild TBI or concussion. Updated September 15, 2025. cdc.gov/…/response/index.html
- 3Living Concussion Guidelines (Ottawa Hospital Research Institute). Management of prolonged symptoms: guideline for concussion and prolonged symptoms in adults, section 5. Last updated April 2023. concussionsontario.org/…/management-of-prolonged-symptoms
- 4Benfield E, Teague C, Moadab N, Hanks R. Talking to people about your traumatic brain injury (TBI). Model Systems Knowledge Translation Center. 2024. msktc.org/…/talking-people-about-your-traumatic-brain-injury-tbi
- 5Headway (UK). Supporting children when a parent has had a brain injury. Booklet; next review 2025. headway.org.uk/…/supporting-children-when-a-parent-has-had-a-brain-injury-e-booklet.pdf
- 6Rouse MH. How to talk to kids about a parent’s brain injury. Child Mind Institute. Last reviewed November 6, 2023. childmind.org/…/how-to-talk-to-kids-about-a-parents-brain-injury-or-illness
- 7Gamgee J, Runacres J, Norman A, Pradhan P. The secondary impact of mild traumatic brain injury: an interpretative phenomenological analysis of the experiences of family members. The Family Journal. 2023;31(4):634-648. doi.org/10.1177/10664807231164421
- 8Jones K, Theadom A, Prah P, Starkey N, Barker-Collo S, Ameratunga S, Feigin VL. Changes over time in family members of adults with mild traumatic brain injury. Brain Impairment. 2020;21(2):154-172. Published online October 2019. doi.org/10.1017/BrImp.2019.27
- 9Ohan J, Jackson H, Bett R, Farmer GM, Martini A. Experiences and needs of children and adolescents affected by a parent’s acquired brain injury: a systematic review and thematic synthesis. Disability and Rehabilitation. 46(6):1034-1044. Published online March 2, 2023. doi.org/10.1080/09638288.2023.2179673
- 10Defense and Veterans Brain Injury Center. Talking with children about moderate or severe TBI (families). Released June 2012, revised June 2019. biav.net/…/CA-01-Talking-to-Children-about-Parents-w-TBI-Vet-BI-Ctr-2019.0601-1.pdf
- 11National Rehabilitation Hospital (Ireland), Social Work Department. Talking to children about brain injury: a practical guide for families. 2025. nrh.ie/…/Talking-to-Children-about-Brain-Injury.pdf
- 12McGill University Health Centre, MGH TBI Program. When parents have head injuries: helping children cope. 2014. muhcpatienteducation.ca/…/532_en~v~when-parents-have-head-injuries-helping-children-cope.pdf
- 13Temple JL, Struchen MA, Pappadis MR. Impact of pre-injury family functioning and resources on self-reported post-concussive symptoms and functional outcomes in persons with mild TBI. Brain Injury. 2016;30(13-14):1672-1682. doi.org/10.3109/02699052.2015.1113561
This article reflects the safety priorities of concussion recovery and family support education. It is general education, not medical or mental health advice. Many of the family guides cited here were written for all kinds of brain injury, so check official sources and talk with your own care team or a qualified professional about what fits your family. Reviewed October 2026.
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