Brain Fog and Cognitive Symptoms in Children With Lyme Disease
Updated January 2026
Many parents notice something is wrong long before they have a name for it. A child who once learned easily may begin to struggle to concentrate. Homework takes longer. Instructions need to be repeated. Teachers mention inattention or declining performance. At home, the child may seem mentally “elsewhere,” easily overwhelmed, or emotionally reactive.
In children with Lyme disease, these changes are often described as brain fog. While the term is informal, it captures a very real pattern of cognitive dysfunction that can interfere with learning, behavior, and daily functioning.
Importantly, these cognitive changes are usually functional. They do not mean a child is losing intelligence or experiencing permanent brain damage.
This article focuses on children. For a broader overview of brain fog and cognitive dysfunction in both adults and children with Lyme disease, see Brain Fog and Cognitive Dysfunction in Lyme Disease.
“For a broader clinical framework on how Lyme disease becomes chronic, see Preventing Chronic Lyme Disease.”
What brain fog looks like in children
Children rarely describe brain fog directly. Instead, it shows up in subtle and frustrating ways. A child may appear inattentive, forgetful, or slow to process information. They may struggle to keep up with classroom demands or lose track of multi-step instructions.
Tasks that once felt automatic can suddenly require enormous effort. Parents often hear concerns about attention or motivation, while the child insists they are trying their best. This disconnect can create tension at home and school, especially when standard testing does not reveal obvious abnormalities.
For a broader discussion of how Lyme disease affects cognition across all ages, see our overview of brain fog and cognitive dysfunction in Lyme disease.
Why brain fog is often missed or misunderstood
Brain fog in children is frequently mistaken for anxiety, attention-deficit disorders, or behavioral problems. Because routine imaging and laboratory studies are often normal, cognitive complaints may be minimized or attributed to stress or mood.
In Lyme disease, however, cognitive symptoms can occur even when standard tests are unrevealing. Subtle changes in brain function, inflammation, and signaling can impair processing speed, working memory, and mental endurance. These changes may not appear on routine studies, but they are still very real for the child experiencing them.
The neurologic basis of cognitive symptoms in pediatric Lyme disease
Lyme disease can affect the central nervous system in ways that disrupt how the brain processes information. Immune activation, neuroinflammation, and altered neurotransmitter function may interfere with attention, memory, and executive functioning.
In children, whose brains are still developing, these disruptions can have a disproportionate impact. The result is not a loss of intelligence. Rather, it is reduced cognitive efficiency, especially during periods of stress or fatigue.
Cognitive overload and emotional regulation
Cognitive strain and emotional regulation are closely linked. When a child is struggling to process information or sustain attention, the nervous system can become overwhelmed.
This overload often contributes to irritability, emotional outbursts, or withdrawal. In some children, it may appear as oppositional or defiant behavior. What looks like misbehavior may actually reflect a child who has reached their cognitive limit and cannot manage additional demands.
Cognitive overload can also contribute to emotional dysregulation and oppositional behavior in children with Lyme disease.
School performance and learning challenges
School environments place sustained demands on attention, processing speed, memory, and sensory tolerance. For a child experiencing brain fog, these demands can quickly become exhausting.
Teachers may notice declining grades, incomplete work, or difficulty following classroom routines. Parents may observe school avoidance, academic anxiety, or a sudden drop in confidence. These challenges do not reflect laziness or lack of effort. They reflect a nervous system struggling to meet expectations it previously handled with ease.
If school refusal is part of your child’s picture, see our related article on school refusal in children with Lyme disease.
Fluctuation and unpredictability of symptoms
One of the most confusing aspects of brain fog in children is its variability. A child may function well one day and struggle significantly the next.
This fluctuation can lead adults to assume inconsistency or lack of motivation. In reality, symptom variability is a hallmark of neurologic and immune dysregulation. Cognitive capacity may change depending on sleep quality, stress, physical exertion, or immune activity.
Overlap with immune-mediated neuropsychiatric syndromes
Some children with Lyme disease experience cognitive symptoms alongside abrupt behavioral or emotional changes. These presentations may overlap with immune-mediated neuropsychiatric syndromes such as PANS.
While diagnostic labels vary, the unifying theme is immune and nervous system dysregulation affecting cognition and behavior. Recognizing this overlap helps families and clinicians move away from rigid categories and toward a more integrated understanding of the child’s symptoms.
Why reassurance matters
Parents often worry that cognitive symptoms signal permanent damage or long-term decline. In most cases, this fear is unfounded.
Brain fog in children with Lyme disease is typically functional and potentially reversible. With appropriate recognition and support, many children experience gradual improvement as neurologic stability returns. Progress may be uneven, but improvement is common.
Supporting children with brain fog
Children benefit most when their symptoms are acknowledged and validated. Reducing unnecessary pressure, adjusting expectations, and providing appropriate academic accommodations can significantly reduce stress on the nervous system.
Understanding that cognitive symptoms are part of illness — not a failure of effort or character — helps preserve self-esteem and emotional well-being during recovery.
Relationship to persistent symptoms
In some children, cognitive symptoms persist even after initial treatment for Lyme disease. This does not necessarily indicate ongoing infection. Instead, it may reflect continued nervous system or immune dysregulation.
Recognizing persistent cognitive symptoms as part of a broader post-infectious pattern allows for more thoughtful evaluation and avoids dismissal or blame.
Key clinical takeaways
Brain fog in children with Lyme disease reflects neurologic and immune dysfunction rather than loss of intelligence or motivation. Cognitive symptoms may affect attention, memory, processing speed, and school performance, often fluctuating over time. These challenges frequently overlap with emotional and behavioral changes and benefit from a compassionate, systems-based approach.
Parents often have practical concerns about how brain fog affects daily life, learning, and recovery.
Frequently Asked Questions for Parents
Is brain fog in children with Lyme disease permanent?
In most cases, no. Brain fog in children with Lyme disease is typically functional rather than degenerative and often improves over time as neurologic stability returns.
Why does my child seem better some days and worse on others?
Fluctuation is common and reflects changes in sleep, stress, immune activity, and cognitive load. Variability does not mean a child is exaggerating or regressing.
Can brain fog affect behavior or emotions?
Yes. When cognitive demands exceed a child’s neurologic capacity, frustration, irritability, emotional outbursts, or withdrawal may occur.
Why are tests often normal if my child is struggling cognitively?
Standard imaging and laboratory tests may not detect subtle changes in brain function or inflammation. Normal results do not rule out real cognitive symptoms.
Will school demands make brain fog worse?
In some children, sustained cognitive demands can worsen symptoms. Understanding this helps families and schools adjust expectations and reduce stress during recovery.
Selected links
Pediatrics Skogman BH, Ernerudh J, Forsberg P, Bergström S. Long-term clinical outcome after Lyme neuroborreliosis in childhood. 2012;130(2):262–269. Pubmed
Journal of Neuropsychiatry and Clinical Neurosciences Tager FA, Fallon BA, Keilp J, et al. A controlled study of cognitive deficits in children with Lyme disease. 2001;13(4):500–507. Pubmed
Pediatrics Vázquez M, Sparrow SS, Shapiro ED. Long-term neuropsychologic and health outcomes of children with facial nerve palsy attributable to Lyme disease. 2003;112(2):e93–e97. Pubmed
Pediatrics Bloom BJ, Wyckoff PM, Meissner HC, Steere AC. Neurocognitive abnormalities in children after classic manifestations of Lyme disease. 1998;102(4):E52. Pubmed
Children with Lyme
Two children who contracted Babesia from their mothers
How Do I Parent or Work With Lyme Disease? When Survival Becomes the Job
What’s your approach to Lyme brain? Methylene blue seems to help but really nothing has helped me.
I have had to individualize treatment and still Lyme and co-infections remain challenging
I wish there was a one size fits all
My son has schizoaffective disorder from a Bartonella infection, no treatment has helped so far, he has had antibiotics, ABARTS, wholistic drops, nothing helps & he’s getting worse
I am sorry to hear your son remains ill. I hope you find a solution
How “early” is early diagnosis and treatment? My daughter’s Lyme seems to have been reactivated with a Covid acute infection in March 2022 and it is only in November/December 2024 that she has had her diagnosis of Lyme and Bartonella coinfection having thought this was only Long Covid all along. Despite the fact that she is now receiving individualized antibiotic treatment, our fear is that because of the delay in diagnosis it could be too late to recover without any sequelae. We are in the UK.
I have Lyme disease who are sick for years who did well with oral antibiotics
This is me !!!! Is there a replay or a way to watch these informative videos? I missed the initial airing
Thanks for your feedback. I have been posting short videos covering common sense Lyme disease cases and questions. Stay tuned
I have been severely struggling with Morgellon’s Disease for the last 2 yrs. The 16 months were unbearable. I was bedridden & in tremendous pain. The things that were coming off my skin were sheer terrifying. My anxiety was at all time new high. I felt panicked, anxious, petrified, alone & isolated just constantly waiting for the next ball to drop…and it always did, usually worse than the previous time. I began to feel frayed like I was coming apart at the seams. The longer I struggled with this disease going to doctor after doctor, ER after ER, and urgent cares, I began to feel so hopeless and helpless. The more the doctors said there was nothing wrong with me, and this was just delusions of parasitosis, the more my family turned on me & refused to believe me, let alone support me. They actually forced me under duress to get not one, not two, but three psych evals in just over 6 months. If that wasn’t bad enough, again under complete and total duress, they forced me to sign my rights to my son over to my mom, so they could have me committed! Anyone who knows me, knows my son is my everything…my heart, my soul, my whole life. All of this led to depression eventually. There’s just so much one person can take. I passed ALL 3 psych eval with flying colors! The psychiatrist REFUSED to admit to psych ward. He tried explaining to my family that I did have severe anxiety & had fallen into a depressive state due to my physical ailment, which he believed was a chronic illness. He went on to say what I needed was to find the right doctor to diagnose & treat me and people around me to support me during this difficult time. Well, that wasn’t received. My sister went on to threaten him by stating that if he didn’t commit me she and the rest of my family would be calling CPS (they were already in contact with them at that point) and make certain that a 12 yr old boy would be taken from his home. The psychiatrist refused to back down, so my sister stormed out leaving me with no ride home. I haven’t spoken to my sister in 17 months and I don’t think I will ever speak to her again. There’s no coming back from this.
I’m telling you my back story, so you can see what a struggle and challenging time this has been. Most Morgellon’s patients have a similar story. It shouldn’t be this way. When someone suggested you in one of my Morgellon’s support group on FB, I felt a glimmer of hope for the first time in 2 yrs. It was an amazing feeling! Do you treat Morgellon’s? Also, I have NJFamilyCare Insurance. Do you accept that? This disease has taken everything from me—my family, my job, my money, my looks, my self esteem, my self worth, my confidence, etc. All I dream of anymore is getting my life back…getting back to normal. If you could help me get there, I would be eternally grateful. 🙏
You are welcome to call my office at 914 666 4665 with you question
You forgot a few! According to the National Institute of Health, under Babesia alone it can also cause uncontrolled and uncontrollable laughing or crying, anorexia, abnormal sensitivity to being touched and light sensitivity. There are others, but they aren’t necessarily brain related.
The list gets pretty long once one looks deeper to the neuropsychiatric and autonomic findings in Lyme disease and co-infections.