Head feels like it will explode daily. Severe cognitive difficulties
I have been dealing with constant head pressure in the back of my head for over a year. It has gradually gotten worse over time, and with this negative development came decreased cognitive function as well. I am not as sharp as I used to be, and my memory is extremely poor. I also cannot seem to feel joy anymore no matter how positive my mindset is. Bear in mind that I am only an 18-year-old male, so I am still young. I often find myself zoning out in my own thoughts as the pressure and pain gets worse. I am hardly present in the current moment; therefore, I really struggle to be mindful and live in the present at all times. As I type this, I find myself struggling to sharply think of how to compose this message. Anyway, the symptoms don't stop with my head. I also feel like I'm out of breath when I talk, and I have on-and-off debilitating anxiety that really gets me down in the dumps. Also, my limbs will just feel restless and achy randomly without any clear explanation. I have seen many doctors and found no relief. Pain killers and supplements are futile. I have only had an MRI laying down, but no chiari malformation was spotted, nor were there any other abnormalities. This chronic pain I deal with in my head makes me deal with a huge mental challenge from day to day. I have gone through the psychiatric route and have found no relief either, despite numerous therapy sessions and numerous (5-6) antidepressant medications. Currently, I struggle mentally from day to day and dread each day. I go to bed as early as I can (8:00 PM) to escape the chronic symptoms. All in all, these symptoms make me feel like I am going insane. I am so desperate for my life back and I know living life is worth so much... that is why I am still here typing this message. However, I cannot live like this forever... this is UNBEARABLE and I need help. Any thoughts?
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October 1 2020 cxvid hit me. Since then 24 x 7 headaches and migraine with auras, pressure on brain (atmospheric pressure relate), brain on fire, brain fog, dizzy, tension headaches (PT Dry Needling fixed) blah blah blah
My head pain/ symptoms puzzle has many pieces.
The last year I’ve been working with Neurology and now I’m looking to add working with Immunology (cell level).
Here are a few papers I’ve found recently that are making sense.
Papers -
12/11/2024 - Persistence of spike protein at the skull-meninges-brain axis may contribute to the neurological sequelae of COVID-19 (Graphic abstract very interesting)
8/16/2025 Comparative Analysis of Long COVID and Post-Vaccination Syndrome:
2/19/2025 - A small number of people report chronic symptoms after receiving COVID-19 shots. A new study provides clues for further research.
10/19/2023 (video) Harlan Krumholz and Akiko Iwasaki (Rishi Shiah, Lilo Wu, and Adith Arun) discuss preliminary findings and answer questions from LISTEN participants.
I listed the Symptoms Long Covid – PVS post-vaccination syndrome (very interesting)
8/25/2025 Immunologist: Hope for ME/CFS and post-Covid, research needed
Akiko Iwasaki "... She sharply rejected views that ME/CFS or post-COVID might not be somatic illnesses."
2/19/2025 - A small number of people report chronic symptoms after receiving COVID-19 shots. A new study provides clues for further research.
12/11/2024 - Persistence of spike protein at the skull-meninges-brain axis may contribute to the neurological sequelae of COVID-19
https://www.cell.com/cell-host-microbe/fulltext/S1931-3128(24)00438-4
Highlights
SARS-CoV-2 spike protein persists in the skull-meninges-brain axis in COVID-19 patients
Spike protein is sufficient to induce brain pathological and behavioral changes in mice
Spike protein enhances brain vulnerability and exacerbates neurological damage in mice
mRNA vaccines reduce, but do not eliminate, the spike burden
Summary
SARS-CoV-2 infection is associated with long-lasting neurological symptoms, although the underlying mechanisms remain unclear. Using optical clearing and imaging, we observed the accumulation of SARS-CoV-2 spike protein in the skull-meninges-brain axis of human COVID-19 patients, persisting long after viral clearance. Further, biomarkers of neurodegeneration were elevated in the cerebrospinal fluid from long COVID patients, and proteomic analysis of human skull, meninges, and brain samples revealed dysregulated inflammatory pathways and neurodegeneration-associated changes. Similar distribution patterns of the spike protein were observed in SARS-CoV-2-infected mice. Injection of spike protein alone was sufficient to induce neuroinflammation, proteome changes in the skull-meninges-brain axis, anxiety-like behavior, and exacerbated outcomes in mouse models of stroke and traumatic brain injury. Vaccination reduced but did not eliminate spike protein accumulation after infection in mice. Our findings suggest persistent spike protein at the brain borders may contribute to lasting neurological sequelae of COVID-19.
Graphic abstract - Click paper link for graphics – very interesting
8/16/2025 Comparative Analysis of Long COVID and Post-Vaccination Syndrome:
https://www.medrxiv.org/content/10.1101/2025.08.14.25333639v1
“Question - What are the similarities and differences between long COVID and post-vaccination syndrome (PVS)?
Findings In this cross-sectional study of 682 individuals, machine learning models identified distinct symptoms between long COVID and PVS. Long COVID was characterized by brain fog, altered sense of smell, and shortness of breath, while PVS was associated with burning sensations, neuropathy, and numbness.”
Feb 19, 2025 - A small number of people report chronic symptoms after receiving COVID-19 shots. A new study provides clues for further research.
https://news.yale.edu/2025/02/19/immune-markers-post-vaccination-syndrome-indicate-future-research-directions
“COVID-19 vaccines have been instrumental in reducing the impact of the pandemic, preventing severe illness and death, and they appear to protect against long COVID. However, some individuals have reported chronic symptoms that developed soon after receiving a COVID-19 vaccine. This little-understood, persistent condition, referred to as post-vaccination syndrome (PVS), remains unrecognized by medical authorities, and little is known about its biological underpinnings.”
(click link to read more)
10/19/2023 Harlan Krumholz and Akiko Iwasaki (Rishi Shiah, Lilo Wu, and Adith Arun) discuss preliminary findings and answer questions from LISTEN participants.
https://medicine.yale.edu/ycci/listen-study/video/
The Yale LISTEN Study Town Hall: October 2023
The entire Town Hall is very interesting, here are 4 sections I found enlightening.
8:00 minute - Difference in Percent of Participants Experiencing Symptom (Long Covid – PVS post-vaccination syndrome; Note: the graphic chart is informative)
Long Covid –
Memory problems, Changed sense of smell, Brain fog, Shortness of breath, Cough, Sore throat, Excessive fatigue, Difficulty speaking properly, Changed sense of taste, Fatigue, Congested or runny nose, Phantom smells, Runny nose, Phlegm in back of throat, Headache, Constant thirst, Night sweats, Hypersomnia, Confusion, Insomnia, Hair loss, Dry scalp or dandruff, Dizziness, Throat pain or discomfort, Postnasal drip, Exercise Intolerance, Wheezing, Swollen hands or feet, Cold/burning lung sensation, Changes in voice, Phantom tastes
PVS -
Loss of hearing, Suicidal thoughts, Feelings of impending doom, Palpitations, Tinnitus, Numbness, Internal vibration, Neuropathy, Burning sensations
16:00 minute - Implications
18:33 minute - Hypothesis
37:00 minute - Hope next 6 months
(continue)
page 2
August 25, 2025 Immunologist: Hope for ME/CFS and post-Covid, research needed
Akiko Iwasaki "... She sharply rejected views that ME/CFS or post-COVID might not be somatic illnesses."
(Akiko Iwasaki gives me HOPE for recovery. Google her – very interesting)
(Note: Original article in German, this is translated link to English)
https://science-apa-at.translate.goog/power-search/17729239753393598891
“At the International Congress of Immunology (IUIS) in Vienna, immunologist Akiko Iwasaki of Yale University (USA) expressed hope that treatment options can be found for at least some of those affected by conditions such as ME/CFS and long/post-COVID. In an APA interview, she emphasized that the causes must be addressed. She sharply rejected views that ME/CFS or post-COVID might not be somatic illnesses.”
(click link to read more)
Feb 19, 2025 - A small number of people report chronic symptoms after receiving COVID-19 shots. A new study provides clues for further research.
https://news.yale.edu/2025/02/19/immune-markers-post-vaccination-syndrome-indicate-future-research-directions
“COVID-19 vaccines have been instrumental in reducing the impact of the pandemic, preventing severe illness and death, and they appear to protect against long COVID. However, some individuals have reported chronic symptoms that developed soon after receiving a COVID-19 vaccine. This little-understood, persistent condition, referred to as post-vaccination syndrome (PVS), remains unrecognized by medical authorities, and little is known about its biological underpinnings.”
(click link to read more)
It’s a journey, Best Wishes for Your Journey!
🍀
Graphics
I’ve considered long covid as a possibility before. However, I’ve mostly rejected it for four reasons.
1. I don’t think long covid would go away for 3 hours from a massage to the back of the head and spine.
2. The pressure and brain fog come from the back of my head. The headaches from long Covid seem to have more of a tension headache pattern rather than localized to one spot.
3. I haven’t had Covid to my knowledge (which I understand doesn’t remove long covid as a possibility, but it makes it more unlikely). I am immunized plus boosters, however.
4. I don’t have some of the most common long covid symptoms, such as post-exertional malaise, chronic fatigue, or respiratory issues (although this doesn’t remove long covid as a possibility either, as it can exhibit a wide range of symptoms).
If nerve blocks don’t make a difference, I will reconsider long covid as a possibility. But for now, I’m focused on either CCI, ON, or CCI and ON.
As for PVS, I don’t have a majority of those symptoms, so I don’t believe I have that. If I do have more of those symptoms, I’ll reconsider PVS.
I do thank you for weighing in to help diagnose whatever is going on. Any suggestion is appreciated and helpful. I’ll try to remember to inform you if I reconsider long covid (I say “I’ll try to remember since my memory had been wonky lately).
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2 Reactionsnathansmith7143
Sorry, this is a late reply, only just came across your post.
But I've been suffering very similar symptoms which started summer last year (started about a week after a fall) and as you described has been horrendous to live with. To cut a long story short, seen many doctors, consultants, ENT, CT scan, MRI nothing abnormal found. Out of desperation I went to see a chiropractor last October and for the first time made some progress with the symptoms. The chiropractor diagnosed as 'occipital neuralgia' - 'sub occipital trigger points' in the neck. Subsequent treatment has substantially reduced symptoms, although not yet totally symptom free. I also found using a neck stretcher brace for 10-15 minutes at a time helped.
Whilst the cause of my symptoms may be different, a chiropractor check is worth a try if you are still suffering. Note: my chiropractor has only used gentle therapy to treat this condition (no neck cracking!).
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3 ReactionsHello, @aw1, and welcome to Mayo Clinic Connect. Sorry to hear your symptoms have been horrendous to live with.
Thanks for the suggestions for @nathansmith7143.
You may also want to check our these Mayo Clinic Connect discussions on occipital neuralgia:
- Occipital Neuralgia Relief https://connect.mayoclinic.org/discussion/occipital-neuralgia-relief/
- Occipital Neuralgia dizziness and vertigo https://connect.mayoclinic.org/discussion/occipital-neuralgia-dizziness-and-vertigo/
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4 ReactionsThanks Lisa.
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2 ReactionsThis sounds almost identical to my issue. We've basically went thru all the same tests but I've also not had my neck or spine checked. The severity of mine comes and goes with short periods of time with me basically feeling normal-ish and damn, that's so nice.
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1 Reaction@im70
Aimovig for migraines? Ill like some info please
@ashleyfierro - welcome to Mayo Clinic Connect.
Here is some Mayo Clinic information on this medication,
- Erenumab-aooe (subcutaneous route) (Aimovig) https://www.mayoclinic.org/drugs-supplements/erenumab-aooe-subcutaneous-route/description/drg-20443746
Do you have migraines, ashleyfierro? If so, what are your most common symptoms?