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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Sorry for delay - migraine had knock me out...
Not sure if you have had this - My Neurologist ordered a CT Scan with imaging, to see if blood vessels in brain were blocked. It's an IV fluid something that gets pushed into vein while in the CT machine.
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1 Reaction@fourleaf - how did your migraine come on, and how long did it last? Did anything provide some relief for you?
Good Morning Lisa,
It came on as increased food cravings, increased fatigue, nausea, auras (light flashing or prism - color separation), numbness hands and arms (dropped cellphone and tablet a few times), light sensitivity, dizzy, wake up sweating, brain ice pick stabbing and throbbing.
Lasted 10 days.
Relief - stay inside, rest throughout day, triptan, Vyepti Infusion have to wait 3 months for next (had two migraine infusion but they didn't last more than 3 days).
My new normal since 2020, headaches 24x7, poor sleeping (wake up every 1 to 2 hours), fatigue, loss of taste and smell (which is weird when I get the phantom smells - something burning), brain on fire - burning sensation after reading for 30 to 45 minutes or concentrating, throbbing headaches, thirsty, brain fog, tremors internal and hands, depression, dizzy, light headed, motion sensitivity, nausea, eye stutter (and dropped frames when seeing object in motion). I have had tinnitus since 1978 and allergies 1980 - two sinus surgeries 1998 and 2025.
Try to put symptoms in back of mind so I can get anything done, even if it's only one or two things a day.
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2 Reactions@lisalucier
To clarify on food and loss of taste.
Everything taste like plain oatmeal. Which is making it easier on grocery shopping. I now shop for texture - crunchy, crisp, etc. Apples; Fresh Vegetable Carrots, Green Peppers, Romaine Lettuce; Nuts. I don't dwelling on what I can't do, what can I do (that took four years).
I found out eating a salad recently, what I thought was a green pepper, was a large jalapeno pepper. All I could tell it was crunchy, until my tongue and lips started to burn. I had a good laugh out of that.
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2 Reactions@aw1 I'm writing this message to ask some questions, as I have many of the same symptoms as well, but I have yet to be diagnosed (plan to be diagnosed in ~3 months).
You mention you had similar symptoms to Nathan. Do your Occipital Neuralgia symptoms include the same depersonalization issues that Nathan had? I'm certain I have those depersonalization issues, and you also having them would make me consider ON as a possibility even more. Also, how would you describe your ON pain? I've been looking into ON forums, and they mainly describe their pain as nervous in nature (zappy, shocking, sudden). Some describe it as only pressure, but that seems rather rare. Do you have the same constant pressure that Nathan described? Or is it more zappy and nerve-like?
Any answer to these questions would be greatly appreciated!
@matthew9324
Hi Matthew, sorry to hear you suffer many of the same symptoms.
Yes, I do suffer the same constant pressure that Nathan described. It does vary intensity but rarely goes completely. Worse when concentrate on an activity for a period of time. I was very sensitive to noise some months ago but at least that symptom has reduced now. I did suffer zappy horrible pains in the first weeks of the constant pressure which was probably why I had an MRI. I also had a CT scan with dye to check blood flow. But nothing abnormal was found. I've also recently seen a vascular consultant who advised my issue isn't vascular and still waiting on neuro referral for nearly a year now.
I think I have some but minimal depersonalisation issues. I'm still seeing the chiropractor and also a massage therapist who has knowledge of treating injuries. Chiropractor is not sure if ON is all or part of the cause. I would say on a scale of 1 to 10. 10 being the worst. When I started seeing the chiropractor and using a neck stretcher last October my symptoms dropped from 10 down to 5 but needs regular use of the neck stretcher. A few weeks ago I then also started weekly with the massage therapist (chiropractor approved) and the symptoms have dropped between 0-3 for 1-2 days after treatment but returns to 4-6.
I do find exercise helps, cardio machines at gym, walking, swimming. I try do include something every day. But the underlying condition is not easy to live with as is invisible to others. With no definite diagnosis and has been going on for over a year now. An ENT specialist mentioned I may also be suffering from Post Concussion Syndrome which is difficult to diagnose. Anyway, hope this is helpful.
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1 Reaction@aw1 Thank you for your response! I'll be sure to keep your points in mind. I wish you the best of luck.
Hoping you have found a solution by now and sorry for oversimplification here, but have been going through exact same thing and just found that I was severely dehydrated. Having water (even when I do think I have had enough) has been helping to some extent. Please see if this is something that may apply to you!
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1 ReactionGo to an MFR therapist try a couple until you get a good one. They need to strengthen your body and realign the muscles for you so you can strengthen your own body. The muscles glued together as we age and they need to be unglued. When they get unglued the pressure and painstops. Your balance returns.
Hi, 40m here. Sorry to hear of your ailments. I have been experiencing something very similar since Sept 5. Pressure is mostly in my forehead area. It has been constant and varying in severity but its always there. Then came the waves of "anxiety" just a feeling of immense mental discomfort. Complete lack of appetite or any desire at all. Stomach discomfort constipation, insomnia, breathless when talking, and a host of others. My last trip to urgent care they gave me some cocktail that included toradol. I felt pretty good for like 24 hours before it came back. It has been much less severe and thankfully has not returned to the previous extremes. Thinking the toradol helped, I began taking 800mg ibuprofen daily and they seemed to really help. Able to eat and sleep much better but still no appetite. Even a few moments where i acrually felt good, like myself but they came by and went quickly. They were a nice reminder of how things were tho. Triptans did nothing. Brain mri clean. Sinus ct showed some inflammation and a possible csf leak, but ent said it looked OK and my nose isnt usually running. Neuro has me on a course of prednisone right now, 60mg seem to have a similar effect as the ibuprofen, but the pressure is still constant but the other symptoms are very quiet. Gi had no answers, acupuncture and herbal extracts, vitamins, supplements, and still at a loss. I do vape and I cleaned my shower with bleach before symptoms began but still struggling to find anything else that effects the pressure one way or another. I will be sure to keep you updated if anything else and please do the same. Best of luck to you in your search.
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