Head pressure is ruining my life

Posted by amandanap1 @amandanap1, Dec 1, 2023

Hello, im hoping that maybe someone can shed some light on this or offer advice if you have experienced the same thing as me.

For almost a year I have been dealing with unrelenting, severe head pressure. Not headaches, though I do get those sometimes. The head pressure is 24/7 and it lasts for months at a time, I get a week off, then it comes back even worse than before.

My symptoms:
head pressure
lightheadedness
vision disturbances (blurry vision, darkness around the edge of vision)
migraines
It feels as if my head is being squeezed and going to explode. It is extremely difficult to do daily activities, I cant concentrate, its taking my life from me. I have had an MRI, numerous CT scans and a lumbar puncture, all clear. If anyone has gone through something similiar and have found something that helps, I would love to hear it.

Interested in more discussions like this? Go to the Brain & Nervous System Support Group.

Profile picture for charl215 @charl215

@rwinney hi sorry know this is old did you find anything that helped?

Jump to this post

Hello @charl215. No worries about the post being old. Yes, for me, learning not to fuel the fire was a helpful first step. In other words don't give attention to symptoms AKA no pain behaviors. Pain behaviors are anything you do say or think that remind you of pain. Don't access the network. Stress management, cognitive behavioral therapy, physical exercise and learning how to properly breathe with diaphragmatic breathing we're all and still are important tools in my management. I realized that less was more in the medicine world and through Lifestyle Changes in forming new habits and the way I viewed pain helped reduce symptoms and gave me more power and tools to learn how to manage. Another important piece is positive distraction. Humor, fun... things that give your brain a vacation because pain is tough and you got to pull out all the stops for it. Hope this helps! Please don't hesitate to let me know if you have questions. Stay hopeful. 😊

REPLY
Profile picture for charl215 @charl215

@rwinney hi sorry know this is old did you find anything that helped?

Jump to this post

@charl215 Also, here's info on progressive muscle relaxation. Knowing how to release tension can be super helpful, especially for migraine.
https://www.webmd.com/sleep-disorders/muscle-relaxation-for-stress-insomnia
Have you tried any types of relaxation methods?

REPLY

Did this go? Did they ever find out ehat it was?

REPLY
Profile picture for Rachel, Volunteer Mentor @rwinney

@charl215 Also, here's info on progressive muscle relaxation. Knowing how to release tension can be super helpful, especially for migraine.
https://www.webmd.com/sleep-disorders/muscle-relaxation-for-stress-insomnia
Have you tried any types of relaxation methods?

Jump to this post

@rwinney thank you very much. I have tried it all 🙁 it just doesnt go. I joined yoga and pilates too. Done acupuncture. Physio. Its their constant.

REPLY
Profile picture for charl215 @charl215

@rwinney thank you very much. I have tried it all 🙁 it just doesnt go. I joined yoga and pilates too. Done acupuncture. Physio. Its their constant.

Jump to this post

@charl215 you say it's been about 5 months, right? Are you working with a neurologist yet?

REPLY
Profile picture for cl24 @cl24

Omg...I sometimes feel like I'm the only one who suffers like this. I've had migraines for about 5 years now. But this past year has been the absolute worse. I literally live with the horrible pressure...dizziness ...blurred vision, vomiting & horrible pain every single day now. And I've tried everything from triptans, muscle relaxers, monthly shots, Botox & most recently vylepti. Tho the botox & vylepti relieve a bit for a few weeks. Nothing has done much for relief yet & I really have no life anymore. I'm in soooo much pain everyday now, I just don't know what to do....I'm so miserable 🙁

Jump to this post

@cl24 I am experiencing the same. I am hoping for a cure for all of us one day. Try to remain as positive as possible even though it’s hard.🤗🙏

REPLY
Profile picture for Rachel, Volunteer Mentor @rwinney

@charl215 you say it's been about 5 months, right? Are you working with a neurologist yet?

Jump to this post

@rwinney yes neurologist and ent surgeon and physiotherapist and sports therapist. Neurologist just prescribes me medication but it doesnt do anything been on lots.

REPLY
Profile picture for charl215 @charl215

Hi I know this is old sorry but did you ever find out what it was. Ive had this for like 5 months now head ct ans head mri all clear. Having physio nothing works. Did you find out or something that works thanks?

Jump to this post

@charl215
I have been thru many many CT Neuroligist. No one can figure me out. Gabipintin took the pressure to a lessor pressure. So NO they did not find anything and I am on month 9 still trying to figure this out. I had to take up smoking Canibis it takes my mind of the pressure I got off all the meds the doctors subscribed to me and just smoke it is relaxing and so far the best I can do. please let me know if you figured something out.

REPLY
Profile picture for tamjojoadar @tamjojoadar

@charl215
I have been thru many many CT Neuroligist. No one can figure me out. Gabipintin took the pressure to a lessor pressure. So NO they did not find anything and I am on month 9 still trying to figure this out. I had to take up smoking Canibis it takes my mind of the pressure I got off all the meds the doctors subscribed to me and just smoke it is relaxing and so far the best I can do. please let me know if you figured something out.

Jump to this post

@tamjojoadar oh gosh really bless ya. Sorry to hear that im in the same boat another mri scan next week. Will do ill take a note of it and let you know if get anything else. Yes they was going to put me on that and have gave me noritrpyline instead. Ive been on amitriptyline but that made me dizzy. Honestly its constant.

REPLY
Profile picture for Rachel, Volunteer Mentor @rwinney

Hello @charl215. No worries about the post being old. Yes, for me, learning not to fuel the fire was a helpful first step. In other words don't give attention to symptoms AKA no pain behaviors. Pain behaviors are anything you do say or think that remind you of pain. Don't access the network. Stress management, cognitive behavioral therapy, physical exercise and learning how to properly breathe with diaphragmatic breathing we're all and still are important tools in my management. I realized that less was more in the medicine world and through Lifestyle Changes in forming new habits and the way I viewed pain helped reduce symptoms and gave me more power and tools to learn how to manage. Another important piece is positive distraction. Humor, fun... things that give your brain a vacation because pain is tough and you got to pull out all the stops for it. Hope this helps! Please don't hesitate to let me know if you have questions. Stay hopeful. 😊

Jump to this post

@rwinney I would suggest Clincial Massage Therapy. once a month I go, the best help, relax
she works on my head, shoulders.. Best to you. I suffer from ON very painful, I agree with our attitude can change help or hurt us. I have made a practice of not telling anyone expect my husband I am feeling bad, I know it will get getter, I do take nerve block shorts, do
exercise daily for neck and head. try and relax, it doesn't come easy.
Thinking about you a fellow sufferer. From Northern Ca.

REPLY
Please sign in or register to post a reply.