Something behind my head...

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WanderingAround

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Hey guys, I wasn't sure where to post this (yes, I looked through all the sub topics), so I decided to go with General Health.

It's been on and off for as far back as I can remeraber, but it's gotten quite bad in the last couple months. I feel as if something is floating/being behind my head and upper spine. Sometimes I feel as if something is behind me, but it's usually just my upper back/head area. I know nothing is there, and I'm not "frightened" of it, and I don't particularly believe in paranormal activity so don't bring that up, please. I'm just wondering if anyone has had this/heard of this. I haven't been able to find anything on google.

Thanks
-Wandering
 
believe it or not, i DO understand exactly what you are describing. have you ever mentioned this 'perception" to your doc at all since this has been such a long ongoing feeling? the mere fact that what you seem to be actually perceiving simply is not a normal thing, i would possibly try seeking out a good neurologist perhaps?

there would more than likely(just to actually 'percieve" that anything is 'there' or percieving things like you are) some level of neurological affectation either from the brain, spinal cord or very particular nerves. so a neurologist would simply be a really good place to start in finding out just exactly what is really generating this perception? i can tell you just from my own experience with being born with what was a glob of blood vessels inside of my spinal cord, this created/generated really strange 'perceptions' for me like someone was actually trying to pry off my right shoulder blade with a crow bar or something? this really insane prying sensation that felt VERY honest to god sooo real to me it was almost like there was someone always standing behind me justa pryin away like 24/7? this prying thing did not actually even start until after the MRI was done and lasted about two years?

had no clue i even had this glob called a cavernous hemangioma til it simply showed up upon a c spine MRI that i had done when i herniated a disc in 2001? but my neurosurgeon told me that this little sucker WAS possible to create "perceptions' of things ONLY because it was IN my spinal cord. who knew? this "prying perception" DID finally go away after i ended up having to have the glob resected becasuse it was bleeding. but since then, i have found other little 'perceptionary feelings" of stuff just becasue of the spinal cord injury now. its kinda what it does depending upon what was impacted.

i am in no way saying that you have what i had, but i most certainly would seek out a good neuro and a possible MRI being done on the brain and the c spine at least. honestly, ya just have no real clue as to what we can have going on inside of our own bodies til ya get that good look inside any given area(for this, a good contrasted MRI would be great for both brain and c spine). hopefully whatever this is being generated by can at least be better explained for you. but DO get this better evaluated by at the very least, a good neurologist. good luck in finding the source of this, and please DO let me know just what you find out,K? FB
 
Sensory perception.Yes,have had similar experiences with that,especially when I was a little younger,like in my 20's.Seems to have dimmed,or at least I do not notice this anymore.I had several tests done,nothing was ever found.Seems like feelbad has some good sound info and advice.Hope you find what is troubling you!Have a good day too.
 
Thank you very much to both of you!
That is a lot of good information, feelbad. I'm glad you got it sorted out, mostly.

I think I'll bring it up with my health care provider next time I go, and see if she thinks anything might be amiss.
 
glad to help believe me. do not "just' mention or bring this up to your doc, make certain this perceptionary "thing' finally gets evaluated. if someone like only a mere primary feels that what you are feeling/displaying is not real critical or important, only because they do NOT have a freaking clue? they in most cases, wont 'do' for you the patient just what really IS NEEDED becasue they have never dealt with it or had any other patients who have what you are? and this just IS where YOU have to become your own advocate.

this is why you really DO need a referral to a neuro to start and that MRI of the brain and at the very least c spine level too? to simply even 'percieve" what you have and for soo very long just is usually a "something' that has possibly been there awhile too? but it does need to be MRIed just to see what is or is not possibly generating this that IS "seeable" upon MRI. this can be some issue with the actual cranial nerves too that run thru and innervate the sensory area where this is being 'felt' as well? but i really do personally feel just based upon how you described this and what i KNOW i was able to truely perceive as soo flippin real, that this has to be something neurological. so, MRI and a neuro referrals would be the very best ways to just get this identified.

you just gotta start somewhere here and this really IS what i would do if i were feeling/percieving things just knowing what I went thru before too? i just had NO freakin clue til i found a highly experienced with what I just had neurosurgeon who had seen what i had hundreRAB of times in my cord simply explain what IS possible to 'feel' with anything IN your spinal cord(but it is not 'only' cord stuff that can do this, that brain also has this capability depending upon what particular area may be impacted with "something"). he was also my third opinion too. he simply just had over 30 years of experience in TONS of the "neurological strange and insane stuff" since he was head teaching prof at the U of MN here too, also head of neurosurgery. i WAS dang lucky let me tell ya. the other two NSs i saw were just hugely under experienced with these and could not tell me much at all. the patients any given type of specialist simply sees and has REAL hanRAB on experience with over years during their own practice really ARE the best teachers to the specialists, ya know what i mean?

it was sheer durab luck that i actually was able to find this particular NS since he was going to retire in just a couple years after he did my resection surgery. things just 'came together" in all the right ways in even finding that 'perfect' doc for ME and MY problem. and that IS the key here with anything that YOU may have? getting a good specialist who simply does have the most experience in what YOUR problem actually just "is'.

but DO give your primary a bit of a push if it comes to that. you just DO need to at least to start, get the MRIs done to see if anything shows up? then let that MRI dictate from there just 'who" you see next. OR, if the primary wont go that route first. get a referral TO the neurologist who WILL want to do those two areas with an MRI scan and WITH contrast, esp for the brain.

what this really basically comes down to hon is in order to just even percieve what you are and have been for so long, something would have to be 'generating it'? testing and ruling in or out comes next. good luck with the primary WA, and please DO keep us posted. FB
 
Wow, feelbad, it looks like you went through a lot to get that sorted out. I'm really glad you did though. I'm still under my parents' insurance for a couple more years, so I ought to get it sorted out now rather than later I suppose.
I won't be able to go for a few months but I'll post back if something comes up.

Thank you for your awesome posts!
 
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