I had labyrinthitis vertigo and this video explained so well the weird symptoms I experienced. The nausea at the start, the two weeks ir so of spinning, inability to track objects, difficulty telling the difference between forward and backward movement. The vestibular ocular reflex defect made me feel like my reality was on a half second delay. It took about 5 or 6 weeks for all the symptoms to completely go away, and even then I'd have trouble balancing, walking across a room in the dark. It's an very odd sensory experience because it's a system that works so seamlessly most of the time that you forget it exists. Vertigo was a much stranger experience and more reality altering than when I scatched my cornea and couldn't see for a week, or had a plugged ear from an infection. There's no great work-around when the vestibular sensory system is messed up, if you know what I mean.
My history of neurological disorders is probably worse than most guys who've posted here. Suffered a serious car crash aged 6. Thereafter developed a brain tumour - as a result have had to live with epilepsy for 42 years. Had 2 major brain operations in 1987 & 1992, however despite all that still enjoyed an active & normal - did kick boxing for many years but Fast fwd to feb 2021, i took a punch to the jaw, which my neurologist of 20 years diagnosed as Pcs. The pcs felt worse than my epilepsy - symptoms were brain fog, concussion, headaches, ear ringing, noise sensitivity & lack of balance / disequilibrium. I was out of work for 4 months, and returned in July 2021. My symptoms were brain fog, confusion, headaches, disequilibrium / balance issues and ear ringing. When it first happened, i felt like a zombie & disconnected, as if i was in a trance - the dizziness, brain fog, confusion, ear ringing, sensitivity to noise was very debilitating. My vestibular & occular faculties were badly disrupted. I have good days & bad days but i feel the symptoms are gradually getting better. Just the waywardness & lack of co ordination can sometimes be frustrating. I've spent over £1,000 in private treatment, consulting an Ent surgeon, cervical chiropractic doctor & undergoing vestibular rehab, (which has only slightly helped) - i believe it comes down to willpower. Also i dont get depressed anymore. The more anxious, fatigued & emotional you feel, the worse the symptoms. Be optimistic & believe with conviction you'll get better. I used to be a desktop support & telecomms engineer but can no longer do that - instead i've been given confined to a desk based job. I know its really upsetting & demoralising but if i can survive 2 brain operations, whilst suffering from epilepsy for over 40 years and live with a brain tumour, then in comparison this is nothing. There certainly is hope. I wish you & all other concussion / post concussion sufferers speedy recoveries.
Thank You Steve, I have severe Vestibular Damage due to Gentamicin Toxicity, I've saved your video to show my family members & friends so they can better understand my condition.
@@dannym6552 I was given Gentamicin due to serious infection from a perforated bowel to save my life, as I was so ill, no one noticed that the Gentamicin was affecting me. Now I need to be vigilant so I don't have any further exposure to any Aminoglycoside Antibiotics. Do the best I can each day, each day is physio for me, there are people far worse off than me.
Sharon - Mine has me doing some too ! I have also been having my neck & spine gently adjusted by a chiropractor and that seems to be helping, also - I was so dizzy, bad migraines & tinnitus all summer - it’s such a relief to be getting back to normal - I’m not 100% for sure, but better !
Is there anywhere in the US where the Electrovestibulography (EVestG) is being used. It measures vestibular response to horizontal pursuit and saccadic eye movements. Thanks!
I understand the complexity, but you should at least come up with a treatment of an infected balance nerve. Had that 2 weeks ago and it was both traumatic and scary and required hospitalization.
I have all the symptoms of CTE and fall all the time . Recently broke my hand in a fall . Being checked for MS also .Can not even close my eyes and stand up without falling . Don’t understand why . Ty for the video .
Any updates? And had you fallen at some point and lost consciousness/ hit your head? Has anyone in your family ever had any similar experiences and have you ever endured a stroke before?
BrainFacts.org, amazing explanation. This was mentioned 1400 years ago about Inner Ear and it's balance. Allah says:[Quran 18.11] Then We hit on their ears in the cave for a number of years.
![Anatomy | Physiology of the Utricle & Saccule [Otolithic Organs]](http://i.ytimg.com/vi/5iZAnn5HlVw/mqdefault.jpg)
![Anatomy | Physiology of the Utricle & Saccule [Otolithic Organs]](/img/tr.png)
I had labyrinthitis vertigo and this video explained so well the weird symptoms I experienced. The nausea at the start, the two weeks ir so of spinning, inability to track objects, difficulty telling the difference between forward and backward movement. The vestibular ocular reflex defect made me feel like my reality was on a half second delay.
It took about 5 or 6 weeks for all the symptoms to completely go away, and even then I'd have trouble balancing, walking across a room in the dark.
It's an very odd sensory experience because it's a system that works so seamlessly most of the time that you forget it exists. Vertigo was a much stranger experience and more reality altering than when I scatched my cornea and couldn't see for a week, or had a plugged ear from an infection. There's no great work-around when the vestibular sensory system is messed up, if you know what I mean.
I'm on my 4th month. Is different for some people. And then there's people that never recover
I'm 5 weeks into this. That delayed VOR is something I never imagined and hard to describe to anyone besides my physical therapist.
@@ErikaAnderson1 How are you now? Any improvement?
My history of neurological disorders is probably worse than most guys who've posted here.
Suffered a serious car crash aged 6. Thereafter developed a brain tumour - as a result have had to live with epilepsy for 42 years. Had 2 major brain operations in 1987 & 1992, however despite all that still enjoyed an active & normal - did kick boxing for many years but Fast fwd to feb 2021, i took a punch to the jaw, which my neurologist of 20 years diagnosed as Pcs. The pcs felt worse than my epilepsy - symptoms were brain fog, concussion, headaches, ear ringing, noise sensitivity & lack of balance / disequilibrium. I was out of work for 4 months, and returned in July 2021. My symptoms were brain fog, confusion, headaches, disequilibrium / balance issues and ear ringing. When it first happened, i felt like a zombie & disconnected, as if i was in a trance - the dizziness, brain fog, confusion, ear ringing, sensitivity to noise was very debilitating. My vestibular & occular faculties were badly disrupted. I have good days & bad days but i feel the symptoms are gradually getting better. Just the waywardness & lack of co ordination can sometimes be frustrating. I've spent over £1,000 in private treatment, consulting an Ent surgeon, cervical chiropractic doctor & undergoing vestibular rehab, (which has only slightly helped) - i believe it comes down to willpower. Also i dont get depressed anymore. The more anxious, fatigued & emotional you feel, the worse the symptoms. Be optimistic & believe with conviction you'll get better. I used to be a desktop support & telecomms engineer but can no longer do that - instead i've been given confined to a desk based job.
I know its really upsetting & demoralising but if i can survive 2 brain operations, whilst suffering from epilepsy for over 40 years and live with a brain tumour, then in comparison this is nothing. There certainly is hope. I wish you & all other concussion / post concussion sufferers speedy recoveries.
@@escoba1971 I’m going on 4 months , did you ever improve an how long did it take
Thank You Steve, I have severe Vestibular Damage due to Gentamicin Toxicity, I've saved your video to show my family members & friends so they can better understand my condition.
🌹 how did you get a gentamicin poisoning 😔🧐
@@dannym6552 I was given Gentamicin due to serious infection from a perforated bowel to save my life, as I was so ill, no one noticed that the Gentamicin was affecting me. Now I need to be vigilant so I don't have any further exposure to any Aminoglycoside Antibiotics. Do the best I can each day, each day is physio for me, there are people far worse off than me.
@@dannym6552 Gentamicin is well known for potential ototoxicity.
@@juliemathieson6289 So sorry. That must be miserable. Hope your nausea is under control.
off balance for 2 years, therapist showed me exercises for my eyes, it worked!
Sharon - Mine has me doing some too ! I have also been having my neck & spine gently adjusted by a chiropractor and that seems to be helping, also - I was so dizzy, bad migraines & tinnitus all summer - it’s such a relief to be getting back to normal - I’m not 100% for sure, but better !
Great information thank you so much for your feed back on vestibular system.
best explanation of otoliths hands down
I never knew that the ear system was so complicated. BTW, can the vestibular system be affected by cervical osteoarthritis at high levels?
Thank you Steve!
Fantastic explanation. Thank you!
i have idiopathic generalized epilepsy give me some suggestions sir for not get exitation
We do know why motion sickness happens; it's a threat response from the brain, much like pain, due to the mismatch in sensory information
Is there anywhere in the US where the Electrovestibulography (EVestG) is being used. It measures vestibular response to horizontal pursuit and saccadic eye movements. Thanks!
Thank you Steve.❤😀
Thanks alot !! Thats really helped me for studying!
Excellent video
Thank you
Good 😊
Thank you!!
I understand the complexity, but you should at least come up with a treatment of an infected balance nerve. Had that 2 weeks ago and it was both traumatic and scary and required hospitalization.
He's a neuroscientist, not a doctor.
And I am Karina and I like you. Thanks for sharing!
Hi karina
I have all the symptoms of CTE and fall all the time .
Recently broke my hand in a fall . Being checked for MS also .Can not even close my eyes and stand up without falling . Don’t understand why .
Ty for the video .
Any updates? And had you fallen at some point and lost consciousness/ hit your head? Has anyone in your family ever had any similar experiences and have you ever endured a stroke before?
I’ve seen enough CZcams videos of people trying to stay upright and composed on ice to know that the vestibular system doesn’t exist. 😊
how neurons are exites in our brain sir
How could that be your name
BrainFacts.org, amazing explanation. This was mentioned 1400 years ago about Inner Ear and it's balance. Allah says:[Quran 18.11] Then We hit on their ears in the cave for a number of years.
Allahuakbar!
Brain