Ménière’s disease has ruined my life, I’m bilaterally affected, had all treatments including skull surgery that failed miserably! Now house bound. Completely deaf this disease is the worst I would not wish it on my worst enemy.
I am so sorry. I believe I have this in one ear and am working to get the doctor’s to believe that it’s not just BPPV, which is what I’ve been treated for to this point. I hope you find some peace in your state, because I too would not wish even the lesser ailment of one ear’s symptoms on anyone.
Oh wow, i am so sorry to hear that. I have it but not as bad as you have it. I hope it doesnt get worse as i get older. I just turned 60 and have had it since 2013. How old are you ?
A lot of people find relief by getting their necks adjusted with upper cervical care. Especially if you have been in car accidents or hit your head playing sports or slipping on the ice. Any head impact also affects the top bone in your neck the atlas which can cause it to get locked out of position and interfere with the brain stem. It has given me my life back from post concussion issues.
I had this disease due to infection in my root canal tooth. After removing the cap and clearing the infection I’m feeling fine. Please highlight this comment let this help everyone.
This disease sucks I have it and everyday is a struggle, prayers for anyone else who has this shit but I think this video had the best information in a short time.
@@lezelldraai1513 if your asking me? I still have it, I got it from COVID in 2021 but I was told that if it's from a viral infection that niacin and vitamin b1 helped a lot, I took it for 3 months and I only get some dizziness and a little off balance feeling.
I wish there's more awareness about this disease...crazy how someone can get it out of nowhere...and it's incurable... Really hoping for cure one day...
I have been suffering with this crazy disease for more than 4 years now. Tried almost everything but this stubborn disease left you shattered with your buried confidence and ongoing self doubt. You loose all control from your body and get scared all the time. Now I have shifted to ayurvedic medicine which seems to have positive impact. Hopefully it will be cured.
Some days I feel like I'm wearing a pair of brand new squishy running shoes. I get very unstable. That's one sign it's coming on. Yes, this disease is nothing I'd wish on my worst enemy.
That last comment: "as long as you strive to get better..." - You can strive as hard as you like, and certain symptoms, like deafness and brain fog, will just get worse, or you will develop vestibular migraine, which adds insult to injury. What kind of striving are you suggesting? It's a chronic, erratic, deteriorating condition that can be very disabling and isolating. It's also invisible to a great extent, and there is no concensus as to its cause.
How do you know that you've developed vestibular migraines? My doctor thinks I have both but he can't event tell the difference between them to diagnose.
@Elizabeth-yx5on It is difficult to separate the two conditions, and they influence each other, but if your MD is being ramped up by VM, you might notice the following: stiff/sore neck coinciding with louder tinnitus and dizziness, flashes of light and more blurred vision. I often get a numb patch on scalp, too. Tiredness, stress, and foods containing tyramine will bring it on or make it worse. I think I have a permanent VM that ramps up and down, but I keep the worst at bay with 40mg of Propranalol each morning and occasionally evening. Propranolol works well, but side effects can be tiredness and slower meatabolism. There are other migraine meds that might work - even Botox - think I tried Nortriptyline, but it made me feel awful. Do fluorescent lights, like in the supermarket, make you feel bad/sick?
3 months ago I started having spells of vomiting and severe dizziness and feeling seasick...was put on medicine and now walk with a cane to keep my balance..I've tried dozens of suggested cures but so far nothing works...now prepared to have this infliction indefinitely...
I'm 23 years old and i was diagnosed with this disease😢 Really changed my life, made me depressed every day and couldn't sleep for a month. Please anyone who suffers from the same disease, can this disease be cured? And have you recovered now? Please advise me what should I do after suffering from it for one month😢
@@TheKing-rj6ztThat's great to hear! I'm really glad you're feeling better from the vertigo. Take care of yourself and keep up the good progress!! 👍🏻 When I turned 24 it's become part of my life now I'm little better only..but I can't do anything like you youngers.. suddenly vertigo happens and I can't talk loudly breathing problem alao happened. What hurts me most I walk and act like old aged people....But their are old aged people who walk very healthy but they don't have my vertigo 😔 what hurts most is nobody understanding...But one thing I'm happy when I started praying to God He healed my vertigo half not fully!! Please pray pslam 91 everyday
@@kirthika2379 OH dear I know I know how hard it is!!!! I'm soo sorry!! Please check your hb and vitamin D level!!!! Then please visit any Doctor Please be strong.. It's going to be alright!!!
I have been suffering from Meniere's for last 3 years. Have constant ringing ie tinnitus 24hours a day. Unpredictable Vertigo attacks almost every week for 2 years and it lasted for hours , had to go hospital for stemetil vaccine very frequently. I ruined my everyday life. Last month I was bound to bed for whole month due to daily episodes of vertigo, had to go to hospital almost daily. Thats when my ENT suggested surgery . I had Labyrynthectomy last month and after a month my vertigo attacks have stopped. Its to soon to say but my ENT says that vertigo will stop now. Though tinnitus is present and hearing in my affected ear is lost but relief from vertigo was our main motive. I am suffering from balance problem in walking after surgery but my ENT says it will recover as soon as other ear alone will take over the role of balance the body. Hoping that it may be the end of this dreadful disease and life become normal again. I suggest to get surgery if hearing in affected ear is beyond service.
@@daisuki_coco Not good. Not used of it. Got hearing from both ears my whole life. Now suddenly this change. I can't locate the source of sound. All noise seem like they are coming from my good ear . Not a good feeling
@@Jyothsna7868 In recovery stage. Vertigo has stopped since surgery. May be it won't come back. Balance is certainly off and taking time to get to a stable stage. Doing vestibular rehabilitation exercises . Being deaf in one ear is not feeling good
My grandmother has it too! Had it go away on myself for about 8 months but I've had some attacks the past few days. Learning that there's people out there who are going through the same thing in terms of it advancing is comforting.
I had Meniere's for 17 years now on the 1st year I got hit twice by cars when commuting because of this disease thankfully only with minor injuries but it made me dislike leaving my house out of fear that it may happen again. I hated going to school as well because its hard to concentrate and hear teachers now I feel like I'm in a fog its hard to learn anything but I have to keep fighting not for me but for my loved ones.
My first attack came suddenly without any sense that something was about to happen. The room span round and I immediately found myself on the floor feeling nauseous and sweating profusely. The spinning sensation didn't stop so I couldn't get up. It was about ten minutes before I could crawl to my phone to ring for an ambulance as I didn't know what was happening to me. The hospital wasn't very helpful in diagnosing the cause. They suggested I had become de-hydrated. I made sure I was drinking plenty but a couple of months later I had an identical attack followed by another a week later. By now I had come across Meniere's on the internet which seemed to describe my own experience accurately. My doctor agreed it could be the problem so prescribed me Betahistine which I take daily. It is now three years since my last attack occurred so It seems the Betahistine is controlling it.
I was diagnosed with this disease 1 mnth back. Immediately i went to homeopathy and started using medicines,as i have no better option in allopathy for long term Doing meditation and bhramari for better results. Using vertiford 16 tablet for immediate relief as per doctor suggestion. And also doing some yogasana's and exercises which i found in youtube for this disease. I Hope my comment will be usefull for any one. il share the youtube links in the next comment if any one would like to try
I have battled this disease over 25 years with vertigo, fullness in ears especially left, constant tinnitus, balance issues. I take meclizine, diazepam and water pills everyday but now something different is happening. It is like my eyes aren't working right, I was just sitting and bam a sudden violent vertigo and then it stopped. My head even moved with it. Sometimes I feel like speech is being effected. Anyone else experiencing this. My attacks can last for hours or for days it's a battle to keep it a bay. I have had 2 gentamicin shots and a stint in ear. When does it end.
I just started taking ginko and Lions mane along with Lipo flavonoid suggested by my ENT. I am also going to start taking allergy shots to see if that helps. I was really heartbroken when he said there was no cure.
@@sofiabhagat8912 Yes it is 100%. Although i have to admit, i got a call from my Neurologist out of the blue one day and he told me i had the beginning stages of hydrocephalus which is basically water on the brain. I dont think they have anything to do with Vertigo but it has similar symptoms. But if i were you, i would try getting weekly allergy shots along with the items i laid out and see what it does for you.
So my hearing just "went out" the other day. Absolute silence. It's happened before but I wasn't concerned, this is the third time now. For me its a switch, on/off. I cant hear a damn thing. 500db.. WHAT?
I've had vertigo in the past, it's horrible but never accompanied with tinnutus. I woke up a few days ago with a high pitch on my right ear (the type of pitch you get when something loud shocks your ear- like a crying screaming toddler). My right ear now feels pressured too. Sometimes during the day I do not notice the pitch, I try to keep busy. Early this morning I felt the pitch on my left ear too. This is frustrating and I really hope it goes away, cannot imagine living like this.
feel better for 2weeks i was so happy thinking that my vertigo was not caused by Meniere, then it attacked again very badly and i couldn't go to work for 4days
I think I might have this. I always get vertigo on elevators. Or anything that lifts me into the air. I can't use lights at work, because I get vertigo and feel dizzy and lightheaded after using it. Elevators are the worst though. I also have tinnitus
I was diagnosed 4 years ago, I visited several otolaryngologist but finally one doctor prescribed me Serc (Betahistine), I have been taking it for 1 year and the vertigo episodes have substancially reduced in frequency, duration and strength. I am not buying Serc because it is very expensive, but in generic versions (here in Mexico it's easy to find and buy without a prescription) and I am getting 28 pills for 15 usd, that is enough for 1 month. At the begining, some doctors, in Mexico and US prescribed me the Serc for 2 or 4 weeks, but my last doctor told me that this should be for the rest of my life.
Thank you for mentioning Betahistine. I tried it for a while and it seemed to help. I will start taking it again because it is now worse, especially my hearing.
Not sure how i got my 1 day was just getting 1 up and felt dizzy then buzzing in my ears had to grab hold off something before i fell down. But i have felt sick as well but not been sick
I think I have it,because I sometimes get an unexplained fulness in my right ear for some hours and it just magically dissapears without a trace and it comes back after some months (not a eustachian tube dysfunction though)
will Meiners Disease cause Alzheimer’s later on? I’m going to be 47 years old and struggling with this now for a Year now? I was just Diagnosed with Meiners Disease and very Angry thinking it will cause Alzheimer’s later on?
I like your chanel very much because you have many videos that make me learn different types of diseases which eventually makes us safe.That is why I liked and subscribed your chanel.👍👍👍👍👍👍👍
I might have Meniere's disease without vertigo. I have sudden sensorineural hearing loss in lower frequencies, loud high whistling tinnitus, and a feeling and sound of a large underwater bubble in one ear when I shake my head. Can hearing aids help?
I hear a constant tone all the time, dizziness from time to time and the fullness in the ear from time to time. Menieres runs in my family but thankfully i have it only in 1 ear and not both. What a hell to carry on my genes.
The cause is actually the Epstein Barr virus inflaming the cranial nerves, mainly the vagus nerve. The cure is to stop eating many troublemaker foods like eggs, dairy, pork, oils, salt, msg etc and heal with specific fruits and vegetables
I think so too! I’ve had this awful disease for twenty years I was drinking a lot of lemon. Than I stopped had t had a episode for over a year. Three weeks ago I had lemon and I thought I was going to die the vomiting and vertigo was so bad my whole body was shaking..😭😭😭I feel for everyone who had this terrible disease..🙏🙏🙏
Why do they keep banging on about vertigo & dizziness? I don't have that at all. Just the annoying ringing in the ear which is stopping me from sleeping even an hour.
Food is a trigger for me. I've lost 40 lbs in the last three months. I get noise discomfort, tinnitus, hearing loss nausea 🤮. I'm on the struggle 🚍. It's gotten worse every year.
I also have meneires disease. I’ve been through periods where you have all the typical symptoms: loss of hearing, vertigo, nausea, etc etc. I also have bad allergies and am on three meds to control them. The biggest pain was finding a good ENT doctor who understood this disease. Most of them have no clue, they don’t know what causes it and there is no cure. You have to almost teach yourself the dos and donts. Watch your salt and sugar intakes very very important since salt brings on the water. Also if you have meds for allergies take them as directed never miss a pill or spray or shot. I’ve been reading lately there is a correlation between allergies and meneires and personally I’ve found keep your allergies in check and the meneires seems to quiet down. Not go away but at least you get a break. Bright lights are also a trigger. The worst as I’m sure we’ll all agree is the directional vertigo aka “the spinning”. I have to use hearing aids since my hearing has tanked over the last couple of years. They help somewhat. One last thing seems to be some connection between barometric pressure and meneires. Who knows? Apparently no one. I hope some of my findings help someone and we just gotta hang in there!
Ménière’s disease has ruined my life, I’m bilaterally affected, had all treatments including skull surgery that failed miserably! Now house bound. Completely deaf this disease is the worst I would not wish it on my worst enemy.
Are you deaf now
Search Parveen surana on TH-cam you will feel blessed may be you will hear again after his treatment
I am so sorry. I believe I have this in one ear and am working to get the doctor’s to believe that it’s not just BPPV, which is what I’ve been treated for to this point. I hope you find some peace in your state, because I too would not wish even the lesser ailment of one ear’s symptoms on anyone.
Oh wow, i am so sorry to hear that. I have it but not as bad as you have it. I hope it doesnt get worse as i get older. I just turned 60 and have had it since 2013. How old are you ?
I also have this disease. 😢
A lot of people find relief by getting their necks adjusted with upper cervical care. Especially if you have been in car accidents or hit your head playing sports or slipping on the ice. Any head impact also affects the top bone in your neck the atlas which can cause it to get locked out of position and interfere with the brain stem. It has given me my life back from post concussion issues.
I learned in 4 5 minutes the topic I kept hearing and felt was complex in ENT lectures , that's how topics should be taught in classes as well ❤️
I had this disease due to infection in my root canal tooth. After removing the cap and clearing the infection I’m feeling fine. Please highlight this comment let this help everyone.
Wow, can I ask if your root canal was already giving you pain/discomfort?
@@daisyalicia yes i used to get pain most of the times
This disease sucks I have it and everyday is a struggle, prayers for anyone else who has this shit but I think this video had the best information in a short time.
Hi there. Are you rid of Miniers, and if so how did you do it? Im suffering now for years.
@@lezelldraai1513 if your asking me? I still have it, I got it from COVID in 2021 but I was told that if it's from a viral infection that niacin and vitamin b1 helped a lot, I took it for 3 months and I only get some dizziness and a little off balance feeling.
Checked for root canal infection if you’ve done one
@@christbuilds7409how about now?, I have symptoms like this and sometimes I have thoughts of ending it all.
I wish there's more awareness about this disease...crazy how someone can get it out of nowhere...and it's incurable...
Really hoping for cure one day...
Look up the medical medium he tells you the true root cause and how to heal. Many people have healed this fully.
Fr I’ve had it since 2021
@@beepboop9519how are you right now, my mom got it and im so stressed on how i can help her
I have been suffering with this crazy disease for more than 4 years now. Tried almost everything but this stubborn disease left you shattered with your buried confidence and ongoing self doubt. You loose all control from your body and get scared all the time. Now I have shifted to ayurvedic medicine which seems to have positive impact. Hopefully it will be cured.
Which ayurvedic medicine??
Some days I feel like I'm wearing a pair of brand new squishy running shoes. I get very unstable. That's one sign it's coming on. Yes, this disease is nothing I'd wish on my worst enemy.
That last comment: "as long as you strive to get better..." - You can strive as hard as you like, and certain symptoms, like deafness and brain fog, will just get worse, or you will develop vestibular migraine, which adds insult to injury. What kind of striving are you suggesting? It's a chronic, erratic, deteriorating condition that can be very disabling and isolating. It's also invisible to a great extent, and there is no concensus as to its cause.
How do you know that you've developed vestibular migraines? My doctor thinks I have both but he can't event tell the difference between them to diagnose.
@Elizabeth-yx5on It is difficult to separate the two conditions, and they influence each other, but if your MD is being ramped up by VM, you might notice the following: stiff/sore neck coinciding with louder tinnitus and dizziness, flashes of light and more blurred vision. I often get a numb patch on scalp, too. Tiredness, stress, and foods containing tyramine will bring it on or make it worse. I think I have a permanent VM that ramps up and down, but I keep the worst at bay with 40mg of Propranalol each morning and occasionally evening. Propranolol works well, but side effects can be tiredness and slower meatabolism. There are other migraine meds that might work - even Botox - think I tried Nortriptyline, but it made me feel awful. Do fluorescent lights, like in the supermarket, make you feel bad/sick?
The biggest symptom is the false hope that it's treatable, or will ever get better.
Vertigo can make you feel deathly ill. So dizzy.
Vertigo is absolutely terrifying 😪
3 months ago I started having spells of vomiting and severe dizziness and feeling seasick...was put on medicine and now walk with a cane to keep my balance..I've tried dozens of suggested cures but so far nothing works...now prepared to have this infliction indefinitely...
i have meniere's i just got thru a flare up this vid is very useful for making me feel like i can still function on a day to day basis
Such a beautifully animated, informative video! Love the characters, their facial expressions are perfect!! ❤️
I'm 23 years old and i was diagnosed with this disease😢 Really changed my life, made me depressed every day and couldn't sleep for a month. Please anyone who suffers from the same disease, can this disease be cured? And have you recovered now? Please advise me what should I do after suffering from it for one month😢
Im suffering it from almost 5 yrs til now no cure just acceptance and continue to life wishing someday they find cure for this.
Living with it for 41 years now...
It completely took my young life..now turned 24 ... nobody understanding 😢
@@Lisa07-sRobbed mine too, but got better as I got older, i’m 26.
@@TheKing-rj6ztThat's great to hear! I'm really glad you're feeling better from the vertigo. Take care of yourself and keep up the good progress!! 👍🏻 When I turned 24 it's become part of my life now I'm little better only..but I can't do anything like you youngers.. suddenly vertigo happens and I can't talk loudly breathing problem alao happened. What hurts me most I walk and act like old aged people....But their are old aged people who walk very healthy but they don't have my vertigo 😔 what hurts most is nobody understanding...But one thing I'm happy when I started praying to God He healed my vertigo half not fully!! Please pray pslam 91 everyday
@@Lisa07-sI'm Just 20 dealing with this shit in both ears..I hate my life now 😢 i think death is better
@@kirthika2379 OH dear I know I know how hard it is!!!! I'm soo sorry!! Please check your hb and vitamin D level!!!! Then please visit any Doctor Please be strong.. It's going to be alright!!!
I'm Japanese. Every day is painful. I hope you can figure out a cure soon.
Being Japanese ain’t that bad. Hang in there ;)
Get well and be strong!
@@SGUSOMUSAlol
I have been suffering from Meniere's for last 3 years. Have constant ringing ie tinnitus 24hours a day. Unpredictable Vertigo attacks almost every week for 2 years and it lasted for hours , had to go hospital for stemetil vaccine very frequently. I ruined my everyday life. Last month I was bound to bed for whole month due to daily episodes of vertigo, had to go to hospital almost daily. Thats when my ENT suggested surgery . I had Labyrynthectomy last month and after a month my vertigo attacks have stopped. Its to soon to say but my ENT says that vertigo will stop now. Though tinnitus is present and hearing in my affected ear is lost but relief from vertigo was our main motive. I am suffering from balance problem in walking after surgery but my ENT says it will recover as soon as other ear alone will take over the role of balance the body. Hoping that it may be the end of this dreadful disease and life become normal again. I suggest to get surgery if hearing in affected ear is beyond service.
what is it like being fully deaf in one ear?
@@daisuki_coco Not good. Not used of it. Got hearing from both ears my whole life. Now suddenly this change. I can't locate the source of sound. All noise seem like they are coming from my good ear . Not a good feeling
@@Jyothsna7868 In recovery stage. Vertigo has stopped since surgery. May be it won't come back. Balance is certainly off and taking time to get to a stable stage. Doing vestibular rehabilitation exercises . Being deaf in one ear is not feeling good
@@Jyothsna7868 yes for more than a year. Not helped much
@@Jyothsna7868 yes I followed a low salt, low caffeine,zero smoke,zero liquor, zero cheese, zero chocolate diet for long. Didn't help much
my grandmother suffer this, and i had some symptoms since i was a teenager... hope it to not advance much
My grandmother has it too! Had it go away on myself for about 8 months but I've had some attacks the past few days. Learning that there's people out there who are going through the same thing in terms of it advancing is comforting.
I had Meniere's for 17 years now on the 1st year I got hit twice by cars when commuting because of this disease thankfully only with minor injuries but it made me dislike leaving my house out of fear that it may happen again. I hated going to school as well because its hard to concentrate and hear teachers now I feel like I'm in a fog its hard to learn anything but I have to keep fighting not for me but for my loved ones.
Very informative video
Yes this is what I feel anytime anywhere. I'll go to the doctor
Please find a cure as fast as possible! Right now, all i want is to blow my brain out afther hearing Tinnitus all day!
Just apply finger pressure just back of ear. U find a hole , press it 30sec in circular direction❤❤
I know it's terrible ringing in the ears
Check for root canal infection. Worked for me
My first attack came suddenly without any sense that something was about to happen. The room span round and I immediately found myself on the floor feeling nauseous and sweating profusely. The spinning sensation didn't stop so I couldn't get up. It was about ten minutes before I could crawl to my phone to ring for an ambulance as I didn't know what was happening to me. The hospital wasn't very helpful in diagnosing the cause. They suggested I had become de-hydrated. I made sure I was drinking plenty but a couple of months later I had an identical attack followed by another a week later. By now I had come across Meniere's on the internet which seemed to describe my own experience accurately. My doctor agreed it could be the problem so prescribed me Betahistine which I take daily. It is now three years since my last attack occurred so It seems the Betahistine is controlling it.
What does of Betahistine are you on?
I hate this disease I'm sick of the dizziness
Lately mine feels like it just won't stop!!! Food seems to make it worse. Ugh
I was diagnosed with this disease 1 mnth back. Immediately i went to homeopathy and started using medicines,as i have no better option in allopathy for long term Doing meditation and bhramari for better results. Using vertiford 16 tablet for immediate relief as per doctor suggestion. And also doing some yogasana's and exercises which i found in youtube for this disease. I Hope my comment will be usefull for any one. il share the youtube links in the next comment if any one would like to try
How are you feeling now?...what all medicines are you taking?
Check for your root canal infection if you have this disease. Came back to let others know about this
Amazing you say this I’ve had it for 6 months and foound put a month back I have an infection in a root canal tooth
Did this happen to you? You needed a root canal and thought you had Meniers? Also did you already have root canal pain/discomfort or no ?
I only have tinnitus and dizziness. Nothing else. I wonder if it is menniéres as my dad does have it, or of it's something else.
I seem to have this only too
Hey i have the same thing recently been months, you got cured?
Same here, only those 2.
Did u find out if it was something else? I have same
I have battled this disease over 25 years with vertigo, fullness in ears especially left, constant tinnitus, balance issues. I take meclizine, diazepam and water pills everyday but now something different is happening. It is like my eyes aren't working right, I was just sitting and bam a sudden violent vertigo and then it stopped. My head even moved with it. Sometimes I feel like speech is being effected. Anyone else experiencing this. My attacks can last for hours or for days it's a battle to keep it a bay. I have had 2 gentamicin shots and a stint in ear. When does it end.
It’s been 6 months for me 😢
Check for root canal infection. Clearing infection cured my menieres
Bilateral. Wearing hearing aids. Some days much worse than others. Can’t seem to get people around me to understand it is a disability.
Superb explanation......
I have vestibular/Meniere's disease. And i have porphyria , and thyroidproblems, on eltroxins for 32 years now. Was fir surgery 32 years ago
After surgery hv u recovered?
I just started taking ginko and Lions mane along with Lipo flavonoid suggested by my ENT. I am also going to start taking allergy shots to see if that helps. I was really heartbroken when he said there was no cure.
is it helping?
@@sofiabhagat8912 Yes it is 100%. Although i have to admit, i got a call from my Neurologist out of the blue one day and he told me i had the beginning stages of hydrocephalus which is basically water on the brain. I dont think they have anything to do with Vertigo but it has similar symptoms. But if i were you, i would try getting weekly allergy shots along with the items i laid out and see what it does for you.
So my hearing just "went out" the other day. Absolute silence. It's happened before but I wasn't concerned, this is the third time now. For me its a switch, on/off. I cant hear a damn thing. 500db.. WHAT?
lol 500 decibels is like a nuclear explosion going off from 250 feat away.
Just brilliant
I had this for 2 months straight for 3 years, just know that you are not alone and it will get better everybody 🦾.
So every 2 months straight once a year for 3 years?
I've had vertigo in the past, it's horrible but never accompanied with tinnutus. I woke up a few days ago with a high pitch on my right ear (the type of pitch you get when something loud shocks your ear- like a crying screaming toddler). My right ear now feels pressured too. Sometimes during the day I do not notice the pitch, I try to keep busy. Early this morning I felt the pitch on my left ear too. This is frustrating and I really hope it goes away, cannot imagine living like this.
How is it going now?
It got better and I thought that was it. I was wrong, it has got worse now and really frustrating me, it's also affecting my left ear too😔.
@@cm6995 me too. I think it is enf radiation. Smart meter and 5g
Is your tinnitus 24/7?
feel better for 2weeks i was so happy thinking that my vertigo was not caused by Meniere, then it attacked again very badly and i couldn't go to work for 4days
I think I might have this. I always get vertigo on elevators. Or anything that lifts me into the air. I can't use lights at work, because I get vertigo and feel dizzy and lightheaded after using it. Elevators are the worst though. I also have tinnitus
So often they claim menieres is periodic, mine is 24/7, drunk giddy with tinnitus all the time, no let up whatsoever
Yea the vertigo is 24/7, idk where they getting this periodically thing from
Great video, keep it up! #freemededucation
I have this and it's hell on earth. I'm only 24. :(
Same here
Had since I was 21 🫤
I was diagnosed 4 years ago, I visited several otolaryngologist but finally one doctor prescribed me Serc (Betahistine), I have been taking it for 1 year and the vertigo episodes have substancially reduced in frequency, duration and strength. I am not buying Serc because it is very expensive, but in generic versions (here in Mexico it's easy to find and buy without a prescription) and I am getting 28 pills for 15 usd, that is enough for 1 month. At the begining, some doctors, in Mexico and US prescribed me the Serc for 2 or 4 weeks, but my last doctor told me that this should be for the rest of my life.
Thank you for mentioning Betahistine. I tried it for a while and it seemed to help. I will start taking it again because it is now worse, especially my hearing.
@@joannegild8001 it doesn’t help for the hearing, it does for Vertigo
@@albertogamboa9516 Thank you.
Xanax also works
@@TheKing-rj6zt I don’t know if it works for vertigo. But it’s addictive.
Not sure how i got my 1 day was just getting 1 up and felt dizzy then buzzing in my ears had to grab hold off something before i fell down. But i have felt sick as well but not been sick
I think I have it,because I sometimes get an unexplained fulness in my right ear for some hours and it just magically dissapears without a trace and it comes back after some months (not a eustachian tube dysfunction though)
So if i only have it every other week and the vertigo only lasts 5 minutes but the tinitus lasts 20, is it onset of the disease?
will Meiners Disease cause Alzheimer’s later on? I’m going to be 47 years old and struggling with this now for a Year now? I was just Diagnosed with Meiners Disease and very Angry thinking it will cause Alzheimer’s later on?
Pure awesomeness ✨
I don't feel spinning, but i always feel swaying
I like your chanel very much because you have many videos that make me learn different types of diseases which eventually makes us safe.That is why I liked and subscribed your chanel.👍👍👍👍👍👍👍
I'm sick of this it makes me wish for death I can't live with this
Me neither, taking naps is only time I look forward to cause I don’t have to deal with it while sleeping
im feeling like im in an elevator and its not episodic it just doesnt stop and worsens when i look down is this merniere's?
I have Meniers and get a similar feeling,like I’ve got off an escalator! Hope things improve for you soon
why does people not try surgery as the video shows, and they still suffer?I Mean for difficult cases?
Water pills might help, yet it's been suggested that herpes might be to blame and that antiviral medications will help overall.
It’s the worst! Diagnosed after terrible bout of mono.
Please tell me the cure.
In my case it lasted for 3 months only buy the left ear is dead for over an year now
Did you have hearing issues when it originally started?
I might have Meniere's disease without vertigo. I have sudden sensorineural hearing loss in lower frequencies, loud high whistling tinnitus, and a feeling and sound of a large underwater bubble in one ear when I shake my head. Can hearing aids help?
I was so interesting when i was watching 🥺🥺🥺.. Thank you for making medicine easier and funny 🥰🥰🥰
this is so cool
I hear a constant tone all the time, dizziness from time to time and the fullness in the ear from time to time.
Menieres runs in my family but thankfully i have it only in 1 ear and not both. What a hell to carry on my genes.
It's a cause of if you eat or drink Citric acid
How do you know this? This is interesting 🤔
The cause is actually the Epstein Barr virus inflaming the cranial nerves, mainly the vagus nerve. The cure is to stop eating many troublemaker foods like eggs, dairy, pork, oils, salt, msg etc and heal with specific fruits and vegetables
I think so too! I’ve had this awful disease for twenty years I was drinking a lot of lemon. Than I stopped had t had a episode for over a year. Three weeks ago I had lemon and I thought I was going to die the vomiting and vertigo was so bad my whole body was shaking..😭😭😭I feel for everyone who had this terrible disease..🙏🙏🙏
meniere disease got worse recently and i was drinking lemon water everyday.
I will stop drinking lemon water., thank you for this info.
Why do they keep banging on about vertigo & dizziness? I don't have that at all. Just the annoying ringing in the ear which is stopping me from sleeping even an hour.
then you just have tinnitus
Google John of Ohio protocol.
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I wonder how many might also have had Herpes????????????
If that was an attempt at humor, it was a big fail
No actually no humor. There are scientific papers who analysed it light come from the herpes virus. Take l lysin everyone
Parte in italiano che mi interessa ma non vi capisco
Food is a trigger for me. I've lost 40 lbs in the last three months. I get noise discomfort, tinnitus, hearing loss nausea 🤮. I'm on the struggle 🚍. It's gotten worse every year.
yes, gotten worse every year huhuhuhu
I've heard salt can be a trigger. Try cutting your salt intake and drinking more water.
I also have meneires disease. I’ve been through periods where you have all the typical symptoms: loss of hearing, vertigo, nausea, etc etc. I also have bad allergies and am on three meds to control them. The biggest pain was finding a good ENT doctor who understood this disease. Most of them have no clue, they don’t know what causes it and there is no cure. You have to almost teach yourself the dos and donts. Watch your salt and sugar intakes very very important since salt brings on the water. Also if you have meds for allergies take them as directed never miss a pill or spray or shot. I’ve been reading lately there is a correlation between allergies and meneires and personally I’ve found keep your allergies in check and the meneires seems to quiet down. Not go away but at least you get a break. Bright lights are also a trigger. The worst as I’m sure we’ll all agree is the directional vertigo aka “the spinning”. I have to use hearing aids since my hearing has tanked over the last couple of years. They help somewhat. One last thing seems to be some connection between barometric pressure and meneires. Who knows? Apparently no one. I hope some of my findings help someone and we just gotta hang in there!
Vertigo can make you feel deathly ill. So dizzy.