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This sounds like me. Onset was last week. My period was coming on so I figured it was just regular period flu. Ended up in ER diagnosed with Vertigo. Meclizine did nothing. About 50% better now but lights, loud noises, and turning while driving gets me

Thank you for sharing! I was just diagnosed yesterday with atyptical VM (or possible MD if hearing loss presents). It’s nice to have a name to the problem and be able to learn more about what worked for everyone else. Until now it was called vestibular neuritis and I never felt that fit my problem

Symptoms vary from person to person as do triggers but as ive said I don’t think that dizziness is part of VM. I don’t think you can self diagnose this as it’s complicated. Much better to get appt with specialist

Thanks for being so positive and showing that there are plenty of options even when you have to work with restrictions. Great video! 👍

this was the most validating story- thank you so much for sharing it!! So helpful.

I just got diagnosed with vestibular migraine today. And i have all the symtoms that you discussed about especially as u said u had trouble following and felt like an idiot exactly the same as i feel now. But then again no loosing hope atleast not something as life threatening like a brain tumor o something.. thanks for sharing 👍..

What is the eye drop's name?

i love this recipe. I've made it twice. thank you!

Dr Shin looks like Dan Lok.

Thank you for this! I have been from doctor to doctor, was even hospitalized . Thank you ! This helps . Just did VNG testing , awaiting results .

Nice one..need to try..

I need help 😢I’m from Florida and I can’t find a good neurologist that knows about it

My neurologist no even talk to me much 😢she said take Nurtec and I’m having shortness of breath and I don’t find solutions

Great video! My triggers are: Chocolate, fake sugars, i.e., any ingredient that ends in "tol", red wine, and coffee, even decaff! Cheese, ages meats, and nuts and fruits dont bother me. Boy do i miss coffee the most. Do you think ill ever be able to have it again? 😢

Going on four years now with vestibular migraine. Wasn’t diagnosed until Dec. 2023 so it was three years of frustration.

I have been struggling with PPPD / ocular migraine for 20 years Recently last year my pppd got way worse, maybe was triggered because of a vestibular/ocular migraine repetition over time which created a hyper sensitivity to the vestibular system i will share my experience hopefully it helps some of you : Initially i tried getting help with a chiropractic but after a few hours and the next day the trigger points where he pressed made me feel a lot worse to a point where the next day i couldnt even walk without losing balance, so that did not help even tho i did a few sessions. I later tried vestibular physiotherapy for 5-6 month that consist of a combinations of exercice i fully commited to do them and there was no improvement at all. What i noticed is more muscles tension from exercices = more inflammation = more symptoms of dizzness and vertigo. Along side in the period of my chiro and vestibular physio treatment i started talking anti inflammatory supplements and magnesium supplement i tried magnesium oxide for 2 month magnesium glycinate for 5 month 2 differents brands and magnesium theronate and i can tell you from my experience none of these helped me i was having so much problems with my gut health : bloating Nausea, lot of burping, brain fog due to these supplement. What i learned is take care of your gut health: eliminate all the food that make you feel uncomfortable and the ones you can not tolerate it will help you a lot with your brain fog, dizzness and vertigio associated with pppd or migraines During the journey i wanted to mention i also tried going to osteopath which i also did not benefit and at all : more muscle tension after treatement more inflammation more symptoms more vertigo I was also recommended to try acupuncture which led to the same previous results but was effective in helping with muscle tension Overall what really helped me the most is taking care of my gut health and obviously there is a gut brain axis connection linked with PPPD I also wanted to add the big importance of good continuous non interrupted sleep that have a big role in brain regeneration and neurotransmitters good functioning which are responsable of many roles including troubles with balance and vertigo.. i can say that im about 60 to 70% better with my symptoms my tolerance in big visual stimuli stores is better, driving is better, watching action movie which use to trigger my symptoms is better but i still have some symptoms present at a low-mid level I hope you all find this helpful and that your journey to recover gets better, do not lose hope, try what you are comfortable with go step by step but it is possible to get better. I wish you all the best !!!

I’ve been dealing with this for over a year now, finally I have been diagnosed with vestibular migraine and I can now start to take care of myself.

Did you have tinnitus?

Can I just say that I live in the Netherlands. There is a mandatory basic insurance here but health care is then fully accessible to all.. I feel so sorry for those in the US who are dependent on health insurance through their jobs. It is totally unacceptable in a wealthy modern nation where health is not available for all. PS: so far I'm told I probably have Menieres because I've had multiple episodes of sudden dizziness with nausea where I have to lie down quickly & then sleep for hours (anything from 3 to 22hrs) Also have tinnitus & decreased hearing. I take Betahistine, which until recently has worked well...but also know my balance especially riding my bike is becoming impaired. I wish everyone here watching on this channel the very best finding a diagnosis & treatment for their vestibular problem. Vestibular issues are known to be very difficult to diagnose. Like other things it is an invisible complaint so often hard for others to be understanding about.

I get similar but less severe version of symptoms during and after my menstrual cycle. Therefore no one could actually told me there is a version of migraine without headache. After having these episodes for ten years, I got the diagnosis yesterday. I always thought I am having extreme and weird menstrual symptoms. I’m writing here maybe there are people who are like me, not always but periodically experiencing vestibular migraine. Thanks for sharing your story and may you all get better soon.

You just described every symptom I've been experiencing for about a month now. I haven't been diagnosed with vestibular migraines but some days I feel so dizzy I feel like I can't even get up.

You can add some raw chicken legs with skin on, drumsticks ❤

Some of those drugs are not good for people if they are older, they can be linked to dementia

I'm in the uk, and never had a diagnosis of VM, but I've had these symptoms for years, I also get tingling in my face, I wonder if anyone else gets this. I wish we had Dr Beh in the UK. I'm Menopausal due to surgery and I thought the estrogen hrt was causing my symptoms to get worse, when I stopped this I got a horrendous migraine. I have reintroduced hrt gently. Thanks for all the help, perimenopause and menopause have many symptoms similar to VM in a way, like tiredness dizziness palpitations. So it's difficult to tell them apart. Xxx

I just got diagnosed with this last year after Covid. I am on the way to hopefully getting recovered. Glad I found you. Every symptom and your story and symptoms describe me!

This video is super helpful! I've watched it multiple times. Thanks for sharing! 🙂 #livingwithavestibulardisorder

I have tried therapy.

I’m also 30 and was just diagnosed with vestibular migraines . Lost my job and this is giving me the hope I desperately needed

You literally announced all the feelings I’m dealing with. Please send me what you did to help I’m so desperate

I have an exact same story and timeline of events from going to ER getting meclazine, vertigo attacks , physical vestibular therapy that helped until it didn’t ! Now I’m trying to get back to work but can’t shake the vestibular migraines . !

have found you. This gives me hope.

When do you take Cognimag and B2? Do you take it evenings before bed?

I've dealth with this for over 5 years. Bounced around from specialist to specialist until a vertigo/balance disorder specialist diagnosed me with vestibular migraines. Im on 60mg propranolol now per day and im seeing a 95% improvement. Sumatriptan is the abortive medication which eliminates all migraines within 45 minutes. This has gotten the symptoms under control for sure. I went from migraines/vertigo everyday to 1-3x a week. I got my quality of life back.

After our chat today, I tuned in! Thanks for doing this interview, friend! You both help so many! ❤

After our chat today, I tuned in! Thanks for doing this interview, friend! You both help so many! ❤

I am also facing similar symptoms but do not understand that it is vestibular migraine or not. I am on medication for the past one month and the experience is awful. Can anyone help me in this? I have started taking Vertin 24 tablet.

Thank you for your video. I can relate. I’m going through similar situations for the past year. It all started when I got off a ride at Centre Island (the tea cup ride) I was diagnosed with Vertigo. I get Vestibular migraines. Huh Vertigo is a symptom not a diagnosis! I get triggered mostly when I am stressed, tired, motion, loud noises, bright lights, change of weather, moving my head side to side quickly.

Im fully crying, this is such a relief, i was going crazy not understanding whats happening to me. Thank you for sharing your story!

Do you happen to know of any doctors in the Montana area?

I like the hardware - software analogy. Sitting & driving are OK for me but not stores with lot of aisles and merchandise and closed spaces or smaller rooms. Some days are good and some bad. Started 2 months ago with slight throat pain and feverish feeling for one night. Then a few days later all this started. But no ringing in the ear. Imbalance while standing so always stand holding on to the wall or something.

I am a man. It’s not about what sex you are. I have been gas lit, brushed off, talked down to, lied to, ignored, told I was making things up, minimized, etc etc, by dozens of doctors. Male and Female Docs. So NO, it’s not just because you are a woman. I started taking my wife with me to visits, and guess what? Yes I was treated CONSIDERABLY better. The medical industry is full of a bunch of Narc docs. If they can’t put you in a box, then they want you to just get out. It’s an EGO thing. I have been dealing with this abuse now for over a decade and I am in much worse now than when I started this journey thru hell. Living in a smaller city doesn’t help for sure, but that’s not the primary reason for such a corrupt failure of treatment….. Egos…..

Magnesium glycinate is great If can’t tolerate try magnesium oil or magahol on skin

thank you so much for posting this, like many others here when this hits it is so scary and you worry that your life as you knew it is over. Thank you for sharing your experience and everything that worked for you- off to try it now. At least there is hope!

I recently bought Sumac and I love the flavor. It lingers and I like that. I'm just about a week into the diet. My neurologist suggested it. I actually have known about your sight for a while. I just hadn't gotten around to it. The Mediterranean meatballs were delicious. I do know chocolate and caffeine are fine with me. I only do a cup of coffee a day and every drink thereafter is caffeine free. Soy I can do but only limited because my belly says no after a while. Lol I am dairy free but mostly bc my body has retaliated and I can use the restroom. Lol some food we already don't eat bc my middle child has a stoma and those foods can either bulk too much or clog. So like beans and nuts and bananas. Just to name a few. And she's also sensitive to dairy and eggs. So my son is the only one having actual milk. I'm hoping it helps. I don't get dizzy all the time but I'm still hoping this will help with the now 6 migraines a month. I am on meds that have helped a lot because I was getting 11 migraines a month for about 7 years. I was in my early thirties and am now am in my early 40s. I do know that too much sunlight, heat, stress, poor sleep (hello insomnia, yes I have meds for that) and exertion are no bueno for my migraines. The rest I wasn't sure on but that's why I'm trying this diet.

I remember I was about 5 years old, live in Pakistan a small town. I suffer this experience, my parents took me to the local government hospital and they treated me for iron deficiency. Now I am 39 I have come to know that what I suffered was vestibular migraine. I have faced it time by time like whenever I take kidney beans and coffee in high quantities. Thank you for your explanation and awareness ☺️... Stay blessed 🙏

How can I connect with you?

Thank you so much for sharing this. I recently was diagnosed with Vestibular Migraines. Super hesitant to get on medication but Neuro said I could start with Magnesium Glycinate to see if it helps. I will be watching your content to see if I can get ideas on how to approach this holistically. So glad I found you! ❤

Have you ever been checked for MS?

I just dont believe it will ever get better.

That's my story too! I'm stilling trying to find a Dr that will take me seriously!