Are your symptoms NORMAL? FULL LIST of chronic dizziness symptoms PPPD, MdDS, vestibular migraine

[@brookewelsh5912]

I am crying many tears of relief right now. You named symptoms in this video I didn’t know were connected and I felt like I just have so many things wrong with me. I cannot thank you enough for all that you do for us who have been struggling. You are absolutely amazing dedicating your time to research and educating us and I really wish I could meet you because you’re changing my life and I truly appreciate you 💛🙏🏼

[@shaneboswell9872]

This is great for all the people out there still wondering! So glad you mentioned POTS. My symptoms have moved through all of these!! Hang in there people! I am so much better than when this started a year or so ago and felt totally normal today and have many normal days again! The thing that held me back the most was the fear that it was going to last forever or still doubting it’s this or just freaking out that I can’t make it home. Engage in things you enjoy as much as you can and surround yourself with good people and don’t beat yourself for not being there for people like normal. ( I know this is so hard ) like she says in other videos, don’t be a perfectionist about recovery! Thank you again Dr. Yo !!!!!

[@DebsEmmy]

Every symptom I have had/am still having is listed here. Thank you so much, Dr Yo. This stuff is so isolating. You are helping me feel less alone ❤

[@carolinemorrison-ot4fc]

@@DebsEmmy we are here for you! Keep going! You are not the only one! My motto " TOO LEGIT TO QUIT"! shows my age that was an oldie but goodie!!

[@JoannaTremlett]

Me too ! Swaying whilst looking in the mirror..I thought I was going mad ! ❤

[@KellyK-pu3mn]

Great video but how do we fix this?

[@lorrainecraig4748]

For the first time someone has described everything im dealing with. This has actually calmed me down so much hearing it. Thank you so much for all your videos

[@trulyheaven2335]

It’s been almost 3 years for me and I’ve literally experienced almost all of these we are truly special❤❤❤

[@debbieford4685]

Thank God for you and your willingness to make this info available to those of us that the health care system has left behind!

[@kaustavhalder]

You just mentioned everything I have. It’s a bad day today and your video came back with the hope I needed.

[@TylerHardin-sy5tc]

Hope you get better. I’ve had it for years. Hope to start a true recovery soon

[@LindsayForan-h8s]

Such a great video, Dr. Yo! You empower all of us to heal our own bodies.

[@JodiJonespsychicmedium]

This video is so incredibly helpful & validating! I’ve had almost every single one of these symptoms chronically and some are really hard to explain to your friends & family let alone to try and get your Doctor to understand. I think this video should be included in any Medical school training 😂

[@carolinemorrison-ot4fc]

@@JodiJonespsychicmedium Yes. I hope the medical field learns about this soon. Thanks will go to Dr. Yonit for sure!

[@rachellucas5269]

This is great information and should put many people more at ease. Thank you!

[@TheSteadyCoach]

❤️❤️❤️❤️

[@karistownsend8292]

I finally joined! I’m so happy about that, I feel so understood!!

[@Charcharss]

I got vestibular neuritis in March 2023 and then pppd since. Was more or less housebound bed-bound for over a year. Such a horrible thing to have hang in there guys if you are dealing with this. It gets better. I’m doing alot better month on month. I’ve had all of these symptoms 😮 have a few lingering symptoms but the worst is the feeling faint like someone’s pressed a switch in my body. Thanks Dr Yo for all you do ❤ I’m doing so much better thanks to your content ❤

[@judynewman3816]

Thank you, Yonit. This is really helpful for me. I will return to you basic videos on how to recover. I realise it’s my over sensitive neural system, which is comforting.

[@elainewang8418]

Hi Dr Yonit, I was lucky to came across to your channel a year and a half ago and you have helped me so much. Thank you for doing this work and helping so many people. Sending best wishes with gratitude!!!

[@michaelmorgan9009]

Wow, so accurate of the symptoms Im having. Its like you read my medical chart or something lol. Great video Dr Yo

[@Caron-s3d]

I have just about every symptom mentioned here. Three that I don't believe are mentioned: Sensitivity to smells (even the ones I used to enjoy), internal vibrations ( like a giant cell phone is inside me, ughhh)... this goes away when I sit down or lay down.Also, at times, things I grasp with my hands feel squishy... pillows feel way more squishy than I know that they should feel, even hard surfaces sometimes feel kind of that way.😕

[@MichaelHplus]

Great video for helping people feel like they’re not alone and that there is hope. I’ve experienced A LOT of these, and still experience come, though they’re not particularly distressing anymore.

[@Emmeyy-dv5hu]

I really have experienced every single one of these and its so helpful that youve listen them like this because sometimes i forget that your videos still relate to me when my symptoms change and i will start to google again then get myself stuck in a ditch and then remind myself "i can still watch the helpful videos its the same issue Emma" Helps me get back on track with telling myself im safe this is still safe. ❤ Edit: Im also a hypochondriac and EVERY symptom triggers off my fear of it having to be something else and i have a huge fear of anifilatic shock to almost anything..which all plays a cylce of destruction for symptoms and dizziness 😢

[@sandra.diaz.7139]

EXCELLENT video Dr. Yo! This will surely provide some comfort to those who are still wondering if their symptoms are part of 3PD or not. Thank you once again for your wonderful work ❤

[@carolinemorrison-ot4fc]

Thank you! I was told I have fibromyalgia and hashimotos. I wonder if others with NCD have those also. I also got swallowing issues the day of Covid vax. But I feel the dizzy sway came few months b4 that. Weak right ear was told and eustachin tube dysfunction. This week 3 plus years in to this neck tremors...brand new. But I was doing more because due to your help I am feeling less sway daily and I am Amazed. So perhaps I moved around more and neck and spine not ready for me to do this. I think the list you created is Awesome. I hope it shows medical field that we are not reporting falsely. Validation is so helpful. So many of us same symptoms. Thank you for this new video. Feel less alone in my journey to recover. ❤

[@rosaabrilfigueroasaldivar1531]

Thank you for this great video Dr.😊

[@TheSteadyCoach]

My pleasure!

[@JoannaTremlett]

❤❤❤ brilliant explanation as always .

[@AnitaPerrine]

You didn’t mention the depression and anxiety that develops as a result and that keeps symptoms active long term,

[@JoannaTremlett]

@AnitaPerrine nothing worse than being trapped in your own head with just your anxiety for company. ❤️ you aren't alone though and you will get there.

[@sdwl07]

Another good one! Thank you. -Sheena

[@ImranKhan-rs4sk]

Dr. Yo, Can you please, please, please do a video on Eustachian Tube Dysfunction, particularly about plugged sensation of the ears, tubes not opening properly and issues with hearing (low or muffled hearing, where you don't hear certain frequencies very well, either high tones or low tones)? This is so important to me. I have been watching your videos and trying to learn as much as I can about neuro issues that affect the ears. A video on Eustachian Tube Dysfunction would be very helpful. Thank you so much!

[@crispycaptures]

Once I rode in an elevator and after getting out I felt super dizzy as if i was still moving in the elevator and it was such an icky feeling.

[@jmwb4u]

I have that! Currently doing therapy and vestibular therapy thats my finaly step to overcome lets help eachother out!

[@crispycaptures]

@jmwb4u Has Vestibular Therapy helped?

[@jmwb4u]

@@crispycaptures its hard to say because im doing therapy as well so combination of both are usually the most effective route

[@TheSteadyCoach]

Absolutely! It can be totally normal even when someone does not have a neural circuit issue going on. Not fun, though.

[@jmwb4u]

@@TheSteadyCoach do you have a video you talk about somatic symptom disorder i just got diagnosed with this and pppd

[@trinal2299]

Great video!! Thank you ❤

[@DaniEla-of4eo]

So no matter what symptoms and how many of them (when no medical reason), it's always the same cause: a hypersensitive nervous system?

[@Caron-s3d]

Good question! I would also like a clearer answer.x

[@mindyli5974]

hi dr. Yo, i wanted to ask if you can make a video for gentle stretches and exercise specifically for the neck and head region to do to strengthen our muscles for that region as many probably like me always seek to sit against something like a wall or pillows so we have that support and when that support isn't there its hard to sit still and maintain a posture without starting to sway again and maybe exercises or stretches can help strengthen that region to support the weight of your head and keep you still without needing to seek some support for your head and neck at all times. i have tried some but i feel they are too intense and those movements are not specific for those with pppd who already are afraid of such movements, i would appreciate any input thank you

[@carolinemorrison-ot4fc]

I know exactly how you feel. Neck got so weak I felt could not hold head up. Have had some good days but wonder why neck feels it needs support. Some days more recent felt no sway or dizzy. Then i think I got too busy moving my head and neck and now some bad days and some nerve stuff going on. But keeping hope going.

[@DiamondForevah]

I agree, one of my long lasting symptom is feeling exhausted and brain fog when I move my head and neck.. do you have the same?

[@TheSteadyCoach]

Hi Mindy, I often find that when people are dealing with a LOT of anxiety, it's counterproductive and not helpful for me to have them do a bunch of exercises. It makes them focus on the symptoms more, not less. Generally, unless someone has something physical going on, I teach them how to react less to these kinds of symptoms to let the brain know it is making a mistake.

[@torifox3506]

This video has been helpful in listing out and explaining many of the symptoms I’ve been having for several years. It’s a pain to have that rocking sensation even while lying down. The only way for me to sleep is propped up with pillows but this unfortunately causes neck issues 😕 I’m afraid I’ll never be able to lay (let alone walk) normally again.

[@Caron-s3d]

Keep fighting. My fear has turned to anger and determination. Are you getting help from a vestibular therapist?

[@davidrager8813]

Can you please make a movie on Craniel Cervical Instability? Have you seen patients recover from their sensations that have this?

[@TheSteadyCoach]

Hi David, generally I think CCI is being blamed for dizziness and other symptoms when it's something that occurs in many people in the general population who don't have symptoms. While true cervical dizziness IS a thing, it's clearly diagnosable by a skilled clinician and can be effectively treated with PT. When symptoms are weird and follow a neural circuit pattern, the CCI is just an incidental finding IMO.

[@davidrager8813]

@TheSteadyCoach would there be any way we could speak for 15 min via the phone? I have followed you for years now and commented several times. I would be more than willing to pay for the quick session. I would love to get further clarification on a couple of things you have mentioned in your replies to me over the years.

[@carolinemorrison-ot4fc]

@@TheSteadyCoach thank you this helps!

[@teebahabu-zahra2580]

Thanks for this amazing video. Yes, Yes and Yes .... I have all these symptoms Lol. However, i learned until my CNS gets out of this fight or flight mode, just acknowledging these symptoms when they come and moving on with my life helps the best.

[@ozzyalejo]

A very reassuring video. 👍

[@Virgobro]

May we all continue to strive and thrive in 2025🎉

[@aprilmoss4106]

Thank you so much for this

[@Brian-bl3cu]

Do you have opinions on medications that mask symptoms? Benzodiazepines, for example, are commonly prescribed.

[@TheSteadyCoach]

Tricky. Here's my general opinion, but I'm overdue for an updated video. I think they should be used as "assistive devices," to be used as infrequently as possible, not as a cure, and they are often sold to patients as a cure or the only treatment. Benzos definitely have a place in relieving people of the most distressing symptoms on intolerable days, but I think it's not a good idea to take them chronically unless absolutely unavoidable. Not medical advice, just my opinion based on observations of clients. I think doing the other work (dealing with fear of symptoms and other stress) is critical. kzbin.info/www/bejne/hH3RhIF5pcqqnpY

[@janiceince1965]

I call the leg feelings puppet legs. Like I'm a marionette puppet...my arms feel like that too.. Or the vision symptoms like I'm looking through a fish bowl or I have superman vision when I'm outside...

[@lindawright636]

What about symptoms that occur when you are in bed and trying to get to sleep? My eyes are closed so I’m not getting sensory info there and I can either feel a rocking motion or a spinning sensation. It makes it very difficult to get to sleep. Do I just ”ride it out” trying not to fear? Or is there anything else I can do?

[@shivshankar2869]

I practice diaphragmatic breathing and eventually I sleep. And the symptoms are back when I woke up. But good sleep routine is a top priority I guess.

[@shivshankar2869]

1. My very new symptom is feeling a heavy body while walking and sometimes lying down during the night. 2. While lying down on the floor sometimes I feel the gravity on my head is too heavy and the sensation continues for a few minutes and gets better later. This is the scariest symptom I have experienced so far. Could these two symptoms fall under pppd or mdds?

[@magdalenereaves4357]

Thank you so much. I have healed all the other symptoms BUT the legs balance, swaying wobbleness is so much I don’t. I hope this goes away soon it has been a while now.

[@FJano12]

So reason the reason my floaters are more visible and bothersome because my brain cant filter them out properly?( got my eyes checked) Hmm interesting ..

[@TheSteadyCoach]

Yes! As someone who personally has an incredible number of floaters than my ophthalmologist is amazed don't bother me - your brain can filter them out.

[@hiya_ana]

Who have all of those symptoms? (Eye, ear and touch dizziness..etc) I have cfs/me and vertigo is not helping 😭

[@TheSteadyCoach]

So many people!

[@hiya_ana]

​@@TheSteadyCoach It is kind of reassuring that I'm not the only one. I thank you for the work you do 💌

[@SaliTaya-w3r]

Thanks for this video, but the only thing you didn't mention is if the symptoms are 24/7 or more like episodes- Which is more neuro circuit related. I have my symptoms all the time , they aren't changing. I'm dizzy like hell 24/7 for a very long time.. the doctor think it may be pppd , but I'm scared they might missed something cause the symptoms are allll the time and they are super debilitating. Maybe do a video with the subject of 24/7 every minute, hours , days , that never go away. Stuck in the body like another heartbeat.

[@TheSteadyCoach]

24/7 symptoms is the rule, not the exception. Most people start there. kzbin.info/www/bejne/b2a9foiagcmlsJo

[@vikkitownsley4847]

My symptoms are pretty much 24/7. PPPD is neural circuit dizziness

[@SaliTaya-w3r]

​@TheSteadyCoach Do you feel the rocking also when you are laying down? Or only when you sit/stand? I'm going crazy with the symptoms also when I'm just lay in bed. They are there alll the the time no matter what

[@pablocontreras6835]

I need treatment I’ve been dealing with this since I was 15 years old and it’s unbearable please help I was diagnosed with vestibular migraine at the age of 18 and they could never recover 100% now also 45 years old I was diagnosed with PPPD and treatment with medications and with vestibular rehabilitation I didn’t help me at all I’m still the same or worse I need real help I can’t stand this situation anymore help please

[@carolinemorrison-ot4fc]

I feel for you! I have had this 3 plus years but following The Steady Coach was so helpful in making a change in the right direction. The brain and nervous system so tricky. You can recover I feel. Do not loose hope. I have made progress with Dr. Yonits videos. You are so very Brave to have this so long. Perhaps look at foods as triggers too. When I start on chocolate, sugar and more salt I think triggers more vestibular stuff...vestib migraines they said I get. But if I watch what I am eating some I do not get those really bad days. I would say oh gee if I could just cut my head off I would be fine to find some humor to survive this! You are Awesome! Keep going you will get better. ❤🙏👍🏻

[@sandra.diaz.7139]

Don't give up! I am making big changes in my life to get over this terrible condition as I think it's important to attack it from all fronts! Exercise, walking, clean diet, quitting smoking, going to therapy, practicing breathing techniques, improving posture... Don't rely completely on doctors and medicines, YOU have the key to recovery. Examine your life situation and determine what can be improved. This condition has a HUGE emotional component. Most traditional doctors know nothing about it!

[@pablocontreras6835]

⁠Thank you for your words there are days that I would like to take my head out also many years with this and I keep fighting I would like to find even if it is a little relief every day I ask God not to give up and continue

[@TheSteadyCoach]

Please, Pablo, take the free course. It will walk you through how to get started. YOU CAN GET BETTER. thesteadycoach.com/free-course

[@pablocontreras6835]

Hello, now I’ll start doing the course, thank you

[@leonkennedy3398]

Got the delayed vision. Gah so annoying. Cant wait for that symptom to be gone. Makes driving and stores difficult. Used to feel like the world was tilted. Rarely feel that now. That was the worst! Lol

[@JoannaTremlett]

@leonkennedy3398 my delayed vision is just starting to go 4 months after finding Dr Yo ( I took the free course ) it is a very confusing, lonely , anxiety inducing symptom but really will go I promise. X

[@tashaandjacob6836]

Brain pressure anyone????

[@carolinemorrison-ot4fc]

@@tashaandjacob6836 yes had that alot...3rd year now and less of it. Had it daily for long time. Thought perhaps vestib migraine issue.

[@Caron-s3d]

Yes, but it's a lot less frequent compared to when I first got PPPD 3.5 years ago.

[@ianbown3543]

You literally just described every symptom I have ever had :(

[@TerkaTomkova]

Dr. Yonit could you please make a video about how to heal from symptoms that are mostly activated by being stationary? I struggle with having symptoms when laying down / when I’m drowsy tired / sitting / or if I stop walking abruptly or I get this weird dream that I’m rotating on a carousel which wakes me up in the middle of the night and then the whole room is spinning but I’ve been checked for BPV and I don’t have it. I’ve been diagnosed with PPPD. I do walks and movement to help with my symptoms, but I don’t know how to ease the symptoms that appear when I’m sedentary.

[@TerkaTomkova]

I do somatic tracking and I’ve done your course :)

[@beratbra4429]

I can't even be close to a closet, door or wall for that matter without feeling like I just had a serious brain damage or something. I just feel awful and overhelmed by this form of dizziness that I can't explain. Been like this for 8 months. Just changing rooms from living room to bedroom maksmes me significantly more dizzy. Is this a part of neural circuit dizziness? Feels like I am alone with these type of symptoms and I am dizzy constantly on top of this with many other symptoms....

[@funnyvidz9682]

Yes, ne assured IT is

[@TheSteadyCoach]

Absolutely!

[@monikaszigeti4342]

I may have health anxiety.i have panic attacks all the time.and it comes with this dizziness that feels like i escaped teality.not like the world is spinning.and I’m worried because it’s been almost a month of this going.

[@deebo1123]

Do you have to have dizziness itself to qualify? What if you just have the visual and auditory symptoms you described in this video?

[@sandra.diaz.7139]

Great question! I do know that sometimes symptoms move from one to the next (like, for example, one day you have dizziness and the next day dizziness is gone but visual disturbances begin...). Would be great to know if you can actually have PPPD without ever having had the dizziness component (sadly NOT my case but could apply to other people).

[@TheSteadyCoach]

Absolutely can have just the other symptoms! I mention dizziness first because that's the big one people have but I've met many people who don't have dizziness and have the others. One of the clients I saw today has the tilting, headaches and dissociation but no dizziness.

[@tshaika9165]

Hypersensitivity of the senses is also a symptom of autism, I wonder if this makes autistic people more prone to experience these dizziness disorders later in life?

[@TheSteadyCoach]

I co-wrote a book chapter on this last year - stay tuned. I think autistic people often have both the nervous system sensitivity AND lifetime of extra stress that makes them more prone to neural circuit issues.

[@janellrose4882]

Does anyone experience harsh ear pain? In her symptoms of the ear she doesn’t mention pain, however this is something I deal with daily in my left ear and seems reflective of when I feel dizzy. I have been told by multiple doctors I have vestibular migraines but wasn’t sure if ear pain was common.

[@Caron-s3d]

I was actually asked by a Vestibular Therapist if I had ear pain, I didn't at that time. Although,I did have it happen a number of times through out this miserable journey.

[@elwiraboczkowski6591]

Is neural circuits dizziness the same like me/ cfs or fibromyalgia or are they are related?

[@TheNinjaprof]

I am so thankful that you made this video ! I have so many of these symptoms and none of my doctors ever seem to be aware of them or have any understanding of them or how debilitating they are. You often mention ruling out a medical cause for symptoms. I have a medical cause for mine, but it is cervical dystonia which is a "software problem". Would you consider my symptoms to be "neural circuit", even though they are induced by the dystonia?

[@MichaelHplus]

One symptom I had was that my head felt wet 💧. The first time it happened, I had exited my apartment building, felt the sensation, and then looked up to see if an air conditioner was dripping on me. It freaked me out to know the sensation was coming from inside my head. It recurred a few times and then never again.

[@carolinemorrison-ot4fc]

Wet feelings can be nerve related. Use to get this on my legs. Really takes you by surprise.

[@MichaelHplus]

@@carolinemorrison-ot4fc It was during the time when I first got my vestibular condition (rocking or "boat-like" vertigo), and came with some other symptoms like tinnitus and such. That was several years ago and I'm in a good place now (though sometimes I still feel the rocking a bit).

[@sandra.diaz.7139]

HA! I'm so happy to have seen your comment! I get that wet feeling on my legs sometimes and nobody believes me! Thanks for making me feel a bit less of a freak! 😊❤️

[@MichaelHplus]

@ it’s nice to hear I’m not alone in terms of wet sensations (even if mine was not on leg)

[@carolinemorrison-ot4fc]

@sandra.diaz.7139 it is a real thing. Forget what it is called. B4 my dizzy sway issue would get it on my thighs or legs and have to check if pants got wet. Then I read about it and felt better. Nerve related like so many things...hard to diagnos and easy to dismiss.

[@MizaMaximus]

Hi Yonita! Thank you for your priceless video 🤗 I have a question, could dizziness (swaying, trampolinwalk) be a symptom that I am crooked on the right side (right shoulder is lower than the left side). And can C1 and C2 be out of position and cause dizziness? A visit to the chiropractor? Or am I totally crazy? 😂

[@Safely2024]

I would love an answer to this question. I get those episodes. It is horrible

[@TheSteadyCoach]

Most of the time from my experience, issues with the neck and posture are being blamed for symptoms when they're just "normal abnormalities" that many people have that do not cause dizziness symptoms. I don't oppose going to a chiropractor but that is usually not going to solve the problem.

[@MizaMaximus]

@@TheSteadyCoach Thanks for the reply and I wanted to hear your expert lent but I think like you. But after many diagnoses, I finally met a physical therapist who tested me with frenchel glasses and came up with PPPV. (Had vertical nystagmus in the past but it is no longer there) My journey to PPPV took 4 years 😐

[@Safely2024]

@TheSteadyCoach Thank you Dr Yonit. Kindly

[@bellafore6719]

i have what im not sure is double vision or not. It's basically like, if I look straight ahead I don't see anything as double, but then if i look out the window and there's an object like a water bottle in front of it, I see the water bottle as double. is that normal?

[@glitterbrickroad2792]

What about difficulty swallowing? Not the lump in the throat/anxiety kind. I just lose the sensation to swallow. This symptom started after developing pppd. Thank you for all that you do Dr. Yo!

[@carolinemorrison-ot4fc]

@@glitterbrickroad2792 Yep hqppened to me. But for me it happened the day I got Covid vax. Was already off balance few mos b4 some. I had barium swallow tests done and they said u r fine. Nope not fine. My swallow issue on right side of throat. Like I cannot complete a swallow fully. It does get worse and then less. No answers I say its the nerve to my throat somehow causing it. 3 years of it. I report it and no help yet. For me same sensation in throat loss. Not lump or anxiety.

[@glitterbrickroad2792]

@ ugh I’m so sorry you go through that too! It’s honestly my worst symptom. I didn’t get vaccinated but I did have Covid two weeks before developing pppd. I agree that it’s probably a nerve issue, since the cranial/vagus nerves are connected to balance issues as well as swallowing function. And we all know that a balance disorder causes havoc on our nerves.

[@MS-jz2pq]

Has anyone else experienced a feeling like when you get a nicotine rush (for those of you who have ever used tabaco) while looking in the mirror? I know this will sound extremely weird but I have has that feeling ever since my dizziness started out of the blue 3 months ago.

[@ShaneFindlay-w2u]

Hello. It perpetually feels like I have voltage running through my body (accompanied with muscle twitches). Is this a common symptom?

[@carolinemorrison-ot4fc]

@@ShaneFindlay-w2u lately I feel voltage thing and twitches I have gotten. Also this week new to me neck tremors. My symptom list is long. Nothing surprises me any longer. 3 plus years but I will recover too!

[@TheSteadyCoach]

Yes definitely.

[@nuriajuzgadoferreira7897]

Algunos de los síntomas que me han desparecido son, sentir que te vas hacia un lado al caminar,oido tapado,los movimientos más lentos o falta de reflejos solo lo tengo por la noche,la dificultad de mirar pantallas y la sensación de desmayo al estar de pie . Aunque aún tengo muchos síntomas visuales,¿el hecho de superar los demás síntomas significa que estoy recuperándome?

[@JaJa-of6rr]

Can we have the same neurval circuit dizziness in family ( grandma;mother; daughter)… I had no idea about it untill my first experience with vestibul. mig and spoke about it to mother. She told me about grandmother and herself after my attac..?????

[@AnitaPerrine]

What was going on in your life when the symptoms first appeared?? A loss, a perceived failure, a threat?

[@JoannaTremlett]

@AnitaPerrine brain tumour diagnosis for me but I definitely had symptoms a few years before of 3pd as I've had a very stressful life so this was always going to hit at some point. X

[@Caron-s3d]

My (former) doctor tapered me too fast from Xanax, from 4 mg. daily to 1.5mg daily. I choose to remain at 1.5mg daily for fear that going lower could make PPPD worse.

[@SergioManaj]

Is feeling fainting and blood pressure drop also a symptom?

[@TheSteadyCoach]

Yes, see the section on other symptoms, I mention this!

[@jillradovanovic3460]

Why does heat and humidity make it worse

[@AnitaPerrine]

Any kind of stress increases symptoms!

[@TheSteadyCoach]

This explains! kzbin.info/www/bejne/iaW8iJ96e9B5oK8

[@urosale]

How to heal finally, once and for all?

[@urosale]

I was anxious, i think I all got this from anxiety, is it possible that anxiety caused all this? What all are causes?

[@JoannaTremlett]

@urosale reduce the anxiety .xx

[@denisebarrett-zq6cy]

Thank you , another great video , so encouraging and helpful ❤