I had a year in 1976 of such severe psychosis I believed I was possessed by demons, my vision was double, cross-eyed, hallucinating scenes from the holocaust ... utterly lost and terrified until I finally collapsed and had a transformational near-death experience. I know how lonely the ordeal of chronic dizziness can be... I have had it since 2014, and after a year and a half of PT still struggle with it. You deserve more than a purple heart for your bravery.

I am in shock. Literally every symptom that Megan has mentioned is exactly what i have been feeling for the past 6 months. I, too, truly thought i was dying. Thank you, thank you, thank you for this video. I have a doctor appointment in just a few days and Im going to bring up PPPD. Truly, thank you. I have been feeling so hopeless and like I'm struggling to be a good mom while feeling this way

This condition is more prominent in women than men. I’m that exception. I tell you what, so much of this resonates with me. It has helped a lot but it’s still a process healing. I’m so looking forward to just being “me” again. Thank you for posting these videos. I was in that lonely dark place that so many others who have watched this video.

This is so encouraging, I am in tears , to listen to people who KNOW what I am going through and know that there is hope ❤

Oh my god this is literally my same story. Finally starting my healing process. This makes me so hopeful/optimistic.

The head pressure is currently the worst symptom for me. And the fear of the symptoms coming back is so real 😣 I’m at a point where I’m mostly living my life but I still have symptoms. This gives me hope that I can continue to feel better and better.

This just gave me so much hope. It’s so hard to not want to give up on bad days.

I'm in tears in hopes of one day being one of your success stories.

Thank you so much for sharing your story. I have had this so far for 3 months. I got COVID and have had a rocking back and fourth or side to side or on a merry go round 24/7 or feel like I’m drunk and it never stops. I get very anxious when around people in stores. I don’t like going alone. I feel like I need to hold on to someone or something. I did HBO & acupuncture, different meds, lots of vitamins and no success. I finally was diagnosed with a Ear Clinic with PPPD and central vertigo. I am waiting to get into physical therapy. There is a month wait. I have lost my job now because I can’t function like this. My brain isn’t working either. I have migraine headaches and neck aches and panic attacks. I just came across this video and Dr. Yo so am going to start working with these videos for help. I have cried a lot through these last few months and so worried about my job and all of this making it worse. I live outside of Boise, Idaho and appreciate all of the info you are providing. I feel like my friends, family and work do not believe that something is wrong. It makes me feel ashamed. I have all the symptoms you do and they are 24/7. They have never gone away but only get worse. I get really bad anxiety when going in the supermarket that I don’t want to go alone. I am looking forward to being in control. Thank you! ❤️❤️

The 11:00 section talking about looking back and not remembering exactly how bad it was (bad enough to have suicidal thoughts) made me very emotional listening knowing there is promise to get to the other side and be able to look back. I can't wait to be able to look back and recover from pppd. Much respect and love for sharing your story.

Welcome to my world for the past 1.5 years. You just literally listed every symptom I have. You give me hope dear Megan!

Around 15 years of mind body sensations (around 15 to 20 different sensations including PPD, eye stuff, neck stuff, breathing issues, all kinds of different pain, insomnia, digestive issues and on and on). I have spent around $300,000 out of pocket and been all over the US.....finally getting better using work exactly like this and Dan Buglios work!! You are a brave and amazing young women!! Thank you for sharing your journey!

Thank you for sharing this type of content, doctor. Today my 24/7 dizziness stopped. Still working on my recovery and starting to feel happy again. You're videos have helped me a lot. Much love from Mexico City. :)

This is such an encouraging video. I've been dealing with the same things for over 9 years. And I can name the emotional trauma that triggered it along with the traumas that have happened through the years since. This makes so much sense to me. This gives me hope.

This is very similar to my story. Living on a boat. Feeling like walking on a trampoline. Visual disturbances and other weird symptoms (occasionally it felt like the inside of my skill was wet). I’m much better now.

Thank you Megan for sharing your story! I almost have all these symptoms with some additional symptoms. I took the free course and I'm working on it, for a one or two days i would feel fine but then all the symptoms keep coming back and i would freakout but I'm still doing parasympathetic breathing, journaling, VRT and balance tapping. I'll keep reporting about any improvement. Thank you so much for helping people like me❤️

Oh Megan, I’m so sorry you went through such a challenging time. I can relate so so much with your story. I had to laugh when you said “is this some kind of sick joke” because I’ve absolutely had those thoughts too. Gosh, I relate so much to everything you’re describing about the emotional toll it takes on you. I also so badly wanted something to be wrong on my MRI’s because I just couldn’t believe that there wasn’t a physical issue causing all of this. I keep editing this comment the more I listen to your story but it’s honestly so crazy to me how similar our symptoms are or were. I’m still in the thick of it all so this is giving me so much comfort and hope. I’ve had PPPD for 12 years but only just got diagnosed in the end of 2021 when I was so so desperate and sick. Thank you for sharing your story!

I completely understand. For those who don't know about this you look fine . It's so hard to explain. It's been 10months dealing with this myself now. Feels like your life is over. Finally got diagnosed with vm and pppd. This was brought on by chronic back pain and back surgery . I'm waiting for a day to feel completely normal. Waiting for appointments is the worse or have doctors dismiss you. I had to educate my own primary provider. They had never heard of this either. 😕 there needs to be more studies and awareness for this condition. Truly debilitating. I wouldn't wish this on anyone. Like being dead when your alive. You'll have to just live with it. Nothing can be done. I'm so happy your story is positive.

Thank you both so much this is me & I keep thinking there is no escape from the dizziness but you both have changed my mind thank you

Thank you so much to the both of you! I can totally relate to all of this! I have been diagnosed with PPPD, VM, anxiety etc. Debilitating symptoms for 4 to 5 years. I continued to work and tried to pretend I was ok when actually I was living in complete terror! It is so isolating and lonely when medical tests are "normal" but feeling like death can occur at any moment. I have tried every treatment modality, supplement, and exercise I could find. I have spent a lot of money and traveled many miles to see multiple specialist that were of minimal or no help. Since I have found Dr Yo/the steady coach, I have been applying the strategies learned and I am finally starting to heal! I have ways to go but I have notable improvement in multiple areas of my life, not just the symptoms. I have watched every success story on this channel and each one seems to provide me with more hope and reassurance! Dr Yo, I cannot thank you enough for sharing your knowledge and wisdom!

This channel is life saving for me. Thank you for sharing so much information you help me go trough my daily life every day with those videos. I have vertigo 24/7 and started because of stressful events… I wanna work on myself and do normal stuff and this channel help me a lot

I started crying when you did the jaw massage motion bc that’s me non stop and people always ask what’s wrong ?? I just say TMj. I slather my neck and jaw in tiger balm

Thank you so much for this. My symptoms started in approx 2017. I have never heard of PPPD until recently. Up until now I thought it was a vision issue. I have tried prisms, some exercises from a functional neurologist, and so many diets. This gives me so much hope! First just knowing that it’s not an eye issue and also knowing I can heal completely from this. I spent a lot of years stuck in my house and one day decided I can’t stay there anymore and started getting out. That has helped so much but I feel your channel will help me heal the rest of the way. I hope to be able to get back to driving again 👏

💚 Thank you both! I’m in tears. My symptoms started in 2017 and hit violently in 2019. I had to drop out of a masters program, I sold my car, all my children moved out at the same time due to my “illness,” couldn’t work, and have spent 3 1/2 years in my bedroom. After all the tests and lack of care and support, I am headed to Johns Hopkins in July for more testing. I wish I found you earlier. My body is worn out from the physical torture AND the lack of understanding AND lack of support. This is the first time I have felt like I might be ok. Blessings to you and your work🦋

I would never wish what I have on anyone but at the same time it’s a relief to hear that I am not the only one….. Her symptoms are basically exactly the same as mine. I’ve had every test done and seen multiple specialists and have been diagnosed with MD and pppd. If Megan saw the same doctors I have seen she would have been given the same MD diagnosis. I started with a strange head pressure without pain for years (started in grad school) then developed a serious struggle with panic attacks and anxiety……then around the same time as Megan I had a few very strong vertigo attacks, also waking up occasionally with vertigo……these attacks caused me to develop pppd….this has lasted for about ~3 years now…. Discovering this KZfaq channel is a life saver…… I am actually from Florida but have been living in Japan…my diagnosis has come from Japanese doctors…..it has been a wild experience….

All I can say is thank you...😢

Oh my god, I have every single symptom Megan described and I was going crazy. You are such an empathetic person and I have gotten so much better just watching your and dan’s (pain from you) videos and can’t wait for full recovery to happen.

I found it very interesting when she mentioned the time of year when her symptoms improved. My symptoms started in November 2021 then suddenly began improving in the summer around July 2022. I almost felt completely normal until September when they all flooded back again. I always start to freak out about the Holidays starting in the fall. I can never tell if that's the trigger or if I get triggered from knowing I feel lousier in the Fall/Winter.

Thank you so, so much Dr Yo and Megan. I cried tears of utter relief when Megan started to describe her symptoms. Her symptoms are identical to mine in almost every single way. My symptoms started in September 2021. Getting to the bottom of this has been an absolute nightmare but in the back of my mind I kept on thinking surely other people have had this too and there must be an answer. Almost two years later I have finally come across your KZfaq video which has given me the answers and the reassurance that I wasn’t going crazy. After the past two years, I saw a GP, an ENT, a TMJ specialist, a neuro ophthalmologist, an optometrist, an acupuncturist, an Ayurvedic Dr, a physiotherapist, a physiotherapist who specialises in headaches, a massage therapist and a naturopath. The last three professionals have helped me immensely and I’m almost feeling 100% like my normal self again. I think gut health is a very important factor as part time of the healing process with this condition, that’s what the naturopath and I are working on. Best of health to all who is reading this.

This video has really showed me it’s all going to be ok. Megan described every symptom I have especially numbness and feeling like you’re having a stroke. It can be absolutely terrifying but this has helped me realise I’m safe. Aswell as head pressure which also made me feel like I had a brain tumour which is brutally distressing.

Megan is so tough! I’ve been dealing with dizziness for four months and currently have been diagnosed with vestibular migraine and PPPD. I went through terrible vision such as double vision, and blurry vision. Double vision is gone but I still have blurry vision with the supermarket isles. I also have terrible brain fog. I dealt with the tilting and spinning of room but that seems to be gone. I think my neuropathway is messed up and my brain is trying to recoup with living with dizziness. I still have a migraine at the back of my head. Constantly. I’ve seen an ENT doctor, two neurologists, 3 PCPs, 3 eye specialists, and I’ve had an MRI of my head, neck and spine. MRAs, cat scans. I’ve seen neuropthopthomology. Everyday I feel like I’m not here and I am. I hope to get better soon. Currently just taking SSRIs

I feel just how Megan felt. I also want to be a success story. I was out of work the last month and a half. I am back now and struggling. I am definitely not giving up. Thank you both!!😍

I’m going through this about 1.5 years. See No hope or help yet. I get it. I cannot do daily tasks. So tired of doctors just not listening to me and how bad I can’t keep going on like this. I can do absolutely nothing 99% of the time. Hold on to furniture and doorways to get around the house. My house looks like a disaster area. I’m at my wits end.

Thank you for posting this … I’m going through it now since September this year… I feel so bad because my kids are home on they Vacation and I literally cook really and have them serve themselves as I walk fast to my room to lay down 😭😭😭 My head just feels so heavy and I just feel so tired 😭 including having all the other dizzy symptoms 😭

I am so glad you got the help you needed, it's been three years for me to finally find out I have PPPD. I am begining my journey of healing using Neuro plasticity.

I cried so much seeing this video. THIS IS ALSO MY STORY! I've been burnout for the past 9 months and having ALL of the exact same symptoms as Megan. I've been to a neurologist related to the pressure in and on my head and the dizzyness but he couldn't find anything. The people in the burnout Facebook group are very loving but nobody had the same symptoms as me. Hearing Megan's story gives me so much hope!!! There is someone with the exact same symptoms who is cured Thank you so much for sharing!!!!!!!! Greetings Ingrid from The Netherlands

Man, it's great to not feel so alone. I've been dealing with the same for quite some time now too. Thank you for the insight and sharing your experience ❤️

I can one hundred 💯 percent resonate with this as I myself still going through this 😢.. it's been four years for me now this swaying/ rocking dizziness and it can be really frustrating at times, well it was really frustrating and saddening in the beginning for me but these days I've learned to accept this as I still hope and the rest of us to overcome this stupid dizziness. All of her symptoms and more I had also and more..

Im so happy you recovered, im still unfortunately still battling with mine. I actually have the same symptoms but i was diagnosed with vestibular neuritis, but i feel for you, They are terrifying.

So happy for you, Megan. You give us hope. You both were trying to fight back tears, but I assure you there weren't many dry eyes out here. Thank you, both. Be healthy

I have all of those symptoms and some, could be my story. Difference being im older 53 and had to go on a snri as i at my lowest ever. Now i can function, am driving, interacting with my kids (i could only manage a few mins conversation also)supermarket shopping and watching tv etc Was also interested to hear you had the brain zaps, I had my first one the other week, was absolutely intense like my brain was trying to reconnect. I also have had the vertigo spells lasting an hour and my heart rate used to sit in the 90s, highest it got was 112. It has calmed down now and the BREATHING and SOMATIC TRACKING IS A GAME CHANGER DR YO!! I am doing the course and enjoying it, never thought I'd enjoy anything again. I cried hearing your story Megan, I'm absolutely so happy for you. Dr Yo I believe you are an angel saving lives also. I hope to one day when im healed to complete my counselling degree that PPPD took away from me at the end of my first year and specialise in pppd also. Thankyou both and bless❤

I’ve been following you for a while and am amazed how your approach to chronic dizziness resembles mine. I am a mind/body therapist, British but living in France and suffer myself from PPPD. I coach people in French, helping them to get on the road to recovery using similar techniques. Thank you so much for all you do.

This video have been SO encouraging to me, I no longer feel alone (insert crying emoji here) THANK YOU!

I was literally getting ready to ask if Megan had ear fullness and as I was typing, you brought up her ear fullness!!! Thank God for both of you!!! I have been searching and searching for answers. Mine symptoms definitely increased after one stressful event after another along with chronic anxiety. Thank you so much for sharing this information!!

I'm watching and crying, this is unbelievable. Going through the same thing, been almost 2 years now. Seen all the specialist, did all the test, but nothing is working, I don't have a real answer and I feel like I'm crazy. Thank you for this video. Grateful to have found it and I' m working on getting my hope back that it will be over one day.

Thank you Megan for sharing your story and thank you Dr. Yo for giving her the medium to do so. You ladies, are doing the Lord’s work for sure. This one recovery story helped me more than I can say… Although I have not had my swaying sensation for as long as Megan or as severe, I can relate so much to a lot of what she says. All the symptoms and how they would change, bouncing from specialist to specialist. I’ve listened to this at least twice in it’s entirety and in bits and pieces at moments that I’ve just needed a little reminder that it’s possible to recover. Also, I’m shocked to learn, it took Megan over a year to have 1 MRI in the UK. I had 3 MRIs in 6 months, totally unnecessary.

Thank you for sharing your story. I am anxious all my life and i think that triggered my chronic dizziness. Same experience as yours I haven't seen a doctor who knew about PPPD. It makes me anxious even more. Your story makes me hopeful that it is still possible to be normal again.

I'm super dizzy and in Florida! lol So many of Megan's symptoms but never been diagnosed even though I've seen every specialist and had so many scans....currently about to start my journey of journaling...been devouring all of your videos and all of the success stories. I signed up for your free program AND the free trial on Curable. I'm ready to regain myself or a new and improved version of myself again!

Doctor Yo I live in South Africa and all doctors ive been to thought i was crazy. I am going to enrol in your course and be your successes story one day 🙏🏾

I am so happy to watch this Megan and Yonit😍. Megan, your story is testament to how effective Dr Yo’s guidance with this condition can help us on the road to recovery .What you have been through in the last few years has been so hard, but you have got it all under control. You’ve been a good support to me over the past few months, answering my various questions etc…wishing you all the best with your coaching and thank you for sharing your story with us x

I literally have EVERY SINGLE symptom Megan had!!!! 😢😢😢 I feel like this interview was me talking. Ugh!!! I’ve also had this for 3 years and seen every single dr and test out there. this interview was so eye opening for me and gave me hope!! I pray I can heal like her!!! Did she work one on one with you? Or just do your free course? I want to do everything she did!!

I have had all of her symptoms for 4 years!! I can so relate to this interview. Thank you so much for all you do, it is helping me so much.

Thank you for this interview. It’s giving me hope that someday I will get over this. I relate to so much of what Megan describes. Although, Instead, mine started with severe vertigo that landed me in the hospital for 4 days. After Lots of tests and scans and spinal tap. They told me i had vestibular neuritis and it most likely damaged my vestibular nerve. Two months later after a VNG and other testing they said I had 68% hypo function do to vestibular nerve damage. I’ve thrown up countless times in the initial four months experience. I’ve since learned to deal with the constant hungover nauseous feeling without getting throwing up. but it is still so difficult. I’ve been to three different PTs over the 3-1/2 years and I’ve developed a severe fear of falling do to the 7 falls I’ve had. I even tore some muscles in my shoulder and needed to stop seeing PT for the dizziness and instead started seeing a PT for my injured shoulder. I realize anxiety is a huge part of this but I can’t get around the fear of hitting my head or breaking my elbows and wrists. My neurologist has put me on an SSRI and propranolol to help with the anxiety but It has not helped my fears at all. It’s still an insurmountable challenge. I’m hopeful that the things I’m doing on my own now will help more than the crazy things they were having me do… (I’ve run out of PT sessions until next year)

I am very much elated for this young lady’s recovery and the willingness to share her success. She has served as a catalyst for everyone and myself who is experiencing this terrible situation. I am from Florida. Thanks.

This sounds sooo similar to my experience, I’m 10 months in from my initial vertigo attack, trying to be patient and optimistic! Glad you’re doing well Megan!

This gives me so much comfort because I had every single one of these symptoms and a few more. I would love to work with you. I literally feel like she is describing me. I’ve been dealing with this for 3 years now. The last 7months have been worse than usual. I hope I can work with you.

I'm only just starting my journey towards mending myself, thank you for this video it gives me a slight hope.

Glad this channel is doing amazing things, unfortunately a lot of ppl who suffer from this aren’t getting the support or help they need. Cawthorne Cooksey exercises, mild walking and breathing exercises definitely help!

Omg it’s crazy you said that you’re in Florida . I’m actually in Florida’s too, I’m curious what city you live? I could relate to Megan so much with almost everything she was going over , kinda like we’ve lived the same life. It’s been almost 2 years since dealing with this. I’ve been following you the last few weeks and I’ve been able to self diagnosed and been able to start my healing journey . I am very grateful for your channel! I would love to one day be able to do a success story too 🙌🏾😩

Dear Yonit and Megan, thank you so much for your interview. I actually can’t believe I have found this!! Your story, Megan, is amazingly similar to mine. I could be telling my story almost word for word. I am still in the midst of it .. and I have dark days. But your interview has given me hope and I am feeling excitement for the first time in years at the possibility of healing. Like many, I’ve tried it all.. and I’ve been dismissed by medical professionals who don’t believe what I’m telling them, who say it’s all in my head and there is nothing I can do. Thank you for your story.. it is inspirational. I am so happy for you Megan and so grateful for you both.. ❤

Thank you for this. I have a verbatim story, but identical. Today was a day I felt I can’t carry on, but your story inspired me to keep at it.

Thank you so much for this video ! I cried because it's the 1st time I find someone who have the same symptoms as me. I was better for a few month but everything came back (at a lower lever hopefully). I will keep working hard to get back to this better time.

I can relate to your symptoms. I was diagnosed in 2008 with vestibular migraine. It was complete hell and took forever to get a diagnosis. It’s been up and down. Stress definitely triggers my symptoms. I had several huge stressful events, husband’s cancer diagnosis, daughter diagnosed with Type 1 diabetes, and that’s just the tip of the iceberg. I have always been told by my neurologist that I will always have this and learn to deal with it. After seeing your video, I believe there is hope after all these years.

Idk how i came across your page but i suddenly got dizzy after a cold and on going cough i fixed that and than became dizzy in april i literally did ct,mri went too different hospital even at hospital i work at switch doctor it subsided i still had everyday some days nothing than boom its been like since feb bk and same way was before i feel exactly like you lord imma drop dead they can’t find issue smh im so happy i found you 😊😊

Wow. Thank you both SO much for doing this video. Megan your story is so inspiring. I can relate to so much of it. I particularly relate to where you were nine months ago when it seemed like there was no hope and you barely left your room. But like you, somewhere deep inside I also have a tiny little subatomic particle of hope. Some part of me knows that I can get better. I refuse to accept that this is how I will live the rest of my life. And hearing your story helps so much. I could write a book just responding to so many of the things you said! Super-sensitive, health anxiety, bad relationships, all your symptoms…But for now I’ll just say congratulations on your journey, Megan. 😊

I'm in this for 9 years. I think I need you. I'm in Germany. Thank you ❤

It’s really like Megan is giving voice for all of us struggling with this terribly! And you & she of course give us hope through your words thanks a ton for that❤️ I literally cried at few points in the video 😅😅 but yeah, we got this guysss!!!! Love from India 🇮🇳

I would take baths too (and still do) because the water helps mask the boat-like sensations.

So pleased to know of your recovery Megan. Thank goodness you found Yonit! 🙌

Wow I was dianosed with vertigo years ago I always taught I was in another place I stay stressed worried lonely maybe hope yep but thanks so much both of you I’m so proud of your accomplishments

This sounds exactly like me! Down to every little detail of symptoms etc 😳 this gives me hope. Thank you!

Megan! What a story of perseverance. I’m tracking with the same symptoms and the same process. Way to hang in there!! You are learning so much more than just dizziness recovery. I have a feeling you will embody and impart a deep wisdom to others because of what you have experienced. Bravo!!

I can reciprocate with all the symptoms . My symptoms have been 24/7 i feel so drunk like i am high all the time. Can't focus my vision on anything , i start feeling imbalanced unsteady and disoriented, its like my brain is all freezed up, i just can't think of anything it becomes no non functional state. I only feel good when i am lying on bed or there is constant head support or while i am driving. Stillness drives me full in panic mode. I have been having this since 1 year I was also diagnosed with unilateral vestibular hypofunction

Loads of love to this channel and all of us❤❤❤❤❤

Thank you, Megan and Dr. Yo. I have pppd and on top of it, just had two brain surgeries, so the symptoms are the same, but more intense. Currently on a walker because of it. My dr said I can still heal in time and get my balance back. I definitely need to work on my anxiety and sleep issues. Will do the breathing technique. Thank you!

Wow this is exactly what I experienced, thank u , it all makes sense now, been experiencing this for 2 years now

Megan, you are a brave girl! So happy that you are finally healed and of course you would've done it without Dr Yonit. Thanks for sharing your story which is definitely my own story too. I was crying watching this interview..I was diagnosed with MDDS this year 2022. I suffered from this dizzeness and balance issue since 2020. I am hoping that I will be healed also and get back to my normal self..I have so much Faith.🙏🙏🙏

Meghan wow wow wow. This is motivating me. There is healing at the end

I completely understand, I have had this since June of 2022. All of this is so true. I get in my car. N drive n it goes away. But the dizziness I s awful some days.

OMG... This is my story, it has given me hope. Xx thank you both. I will start the free course today. I am in Australia.

Thank you for sharing. I have every symptom that Megan described from swaying, neck and shoulder discomfort, ear fullness, etc. Nov. will be 2yrs from onset. This inspires me to remain positive no matter how many negative stories I read within the various FB vestibular support groups.

Hi, Thank you for sharing your story and also Dr.Yo. Finally, I found that what is my dizziness. One day, the KZfaq automatically showed on my TV. My experience and Megan's experience are exactly same as mine . I live in Canada but I am from Japan. I went and tried to whatever both Dr.s said. I still have it but I feel gradually getting better now. This movement has been on for 3 years and 4 months now! Thank you!

I was diagnosed with vestibular migraine and had PPPD set in afterwards, which was terrifying. Watching this after my symptoms started making their way back just relaxed me so much. The fear of it getting so bad again is real! Thank you Megan and Dr. Yo. ❤

I relate so much to what Megan went through. I have the same exact symptoms as her and I’ve been going through it now and I have been dealing with it for 7 months now. I have really bad anxiety as well as health anxiety and stress before it started and it has gotten worse since the dizziness started. I’ve gone to the doctors so many times and everything has come out normal and i feel like a crazy person because I feel like they don’t know what I’m talking about. They even recommended anxiety meds but I don’t want that to be my first resort. I even started losing hope just like Megan. I’ve been such an emotional person because I just want this to go away and even just started therapy but even therapists never have heard of being this dizzy before. I just want to feel better and have my own success story.

I literally have tears watching you. I have had a lot of trauma over years. First symptoms started post cruise but over a number of years starting in 2022 I have had symptoms not cruise related and thought I was going crazy, thought I was going to die, have even been taken to hospital and told that I had an NSTEMMI due to increased troponin, I told them that I thought I was having a stroke as it was my head, I couldn't walk straight, I felt like I was falling particularly when laying down which set of panick. 2 other trips to hospital after same feelings, told SVT. Sent to cardiologist and nothing wrong with my heart. Most recently high stress and symptoms have started again, the falling feeling scares me. I have also been to have ears checked as i get severe ear aches particularly before periods but nothing wrong with my ears. My GP has started me on ant depressants and valium and believes i have MDDS. I just hope it stops or I may need to go live on a cruise ship :p

Another wonderful success story! Congratulations Megan - you give me hope as I am just starting my healing journey. Thanks so much Dr. Yo!

Thank you! Thank you! Thank you! I have the same symptoms! It's scary!! My eyes move by themselves, they can't focus and now have memory issues also. Everytime I'm dizzy, all the other symptoms get worse. Neurologist gave me otc supplements and told me to come back in four months.

Thank you both for sharing your wisdom, insight and experiences. Megan, your honesty and vulnerability are such an asset to your story. Thank you both for helping so many of us all over the world.

Dr. Yonit, thank you so much for this video. And Megan, thank you for sharing your story. I relate so much to what you've gone through as I've been suffering from chronic dizziness for almost 2.5 years. For me it's always when I'm still and laying down, and I feel better when I'm walking or in a car. I've also had a lot of stress and health anxiety, and have basically been living in my sympathetic nervous system for most of my life. I'm doing all the things you suggest - deep breathing, yoga, living my life - but it hasn't budged and is incredibly hard to live with. Still trying, though, and very glad to hear you made your way out of this. Megan: did you feel worse when reading/using screens? That's a huge trigger for me, and makes my brain feel like it's moving/pulsing even worse. Dr. Yo: I've had numerous doctors see a nystagmus & convergence insufficiency in my eyes, and am currently seeing a neuro-ophthalmologist who follows Dr. Zelinsky's method from the Mind Eye Institute. She has me wearing "brain glasses" as a way to retrain my brain. Are you familiar with this at all? If so I would love to hear your thoughts. I'm having a hard time understanding if the dizziness is a physical issue stemming from my eyes, a nervous system disregulation, or a mix of both. The glasses are super unpleasant but I've gone down so many paths and just desperately want to get better.

Im also Dec 6 too , I suffer from never ending migraine headache , and I am now experiencing a tingling crawling on temple and around my left eye and now its now reaches my whole left side on my face, and experience, and when I sleep I move so much my feet sometimes get colds or warmth.

Megan , I really feel for you because i could really relate to what you went through. I have this constant swaying-on-the-boat feeling. I feel it more when in a resting state and even when laying down trying to sleep thereby i don't much sleep. I can also relate to the heaviness when I walk my body feels as if I am walking with extra weight and feel tipping over. Funny that you mentioned feeling better in the car because i feel the same its movement is distracting. Megan so many things you have mentioned resonate with me even the visual aspect affecting your perception of the world. I went to so many doctors, Ent, Neurologists, Mri, general gp, chiropractors, and physical therapists. Nothing is working. The only abnormal blood work back in June was a low ferritin (iron storage) count, yet I take iron supplements and had a fusion about 3 months ago thereby would be feeling better. The neurologist could only suggest that i am suffering from central vestibular vertigo. and the neck doctor says i have some degenerative. Yet I have to say I have had major stress prior to this condition. I had a rough couple of years, I was living far away from home away from my immediate family, and also in a rough marriage, he put me through chronic stress. Megan I would love to hear from you if possible to seek advice in starting in recovering ..I am also a fellow Sag =) Dec 1 we are survivors. Thank you for doing this video it is very inspiring, it's truly a blessing.

Thanks so much for sharing your message. I finally found Dr yo and your journey about your illness and healing. I've been trying to find people to help me as well. I'm getting better slowly, but knowing this will help me to heal faster. I've been dealing with this for 2 and half yrs. God bless you. I not crazy after all...

Thank you Megan and Dr Yo, this is so encouraging and the best part is I can work on this with community help and you Dr Yo.

Wow! This gives me so much hope - and I’m about to give up. Been struggling with rocking, swaying, pulling and other strange sensations for nine months now. The docs can’t help me - as all their tests are normal. I don’t know what to do!

Oh gosh thank you Yonit and Megan. I can relate SO MUCH to this video and it is literally amazing hearing about you getting through this Megan and to hear where you are now. I had automatic tears lots through this video. So lovely to hear such a positive end to your story. Megan-your written comment about feeling claustrophobic in your own body made me say ‘Omg’ because I had this for so long. I just longed to be able to feel at peace inside and be able to enjoy spending time alone ‘in my body’ and feel at ease. Dr Yonit, I hope you feel forever proud for what you do for this community. You help us find answers when there are none in our everyday lives when we initially see medical professionals . My wish for the future is that medical professionals learn about this and can give people the tools to heal and the positivity that you CAN heal. Thanks both and good luck with your future coaching Megan, it will be lovely to have more people helping like Dr Yo and spreading the word and help over the world !! Please do a world tour Yonit, 😊I’m midlands UK 🇬🇧! X

I understand what you went through. I feel the same everything you did with doctors anything out there to bring me back to myself 😢

I'm so happy for you Megan I've been watching your KZfaq videos and seeing your progress is very inspiring. It gives me so much hope that one day we can also recover and live our lives 🙏🙏

Wow… she’s describing my symptoms exactly. I need to start your program. Been dealing with this for years. I’ve been close to recovered before but never completely and will have symptoms reappear during periods of stress

What a fab interview! Ready for the follow up!!

Thank you for this. The one place where I feel really good (except when lying down) is also in a car!