The uptick of new patients is unbelievable, but we understand. The Virus is a real game changer in the past 4 years - tons of new cases. On a bright note, early happy birthday!!!

Love it!! 🥰 Happy about your hearing 🩷

I discovered it seemed the ease up during colds is that the runny nose actually decongested the sinuses. I once tried cinnarizine (first gen antihistamine) for my nausea and dizziness, it worked but i was so drowsy and then after the med wore off the symptoms came back even worse.

Thank you for this. I was diagnosed a month ago and recently joined the group. Every time I open my FB app, there's a scary post from the group and I've been terrified of what my future holds. Your calm demeanor and matter-of-fact delivery have made me feel a little better. I'll definitely check out more of your videos.

So true. You have no idea communicating on line of what that person’s health history is. A lot of us have more than one chronic illness so you could do harm. Their doctor will look at the whole picture. A lot of meds and supplements people suggest to use I can’t but you must know if you want to try anything….run it by your doctor first.

In reference to my medical condition, I would like to bring to your attention that I was initially misdiagnosed by our company doctor, who is a ENT. Instead of recognizing Meniere's disease, I was simply diagnosed with dizziness, which unfortunately led to the loss of my job. Despite having three separate diagnoses from reputable ENT and neurology specialists confirming Meniere's disease, the company doctor's oversight has had significant consequences for my professional standing.

Cute dogs! Life is better with dogs:)

Thank you for sharing this! I hope you feel better soon! I find that loss of sleep is a flare factor for Meniere's.

You know what I'm done wirh explain what I'm going through to people. I just live my life and if they really care they would understand. ❤

I drink my decafe coffee and I enjoy that.

Dave they think you are crazy and drs are quick to prescribe ssri

What brand & type of hearing aids? Cross or Bicross?

That’s why it’s important to show the bad days as well as the good. Sometimes climbing Mt. Everest might put you in bed for a week.

I'm really glad for you ❤

Every time you said “Whoaaaa” I had a big smile on my face 😊

Thanks Dave. You give me hope❤

In good time! It'll be for the best, cheers!

Any issues with your neck

I had no idea they made hearing aids that double as earphones for things like digital media! Do you get any funny interferences with your tinnitus (if you're experiencing any)? And can you wear them at a concert, too? I remember how inconvenient the ones my grandma had were, and then I became really discouraged when I read that, allegedly, you were supposed to start training your brain to adjust to hearing aids when the hearing loss was still in its beginning stage. They basically said that you couldn't regain long lost frequencies. I guess those were either false news, or research and technology have improved a lot since! These are exciting news and I'm so happy for you; I'll look into it! One request I have for you would be to please put product names, as well as terminology like the name of the procedure you're going to get, into the info box? I couldn't catch some of them and it's important to get the spelling right if you want to look things up. :)

I can't believe this channel exists. I was diagnosed in the early 2000's as a rare (very young) case. There was nothing about it on the internet! And if there was, it was like a one-paragraph encyclopedia entry with no real information. No real people were talking about the experience. Menière's runs rampant on my maternal grandmother's side of the family tree; it stole a decade of my life by way of extreme vertigo attacks, and by being used as a guinea pig for all sorts of contemporary medication. The long-term effects continue to affect me. Sigh.

Just completed post-labyrinthectomy vestibular therapy. It was so very helpful to have heard your advice, and it helped me persevere. You have my heartfelt thanks. I am walking confidently indoors and out, and have resumed driving and daily fitness exercises and swimming. The therapist said I don't need to continue the exercises, but I am concerned I could lose my progress, so I still complete one full set of the exercises daily. It has been over 2 months since my surgery. May I ask, did you continue the exercises after completing vestibular therapy? If not, did you lose any of the progress? Many thanks!

In good time! Rooting for you MD warrior!

I did my phone hearing 3 days ago and everything seemed like it went good but he said he would need my last paysub before he can make a decision? Do you think thats a good sign ill be approved or just something they need no matter anything? And how did your money come? Check or on card? Because they never asked about a card or account number or anything, im just so nervously because i been denied twice already

Thanks a lot for sharing this video and congratulations on getting your hearing back. Sir I watched one of your old videos and you had Labyrynthectomy in your left ear. With hearing aides is it possible to get hearing back in ear which has been operated with Labyrynthectomy? Please clarify . I too had Labyrynthectomy and operated ear is totally deaf.

I’m so happy you love the Oticon. I have a Phonak (not cross fit) power aide and am very happy with it. Btw, the part that goes into your ear is the dome (I know you love when I correct you 😂). For me it always took about 2 weeks to get used to a new hearing aide. Enjoy hearing ❤😊

I’m so glad you love your hearing aids. I hope the pollen and your dizzies get better soon.❤

Thank you so much for sharing this! I had my labyrinthectomy in June this year, and am hoping to get a hearing aide soon. My hearing in the other ear is not quite bad enough to qualify for Medicare to cover the hearing aide. I am trying to decide if it’s worth the cost, without insurance coverage.

I am so very happy for you! I had to have a Cochlear implant 5 years ago and I understand what a difference hearing after not being able to for a good while is.

I have MD like symptoms 6/7 yrs vertigo tinnitus in both ear and hearing loud sound feels like vertigo feeling nervous while driving

Hope you are having a winning Wednesday and that your hearing aids work great♥️

Morning Dave. Yes thats terrible to feeling like that. Really hope en believe you feel better now. That's sound that you have a migraine attack too. I know that feeling. Good luck and God bless.

Hey there Dave, So sorry for a Terrible Tuesday. I'm praying for you that better days are a head for you. This has been a terrible month for me. I'm right there with you. Take care 🙏🤗

I hope you’re feeling better.

Hope you feel better. Cheers!

... feel for You ! ~ This Summer for Me has been 'extremely' Brutal : ( I smiled when I saw your video title, My day was Horrible today too ... Yes, All the BEST for Wed : )

Hi Dave. Tough day here, too. I pray your symptoms from this episode resolve soon.

I’m sorry you had a painful day, Dave. I had a pretty awful day today myself. I’m wondering: do you take a medication specifically for migraines? If so, does it help you? I hope you can have a restful night. 🙏

Hello sir. Sorry to know about your Meniers becoming bilateral. How is your hearing now? Do tou use hearing aids? Can you communicate,walk , do daily chores, go for walk etc?

I love this video! Thank you! Also this change in life is redemptive suffering.

I am so sorry you went through this, I think I know who this person is. Yes, very rude but had good intentions in the beginning. I'm praying that he has a "come to Jesus moment" and he finds peace.

My symptoms are always worse when I don’t sleep for a few days. It’s a vicious cycle for me. Hope you get some good sleep tonight. ❤

Love the drawings! So happy those faces. I became garbage real quick with said person. I wish him well though❤

Sound Pharmaceuticals is please to Announe that thePhase 3 clinical trial involving SPI 1005, a navel anti inflammatory for the Treatment of Meniere's Disease (STOPMD-3) has been completed. Date: 31.07.2024 - Seattle

Thank you for all you do. I have learned a lot from you and others on the group as well. I'm glad you are continuing your KZbin videos. People are going to be the way they are just do what Jesus did, dust your sandels off and keep moving. Praying for better days for you🙏❤️ take care

This videos are much needed. I still can't accept the fact I won't be able to do the things I used to, the fact that this is gonna be the baseline from now on. Gonna try with therapy. Have a great weekend!

Lack of sleep makes things worse, that's for sure, but going to bed and feel like rocking on a boat does not help at all. Thank you for sharing.

Hello sir. Can you please tell how long you had menieres before going for labyrinthectomy.

Your story sounds similar to mine. (I recall the sweating episodes.) Except, I noticed something wrong several years before the massive attack occurred. I'd experienced many smaller duration attacks over the years, that seemed like food poisoning that included vomiting. I'd thought it was food poisoning from a restaurant, even though it dawned on me, that it would be hard to get food poisoning that often. So what else could be the problem? Most GPs don't know much about Meniere's Disease. And none diagnosed it until I had a major attack with massive vertigo and massive vomiting sessions. Still, it took an ENT to diagnose MD. Plus, there were many other signs, such as my balance and spatial orientation wasn't very good over those years and I couldn't understand why. Fatigue and brain fog was and still are major symptoms. I get the big four symptoms often (Tinnitus, Ear Fulness, Hearing Loss, Vertigo & Vomiting). Tinnitus all of the time, some level of ear fulness that ramps up when an attack is near, along with hearing loss. Usually there's a degree of vertigo that ranges in intensity when there's no attack, that hits mind-warping velocity during an attack. In addition to this, I have migraines with aura's, where I temporarily lose most of my eyesight. Some doctors say there's no connection to MD, some think there is a definite connection.