Constant rocking/swaying feeling for 7 weeks and counting

Posted , 12 users are following.

So my illness began about 7 weeks ago now. Initially I experienced two seperate short occurrences of a strange rocking swaying sensation... almost like someone had pushed my brain very hard inside my head so it felt like I was moving but I wasn’t. The first two times it happened were both after hiking, but both times I had been hiking at very low elevations. Then about a week after the second occurrence my symptoms hit full on and haven’t gone away since. I wasn’t sick beforehand, I had no allergies, no migraines, no concussions or head traumas, I had flown a month earlier but had no issues during or after the flight... I felt well the night before, and then wham, it hit and I’ve been feeling like I’m moving ever since. Unfortunately I have been off work for almost the entire 7 weeks and will be unable to return to work until this mystery is solved. I feel like my life has been put on hold. I can’t work, exercise, drink coffee, have a glass of wine... even trying to meet a friend for support is difficult because it’s hard to concentrate on being social when your whole world is moving. This obviously all leads to an insane amount of anxiety and sadness, constant tears and frustration. I want my life back and all the testing and trying to figure out what’s going on is just taking way too long. I’m hoping someone sees this and maybe has had similar symptoms and got a diagnosis or a cure? It’s a long shot but I’m desperate to get my life back. If anyone has any advice or ideas or similar experiences please let me know! So read on for more details on my symptoms, testing and treatments I’ve had so far. 

My symptoms include:

- constant feeling of swaying back and forth, front to back and sometimes up and down with the feeling that my knees will buckle or the ground is falling under me. It’s like being on a trampoline or getting off a carnival ride almost all the time. But having said that it is NEVER a spinning sensation. 

- the above symptoms are a bit better laying down, I feel them sitting up and they are the worst when I stand in one place, for example to do dishes, or the absolute worst when I walk, especially downhill. 

- the “dizzy” symptoms described above are always there to some degree but they vary with how badly I feel them throughout the day. The only time I fully don’t feel them is when I’m sleeping but I have woken up a few times since this happened feeling like I’m moving laying down.

- the more physical activity I do throughout the day the worse the symptoms get.

- the more I look at screens, be it computer, phone or TV the worse the symptoms get. 

- headaches have become an every day occurrence. The worse the dizziness the worse the headache. It’s usually in the temples or sides and back of my head. 

- there is often pressure in my head near the temples and sometimes near my left ear. 

- I have ringing in the ear in the left ear. It only comes occasionally and nothing in particular seems to trigger it. 

- I have had difficulty with my vision being blurry and little spots or shadows in my vision.  Difficulty focusing on things close up, especially if they are moving. 

- It has been very difficult to concentrate. I often have a hazy feeling or head in a fishbowl feeling. Almost like I’m super hung over and my body and brain just aren’t firing on all cylinders. 

- it is difficult to be in really busy places like malls or restaurants or crowded sidewalks. 

- my muscle strength has been greatly diminished over the month and a half this has been happening. There are many days where I can’t even lift an 8lb weight 10 times without my arm muscle going into a spasm. I have been attempting slow and low rep hand weight lifts in an attempt to not completely lose all aspects of my fitness while trying to figure out what is going on. However any attempts at walking for any distance or weights or even physio exercises leave me drained with muscle cramping, numbness/tingling and I often have to sleep after to recover. 

- driving is surprisingly completely unaffected. In fact if there was a time where I actually felt like maybe I might not be dizzy it would be when I’m in the car driving. This seems to make no sense whatsoever to me. You’d think the motion would make it worse, but it almost seems to override whatever is going on with my balance issues. 

Treatments and testing so far 

- Initially I was told it was a viral inner ear infection - treatment with oral steroids and serc. No relief.

- next told it was bacterial inner ear infection. 10 days on antibiotics. No relief.

- next blood testing to rule out anemia and migraines. Given migraine medication. No relief. 

- saw an ENT who feels Ménière’s disease is likely. Received a steroid injection directly into the ear. No relief. I have an appointment for another injection soon. 

- currently waiting on an MRI, a 2nd opinion from a different ENT on Ménière’s being the cause and also waiting on an appointment with a balance specialist. 

- acupuncture was tried twice, no relief.

- an eye exam has been done. No signs of binocular vision dysfunction and the optic nerves tested perfectly. Nearly 20/20 vision.  

- I have been seeing a physiotherapist for balance exercises, currently awaiting an appointment with a new physiotherapist who specializes in vestibular rehabilitation therapy. 

- I have gone for multiple massages for my neck and head as well as cranial sacral massage, all providing no relief. 

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  • Posted

    So sorry I understand what you are going through. I constantly feel like someone is pushing me forward and I stumble around like a drunk. I have a hard time at work looking at computer I can’t go to work a lot because of it. Thank gosh I’ve not been fired. I have had MRI cat scan heart checked ears checked. All the doctors say is it is Ménière. I’m on 2 months since my last attack and still feel this way. When I roll over at night I wake up because the room rocks. I try to leave a light on at night that helps and if I lie completely flat the room spins i can’t do it.   I can’t look up or down without spinning. Or turn my head to fast to the side.  I have watched what I eat stayed away from salt. I  have been doing the exercises with my eyes and I have noticed a difference   I don’t rock as bad now. I don’t have anything to tell you to make it better other than your not alone. I will say I think everyday is a little better but I don’t think this will ever completely go away.   This sounds crazy but when I’m feeling bad about it my dog being there with me helps And I try not to think about it to much because I’m quite sure anxiety makes it so much worse.    Hang in there

    • Posted

      Thanks for the response. I am not 100% certain mine is Menieres yet. If I do find out without a doubt that it's Menieres I will have the ear surgery to make the constantly moving feeling go away. I definitely can't handle feeling like this forever and would rather have hearing loss in exchange for making the dizziness stop. Have you considered the surgeries? Sorry to hear you can't work much. I'm glad you have your dog for comfort, I don't think that sounds crazy at all. The companionship of animals can be very healing. Best of luck, I hope it gets better for you soon!

  • Posted

    I know how you feel and sympathise so much. I have been diagnosed with Ménière’s and had all the usual tests to rule out other things. Even saw a neurologist in case it was MS but the MRI showed no lesions but there was fluid in my right ear which is the one with the hearing loss and tinnitus. I get the horrible drunk feeling and eyes have floaty things in them. Tingling in my head and down my arms. The balance clinic said I was suffering migraines but I never had headaches as such just pain behind my eyes. They said it was my eyes trying to deal with the loss of balance.

    I have recently had the balance rehabilitation therapy which has helped but I am still very off balance most days. Once I try to do things the horrible vertigo starts and I feel nauseous. You need to get a diagnosis so you know what you are dealing with. I live in the UK and appointments on the NHS take months so if you can afford it go privately to see neurologist who specialises in balance issues. I think they are called otoneurologists. 

    • Posted

      Thanks so much! I'm waiting to here back about specialist referral appointments right now. If it is going to be months more of waiting I will pay privately. I'm hoping to not have to miss work for much longer. Have you considered the surgeries available for Menieres?

    • Posted

      Surgeries were never offered to me. Don’t know why. When I was younger it wasn’t too bad but the last few years terrible. I asked my GP to send me to an otoneurologist and after waiting 3 months for the appointment when I got to the hospital he wasn’t there and I saw an ENT woman who sent me for balance tests and then to the balance clinic. I should have insisted on seeing the otoneurologist but you are just so happy to get to see someone who might help but in hindsight I may have gotten better treatment. Got the impression ordinary ENT people don’t know enough about Ménière’s. I take betahistine 16mg 3 times a day to try to stop the bad episodes but I struggle to do very much.

    • Posted

      I'm sorry to hear that. I also agree with your opinion on the ENT's not seeming to know enough about this. In the short time I've been dealing with this it actually has become incredibly clear that all doctors seem to know very very little about vestibular issues. I get looked at like I'm some sort of mystery case a lot. Which isn't exactly a reassuring feeling. I know it is sooooo tiring. I've only been dealing with this for a month and a half and I am absolutely exhausted most days. I can only imagine it must get worse and worse with time and no answers. But if I were you I would push again to see the otoneurologist you didn't get to see. And I would suggest also enquiring about the surgeries to at least see if they are an option for you. This is our lives, sadly we have to advocate heavily for ourselves within the medical systems. I'm tired of having to feel like I'm fighting to have my health taken seriously, but there is no way I'm going to sit here and accept that I'm going to feel this way forever with little to no relief. This link outlines the surgeries available for Menieres near the bottom of the page. They may not be for everyone, but maybe worth a look. https://www.mayoclinic.org/diseases-conditions/menieres-disease/diagnosis-treatment/drc-20374916

  • Posted

     hi mcg0586 sorry to say but once we get this it really never goes away do you get the ringing in the ears too the fullness in the ears the pain in the head doctors told me are now vestibular migraines first told me it meniere,s disease this has been going on for a year every thing you have written down  I have  it no fun I am sorry to say we have to learn to live with this I had to retire from my job because of this sorry it not good news but you are not on your own we are all hear

     

    • Posted

      Thanks for the reply Valerie. I'm only in my early 30s and I have a family, so unfortunately retiring from my job will not be an option. I hope that you will find some relief. If I come across anything at all that provides me with relief from the dizziness I will be sure to share it on this forum.

    • Posted

      hi mcg0586  thanks for your reply it great to have this page to talk to other suffers don't feel so alone do hope you get some relief too

  • Posted

    Have you had a VNG test? VNG can tell if the cause is inner ear like vestibular neuritis or menieres. VNG can be normal between menieres attacks, but it sounds like you are currently symptomatic.

    • Posted

      Hi DizzyLizzy. No, I haven't had this VNG test done. I am currently symptomatic. Do you know if it would usually be an ENT that would do this test? My ENT didn't do much testing before stating he suspected Menieres. He did all the same head and body movement tests as my physiotherapist did. Then he said he was 90% certain it was Menieres and said his best results for helping it had been a steroid injection into the ear. I allowed him to do this because I'm desperate for anything to help. But it didn't help and now I'm regretting trying it because it made my symptoms worse all week. He wants to do another injection this afternoon but I'm going to question him on it because I don't feel he's done enough to rule out other causes. Plus if he can't say for certain that it is Menieres, then why should I be sticking more needles in my ear, especially when the first time he did it, it didn't work. 

    • Posted

      Is the vng test where they put warm and cold water in your ears
    • Posted

      Yes. VNG is a series of tests that monitor the movements of your eyes via goggles that record any nystagmus while visually tracking certain things, and doing positional moves. It includes a caloric test which blows hot air or water into the ears to elicit a normal vertigo response in ears with undamaged vestibular nerve as well. It is a test typically ordered by an ENT. It can specifically point to vestibular issues such as menieres, labrynthitis, BPPV, etc. I've had 2 in the last 3 yrs, both ordered by different ENTs that totally suspected Menieres. They used the results to rule that out. Also, my dizziness is never spinning, so I am told it is most likely not menieres.

    • Posted

      That's part of it- the calories test. There's also the visual tracking and positional testing.

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