Ears are main post Covid complaint

Posted by dloos @dloos, Sep 12, 2023

Anybody else with ears being your main post Covid complaint?

I’m sixteen plus months of feeling underwater with ear pressure. My symptoms started after I thought I was fully recovered from a moderate case of Covid. Six weeks after Covid infection we went to Hawaii. The plane flight seemed to trigger these ear issues.

It started just as the ear pressure thing, but over these last many months it has cascaded into, tinnitus, hyperacusis, dizziness, blurry vision, and just as a bonus I get intermittent swollen nasal passages. It’s as if my whole head is closing up on me. Not surprisingly I’m now pretty anxious because I’m not stable, and the ear pressure and other symptoms continue to worsen.

I see reference to ear issues now and then, but with most people it seems to be their lesser issue. Believe me I count my blessings that I have had very little pain, but my symptoms have me going nuts.
I’d love to hear from any others out there who might be similar to me.
I’ve been to a couple dozen different doctors, and really no one has a clue. I have seen multiple ENTs, Neurologist, Endocrinologist, Audiologist, Optometrist, Ophthalmologist, Naturopath, Acupuncturist, Chiropractors, Vascular Specialist, and of course my PCP. Trust me, I am not an hypochondriac, though it does look like I might be. Until this, many times a few years would go by without my seeing a doctor.
I now know I sure took my good health for granted.
So, if you’re out there, I ‘d like to hear how you’re coping, and if you have found any answers.
Thanks.

Interested in more discussions like this? Go to the Post-COVID Recovery & COVID-19 Support Group.

@koliver

I can definitely relate to your comment! Mine was triggered Sept. 2022 after a 2 week trip into high altitude. I could have sworn I brought back some dreaded disease since my head hasn't been the same since. It's been one issue after the other. It's been like chasing rabbits, being referred from one doctor to the next, having various medical tests/scans, etc. I even ended up in ER with chest pains at which time they did a complete cardiac evaluation. So far, all of my tests have shown no major problems. Pulmonary test showed "minimal" pulmonary disease. At times, I've thought I was loosing my mind, never having had health issues before. THANKFULLY, I found relief using a low dose nicotine patch (3.5 which is half of a 7 mg patch), as well as supplementing with 50 mg of sublingual glutathione and increasing my Vitamin C intake. I was desperate, so I took the chance using this protocol. Strange as it sounds, within 30 minutes of applying the first patch, my head/ears actually opened up clearer than they had been in months! I have continued this for over a month, and have seen 75-80% improvement in my LC symptoms (off balance, head/ear pressure (like helium being pumped into my head), anxiety, brain fog, fatigue, shortness of breath, muscle weakness, joint paint) I have sought out the natural remedies, also adding daily Ashwaganda. I also use CBD oil daily. I've had good luck with Xlear Rescue nasal spray with essential oils for sinus congestion. Mullein leaf tincture also helps the lungs and congestion. I joined 2 social media groups on FB 1) Renegade Research #TheNicotineTest. 2) Long Haul Reset: Long Covid & Spike Injury Treatment. There is an overload of information in these groups that is overwhelming at times, but much of the information has been helpful to me. While being evaluated at a local Rehab facility, I was encouraged to seek out a doctor treating long C. Although I am much better, I plan to follow through with a scheduled appointment the end of this month. I know there are many smart doctors trying to get this nasty stuff figured out, and if by treating me can help others, that's a win!

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I also have ear pressure and anxiety dizziness. I will look into your natural solutions. I am also looking to try a grounding Mat to help inflammation. 9 ent drs later and not on found a problem. Some suggested it was histamine related. So I’m also 2 yrs into allergy shots. No help with that yet. Also told moderate hearing loss so now it will be hearing aids. Please post me if you find the solution. God bless and stay safe.

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@delweb98

I also have ear pressure and anxiety dizziness. I will look into your natural solutions. I am also looking to try a grounding Mat to help inflammation. 9 ent drs later and not on found a problem. Some suggested it was histamine related. So I’m also 2 yrs into allergy shots. No help with that yet. Also told moderate hearing loss so now it will be hearing aids. Please post me if you find the solution. God bless and stay safe.

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I wish I had the solution.
I have been down the road you are on. Two and a half years for me. Allergy meds made me drier, but did not clear my ears.

I have slept on a grounding mat for over a year. While I believe it helps circulation, it has not helped my ears. I also wear hearing aids with minimal help. My hearing loss is mild. It is the pressure and disequilibrium that I find debilitating. I have also developed tinnitus and hyperacusis which makes it difficult to use hearing aids.

My eyes are also somehow involved. I have blurry vision which contributes to dizziness.
I continue to look for solutions and try treatments, but so far no luck.

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@dloos

I wish I had the solution.
I have been down the road you are on. Two and a half years for me. Allergy meds made me drier, but did not clear my ears.

I have slept on a grounding mat for over a year. While I believe it helps circulation, it has not helped my ears. I also wear hearing aids with minimal help. My hearing loss is mild. It is the pressure and disequilibrium that I find debilitating. I have also developed tinnitus and hyperacusis which makes it difficult to use hearing aids.

My eyes are also somehow involved. I have blurry vision which contributes to dizziness.
I continue to look for solutions and try treatments, but so far no luck.

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Do you also use your hearing aids to deliver sound therapy?

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@patriciapardo

Do you also use your hearing aids to deliver sound therapy?

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I do, but I am not crazy about Bluetooth. I do a form of sound therapy with a biomat. The sound is on both sides of my head but not in my ears. I have hyperacusis and sometimes sounds going directly into my ears is just too overwhelming.

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I have the same problem. Literally the same thing happened to me. It was as if the air flight activated tinititus. And it hasn’t gone away since. It feels like it’s getting worse.

After I had Covid in 2021 I started having problems with my ears - sensitivity (the hyperacusis) and I was more prone to ear infections. I had a chronic ear and throat infection for a while. That has gone away at least. But now suddenly tinititus and hyperacusis and I’m 25 years old 😭

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@chaneldelarosa

I have the same problem. Literally the same thing happened to me. It was as if the air flight activated tinititus. And it hasn’t gone away since. It feels like it’s getting worse.

After I had Covid in 2021 I started having problems with my ears - sensitivity (the hyperacusis) and I was more prone to ear infections. I had a chronic ear and throat infection for a while. That has gone away at least. But now suddenly tinititus and hyperacusis and I’m 25 years old 😭

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Also more blurriness (eyes). I thought it was only me.

I don’t know how to live with this - it’s overwhelming.

They are going to do hearing tests next week - don’t know how this will help though

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This all started for me in the spring of 2022. At first it was just annoying, and I continued to live a pretty normal life. Now, I really can’t. I am so sound and light sensitive that being out and around people is almost impossible.
I was given hearing aids. You may find they help a bit, but at your age you probably don’t have hearing loss. I knew I had a little hearing loss, and at first the aids helped me hear my own voice better, and brought me out of the “underwater” feeling. As time has gone on they help me less, and magnify the hyperacusis! Not good.
I am seeing a Neuro Optometrist (blurry vision like you). He feels the virus has done some brain damage just like a concussion or a stroke. I’m undergoing treatment and he assures me that people do get better. It sure isn’t fast.
I also see an Audiologist for help with hearing aids.

None of it has made a big difference for me,(yet) but I’m told there is hope for brain injury, but the recovery takes time.
I hope this encourages you a little. I know just how miserable it is, and it truly does ruin your life. I do believe these symptoms are somewhat rare for Covid. It makes it harder to find care. I have seen dozens of doctors, specialists and therapists over the last two and a half years.
Good luck to you. If I find anything that really helps, I will post.

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@dloos

Thank you so much for taking the time to respond to my post. You can bet that as soon as I respond, I’m out the door for a nicotine patch!! I think you’re saying you cut it in half? Right?
I had read about this but it seemed a little “out there”. Having said that, I’ve tried mushrooms, smoke a little pot, and also pretty much everything you mention in your post. This is a tough one for sure. Even amongst other Long Covid sufferers we’re a little different. It doesn’t sound like such a big deal until you’ve lived with it for months. As you know, it’s a BIG deal, and does make you feel like your mind is going.
I wonder if I should drive (I do a little) because when you have these issues, everything is just off.
I have felt drunk for the past year. Does that make sense to you?
I’ll post how I do with the patch.

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For nicotine, check out the Facebook page Renegade Research first.

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I am not on Facebook, but have read quite a lot about nicotine for LC. I have tried it multiple times, and multiple delivery systems. It doesn’t seem to be right for me.
I have previously posted my reactions.
Believe me, I have tried everything.

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No answers but I add severe headaches to the tinnitus. Also feel like going crazy. Try to stay positive but getting worse. All my Drs. just said see a psychiatrist

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