Help: Sudden Sensorineural Hearing Loss (SSHL) - very scary

Posted by ed140 @ed140, Sep 6, 2019

I just got diagnosed with hearing loss by My ENT. Woke up and hearing was gone in my left ear. I'm being treated with oral and ear injected steriods. Becoming anxious and panicked about recovery. Hoping someone can offer advice or someone who has story of recovery success. I went to an urgent care the day this happened ,the doctor gave me oral steriods and I followed up the next day with an ent. At this moment I feel the sense of sound but its not clear also hear rapid tones , pops and clicks. Previously I heard nothing at all . hope this means the trearment is working.

Interested in more discussions like this? Go to the Hearing Loss Support Group.

@theoalvarado1

I was just diagnosed with SSHL on my right ear. I lost complete hearing in the afternoon of Feb 5th I saw medical attention right away and I have been in 60mg of prednisone from Saturday Feb 8th and asked my primary doctor to keep me on prednisone for 4 full weeks + weening period. Had audiology test and showed moderate to sever hearing loss. I took 2 tests a week apart and didn't show much progress. I was wondering if anyone here has had any experience with HBOT (Hyperbaric Oxygen Therapy) to perhaps try to get some hearing back? It's will be 3 weeks on prednisone tomorrow.

It seems recently, i can scratch the outside of my ear and hear some scratching noise and when people talk now i hear pitching noises of the words that are spoken.

Any help with this is greatly appreciated. Are there any ENT's doctors in this forum?

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I'm sorry you are experiencing this. SSHL is not common. Most hearing loss happens gradually. However, people on MCC have shared their experience with SSNL. You did the right thing by seeking immediate medical attention. It seems that steroid treatment only works if it is given very quickly after the hearing loss incident. However, it does not always work.

It's helpful to know that hearing loss technology has improved greatly over the last few decades. Hearing aids are better than they used to be. Bicross hearing aids can transfer sound from a 'deaf' ear to the hear that hears when there is single sided deafness. So some single sided implants.

If the damage is in the cochlea, which it often is, a cochlear implant may be a possibility. The large majority of cochlear implant recipients have excellent results.

I am unaware of HBOT treatment, but encourage anyone who has experience with this to share what they know.

Was there an incident of some kind that may have caused the SSHL? Were you on an airplane? Were you exposed to extremely loud sudden noise? Is there possibly a genetic connection?

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@julieo4 thanks Julie, no I was not on a plane and was not exposed to any extremely loud sound and not genetic connection. I woke up Wednesday 5th worked at home all day and around 3pm out of the sudden my right ear striped working.

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@nancyjg

Fifty years ago I lost my hearing in my right ear. Diagnosed as Menieres. I did not try HBOT, if they even had it back then. I had had severe vertigo and lost it when I lost my hearing, so I wasn't devastated by the loss. Fast forward a decade or so and I started losing it in my left ear. I was immediately put on Prednisone. This was pre-internet, but fortunately there was an apartment I wanted to rent and I had to pretend I knew the current tenant. He and I had dinner to get to know each other; he was a chiropractor. I come from a famil y of Yale MD's and had been snobbish about chiropractors. He told me the history of chiropractics and that the first person ever treated was a deaf farmhand who got his hearing back. I was desperate. It had been years since our one meeting, but I tracked him down, reminded him of the deaf farmhand and cried, asking him if he could help me get my hearing back. He said he'd try. I felt a cold instrument tap against the back of my neck ( as if it were on a spring) and he manipulated/twisted my head. I heard a horrible crunching sound and felt some heat. I left, went to a movie to sit in the dark to cry, when partway through the movie it was as if the sound volume was cranked all the way up. I had my hearing back! I've had it happen two or three times since and each time a (different) chiropractor helped. But never as much as the first time.

This is a long story, but after 53 years of being deaf in one ear, and losing some in my good ear a few years ago, I've learned that while the science of hearing has progressed, there's really been no progress in treatment. I don't want to discourage you, but give you hope that by going non-mainstream, like to a c hiropractor, might possibly help. I'm still a snob about what doctors I see, but I'm now more open to alternative medicine.

Also, Facebook has support groups for SSSH sbd other hearing issues, with hundreds of people sharing what's worked for them. And they share their cochlear stories. Some good. Some not.

I wish you the very best. If you cannot get your hearing back, I recommend CROS hearing aids (amazing!). And there are now smart glasses with "closed captioning" by Vuzix so you can read what people are saying!! 'They're $500 and I'm getting them as soon as they're back in stock.

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I am trying to inform people about another cause for sudden sensorineural hearing loss with chronic tinnitus which is cochlear migraines, name deceiving because no headache just hearing loss which is triggered possibly by loud noise, stress, poor sleep, foods, etc. Have only found one Dr in Irvine California who understands and treats this. Yes multifactorial causes and approaches for treatment.

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@theoalvarado1

@nancyjg Thanks for sharing your story, I know I am in the beginning stages of dealing with this and I appreciate people’s feedback and learning more about alternative methods of perhaps treating this. ENT doctors still seem like there is no clear answer as to why it happens to certain people and not others.

I am researching other options and continuing my prednisone treatment.

Very much appreciated for sharing your story.

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Dr Djalilian is the ENT who is in Irvine California btw.
My name is Lesley Hirshberg Miller and my daughter had this condition. The Drs in NYC do not seem to know about or treat cochlear migraines. I have tried calling heads of department and the heads of large otolaryngology groups but not getting much help with spreading the information so people can be more informed and better diagnosed and treated.

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@theoalvarado1

@nancyjg Thanks for sharing your story, I know I am in the beginning stages of dealing with this and I appreciate people’s feedback and learning more about alternative methods of perhaps treating this. ENT doctors still seem like there is no clear answer as to why it happens to certain people and not others.

I am researching other options and continuing my prednisone treatment.

Very much appreciated for sharing your story.

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The first ENT I went to told me the SSHL is caused by a virus. When he retired, I changed providers to an ENT at Stanford who said, “Oh yeah. Virus is what we say when we have to come with something, but in reality, the cause is still a mystery most times”.

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Interesting! Back in 1972 I was told the same thing, and then later Meniere's. But what causes Meniere's?

When I see any doctor for any reason and they give me a diagnosis, I always ask, 'What else could it be?' And after they think for a bit and tell me, I ask it again. Some doctors can be lazy, especially with older patients. I once had a doctor tell me what I had was because of my age. I gently told him he was being lazy and asked what would he tell me if I were 50. I got a much better response. Try it!

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@julieo4

I'm sorry you are experiencing this. SSHL is not common. Most hearing loss happens gradually. However, people on MCC have shared their experience with SSNL. You did the right thing by seeking immediate medical attention. It seems that steroid treatment only works if it is given very quickly after the hearing loss incident. However, it does not always work.

It's helpful to know that hearing loss technology has improved greatly over the last few decades. Hearing aids are better than they used to be. Bicross hearing aids can transfer sound from a 'deaf' ear to the hear that hears when there is single sided deafness. So some single sided implants.

If the damage is in the cochlea, which it often is, a cochlear implant may be a possibility. The large majority of cochlear implant recipients have excellent results.

I am unaware of HBOT treatment, but encourage anyone who has experience with this to share what they know.

Was there an incident of some kind that may have caused the SSHL? Were you on an airplane? Were you exposed to extremely loud sudden noise? Is there possibly a genetic connection?

Jump to this post

Please consider cochlear migraine. The name is deceptive because there is no headache.
This has been recognized since 2018.

Dr. Lesley Hirshberg Miller

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Look up cochlear migraines. SSHL with no headache.
Yes there is hope that steroids can help.
There is hope.

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