Tinnitus Caused by MRI

ccpjc

Member
Author
Dec 10, 2024
38
Tinnitus Since
12/2024
Cause of Tinnitus
Acoustic Trauma
Before I begin, I kindly ask that responses avoid comments like "you should have" or "they should have." I am already dealing with my own internal struggles over this.

In September and October, I experienced random bouts of tinnitus in my left ear, accompanied by pressure and pain. By early December, it became more persistent, so I saw a doctor who prescribed antibiotics. However, the pressure and pain persisted despite the treatment.

As I started researching tinnitus, I came across information about acoustic neuroma. Unfortunately, I had nearly all the symptoms associated with it, except for hearing loss. Despite this, I panicked and convinced my doctor to refer me for an MRI.

When I went for the MRI, the technicians had trouble properly fitting the earplugs in my right ear. Although I kept expressing concern, they assured me that the ear protection was correctly placed. The MRI was extremely loud, and when I came out, I noticed tinnitus in my right ear, which had not been present before.

Now, I have finished the antibiotics, and the tinnitus and discomfort in my left ear have mostly subsided. My wife reassured me that I did not have a tumor, and my doctor had advised me to wait until finishing the antibiotics before making further decisions. However, I was in such a state of panic that I went ahead with the MRI anyway. Now, I am left with profound regret, sadness, anger, and a deep sense of trauma over what happened, knowing I may have to live with this for the rest of my life.

It has been five days since the MRI, and the noise in my right ear has been constant. There is also some pain and a strange sensation in that ear. I spoke with a doctor virtually on the same day as the MRI, an ER doctor the following morning, and my family doctor after that. All three told me the same thing: nothing can be done. I asked about Prednisone, but each one declined to prescribe it. Whether it would have helped or not, I will never know.

Now, I am consumed with regret. My sleep is disrupted, the noise is constant regardless of the environment, and I keep replaying the MRI experience in my mind. I told them the ear protection was not properly fitted, but they assured me it was. It was not.

I spoke with a psychologist on Saturday, who told me that I made the decision based on what I thought was right at the time and that I need to forgive myself. However, it is incredibly challenging to do so, knowing I caused this and may have to live with it forever. I want to cry, and I have been trying hard not to break down in front of my kids.

That is my story and my deep regret: I wish I had waited a little longer. While the MRI showed no tumor, I now have this awful reminder of my decisions and mistakes.
 
I'm sure this is something many can relate to, but you can read about my experience with the MRI disaster above.

Right now, I'm in Las Vegas—a trip I booked before developing tinnitus. It's been difficult being here with my family, surrounded by so many people enjoying themselves, while I'm struggling with this constant ringing in my ears. The loud noises around me are only making it worse.

It's hard not to think back to just nine months ago, when I was here with my wife, enjoying everything without a care. Now, my life feels completely turned upside down.
 
Welcome to the forum. It seems the MRI may have caused acoustic trauma, leaving your ears a bit unstable. Sometimes, hyperacusis or reactive tinnitus can develop after acoustic trauma. This is quite common, as many members here report similar symptoms—myself included.

When my hyperacusis was severe, even my wife's soft voice felt piercingly painful. Going to restaurants was a purely nightmarish experience. However, hyperacusis or reactive tinnitus resulting from acoustic trauma often fades over time. I've experienced hyperacusis twice, and both times it faded within a year. So, be hopeful that your condition might be temporary. Try not to get too stressed, as stress tends to aggravate tinnitus. Be patient and allow your ears time to heal.

Sometimes the mental suffering can be so intense that it triggers a fight-or-flight response. When the limbic nervous system is activated, it may interpret tinnitus as a mortal threat. I made this mistake initially and endured a nightmarish existence because of it. However, I now live a normal and enjoyable life. In fact, I wrote my success story, "From Darkness to Light…", where I share many helpful strategies for coping with severely intrusive tinnitus and hyperacusis.

Feel free to check it out to see if these strategies might help you manage your tinnitus. Give it time, take good care of yourself, and stay hopeful. Wishing you a speedy recovery. God bless!
 
I found an online tool that sweeps frequencies from 22 Hz to 8 kHz, and I've managed to pinpoint where my hearing loss is occurring.

In my left ear, I can hear sounds starting at 16 kHz, but nothing at 15 kHz. It starts again at 14 kHz and continues beyond that.

In my right ear, I can't hear anything until 14 kHz.

This confirms that I have hearing damage in both ears, but it's more pronounced in my right ear. That's the ear where my hearing protection failed during my last MRI.

Interestingly, after playing the 16 kHz tone in my left ear, my tinnitus has quieted down. For me, this suggests that my brain is trying to recreate the ~16 kHz tone.
 
Today, I woke up to an alert that my phone is low on storage, so I started clearing out older pictures and videos. As I went through them, seeing myself before this affliction with tinnitus, hyperacusis, and noxacusis brought me to new depths of sadness.

I'm overwhelmed with grief, regret, and pure sadness that this is now my life. This is supposed to be the best time of my life—watching my kids grow up, reducing debt, advancing in my career, and strengthening the bond with my wife.

But it feels like life is over. The ringing never stops, the sounds are unbearable, and I feel like I can't survive this. I'm falling into such a dark and depressed state of mind.

I know it's common for new sufferers to feel this way, but that doesn't make it any easier. This is my struggle now.

I read success stories and understand they represent the minority of cases. I've joined support groups and witnessed the sheer pain and suffering others endure, and it terrifies me that this could be my future too.

I just want my life back—the life I had less than a month ago. But right now, it feels like everything is falling apart, and I can't stop it.
 
32YO here in Texas, dealing with tinnitus and hyperacusis for 2 years. An MRI was my second trauma after the nightclub incident that incited this all. I'm sorry man, auditory conditions are difficult to contend with. For now, to keep on living, carry some foam plugs or Loops with you (search for these on Amazon) and pop them in whenever you feel overwhelmed by sound. There's a migraine connection too with invasive tinnitus and hyperacusis and I learned a lot from reading articles written by Dr. Djalilian on his website (I'm not endorsing his telehealth program one way or another). But his protocol treats invasive tinnitus with a combination of Nortriptyline + Topiramate and/or Gabapentin. You might consider some medication to help you maintain good quality sleep. Mirtazapine has also helped me with that in the past when I was first dealing with tinnitus & hyperacusis.

Over time, I began to re-introduce digital audio like pink and red noise and 'bright noise' on my iPhone via the background sounds function (accessible via the control panel when you swipe down if you have an iPhone). I actually found these sounds soothing, and they masking the tinnitus helped free up mental bandwidth to focus on other things than my suffering with this inescapable condition. If you have hyperacusis, sometimes sound therapy won't agree with you early on. But over time, I found a way to enjoy it. I play it at work to soothe my ears and nervous system in an office environment.

Smart people are researching this condition at Harvard and around the world. Read up on Eaton Peabody Labs and Dr. Susan Shore's bimodal stimulation device. This article gives me hope with regard to tinnitus and hyperacusis. I have normal hearing on paper but likely what's called hidden hearing loss - AKA cochlear synaptopathy. This company is working on a therapy for those of us with this auditory nerve damage but no discernible hearing loss on an audiogram. You should probably see an audiologist to confirm your diagnosis, but just don't sign up for any loudness discomfort level testing, which can be uncomfortable and worsen the condition.

Good luck. You're definitely not alone.
 
32YO here in Texas, dealing with tinnitus and hyperacusis for 2 years. An MRI was my second trauma after the nightclub incident that incited this all. I'm sorry man, auditory conditions are difficult to contend with. For now, to keep on living, carry some foam plugs or Loops with you (search for these on Amazon) and pop them in whenever you feel overwhelmed by sound. There's a migraine connection too with invasive tinnitus and hyperacusis and I learned a lot from reading articles written by Dr. Djalilian on his website (I'm not endorsing his telehealth program one way or another). But his protocol treats invasive tinnitus with a combination of Nortriptyline + Topiramate and/or Gabapentin. You might consider some medication to help you maintain good quality sleep. Mirtazapine has also helped me with that in the past when I was first dealing with tinnitus & hyperacusis.

Over time, I began to re-introduce digital audio like pink and red noise and 'bright noise' on my iPhone via the background sounds function (accessible via the control panel when you swipe down if you have an iPhone). I actually found these sounds soothing, and they masking the tinnitus helped free up mental bandwidth to focus on other things than my suffering with this inescapable condition. If you have hyperacusis, sometimes sound therapy won't agree with you early on. But over time, I found a way to enjoy it. I play it at work to soothe my ears and nervous system in an office environment.

Smart people are researching this condition at Harvard and around the world. Read up on Eaton Peabody Labs and Dr. Susan Shore's bimodal stimulation device. This article gives me hope with regard to tinnitus and hyperacusis. I have normal hearing on paper but likely what's called hidden hearing loss - AKA cochlear synaptopathy. This company is working on a therapy for those of us with this auditory nerve damage but no discernible hearing loss on an audiogram. You should probably see an audiologist to confirm your diagnosis, but just don't sign up for any loudness discomfort level testing, which can be uncomfortable and worsen the condition.

Good luck. You're definitely not alone.
I appreciate you taking the time to write this. As I sit here in my own personal struggle, I've been reading through a lot of information, including all the recommended treatments. I've noted them down, including medications that others have reported success with, and I plan to share the entire list with my doctor.

I'm even considering surgery if it could help alleviate the hyperacusis or noxacusis.
 
I developed tinnitus from an MRI four years ago. Hopefully, yours will be temporary.
 
I developed tinnitus from an MRI four years ago. Hopefully, yours will be temporary.
I'm sorry you're going through a similar experience. I'm praying and hoping, but deep down, I know it's probably here to stay.

The doctor I spoke to right after my event said it might take up to three weeks to resolve. If it doesn't stop by then, it's most likely permanent. Three weeks will be up in three days.
 
I'm sorry you're going through a similar experience. I'm praying and hoping, but deep down, I know it's probably here to stay.

The doctor I spoke to right after my event said it might take up to three weeks to resolve. If it doesn't stop by then, it's most likely permanent. Three weeks will be up in three days.
Hang in there! There are so many stories of improvement, sometimes gradual and other times sudden, that happen over months or even years. One month is just the beginning of the journey. Think of this as a marathon, not a sprint.

The TPP formula (Time, Protection, Patience) is your best approach:

Time: Allow plenty of time for things to resolve naturally. Healing can take a long time, so don't rush the process.
Protection: Use earplugs or earmuffs in loud environments to safeguard your ears. The goal is to avoid any further trauma.
Patience: Be patient with yourself and the process. Progress takes time, but improvement is possible.

Stay hopeful and take it one step at a time!
 
I appreciate you taking the time to write this. As I sit here in my own personal struggle, I've been reading through a lot of information, including all the recommended treatments. I've noted them down, including medications that others have reported success with, and I plan to share the entire list with my doctor.

I'm even considering surgery if it could help alleviate the hyperacusis or noxacusis.
Sir, with all due respect, you may want to stop. Stop researching surgeries. You experienced acoustic trauma, an injury caused by noise, during the MRI just a month ago.

Give your ears and psyche time to heal. Pursuing surgery so soon could potentially worsen your condition, leading to unimaginable levels of suffering. Please take it slow.
 
Sir, with all due respect, you may want to stop. Stop researching surgeries. You experienced acoustic trauma, an injury caused by noise, during the MRI just a month ago.

Give your ears and psyche time to heal. Pursuing surgery so soon could potentially worsen your condition, leading to unimaginable levels of suffering. Please take it slow.
I wish I could, but my life has turned into a kind of hell I never thought possible. I performed a TFI test and scored 90/100. I'm not sure I've seen anyone score that high before.

My tinnitus has gotten progressively worse over the past week. It's so loud that I hear it clearly on my left side, but when I plug my ears, I can tell it's actually radiating from my right side.

I'm reaching new lows I never thought I could. For the first time in my life, I feel completely hopeless. As I write this, I can't imagine living like this. It breaks me to even think about saying goodbye to my family and my life.

I've read the stories from people on here who got into clinical trials and found relief, and it crushes me to know that because of where I live, I'll never have that opportunity.

After my injury, I begged for steroids three times and was told no every time. I'm certain they could have helped, based on the stories of others who benefited from them.

I don't know how I can keep going. I feel like I can't survive this affliction. All I wanted was to rule out something bad in my head, not make things worse—and yet, that's exactly what happened.
 
I wish I could, but my life has turned into a kind of hell I never thought possible. I performed a TFI test and scored 90/100. I'm not sure I've seen anyone score that high before.

My tinnitus has gotten progressively worse over the past week. It's so loud that I hear it clearly on my left side, but when I plug my ears, I can tell it's actually radiating from my right side.

I'm reaching new lows I never thought I could. For the first time in my life, I feel completely hopeless. As I write this, I can't imagine living like this. It breaks me to even think about saying goodbye to my family and my life.

I've read the stories from people on here who got into clinical trials and found relief, and it crushes me to know that because of where I live, I'll never have that opportunity.

After my injury, I begged for steroids three times and was told no every time. I'm certain they could have helped, based on the stories of others who benefited from them.

I don't know how I can keep going. I feel like I can't survive this affliction. All I wanted was to rule out something bad in my head, not make things worse—and yet, that's exactly what happened.
I know this is really tough. Believe me, I understand. We all do.

Please do whatever you think is best for you. I truly hope things start to calm down, and I believe they can if you just give it some time.

Hang in there, for your family and for yourself. I am rooting for you!
 
I can't believe there's a new layer of hell to tinnitus. Yesterday, and continuing through today, my tinnitus has become reactive—but not just any type of reactive.

If I tense my muscles, it gets worse, even if it's just in my foot or hands. Any noise at all makes the tinnitus increase.

Please, please, please tell me this goes away. I'm crying and feeling like I'm about ready to give up on everything.
 

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