Four Months into Severe Tinnitus, Reactivity, Hyperacusis, Dysacusis and Visual Snow

vikaspratap

Member
Author
Dec 15, 2024
3
Philadelphia, PA
Tinnitus Since
08/2024
Cause of Tinnitus
Not really sure
Hello, everyone,

My tinnitus started around August 20th, and at first, it was really mild. I could only notice it if I blocked my ears or was in a very quiet room. It sounded like an air-blowing or whooshing noise in my head and was easily maskable with a running fan.

A week later, I visited an ENT, who checked my ears and performed a hearing test. Everything was normal, with no hearing loss detected. The ENT prescribed Methylprednisolone to address any potential inflammation in the ear, but it did not help.

Four days after that visit, my tinnitus increased, and I went into panic mode, unable to sleep for two days. I reached out to my PCP, who prescribed Belsomra to help me sleep. It worked the first night but stopped working after the second night. That same week, I went to a restaurant and noticed the noise from the speakers caused a humming sound audible only to me, not to the people around me. Later, I learned this was dysacusis.

On the same day, I took a train home and realized the sound inside the train triggered hyperacusis, making everything seem unusually loud. I decided to stay home for a few days to rest my ears, but things only worsened. I was barely getting one to two hours of sleep, even with sleeping aids.

A week later, I visited another ENT, who suggested getting an MRI to check for abnormalities. The MRI and MRV results came back normal. I then began taking supplements like Magnesium and Zinc to see if they would help.

Second Month

Since sleep was a major issue, I was prescribed Ambien (10 mg), which allowed me to sleep for five to six hours—a significant improvement compared to the one to two hours I had been getting. However, my dysacusis and hyperacusis continued to worsen, though my tinnitus was still manageable at this stage.

I took short-term disability leave from work because it became impossible to focus. By the end of the month, my tinnitus began increasing daily. I saw a tinnitus specialist who matched my frequency at 15 kHz, noting that it was very high but not something to worry about. They suggested using masking sounds and exercising daily for a month.

Third Month

New symptoms emerged—a very high-pitched, sharp hissing in both ears and a metallic humming in my right ear. These additional tones made everything much worse.

I tried acupuncture, Ayurvedic medicine, and homeopathic remedies, but none of them helped. I was also prescribed Amitriptyline and Gabapentin, but neither provided relief. During this time, I started feeling very depressed, and suicidal thoughts began to surface.

I am married, and my wife has been incredibly supportive, but this has been hard on her as well since she has struggled with depression in the past. I have always been a positive person and never dealt with depression before, although I have experienced anxiety in the past.

Fourth Month

Things took a turn for the worse when I took a flight. The tinnitus became unbearable, with 4–5 distinct tones constantly present: air-blowing, sharp hissing, loud metallic humming, and a high-pitched laser beam sound.

I can no longer handle sounds above 65 dB, and in early November, visual snow started appearing. Initially, it was very light static, but it has worsened significantly. Now I see more floaters, extreme blue-field entoptic phenomena, and my night vision has deteriorated with starbursts and static-like interference.

I reached out to Neuromed, as they seemed to be the only ones familiar with conditions like mine. They prescribed Nortriptyline (currently on 60 mg) and Ambien, as it is the only medication that helps me sleep.

Current Situation

I am not sure what caused this in the first place. It started suddenly on a Sunday afternoon. I do not smoke and only drink occasionally.

I cannot sleep naturally anymore because of the unbearable hissing in my head. I miss that natural feeling of sleepiness and the ability to rest. I have a passion for cars, but I cannot enjoy driving anymore because the reactivity of my condition makes it unbearable.

As this condition worsens, I feel like I am losing hope every day. The physical torment has become overwhelming, and I do not know how to survive this anymore. I cannot imagine leaving my wife and family behind, and I do not want my loved ones to suffer.

I truly feel the pain of everyone here who is also struggling with this dreadful condition. I am sorry for venting so much, but I am really hoping there will be a cure or treatment for us in the near future.

Take care, and know you are not alone.
 
Hello,

I noticed you mentioned trying Ayurvedic medicine. It is worth noting that Ayurveda often takes time to show results and usually involves panchakarma for optimal effectiveness.

The tinnitus I experience changes throughout the day and from day to day. Over the past few months, it has fluctuated between low moderate and severe, although it has thankfully improved from the catastrophic level it was at when it first developed 13 years ago.

I am planning to spend two months in India for panchakarma treatment. When I underwent this treatment last February and March, it reduced my tinnitus to a mild or moderate level. Unfortunately, it has slowly crept back up in recent months, possibly due to the colder weather and less time spent outdoors, which usually helps me relax.

You are in a tough spot, and as you know, sleep is critical. To help with relaxation, you might try applying vata oil to your scalp. Massage it in well, then wash it out in the shower. A warm bath with Epsom salts may also help with calming your system.

I recommend avoiding caffeine. Personally, I find that using a computer, possibly due to the blue light, sometimes worsens my tinnitus. For relaxation before bed, try having warm milk (or almond milk, if you prefer) with spices like nutmeg, cardamom, and turmeric about an hour or two before sleep.

I use melatonin and valerian as sleep aids, as they are milder alternatives to Ambien, which I had a bad reaction to. Some years back, I resorted to Klonopin and Gabapentin. While I have reduced my dosage over time, I still rely on these medications, hopefully not forever.

For tinnitus relief, I use hearing aids with pink noise, which helps a bit. Playing ocean sounds on my phone or a sound machine also aids my sleep.

When flying, I rely on noise-canceling headphones, which make a big difference. I also carry silicone earplugs for loud environments like movie theaters.

Regarding visual snow, I do not have any personal experience with it, but I suggest searching forums to see what others have tried.

Wishing you the best,
Stephan

Let me know if you need further adjustments!
 
Are there any days when the hissing decreases?

I would suggest trying Klonopin for sleep and anxiety instead of Ambien to see if it makes a difference. I truly feel for you; you are in the early stages, and I believe the intensity can lessen over time. You might also consider reducing your salt intake, as it could potentially help.

Additionally, try getting a Swedish massage. It stimulates the central nervous system and might provide some relief.
 
The hissing in my ears sometimes decreases when I wake up in the morning, but it goes back up once I start engaging in activities. It feels like my tinnitus worsens when my brain is more active.

Living like this has been incredibly difficult, especially with the addition of visual snow. I see static everywhere, and the constant buzzing and hissing in my ears make me feel utterly overwhelmed. I struggle to enjoy simple things like listening to music, watching TV, or even driving.

This situation has taken such a toll on me that I often feel hopeless.
 
As this condition worsens, I feel like I am losing hope every day. The physical torment has become overwhelming, and I do not know how to survive this anymore. I cannot imagine leaving my wife and family behind, and I do not want my loved ones to suffer.
Welcome to the forum. I'm sorry to hear that you're suffering from tinnitus and its many symptoms. I can relate, as I experienced many of the same challenges during the first year of my struggle with ultra-high-pitched tinnitus and severe hyperacusis.

My left ear has lost all hearing, yet it constantly produces a loud, humming, jet-engine-like tinnitus that rings 24/7. In my right ear, the tinnitus is an ultra-high-pitched sound, like a dentist's drill but ten times worse. On top of that, I suffered severe hyperacusis—twice. Even the soft voice of my wife was painful, and everyday noises like the TV, driving, dishwashing, or being in a restaurant became unbearable.

Having already battled chronic anxiety and panic disorder for decades before developing tinnitus and hyperacusis, the constant, intense ringing triggered relentless anxiety and panic attacks, each with its own set of debilitating symptoms. It was a nightmarish existence during that initial stage. How does one live with such unlivable conditions? It felt so hopeless that I had to rely on benzodiazepines, antidepressants, and sleeping pills just to get through each day. Even now, recalling those days of despair and dread brings tears to my eyes. I never thought I could recover. Yes, those dark, suicidal thoughts crossed my tired and depressed mind more than once.

However, today, I live a normal and deeply enjoyable life. I travel extensively, dance with my dear wife, tend to my garden, go salmon fishing, play badminton regularly, and sing with my folk guitar. Life after the nightmare is truly good. I've even written two success stories to share the strategies that helped turn my suffering around. For brevity, I encourage you to read those stories, as well as the stories of others, to inspire hope and healing.

Be patient with yourself. Your body needs time to heal and adapt to these new, alien sounds and conditions. Hyperacusis and reactive tinnitus often reduce in intensity or even fade away over time, typically within a year of onset. I've experienced hyperacusis twice, and both times it faded completely within a year.

If you're interested, please check out my stories: "From Darkness to Light…" and another detailing my experience with sudden sensorineural hearing loss (SSHL) when my left ear became deaf. Remember to stay positive and patient. Hold on to the hope that better days lie ahead.

Take good care of yourself, and may your recovery be swift. God bless.

 
It seems like your nervous system is on overdrive.

I'm currently dealing with my second onset and struggled a lot for two months. I was hypersensitive and even felt suicidal at times.

Then I watched a video on YouTube, and the next day, I found myself not caring about the tinnitus. And guess what happened? It was reduced by half. That was just a week ago. Today, it was completely silent. It came back while I was writing this, but I'll do 10 minutes of controlled breathing, and it should go down again.

You need to focus on calming your body through meditation and breathing techniques.

Whether it's placebo or snake oil, I don't care—it works. And to think, I once believed my life was over.

 
Welcome to the forum. I'm sorry to hear that you're suffering from tinnitus and its many symptoms. I can relate, as I experienced many of the same challenges during the first year of my struggle with ultra-high-pitched tinnitus and severe hyperacusis.

My left ear has lost all hearing, yet it constantly produces a loud, humming, jet-engine-like tinnitus that rings 24/7. In my right ear, the tinnitus is an ultra-high-pitched sound, like a dentist's drill but ten times worse. On top of that, I suffered severe hyperacusis—twice. Even the soft voice of my wife was painful, and everyday noises like the TV, driving, dishwashing, or being in a restaurant became unbearable.

Having already battled chronic anxiety and panic disorder for decades before developing tinnitus and hyperacusis, the constant, intense ringing triggered relentless anxiety and panic attacks, each with its own set of debilitating symptoms. It was a nightmarish existence during that initial stage. How does one live with such unlivable conditions? It felt so hopeless that I had to rely on benzodiazepines, antidepressants, and sleeping pills just to get through each day. Even now, recalling those days of despair and dread brings tears to my eyes. I never thought I could recover. Yes, those dark, suicidal thoughts crossed my tired and depressed mind more than once.

However, today, I live a normal and deeply enjoyable life. I travel extensively, dance with my dear wife, tend to my garden, go salmon fishing, play badminton regularly, and sing with my folk guitar. Life after the nightmare is truly good. I've even written two success stories to share the strategies that helped turn my suffering around. For brevity, I encourage you to read those stories, as well as the stories of others, to inspire hope and healing.

Be patient with yourself. Your body needs time to heal and adapt to these new, alien sounds and conditions. Hyperacusis and reactive tinnitus often reduce in intensity or even fade away over time, typically within a year of onset. I've experienced hyperacusis twice, and both times it faded completely within a year.

If you're interested, please check out my stories: "From Darkness to Light…" and another detailing my experience with sudden sensorineural hearing loss (SSHL) when my left ear became deaf. Remember to stay positive and patient. Hold on to the hope that better days lie ahead.

Take good care of yourself, and may your recovery be swift. God bless.

Thank you so much for your encouraging words, Billie. The people around me have been really supportive, which has been helpful, but at times, the constant shouting of these multiple tones feels isolating. I've been on Nortriptyline for a month, but it hasn't improved anything. Meanwhile, the visual disturbances are getting worse every day.
 
You're most welcome. You may want to search the forums for discussions on visual snow or floaters. These topics have been covered before, and even Markku, the founder of Tinnitus Talk, shared his experiences with visual snow and floaters some time ago. If you search for "visual snow Markku," you'll find several prior discussions.

This condition seems to be quite common among tinnitus sufferers. Have faith that things will improve with time, especially if you follow some of the advice shared by forum members. In the meantime, try not to stress too much. With patience, these conditions may fade, or your perception of tinnitus may improve, making it easier to live a normal life again.

Stay hopeful!
 

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