5 Things You Should Know If You Have Tinnitus

Mike interviews @treblehealth about the 5 things you should know if you have tinnitus.

Bob (the tall one) has been diagnosed with Ataxia. It affects his balance and his speech, but does not affect his thinking. We appreciate your understanding and support!

~~~~ Video Chapters ~~~~

0:00 Ben Thompson Introduction
0:36 5 Things You Should Know If You Have Tinnitus
0:47 Things to Know If You Have Tinnitus - #1
1:28 Things to Know If You Have Tinnitus - #2
1:59 Things to Know If You Have Tinnitus - #3
2:18 Things to Know If You Have Tinnitus - #4
2:54 Things to Know If You Have Tinnitus - #5
3:38 Treble Health Website & Contact Information
4:22 End Screen

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[JeanieD]

I’ve had tinnitus since my teens, from repeated exposure to loud music - over 40 years now. Sure, it’s not permanent- it’ll definitely stop when I’m dead.

[sarapanzarella]

Thanks for bringing awareness. We are all waiting on a real breakthru. I think this can help some and I have ‘habituated’ most of the time but it still affects my quality of life and I would love to have a few moments of silence.

[sherrieschmidt]

Listening to this and my tinnitus simultaneously. 👍🏼

[Raymond.Butler]

My tinnitus is a part of me and if it isn't going to drive me crazy, I've had to learn to ignore it and get on with life. I like peace and quiet atmospheres, though my ears are ringing every second of every day, it does not stop anything. I don't allow any disability to stop me, because the simple fact is no one else is going to watch out for my family, but me, so I adapted, it ain't easy, but life waits for no one, for any reason.

[endcomingsoon]

I was suffering of anxiety and tinnitus have been a blessing in disguise. I’ve been having tinnitus fue about 1 year so far, when it’s quiet I can’t get anxious, since I hear the tinnitus and I thank God I don’t have a chance to think anxious stuff.

[zachmatt]

I have tinnitus that correlates 100 percent with neuropathy pain. It usually precedes the onset of neuropathy pain by about one minute. If the neuropathy pain subsides, so does the tinnitus. I've mentioned this to multiple doctors, including three neurologists, my EN&T doctor, and primary care doctor. None had ever heard of of this correlation, nor offered any explanation.

[spenceh]

I’ve been living with tintinus for 20yrs and I’ve been seen by both ENT and an audiologist and none have been able to help. I just mentally dealt with it

[InSearchofTruththruJesusChrist]

I developed tinnitus after covid. The CEO of Texas Roadhouse later committed suicide after suffering a sudden onset of tinnitus following covid. I cried for that man as I knew exactly how he felt. I am two and a half years post onset and dealing with it as best as possible.

[bobcat]

It’s permanent. If you got it from a loud noise, a bunch of testing is unnecessary. After months your brain learns to tune it out until something reminds you of it, like this video.

[stephaniecarrow]

I have found the masking videos online to be very helpful ~ especially the ones put out by Dalesnale. He's an audio engineer and has vids that cover a full spectrum of sound. They've helped me sleep at night. I've also heard that listening to these sounds that match the sounds in one's head helps to retrain the brain, and that actually has helped at times.

[annlaurel]

Thank you for sharing this Bob and Brad.
I could say that i had tinnitus about 5 months ago but it’s not bothering me as much as in the beginning . i got this from the vertigo attack i had then. I am dealing with it everyday and trying not to stress out so much. No cure🥲

Thank you Bob and Brad. Love you guys! Until next video!

[tobygathergood]

I've had Tinnitus in both ears for the last 24 years, it never ever stops and has become worse over time. The doctors say they have no cure and can't do anything for me. I have been to hearing therapists...no use. I use a fan to help me sleep at night and have done so for as long as I've had the condition. Mostly I just try to ignore it.

[slk]

Gave my mother magazine was passing out from what was to be tinnitus, ,Thank you for putting up great videos that will help

[cathyfield]

My tinnitus developed suddenly when I was 12. When I recovered from a bout with tonsillitis I had the ringing in my ears. I decided to make friends with it and use it as my personal white noise. That was 58 years ago. I miss silence now and again, but the ringing no longer distracts me.

[lrajic]

I sometimes get a flutter sound. There's no bug. It drives me nuts. Dr couldn't diagnose.

[victoriabarclay]

I’ve had it for 30 years. Worse in one ear where I also wear down my night guard. It’s a low hiss, so I’ve gotten used to it. Sometimes it gets worse if I’m Sick, but that’s so rare I don’t even recall what that was like anymore. I’ve learned to Live with it without ant problem. I’m luckier than sime

[ksmith]

I had it for the first time after a 5 hour flight just a few days ago. Lasted about 24 hours. Sounded like a whooshing sound or like an air leak. Hope it doesn't come back!

[justanothergigi]

Both my husband and I suffer from this. For me doing the thumping exercises on the back of my head (found online) work great for me and cuts it down a lot. The same exercise does not work for my husband. I think his is more jaw related and mine more inflammation/nerve.

[lokipokey]

Two audiologists have told me that my tinnitus is caused by my brain re-creating the frequencies that I can no longer hear. Makes sense to me based on experience. I went from a mild loss of low frequencies (and low-frequency tinnitis) in my right ear in January 2018, to 98% deaf with no hope of help from hearing aids by May 2018. January I performed at Carnegie Hall, and by May I'd quit my singing group. Now I live with extremely loud tinnitis in almost every frequency on my right (totally deaf) side.
People with cochlear implants have told me that they've had tremendous relief from tinnitus after getting the implant(s.) But I can't get Medicare to pay. They say that my hearing in my partially deaf left ear is too good for me to get my entirely deaf right ear fixed :( So I turn my head a lot, and live with the screeching and booming.

[brokenwrench]

I’ve been dealing with it since I was 12 when my left ear was injured in a hunting accident and then growing up around guns, Motorsports, music and aircraft. I’ve seen the usual de’s and specialists, none have helped. Tue only way I can sleep is with multiple fans at different distances and speeds to mask the constant ringing. I know one day it will lo drive me insane 🤪