I've had tinnitus in my left ear for about six months now. I was hoping it was the result of an earwax impaction or something, but after having several specialists look at my ears, test my hearing, and getting an MRI to check for tumors, the overwhelming medical consensus of the cause appears to be "I dunno", and at this point I have given up on it being temporary. About 95% of the time, I can fairly easily just tune…
Tinnitus Neuromodulator
231–240 of 256 posts
Re: Tinnitus Neuromodulator
#232Earlier quoted context omitted.
So... what? Everything causes dependence one way or another. What is the point of a substitute to "use all the time". It even reads funny to me. I would like you to explain what you meant by that. And what would you recommend as a great substitute of benzodiazepines (that are effective AND safe to use at all times)?
Parent comment is right. I’ve used Lorazepam to treat tinnitus. It’s not worth it. In the long run it raises your base anxiety level. Currently I’m experimenting with Tizanidine.
It might not be worth it to you, it might be worth it to someone else.
I would still like to hear about this substitute that is both effective and can be used "all the time".
Tizanidine causes "dependence", too, by the way.
Funny you mention Tizanidine, because that is what I want to try as well for my MS-related muscle spasticity.
Alprazolam works, but I have been using it for years and it would be great to finally get off of them. It does not last long either, and longer acting benzos don't work for me for some reason. I tried diazepam, which was supposed to be just perfect, but it did not work at all. :(
In any case, hoping tizanidine will work for me, we will see.
Let me know if tizanidine works for your tinnitus though, my mom has been "suffering" from it for a long time now.
Re: Tinnitus Neuromodulator
#233I've had tinnitus in my left ear for about six months now. I was hoping it was the result of an earwax impaction or something, but after having several specialists look at my ears, test my hearing, and getting an MRI to check for tumors, the overwhelming medical consensus of the cause appears to be "I dunno", and at this point I have given up on it being temporary. About 95% of the time, I can fairly easily just tune…
Re: Tinnitus Neuromodulator
#234I suddenly lost the hearing in my left ear at the age of 24. One moment I was fine, eating a slice of pizza, the next moment I suddenly could sense something was wrong. I tried to stand up and walk, but my balance was gone. My ear felt full and there was a strange metallic echo. I waited about 24 hours and it hadn't gone away, so I went to the urgent care. By that time, just standing up was enough to cause me to vomi…
This mirrors what turned out to be the onset of my pulsatile tinnitus – especially the "strange metallic echo". I remember sitting at my desk listening to the radio when I noticed it sounded like the radio's speakers were slightly out of sync with each other. I took my headphones off and listened, and my coworker's voice sounded metallic and robotic, almost exactly like a dalek from Doctor Who.
By the time I got to the doctor (same day), the metallic echo had passed but I had that fullness feeling in my ear that you describe and my doctor couldn't diagnose. Long story short, I'm not completely deaf but I have reduced hearing and permanent pulsatile tinnitus in my right ear.
I've had regular tinnitus since I was a kid, and I've thankfully been able to adjust to hearing the sound of my own heartbeat in my ear at all hours of the day without too much trouble. But when I describe what it's like to friends and family, I like to joke that it's like the heartbeat in Edgar Allan Poe's The Tell-tale Heart.
> I am now 40 years old and have lived with being single sided deaf for half my life. Initially I didn't think much of it. I've slowly realized it has had a profound impact on my personality and sense of identity. I am much less social due to the difficulty I have hearing in group settings. Conversations are frustrating because it takes so much effort to hear the other person properly.
My reduced hearing has affected me more than I thought it did, and I've only come to realize it very recently. It's difficult for me to help my wife with her birding hobby because I'm always pointing in the wrong direction, for example. It also takes a lot of my patience not to get irritable when she's trying to talk to me while we're watching tv or listening to a book in the car, because I have a hard time tuning out things I can hear in my good ear and focusing on her with my bad ear.
Re: Tinnitus Neuromodulator
#235Earlier quoted context omitted.
A message of hope. I got mine in my 30's too. The first week I thought I was going crazy, and this was the end of my life. I was shocked, I couldn't go to work for a whole week. I then saw a doctor who said to me: "Man, I've got tinnitus since 20 years and I barely hear it anymore. The more you accept it, the more it'll fade." A decade later, my own experience is exactly this. I accepted it as one of the body malfunc…
I've always been someone who hears high pitched noises that "normal" people don't. I'm also in my 30s, and I'm sure those "teenage alarms" in Japan would work on me. I was the one who would walk up to a CRT and turn it off when everyone else thought it already was. What helped me accept (and ignore) tinnitus was realizing that I had already grown accustomed to tolerating that sound indoors. When's it's something you…
Re: Tinnitus Neuromodulator
#236I've had tinnitus in my left ear for about six months now. I was hoping it was the result of an earwax impaction or something, but after having several specialists look at my ears, test my hearing, and getting an MRI to check for tumors, the overwhelming medical consensus of the cause appears to be "I dunno", and at this point I have given up on it being temporary. About 95% of the time, I can fairly easily just tune…
Re: Tinnitus Neuromodulator
#237I've had tinnitus since 2018. I got used to it. it's not the worst thing for me. I'm 5'2" bald guy LoL If you're suffering from tinnitus, remember, at least you're not bald and 5'2" tall.
Re: Tinnitus Neuromodulator
#238Earlier quoted context omitted.
Even 80 mg of benfotiamine a day is too potent for me, giving me anxiety. 40 mg is more tolerable. I do take plenty of magnesium, zinc, and P5P. Be careful taking the basic non-P5P form of B6 because it risks causing serious neuropathy in the long term. Benfotiamine is more for managing damage from high glucose. I acknowledge your experience, but if your nerve damage is not from metabolic concerns, I am skeptical. Wh…
the older i get, and more in tune with my body i become, the more i'm thinking everything is connected to metabolism... it is, after all, the primary thing life does as it relates to energy. the b vitamins, and specifically b1 is a precursor/cofactor in almost every metabolic pathway. i only high dosed it for a couple months, just taking 150mg with ala daily now, but my tinnitus that i've had for 20 years is gone unl…
As for ALA, I take the r- fraction form.
Re: Tinnitus Neuromodulator
#239Earlier quoted context omitted.
I feel you. Here’s things you can try (in this order): - Cut stimulant use (coffee, energy drinks) and alcohol - Drink plenty of water - Check blood pressure - Talk to a dentist and check if you grind teeth or suffer from jaw stiffness - Supplement Magnesium (chelated/glycinate, 300mg/day) I’m ignoring issues of the ear canal (wax, secretions) since you mentioned it. Studies point to tinnitus being either caused by c…
Mine came on when I was about 12 years old and I'm convinced it was brought on by severe anxiety. At the time my life had changed dramatically. My parents split. Moved to an area adjacent to government housing projects, through which I had to travel everyday to school, and I was, by virtue of unfortunately being wrong color, beaten daily by gangs of hooligans. I ended up sneaking through a slightly wooded area like a…
Re: Tinnitus Neuromodulator
#240Keep at it, I think you're on to something!