I take two capsules per day, at 600 mg. each, for a total of 1,200 mg. per day. The brand I take is NOW NAC.
Karen do you take two capsules at once or 1 twice daily?
Thanks!
I take two capsules per day, at 600 mg. each, for a total of 1,200 mg. per day. The brand I take is NOW NAC.
I know this post is old, but I also have reactive form of tinnitus. Just wondering how @valeri is doing now? My T reacts to all sorts of other sounds, loud group of people, television (especially), the car radio, road noise when driving, my heater or ac in the car, faucets, keyboards etc. I do not necessarily feel pain in my ears though, just the hissing T gets louder as it attempts to compete with the exterior sounds. Mine is newer onset- 9 weeks and already I've noticed some improvement. Some days it does not react or if I'm busy I don't notice the reaction and most of the time I can watch TV still for an hour or so and I just deal with the reacting which is an improvement since it started because I was unable to do this for the first month. I have also been able to tune out my T occasionally while watching TV if I'm very interested in the show although usually it's always there and more high pitched then the tv. I really hope it continues to improve for me and am grateful so far I'm not having any difficulty sleeping.
I'm very sorry you suffer with reactive tinnitus. I understand how difficult it is.Hi, @valeri. I know this is an old thread, but I am massively struggling with reactive tinnitus. I'm having a similar experience to what you described. Did this ever improve for you?
Unfortunately, I haven't found anything that provides relief. It is not maskable and reacts to all external noise. I am holding out for a cure at this point.I'm very sorry you suffer with reactive tinnitus. I understand how difficult it is.
Mine has been on/off, starts with burning pain and my ears feel as if acid has been poured in them.
The only thing that helps me, in the lack of Trobalt, is benzo Rivotril. It doesn't go away but takes the edge off.
I'm expecting my next round of reactivity to start soon.
It's impossible to mask.
Did you find anything that gives some relief at least?
Initially, I was prescribed anti-anxiety meds to help alleviate the burden. It worked for a little while (didn't reduce the volume but made me care less), but mine has worsened severely over the last four months. Now, I'm not sure if the worsening was attributed to the meds or if it was going to happen regardless. I try to spend as much time in silent rooms as possible now because of how bad the reactivity is.
Do you know what caused it? Have you tested your hearing via an extended audiogram?Thanks Emgee. It hasn't improved at all in 3 weeks which is scary.
What did we do to deserve this hell?Reactive Tinnitus is one of the worst sub-types to have, as it is virtually non-maskable (ask me how I know)
The louder the ambient sound, the louder the tinnitus volume and the higher/sharper the pitch.
It literally feels like a sharp knife cutting into back of the brain, as that is where the sound seems to be coming from (at least in my case)
I also get the bonus of the "hot ears", which I attribute to the fact, that the sound is travelling backwards (originates inside the head, clashes with sounds coming from outside and pushes through all the way out).
When someone says that they can mask their tinnitus by just "turning on the fan", it makes me realize that we have two separate conditions under the same name (which is part of the reason why the outside world still thinks that tinnitus is the same for everyone).
Not being able to mask is a huge game changer psychologically, as the sufferer is unable to get away from the sound.
Throw in the destroyed sleep and you have a 24/7 hell on earth with no way to escape except for one.
It's possible you have a loss in the upper frequencies which is often untested for. Or, you may have synapse damage which would also go undetected.Yes, three LOUD M80 fireworks set off by a neighbor on 4th of July. Started immediately after. And I've always been so careful with my ears. No significant hearing loss detected.
Mine is also electrical. It's awful.@Emgee
I sure hope it improves. Sounds like loud electrical buzzing right now. My ear feels angry/raw. Hard to describe. I have wondered about hearing loss in upper frequencies and also in other parts of the auditory system. If I've seen zero improvement in three weeks, does that mean there is still a chance for improvement? Thanks so much for the support.
@Emgee can tinnitus go away 100%? I'm 6 months in and just getting quieter days but I do think my ears are reactive.It's possible you have a loss in the upper frequencies which is often untested for. Or, you may have synapse damage which would also go undetected.
Either way, you're still in early days. Have hope that it can improve. Give it time and protect your ears. Reach out if you have any questions.
Sorry to hear that, Tara. This can be a terrible condition indeed. Can tinnitus go away completely? Sure, but generally that is not the case. Most often, it does improve over time though. It is a great sign that you are experiencing quieter days, especially considering you have only had it for six months. Six months is actually not long at all with tinnitus. You are still on the fringe of being in the acute phase. The most likely outcome is that it will continue to improve as time goes on. Wishing you quieter days.@Emgee can tinnitus go away 100%? I'm 6 months in and just getting quieter days but I do think my ears are reactive.
I'm just missing silence like crazy and this thing is so maddening, I don't see how it just stops. It's ruthless.
@Emgee I'm only 32. I can't imagine living with this forever! I just can'tSorry to hear that, Tara. This can be a terrible condition indeed. Can tinnitus go away completely? Sure, but generally that is not the case. Most often, it does improve over time though. It is a great sign that you are experiencing quieter days, especially considering you have only had it for six months. Six months is actually not long at all with tinnitus. You are still on the fringe of being in the acute phase. The most likely outcome is that it will continue to improve as time goes on. Wishing you quieter days.
I'm only 23. I know the feeling.@Emgee I'm only 32. I can't imagine living with this forever! I just can't
I'm very sorry you suffer with reactive tinnitus. I understand how difficult it is.
Mine has been on/off, starts with burning pain and my ears feel as if acid has been poured in them.
The only thing that helps me, in the lack of Trobalt, is benzo Rivotril. It doesn't go away but takes the edge off.
I'm expecting my next round of reactivity to start soon.
It's impossible to mask.
Did you find anything that gives some relief at least?
Consider:@Harley I agree. I've had maskable tinnitus for 15 years. This new piercing hiss is hell on earth.
@Emgee it's terrible. I never imagined I'd have this. But who does I guess?I'm only 23. I know the feeling.
Odds are you won't have to live with this forever, especially considering the advancements being made in the hearing regeneration space.
That is a very good question.What did we do to deserve this hell?
Hi there,Hi @DebInAustralia, hope you are doing well this week. Curious what else you may know about laser therapy? Is this practiced in clinics or are there home devices users have talked about on Tinnitus Talk?
You can read the experience of @GBB.Hi @DebInAustralia, hope you are doing well this week. Curious what else you may know about laser therapy? Is this practiced in clinics or are there home devices users have talked about on Tinnitus Talk?