• This Saturday, November 16, you have the chance to ask Tinnitus Quest anything.

    The entire Executive Board, including Dr. Dirk de Ridder and Dr. Hamid Djalilian are taking part.

    The event takes place 7 AM Pacific, 9 AM Central, 10 AM Eastern, 3 PM UK (GMT).

    ➡️ Read More & Register!

Any Recommendations on How to CONTINUOUSLY (Day After Day) Stop Considering Tinnitus a Threat?

Do you think that everybody can habituate to their tinnitus? If not, why not?
Do you think anti depressant meds changes a person's mental health? If not, why not?
Do you think that a person may be able to habituate easier to tinnitus with a change in their brain chemistry due to taking AD meds?
First? No I don't, but then maybe "habituation" is dependant on many things, not all of which are present in equal measures for everyone. I sort of think that habituation has become a bit of a buzzword, and its meaning is different from sufferer to sufferer. Second? I've seen anti-depressants described (not derisively) as a band-aid and as a legit strategy for dealing with an otherwise insurmountable crisis. I do agree that this is a positive for their use. I've got some history working in mental health some years back, and I've seen depressions that were so intense that there was no other way. I think real mental health issues are physiological as much as psychological and demand a physiological solution before any psychological approach will ever have a chance. As to your last point there, I find that harder to answer. I think tinnitus can take you down psychologically to the point where your brain function alters itself at which point one becomes locked in a feedback loop where the tinnitus feeds the negative processes which draw attention to the tinnitus etc. I guess the thing about mental health is that, like any medical condition, there are layers of coping/management strategies which get us by until something breaches that last line of defense, at which point outside intervention becomes the only option. ADs, benzos etc certainly have a role in breaking that cycle.
I have known several medical professionals that believe the smartest doctors are high functioning autistics with Asperger's. These same doctors generally have the worst bed side manner.
I've certainly seen this play out in real life. The Medicos you mention here are absolutely right.
 
Hey Melissa, I'm just adding a dose of reality to your positivity. We can all sing kumbya and habituate together without meds and too bad for those that can't. We are all friends here but if we don't agree, its ok to share our views and agree to disagree. I believe the truth has some relevance and cheers to your positivity.

Whoa, no need for the sarcasm! My experiences are just as real as yours. Please don't presume that your perception of reality can be extrapolated to others. Wasn't that what you critised me for? Signing off now, love and light x
 
Whoa, no need for the sarcasm! My experiences are just as real as yours. Please don't presume that your perception of reality can be extrapolated to others. Wasn't that what you critised me for? Signing off now, love and light x
I wasn't being sarcastic.:) In spite of your believe in free will, some people can't habituate without AD meds. You can color it, you can put gingerbread around it....invite the tooth fairy to hang out and sing nursery rhymes, them is the facts. Some people can't by force of will quell their anxiety and quiet their contempt to 'allow' habituation without a change in the brain chemistry brought about by medication. Btw, some people can't get on an airplane without medication either as much as they want to whereas the vast majority hop on with a smile.
 
I agree with much of your post including OCD and tinnitus which may in fact be related and why so many struggle with habituating.
But where I disagree is...you infer that mental health is a choice...something you can choose, will or order up. No, mental health isn't a choice or all the profoundly mentally ill people throughout the world including those in institutions could be cured by so called positive thinking seminars...lol. Mental health can't be willed just like habituation often asked about can't be chosen or willed. Good mental health is a reaction to normal brain chemistry which eludes many with tinnitus. This is when drug intervention is required to restore brain chemistry to allow acceptance and less hyper focus and allow habituation. Further...staying on AD meds for life isn't always required to maintain habituation. Once new behavior patterns and neural pathways are forged, sometimes a given patient on AD meds can go off or dramatically reduce dosage whereby mental homeostasis can be maintained.
Not at all what I am saying or inferring. Mental health can be worked on through medication and/or counseling. No one need suffer alone there is support available.
 
Not at all what I am saying or inferring. Mental health can be worked on through medication and/or counseling. No one need suffer alone there is support available.
My quote wasn't addressed to you so not sure why you responded to me.
The point is I believe, too many suffer alone trying to gut it out like Melissa when seeking professional help would improve mental health by medication and/or counseling like you correctly say..
 
My quote wasn't addressed to you so not sure why you responded to me.
The point is I believe, too many suffer alone trying to gut it out like Melissa when seeking professional help would improve mental health by medication and/or counseling like you correctly say..
You quoted me. Said you agreed with some of what I said and then disagreed with some of it. Maybe you forgot. It was at the beginning of this thread.
 
@JasonP

Have you tried a mood stabilizer? You really need a good psychiatrist to sift through what will work best for you. Unfortunately, a really good one is hard to find
 
I wasn't being sarcastic.:) In spite of your believe in free will, some people can't habituate without AD meds. You can color it, you can put gingerbread around it....invite the tooth fairy to hang out and sing nursery rhymes, them is the facts. Some people can't by force of will quell their anxiety and quiet their contempt to 'allow' habituation without a change in the brain chemistry brought about by medication. Btw, some people can't get on an airplane without medication either as much as they want to whereas the vast majority hop on with a smile.

I'm really not anti-meds at all. I was on and off SSRIs for over a year but unfortunately they didn't help. The only choice I had was trying to change my mindset and thinking patterns. I thought that CBT and all of that kind of stuff was bullsh*t but, with no other options, I decided I would just try and buy into it as best I could. It did help but finding a support group where I could talk to other people and vocalise my thoughts was the best help for me. People that had already weathered the storm and managed to forge lives for themselves helped me see things that I couldn't on my own - that there was a way through and life was worth living. I guess maybe I see habituation via changing thought processes as a more long-term solution...but def not critical of those that need meds.

I'm a valium and double-shot of whiskey flyer
 
I'm on lamictal. If it weren't for tinnitus I would be doing pretty good.
Then you are doing pretty well:) You have to give yourself credit for that, because I am guessing that there was a point where you couldn't say that. You must have done something to get yourself this far.

I was freaking out for a long time when I first got T. Sometimes I still freak out. The things that help me the most are to not think about having to deal with the t beyond today. If I think about having it forever or losing my hearing altogether. I start losing it, so I don't let myself get that far in my thoughts. I couldn't stop thinking about it for a minute at first, now I can tune it out for a while. Maybe in 5 years it will bother me even less. The other thing I did at first was to ask myself what I would be doing if I didn't have T and then do whatever that was. Now I just do what I am going to do and don't have to ask myself anymore. Idk maybe some of this could help you. Hope it starts getting easier for you.
 
Then you are doing pretty well:) You have to give yourself credit for that, because I am guessing that there was a point where you couldn't say that. You must have done something to get yourself this far.

I was freaking out for a long time when I first got T. Sometimes I still freak out. The things that help me the most are to not think about having to deal with the t beyond today. If I think about having it forever or losing my hearing altogether. I start losing it, so I don't let myself get that far in my thoughts. I couldn't stop thinking about it for a minute at first, now I can tune it out for a while. Maybe in 5 years it will bother me even less. The other thing I did at first was to ask myself what I would be doing if I didn't have T and then do whatever that was. Now I just do what I am going to do and don't have to ask myself anymore. Idk maybe some of this could help you. Hope it starts getting easier for you.

Very cool. I like that idea!! My hearing aides with maskers sometimes help too but its way better when I have it mentally under control. I really like the way you think there. It is something I would need to work on. :)
 
I'm on lamictal. If it weren't for tinnitus I would be doing pretty good.
I'm on Lamictal too, although tapering down from 100mg to 25mg. I agree with @stophiss that some people with OCD and pre-existing anxiety /depression (like me) may need a AD to control the mental disorders, but the problem is which one? The last psychiatrist I've seen wanted to try Zoloft which I had taken previously and didn't like. Lamictal seems pretty clean but the SSRI's give me too many side effects for some reason. Maybe I should try Wellbutrin or Remeron again? I do fear the side effects like many people here.
 
If I think about having it forever or losing my hearing altogether. I start losing it, so I don't let myself get that far in my thoughts.
Yes. Likewise. With hyperacusis thrown in though, losing my hearing sounds like a valid option sometimes.
 
I'm really not anti-meds at all. I was on and off SSRIs for over a year but unfortunately they didn't help. The only choice I had was trying to change my mindset and thinking patterns. I thought that CBT and all of that kind of stuff was bullsh*t but, with no other options, I decided I would just try and buy into it as best I could. It did help but finding a support group where I could talk to other people and vocalise my thoughts was the best help for me. People that had already weathered the storm and managed to forge lives for themselves helped me see things that I couldn't on my own - that there was a way through and life was worth living. I guess maybe I see habituation via changing thought processes as a more long-term solution...but def not critical of those that need meds.

I'm a valium and double-shot of whiskey flyer
Cool. What I like about you Melissa is you defend your viewpoint well and you make several good points.
Since about 30 % of America's population is on AD med's...and by the way a salvation for many and scourge for other's...probably a good thing they exist. And Greg I believe is spot on about the term habituation as well. I feel the same way. Habituation IMO is simply acceptance which btw it pretty impossible in the face of acute anxiety or depression which accompanies a cry for help on this forum too often. I also put CBT...not in the bullshit camp completely but rather something like habituation which can come by more naturally with time. If you think about it, we arrived the same way. I didn't attend any support groups however but there is much great advice shared here that has helped me and honestly, I adjusted to T because I encountered something harder to adapt to a couple of years ago...nerve damage in my face due to a tooth extraction which I suspect precipitated my tinnitus or was at least part of the perfect storm because the nerves run so close to the nerves related to the hearing apparatus. So I have been the habituation thing before but it wasn't related to tinnitus...and neuropathic pain is in some ways much worse than tinnitus...again depending on magnitude of each.

Yes, time heals to a degree. Most don't habituate in a week as you infer. It takes time for the mind to come to terms with a most unwelcome intruder that we have no control over. There is grieving, anger, fear...a gamut of emotion that can spiral someone new to tinnitus in particular out of control into anxiety attacks and we both know what that is like...there is no worse feeling or more desperate place to be. Some can cope without medication but many can't and are greatly helped with meds to get to a more peaceful place of acceptance.

Most of all, I am glad you are better and you have come here to share your story which helps so many.
I have never taken a valium but whoever invented Xanax and Ativan should be knighted.:)
Be well Melissa.
 
I'm on Lamictal too, although tapering down from 100mg to 25mg. I agree with @stophiss that some people with OCD and pre-existing anxiety /depression (like me) may need a AD to control the mental disorders, but the problem is which one? The last psychiatrist I've seen wanted to try Zoloft which I had taken previously and didn't like. Lamictal seems pretty clean but the SSRI's give me too many side effects for some reason. Maybe I should try Wellbutrin or Remeron again? I do fear the side effects like many people here.
What AD med's indeed...including what dosage? $64K question for sure. Everybody brings a different mental pre-disposition and different brain chemistry and so which med is most effective and as important, which med will not make their tinnitus worse short or longer term. This is almost unknowable as to what is best. For the countless ten's of thousands on AD med's there maybe in most instances a best med or better dosage for each individual.

All one can do is inform themselves the very best they can. Confer with a tinnitus and med expert like glynis, search this forum for side effects, search the web, and try to find the most enlightened therapist. Not an easy task for sure.
 
While I don't have a success story to report yet, I believe that the way to go is through learning, not willing.
In some cases, for some people, it might be possible to force a change in outlook through willpower. But in most cases it's not. I myself have very little control over how I feel about a subject, but I suspect some have it easier.
Most people can learn, though. And once something is learned, really learned, whether it's a fact or a habit, it affects us profoundly.
We need to teach ourselves that T isn't a threat in order to react to it in a reasonable manner. Or better still, not react to it at all.

The late great anthropologist Mary Douglas said about the concept of dirt that it's "matter out of place". Anything can be dirt as long as it's not where it should be. Pebbles aren't dirt on the gravel road, but on your kitchen floor? You get the idea. Tinnitus is perceived as a noise disturbance because we feel it's "out of place". And we react as if we should do something about it. If we could go to the doctor and ask for the pill to take it away, that would be fair enough. But at this point, that's tragically not an option. Coping is our best bet.

We need to teach ourselves that tinnitus isn't out of place. The sound is coming from me. I'm making it. Tinnitus is me, I am the tinnitus. There is no line that can be drawn between the two. And if you want it to truly go away, I don't think that's impossible, but not without this understanding. Tinnitus isn't a thing. Treating it like a thing is misguided and will warp your outlook in a negative manner.
That's part of the reason, I think, why the back to silence method is effective, you don't treat the T as a thing, but acknowledge your reaction to it. Which is entirely real and legitimate, in other words, positive.

Therapy is one way of going about this, but it's not always easy to get a therapist, let alone one with experience in this field. Luckily, meditation and mindfulness can be practiced by anyone, anywhere, and can be very helpful. Part of mindfulness is accepting your entire experience, even the painful and scary parts.

I've been using meditaton apps lately, and they have helped me reinforce feelings I had mostly forgotten about. For instance, I'm usually one who shrugs at gruesome news from around the world. But a "compassion" exercise in Stop, Breathe and Think suddenly had me in tears over Syria. After a good meditation session, my T feels softer, probably because my focus is more balanced. In time, I hope this can be more permanent.

I would rant more, but I have to go to work.
 
While I don't have a success story to report yet, I believe that the way to go is through learning, not willing.
In some cases, for some people, it might be possible to force a change in outlook through willpower. But in most cases it's not. I myself have very little control over how I feel about a subject, but I suspect some have it easier.
Most people can learn, though. And once something is learned, really learned, whether it's a fact or a habit, it affects us profoundly.
We need to teach ourselves that T isn't a threat in order to react to it in a reasonable manner. Or better still, not react to it at all.

The late great anthropologist Mary Douglas said about the concept of dirt that it's "matter out of place". Anything can be dirt as long as it's not where it should be. Pebbles aren't dirt on the gravel road, but on your kitchen floor? You get the idea. Tinnitus is perceived as a noise disturbance because we feel it's "out of place". And we react as if we should do something about it. If we could go to the doctor and ask for the pill to take it away, that would be fair enough. But at this point, that's tragically not an option. Coping is our best bet.

We need to teach ourselves that tinnitus isn't out of place. The sound is coming from me. I'm making it. Tinnitus is me, I am the tinnitus. There is no line that can be drawn between the two. And if you want it to truly go away, I don't think that's impossible, but not without this understanding. Tinnitus isn't a thing. Treating it like a thing is misguided and will warp your outlook in a negative manner.
That's part of the reason, I think, why the back to silence method is effective, you don't treat the T as a thing, but acknowledge your reaction to it. Which is entirely real and legitimate, in other words, positive.

Therapy is one way of going about this, but it's not always easy to get a therapist, let alone one with experience in this field. Luckily, meditation and mindfulness can be practiced by anyone, anywhere, and can be very helpful. Part of mindfulness is accepting your entire experience, even the painful and scary parts.

I've been using meditaton apps lately, and they have helped me reinforce feelings I had mostly forgotten about. For instance, I'm usually one who shrugs at gruesome news from around the world. But a "compassion" exercise in Stop, Breathe and Think suddenly had me in tears over Syria. After a good meditation session, my T feels softer, probably because my focus is more balanced. In time, I hope this can be more permanent.

I would rant more, but I have to go to work.
Newloud,
Agree on many fronts you write about and of course the cornerstone I have written above is that willfulness rarely works as you reinforce. First reaction to tinnitus is...what the hell is this and am I going to die from this? From there is a long slog to acceptance with many bumps in the road.

Can you tell us about your Asperger's...where you are on the spectrum...when you were diagnosed and how it affects your life as objective as you can be about it?

Be well.
 
I'm on Lamictal too, although tapering down from 100mg to 25mg. I agree with @stophiss that some people with OCD and pre-existing anxiety /depression (like me) may need a AD to control the mental disorders, but the problem is which one? The last psychiatrist I've seen wanted to try Zoloft which I had taken previously and didn't like. Lamictal seems pretty clean but the SSRI's give me too many side effects for some reason. Maybe I should try Wellbutrin or Remeron again? I do fear the side effects like many people here.
Good question. I don't know. There is a med called Riluzole I would like to try but my doc won't prescribe it for me. I know people with liver damage can't take it ànd it would be for off label use but still...would be interesting for me to try at a low dosage just to see. They did some off label studies on it that are on the net for depression and things lIke that. If you read up on it let me know what you think.
 
That's part of the reason, I think, why the back to silence method is effective, you don't treat the T as a thing, but acknowledge your reaction to it. Which is entirely real and legitimate, in other words, positive.

I'm following how it's real and legitimate, but I fail to see how that makes it positive. "Positive" is not another word for "real and legitimate" - unless I'm using the wrong dictionary?

My reaction to my T is definitely real and legitimate, and I know well it's within me and is not life threatening, but it doesn't mean it's positive. I don't see the logic there.
 
Good question. I don't know. There is a med called Riluzole I would like to try but my doc won't prescribe it for me. I know people with liver damage can't take it ànd it would be for off label use but still...would be interesting for me to try at a low dosage just to see. They did some off label studies on it that are on the net for depression and things lIke that. If you read up on it let me know what you think.
Okay, I will look into it. Nortriptyline seems to help but the dry mouth is bad. My awakening noise is hard to take but then it settles down quite a bit and have been taking Robaxin also. My primary Dr. doesn't want me on too many CNS depressants.
 
I might have been using the term a bit awkwardly, but what I meant was that it is actual, something you can work with and acknowledge. "Positive" doesn't have to mean "good" or "pleasant". I mean, one can be HIV positive, right?
 
There is a med called Riluzole I would like to try but my doc won't prescribe it for me
I see that Riluzole is used to treat ALS, which would make our tinnitus seem minor in comparison to that dreadful condition. Head noise is bad enough. Maybe the side effect profile of Riluzole is too dangerous in your Dr.'s opinion?
 
I see that Riluzole is used to treat ALS, which would make our tinnitus seem minor in comparison to that dreadful condition. Head noise is bad enough. Maybe the side effect profile of Riluzole is too dangerous in your Dr.'s opinion?

She probably saw ALS and freaked out. Basically, if people have liver problems, it probably is not a good idea to use the drug. However, I don't have liver problems. These are the only side effects I would be concerned with:

Adverse Effects
>10%
Asthenia (16-20%)

Nausea (16-20%)

Skeletal weakness (19%)

Decreased lung function (11-15%)

Source: http://reference.medscape.com/drug/rilutek-riluzole-343067#showall

My thought was that if I took a low dose, those issues might be light or not happen at all. They are all 20% or lower.

According to these studies on OCD, depression, anxiety, etc. it says there was no adverse affects except for the people with liver problems. I wonder if those adverse affects above were for people taking it for ALS which means their brains are acting different I imagine.

Source: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2958461/table/T1/

My thinking is, that if I can remove some excess glutamate, maybe the T would be lower. I don't think that would fix everything but it might help some.
 
Newloud,
Agree on many fronts you write about and of course the cornerstone I have written above is that willfulness rarely works as you reinforce. First reaction to tinnitus is...what the hell is this and am I going to die from this? From there is a long slog to acceptance with many bumps in the road.

Can you tell us about your Asperger's...where you are on the spectrum...when you were diagnosed and how it affects your life as objective as you can be about it?

Be well.
If there's a separate aspie spectrum I'm not aware of it. But I guess I would be someone with "mild" Asperger. I'm living by myself, dress normally, working, blending in (or so I think). Unless you were an expert on the subject you wouldn't be able to tell - only a few close friends have suggested that I might be one. Aspie traits are rampant in the family, though. I am professionally diagnosed, after my therapist suggested it might be worth looking into. Diagnosed at 33.

I guess it affects me in that "wrong planet" kind of fashion. I never quite got other people, how they could live the way they do, and where I could fit in. I realized at one point that people aren't complete phonies, though, but that most are a bit different from myself. Always struggled with depression, anxiety, sleeping. Underachieving (from a normal point of view).
 
If there's a separate aspie spectrum I'm not aware of it. But I guess I would be someone with "mild" Asperger. I'm living by myself, dress normally, working, blending in (or so I think). Unless you were an expert on the subject you wouldn't be able to tell - only a few close friends have suggested that I might be one. Aspie traits are rampant in the family, though. I am professionally diagnosed, after my therapist suggested it might be worth looking into. Diagnosed at 33.

I guess it affects me in that "wrong planet" kind of fashion. I never quite got other people, how they could live the way they do, and where I could fit in. I realized at one point that people aren't complete phonies, though, but that most are a bit different from myself. Always struggled with depression, anxiety, sleeping. Underachieving (from a normal point of view).
Thanks. There is a very bright however somewhat tortured young lady on this forum with Aspergers. I would love to know her IQ...seems to be in the genius range by the way she writes.
She is hyper sensitive to all sensory input in her body and constantly searching for ways of coping with her view of the world.
I theorize that my older brother is a high functioning Asperger's however he has never been formally diagnosed.
Do you excel at science...do you have graduate degrees?
Mental health challenges as discussed only make the challenge of tinnitus more daunting.

Wishing you well and thanks for sharing.
 
Yes. Likewise. With hyperacusis thrown in though, losing my hearing sounds like a valid option sometimes.
Lol. You don't want to lose your hearing. When my T first started I thought I would rather lose my hearing. I'm already deaf in one ear. Then, I started feeling like I couldn't hear very well in my T ear and it was pretty scary. Now I would say that I would take T over hearing loss any day.
 
Any suggestions to stop considering it a threat and start having more "clear thinking".


Jason you have received so many great replies and suggestions. Your thread here is one of the most informative threads right now. Stophiss's responses and information is right on the mark in many ways. And it is great that everyone is listening and giving back information.

Stophiss...good job. (I know I haven't opened my pm yet. You can ask Marku or Steve for my email. And I can explain in greater details)

Jason...your first post had the above question. I have reread this thread a few times now. I am new here and back into support board after a very long break so I am rusty. My first reaction to that question is: Simply stop trying.

What I mean is this. Sometimes we create more brain fog by continued "trying". There must be some way...there must be something I can stop eating or drinking or doing...there must be some answer as to why the tinnitus is such a threat to our brains and living existence.

This isn't easy. I was housebound for a year. My once privileged life was taken away in a single day. It would never be the same for me. Ever. Days spent in a closet rocking back and forth in tinnitus/hyperacusis agony and pain. And the visits to even top "specialists" only reinforced my issues. This was back in 2002. I could not drive. I lost so much of myself. I lost so much.

I digressed a bit. Sorry.

It is hard to explain the ability to stop trying. It is like you mentioned when your tinnitus was not so bad you were much better. Then you realized it was better and the cycle started again?

I believe in the right medications be it Antidepressants or Xanax. The problem is I had high anxiety they wanted to treat with ADs. I was not depressed in the clinical sense. I was over ridden with anxiety. That was what needed to be treated before I could move forward and get more help.

It saved my life. So many here will be against this because of the horror stories of addiction. So usually I say nothing. I understand their point of view. But if I wanted my life back I knew this was my safe option that my doctor and I worked on. Xanax saved my life back then. Just like diabetics need their medication.

But had I listened the the negative stories I would not be here today.

So when did I stop "trying" to over come that "threat" from tinnitus? It is an ongoing process for me. I accept good days so much more now. And the bad days...are a bit less frightening now. A baseball bat to the head helped. : ) Kidding about that of course.

Another example you know when you have forgotten the name of an actor in a particular movie? You can see the face. The name is so there but just gone and the harder you try to recall it the more aggrevating it becomes. And finally you just stop thinking about it for some reason. And out of nowhere suddenly the name pops into your brain. Crazy.

Back to the medication you guys are talking about. I don't know much about ADs. But some of the replies here are very good.

You really sound like a smart guy. You will get back normal in some sense soon.
 
Jason you have received so many great replies and suggestions. Your thread here is one of the most informative threads right now. Stophiss's responses and information is right on the mark in many ways. And it is great that everyone is listening and giving back information.

Stophiss...good job. (I know I haven't opened my pm yet. You can ask Marku or Steve for my email. And I can explain in greater details)

Jason...your first post had the above question. I have reread this thread a few times now. I am new here and back into support board after a very long break so I am rusty. My first reaction to that question is: Simply stop trying.

What I mean is this. Sometimes we create more brain fog by continued "trying". There must be some way...there must be something I can stop eating or drinking or doing...there must be some answer as to why the tinnitus is such a threat to our brains and living existence.

This isn't easy. I was housebound for a year. My once privileged life was taken away in a single day. It would never be the same for me. Ever. Days spent in a closet rocking back and forth in tinnitus/hyperacusis agony and pain. And the visits to even top "specialists" only reinforced my issues. This was back in 2002. I could not drive. I lost so much of myself. I lost so much.

I digressed a bit. Sorry.

It is hard to explain the ability to stop trying. It is like you mentioned when your tinnitus was not so bad you were much better. Then you realized it was better and the cycle started again?

I believe in the right medications be it Antidepressants or Xanax. The problem is I had high anxiety they wanted to treat with ADs. I was not depressed in the clinical sense. I was over ridden with anxiety. That was what needed to be treated before I could move forward and get more help.

It saved my life. So many here will be against this because of the horror stories of addiction. So usually I say nothing. I understand their point of view. But if I wanted my life back I knew this was my safe option that my doctor and I worked on. Xanax saved my life back then. Just like diabetics need their medication.

But had I listened the the negative stories I would not be here today.

So when did I stop "trying" to over come that "threat" from tinnitus? It is an ongoing process for me. I accept good days so much more now. And the bad days...are a bit less frightening now. A baseball bat to the head helped. : ) Kidding about that of course.

Another example you know when you have forgotten the name of an actor in a particular movie? You can see the face. The name is so there but just gone and the harder you try to recall it the more aggrevating it becomes. And finally you just stop thinking about it for some reason. And out of nowhere suddenly the name pops into your brain. Crazy.

Back to the medication you guys are talking about. I don't know much about ADs. But some of the replies here are very good.

You really sound like a smart guy. You will get back normal in some sense soon.

Great response. I am so glad you find this thread informative. I have been on here a while now and can't believe I never asked this question before! I think it is because I was so consumed with finding a cure or ways to lessen tinnitus. I remember a couple of times I got angry and wanted to vent a couple of times. If you are interested, I put together a thread about caffiene, melatonin, anti-depressants, and benzo's affect on sleep which can affect tinnitus. If you do read it, please let me know what you think. :) I have updated it since I posted it the first time.
 

Log in or register to get the full forum benefits!

Register

Register on Tinnitus Talk for free!

Register Now