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I developed this issue a few years ago after exposure to loud noise where my right ear perceives certain notes or frequencies as slightly sharper in pitch compared to my left ear. I've already been living with tinnitus for over ten years which I've learned to cope with, but this new condition...

Hey all, I'm really curious to know if Lenire might help with other tinnitus related problems like pulsatile tinnitus, TTTS, hyperacusis, diplacusis, etc?

Hey all, I'm really curious to know if Dr. Shore's treatment might help with other tinnitus related problems like pulsatile tinnitus, TTTS, hyperacusis, diplacusis?

I just wanted to warn anyone who thinks of taking Ashwagandha. While researching if I should take this or not, I found a bunch of accounts of people who took Ashwagandha and ended up with chronic SSRI syndrome. I personally would steer well clear of this drug/supplement.

I was prescribed Pregabalin by my psychiatrist for sleep and anxiety. I have been taking it for 4-5 months. In July I started getting some hearing distortion but I didn't relate that to the meds. My tinnitus usually gets worse some way each year. I have all sorts of tinnitus sounds, TTTS and...

Is there a chance that this future treatment might be able to help those of us with problems like hyperacusis, TTTS, hearing distortion? I have learned to live with tinnitus. I can cope with it fine but these other conditions are what make my life a living hell. This is what i really hope to...

somone on here said that getting this surgery would make your tinnitus more noticable similar to how when you put ear plugs in, is this right?

Does no one else recognise these symptoms?

I have tinnitus and hyperacusis but I also have something which I need help finding answers to, I need to see if I can maybe treat it or find out why it's happening. What I hear is a low level blood rushing/roaring and bubbling which is amplified when I hear external sounds over a certain...

Did they mention whether this would help people who have pulsatile tinnitus and hyperacusis?

I do get it with music too at certain frequencies but speech seems to be ok. I was addicted to an ototoxic drug also noise exposure and it runs in my family

What's so bad with menieres compared to someone living with severe T and H?

Ive had tinnitus for 6 years got H in the summer and now past few weeks this. At certain frequencies or pitch I hear a bunch of tones from my tinnitus now in almost every outside sound apart from voices or music. It's a nightmare and the doctors do nothing. I started to research the nitrous...

I'm 27 I've had tinnitus for 6 year and it's gradually got worse and worse I have multiple different tones in both ears I find it hard to count them. I was habituated after those first few years and coping but all that changed In the summer last year I developed pulsatile like tinnitus that...

Hearing stuff like this is one of the few things that helps me cope with my tinnitus, learning about others who have conditions far worse than mine(fibromyalgia,ALS,ClusterHeadaches) give me some perspective and makes things seem atleast not as bad as they could be. Doesn't stop the screaming in...

Just wondered if anyone here claims ESA because of T and if so what is your experience of it? Cheers, Tom

Must say I love your avatar picture so much! made me chuckle hehe :)

I don't care about a cure right now all i want is a reduction in volume so i can live a normal life just like everyone else

I would be curious to know what happened with the drug user group? And did it say what drugs they were currently being prescribed?

This is just my experience but I was on a set of anti depressants when i like you decided to come off them, my GP told me that the dose was low enough for me to come straight off cold turkey with no hassle. Unfortunately this was far from accurate the withdrawal effect were to put it lightly a...

I love to cook also a huge gamer I love this game Dayz at the moment if anyone here plays it let me know If you want to add me on steam :)

Is there date i can mark on my calender for when the next big update on autifony will be or when phase 2 trials start?

If Autifony fail to come up with a working treatment for chronic tinnitus then I'm going to gather as much media as i can and stage my suicide at wherever their head offices are maybe then people will understand just how serious this "condition" really is

I got referred to an ENT on the NHS February this year didn't hear anything back from them until last month saying i had an appointment in June.

"I'm cautiously optimistic about Autifony, but as it's not even in phase II yet, we're talking nearly 10 years IF it's proven effective." 10 years? how so? I remember people saying that If It was proven effective it would be more like 3 or 4 years

Yea, I've had the same experience where I have been up all night then the next day doze off in the middle of the afternoon only to wake up with it screaming at me much louder than before

To the original poster Is the actual volume of your T lower now? And do you attribute the am-101 gel to the reduction in volume?

If anyone has tried this device please let us know If It worked or not in reducing the volume of tinnitus

When can we expect to see the results of phase 3?

I got excited for a minute but I then I noticed this thread was started back in 2012. Is this form of treatment actually available or Is It still being developed and when If ever will It be ready?

Hi, I just made an account to ask when we could expect to hear the results of the phase 1 trial autifony are doing? I am suffering alot right now and this is the one thing keeping me from giving up hope, so any replies would be greatly appreciated. Thanks.