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Goodbye everyone, this is a fight I can’t fight anymore.

Honestly feel pretty sad, not only do I know I have sound induced T but now I think I have Tmj

I used to post research information on Facebook tinnitus groups but got little response/got comments that there will never be a cure etc. I don't know if it’s just me but it seems like a lot of them there like to drown in their negativity instead of addressing their issues. I gave up and left...

Cracking up a cold one with the boys

Hit or miss

I need some milk

I’m a bit curious if they have a requirement to have the participants to stay away from sounds to see if it reflects the results from the injections.

Having not one but two incurable conditions is just awful. Made me realize that Tinnitus isn’t the only thing that should get more attention

They’re just cringe content for me now and the FB groups. I was in mostly in all of them but left since they just seem to go in circles.

A shooting that had happened. Multiple guns involved

Right now it’s not super super bad. I just know I don’t hear what I use too. By the time I’m like 30 it’ll be really awful I believe.

I kinda hope I become friends with someone born deaf so they can teach me their ways

Naruto is my favorite. I don’t like the new series though

Lil sample of the thousands of pictures I’ve taken.

I try my best to take good pictures but I sometimes rush a bit too much. All I could take pictures of is nature and dogs lol

Ya boy just became a Benefactor

My dogs abuse me on a daily basis

I’m still salty after the lil stunt ata pulled. After like 50 years they still aren’t very known even though apparently 1 in 6 people have it ?

What do people in the ATA even do on a daily basis? I’m not 100% on what they even do to raise awareness and gain funds other than getting very few volunteers to do support group meetings for them. For example what did they do before the A Star Is Born movie? Do they just milk things that...

Dank memes always makes me happy

https://www.ata.org/research-toward-cure/research-program/past-ata-funded-research This shows where ATA gave money too. I still believe their awareness strategy is complete trash as well as their decision making,it’s just sad. BTA does a better job in my opinion from the things I hear (read)

I think it’s best to let the results do the talking at this point. Sorta seems a lot being said is speculation in my opinion

I find that a bit disgusting honestly

I was exactly the same and always heard like Charlie Brown for awhile when people talked

A bit curious. I've been having some thoughts ever since I got all three (tinnitus, hyperacusis, hearing loss) and I also don’t exactly have the best vision either. I work with older dogs and sometimes we get dogs that are both blind and deaf. That’s when I get most of my negative thoughts...

I think I do ,I have at least 4 different sounds and I had the ringing before I had been exposed to loud noise exposure which made the noise a whole lot louder. I kinda thought before my hearing was normal. Then I read up about tinnitus after the noise exposure

How many people was this out of?

I was thinking the same but also think that doctors just look over your overall heath then send you to a specialist if need

Yeah like around August/September from what this article says which is from March 10th 2017 https://hsci.harvard.edu/news/progress-toward-treatment-hearing-loss

I agree but I’m not sure how that would happen. I know BTA does a good job with awareness. Not sure about ATA, from what I see they don"t do much, other than do meetings instead of events to spread awareness.

Yeah I use to have really really bad anxiety but I never had this sound. As soon as I got more confidence stupid me ruin my hearing from noise exposure this one time and now my anxiety is coming back. Overall I don’t understand how people say they got this from anxiety. When I would be too...

Whoever puts money in would definitely be rich soon enough lol

How

Not sure if they go by something else but this is what I’ve read from last year articles https://hsci.harvard.edu/news/harvard-researchers-regenerate-sound-sensing-cells-mice-hearing-damage...

I believe HSCI also in August I think

If there was large enough movements and publicity the government wouldn’t have any other choice than to help veterans since it’s #1 problem they come back with. But as I see it there’s not really any process of that happening currently

Anyone seen an update with the REGAIN eu project ? Last I’ve seen was that they were recruiting

Fibroblasts, reprogramming, pluripotent stem cells and suddenly hear again? What sounds like disconnected words might soon become reality. Professor Löwenheim from the University Hospital Tübingen reports on current research. -07: 38 quality 360p 480p 720p speed 0.5x 1.0x 1.5x 2.0x...

Imagine all that money going towards research. We would definitely know more about tinnitus and how we can stop it.

I just find it interesting so I watch a bunch of documentaries about their minds and crimes.*hopefully will be a future detective*

Kinda wish I was able to be frozen and brought back to read the end result of these studies and trails

I just can’t wait until Harvard starts doing their testing this year!

I think because if they fix the hearing loss issues, T might be fix with it? I’m not entirely sure I’m assuming that’s why

“Although one or more drugs that might temporarily or permanently repair inner-ear damage and restore hearing loss is still several years away from commercial availability” 7 years is too long for me. 5 or less is better:mad: anyways I’m glad that I’ll most likely won’t have this all my life...

I think your money is better off being donated to an association that wants to cure or give better treatment with people that have tinnitus. Stuff like that is mostly baloney.

So it’s at phase 2 when we’ll know if this treatment actually works ?

Isn’t frequency therapeutics working for those that have chronic tinnitus and hearing loss not just acute ?

What makes you think that?

They all had cochlear implants ?

I’m so happy !! So now it’s going into phase 2 ? I’m not exactly sure how the process goes

I have once because I was new and wanted to get help knowing I might have this for a long time. I contacted and got a response from one person which was from Regain CEO I believe. ATA, Harvard, etc haven’t replied. Just curious if any of you have done the same as well or if you still try to...

https://www.genengnews.com/gen-news-highlights/stem-cell-restoration-of-hearing-loss-might-be-a-double-edged-sword/81255139 https://hsci.harvard.edu/news/progress-toward-treatment-hearing-loss https://www.regainyourhearing.eu/trial/...

From what I’ve read is that Harvard University And Regain Project both we’re able to bring back hearing in animals and now going to start testing on people. Supposedly they were able to regrow the hair cells with stem cells and some brain cells I believe but another article was talking about how...

I believe there will be cures soon from certain causes of T. How I see it is we know whole lot more than what we did before. For example stem cells that helped other animals hear again from too much sound and soon to be tested on people. That's a step forward. We didn't have that around before...

I'll be making a video soon to raise awareness and I was wondering if you have any ideas or anything I should add. I kinda have an idea on what to do but still planning it out.

Has anyone heard of an update with project ?

I'm feeling pretty happy when I read about how both Harvard and REGAIN project were able to regrow hair cells on animals then testing on people soon sometime this and next year. Just wish there was an update, I'm only getting articles from March/Feb. What's your thoughts?