Introducing Tinnitus Quest

Whether it is temporary or prolonged depends on how the limbic system and conscious brain respond. If they interpret it as an important signal of danger, it becomes prolonged. If not, it typically fades after a few hours or days.
Yeah, except it doesn't. That explanation sounds incredibly shortsighted, especially for people with an unknown or idiopathic cause. You might never identify the root issue, and the tinnitus could progressively worsen due to factors like autoimmune conditions, viral infections, hydrops, presbycusis, or many other ear-related diseases.

There's a specific malfunction occurring, and it doesn't care how you interpret it—it just does what it does.
 
Strange that it costs £110 to access that 2015 paper; I'm able to view the full document clicking your link.

I'm not overly familiar with Rauschecker's most recent work, but the tinnitus paper of his that I generally draw on is this one. I've read comments that it's an overly complicated paper - and I agree it's not an easy read. But where Jastreboff talked about tinnitus distress as a kind of sub-conscious/conscious reaction that a patient can ultimately talk their way out of (but hey, if they can't, it's their fault), Rauschecker paints a subtly different picture. With him I think tinnitus becomes physiological and not something a patient can mitigate by chatting to a psychologist.

Jastreboff is cited by so many researchers, it's almost painful. At the very least, though, I do believe his work can be credited for taking tinnitus beyond the cochlear and into the brain. This is why I'm quite excited about Dan Polley joining Tinnitus Quest. I think the more scientists focus on tinnitus as being a brain issue, the better.

I spent a couple of years putting together some thoughts about all of this and about how aspects of the Rauschecker paper seemed to tie in with various other tinnitus happenings coming down the pike. The result is a layman's thesis on a proposed method of action for tinnitus. It's published here on this website free to read if you're interested.
Ah, it's actually £110 to purchase the Textbook of Tinnitus (published in 2024), a collection of articles by various authors, including Rauschecker. His chapter spans pages 221–230 and costs only £19, which I might buy out of curiosity.

I've downloaded your Tinnitus Gating Model and plan to print it for a thorough read. This year, I'm determined to eliminate my tinnitus, and I genuinely believe I can achieve this as long as I stay focused and avoid distractions.
Yeah, except it doesn't. That explanation sounds incredibly shortsighted, especially for people with an unknown or idiopathic cause. You might never identify the root issue, and the tinnitus could progressively worsen due to factors like autoimmune conditions, viral infections, hydrops, presbycusis, or many other ear-related diseases.

There's a specific malfunction occurring, and it doesn't care how you interpret it—it just does what it does.
That's why I said 90% of cases. Most of the time, tinnitus is caused by acoustic trauma or possibly a head injury. The rarer causes, such as Meniere's disease or the conditions you mentioned, require more specialized care to address the underlying issue.
 
Is there any possibility of seeking funding from militaries worldwide
@Fazdoll, the funding should primarily come from tinnitus patients rather than organizations. While ex-servicemen are welcome to contribute, the main goal is to prioritize donations from patients rather than relying on organizational funding.

Currently, much of the focus is on engaging with patient groups, encouraging them to sign up and contribute.
 
I would like to request that Tinnitus Quest interview/reach out to Dr. Kelly Assouly and/or Dr. Matthew Carlson regarding the efficacy of extracochlear devices. In fact, together, would be absolutely insane although unlikely with how busy they are.

Dr. Carlson has previously published on the topic here.

Dr. Assouly has previously published research summarizing the literature here.

Both are currently investigating the efficacy of extracochlear devices providing electrical stimulation, in turn providing tinnitus suppression.

Dr. Carlson published a patent in 2017 for such a device.
 
This initiative inspired me to join this forum.

First and foremost, I want to express my heartfelt gratitude to everyone contributing to this project. Your efforts mean so much!

The reason I registered is that I felt compelled to share this message. While it may echo sentiments expressed countless times before, I still wanted to add my voice and make a small contribution.

To share a bit about my background: I have been reading success stories here over the past 20 days because my mild tinnitus of 15 years (out of my 33 years of life) decided to spike and evolve into a moderate case as we entered the new year. Perhaps it got excited at the thought of celebrating its 15th anniversary, who knows? While it is not yet severe, I hear my new fluctuating, piercing sound most of the time, and some days have been particularly challenging. To cope, I have sought out positive and uplifting perspectives on tinnitus.

That leads me to this: It took me 20 days to realize that "Tinnitus Quest" exists, despite frequently lurking here. As soon as I discovered it, I became a monthly donor. But honestly, I could have easily missed it altogether.

Let me digress for a moment: I am absolutely convinced that science can solve tinnitus. If the brains of most sufferers were once in a state where they did not generate random signals causing this unwanted noise, then, in theory, they can be reconfigured to return to that state or a similar one. For the fortunate people whose tinnitus resolves on its own, I believe this is exactly what happens. For many others, though, that process does not occur automatically and requires a push from science. In other words, I believe the solution already exists in theory and is waiting to be discovered.

The timeline for that discovery, whether it is 10, 20, or 50 years, will depend on a combination of factors:
  1. How much visibility tinnitus and its cure receive in mainstream media (including how much profit the industry believes it could generate).

  2. How much coordinated effort is directed toward finding a cure.

  3. The biggest factor: how much funding is invested.
An initiative like Tinnitus Quest has the potential to address all these factors, but its ultimate impact will depend on the traction and publicity it receives. For this reason, I believe spreading the word about Tinnitus Quest is one of the most beneficial actions any tinnitus sufferer can take this year. With increased exposure, funding will naturally follow. Visibility is absolutely critical to its success.

At the risk of sounding overly idealistic, I believe every individual can make a meaningful difference. Here are a few ideas that came to mind during a quick brainstorming session:
  1. Maximize visibility on this forum.
    For example, members could highlight Tinnitus Quest in their signatures. It is essential to convey its purpose at a glance. Something like "Fund Tinnitus Research" or "Support the Search for a Cure" would immediately catch attention and resonate with readers.

  2. Leverage the power of social media and the internet.
    Social media is an incredibly powerful tool. Reaching out to influencers, YouTubers, and educational channels with millions of subscribers could make a significant impact. For instance, channels like CrashCourse or Kurzgesagt often cover topics related to biology, medicine, and science. There are many similar creators with a focus on learning and advocacy, and I believe some would be willing to help. This could potentially lead to partnerships, sponsorships, and most importantly, increased publicity.

  3. Engage with the real world.
    Simple actions like distributing flyers at local concert venues or reaching out to military hospitals about Tinnitus Quest could also help spread the word.
I hope this post does not come across as too scattered, ambitious, or pushy. My intention is simply to share my enthusiasm for this incredible initiative and contribute these ideas. Anything that actively seeks to change the status quo is a win in my book, and I sincerely hope Tinnitus Quest gains significant traction this year.

A cure might not arrive in the immediate future, but with sustained effort and collective action, we may bring it much closer than we think.

Peace to all of you. Take care, stay strong, and let us work together for a brighter tomorrow!
 
First and foremost, I want to express my heartfelt gratitude to everyone contributing to this project. Your efforts mean so much!
@SafeMusicFan, thank you! Posts like this, from people like you, are what inspire people like me. The volunteers at Tinnitus Quest work hard and with purpose, but without support from the community, our efforts would be in vain. Thank you for joining us in this mission!
 
I've started donating. I hope my contributions help.
@ccpjc, donations truly make a difference. For example, a typical donation to a typical charity might be $10, with around 10%—or $1—allocated to research projects.

Our goal, using a volunteer-driven, multi-board model, is to allocate 80–90% of donations directly to research projects. Of course, there are some necessary costs, mainly for administrative duties and registration fees.

This means a $10 donation to Tinnitus Quest could have the same research impact as a $70–$80 donation to other charity models.

Traditional charities often have many salaried staff, physical overhead costs, and use surplus funds to provide support services.
 
I just started donating—wishing you all the best! I'm manifesting a successful event in the future where I can give you a fist bump, @Nick47.
 
Hello,

I am interested in Tinnitus Quest and am considering making a donation. Could you let me know when funding is expected to take place? Also, when might we see outcomes from Tinnitus Quest, such as studies or investments in treatments?

Will the funding and financial details of Tinnitus Quest be publicly available so we can see what you are working on?

Sorry for all the questions; I am just very interested in the project.

I hope you are all doing well these days.
 
Could you let me know when funding is expected to take place?
@MrRing, hopefully this year we will be able to start allocating grants. This depends on how much we have raised and the quality of the pitches received.
Also, when might we see outcomes from Tinnitus Quest, such as studies or investments in treatments?
I'm not really sure what you mean. Is this answered above? Successful applicants can begin studies ASAP, providing they have ethical approval.
Will the funding and financial details of Tinnitus Quest be publicly available so we can see what you are working on?
The tinnitus community will be kept fully updated as soon as grants are approved by the Executive Board. Researchers have to provide updates every 3 months.

In order to stay updated, it is strongly advised to subscribe to the newsletter on the website, YouTube and other Tinnitus Quest social media profiles.

I hope this is helpful.
 
is there an update on the donations received so far? Will there be a way to track this on the website?
Hi @Cyborg, we have been receiving steady donations since our launch last summer. Momentum is building as patients realize they finally have a research-focused organization run by volunteers.

There will be some updates during Tinnitus Week, which takes place next week.
 
Tinnitus Quest is all over the news in Norway today. Great work, Jack Rubinacci and Gaute Ormåsen!


They are also appearing on TV.

Unfortunately, there is a doctor at the end who claims there is no further need for research because tinnitus is already well understood. He also states that inhibiting the activity of the neurons responsible for tinnitus is not possible. I guess he is a staunch believer in CBT and unaware of recent research, such as the work done by Hamid Djalilian.

This was quite provoking because, on one hand, you have a foundation encouraging people to donate based on its belief in science and the development of treatments. On the other hand, you have a doctor essentially saying there is no point in donating to research.

I wish the article had focused solely on Tinnitus Quest without including opinions from people stuck in another century.

Other than that, this was very uplifting!
 
Tinnitus Quest is all over the news in Norway today. Great work, Jack Rubinacci and Gaute Ormåsen!


They are also appearing on TV.

Unfortunately, there is a doctor at the end who claims there is no further need for research because tinnitus is already well understood. He also states that inhibiting the activity of the neurons responsible for tinnitus is not possible. I guess he is a staunch believer in CBT and unaware of recent research, such as the work done by Hamid Djalilian.

This was quite provoking because, on one hand, you have a foundation encouraging people to donate based on its belief in science and the development of treatments. On the other hand, you have a doctor essentially saying there is no point in donating to research.

I wish the article had focused solely on Tinnitus Quest without including opinions from people stuck in another century.

Other than that, this was very uplifting!
Yeah, the doctor is hugely disappointing. Unfortunately, when it comes to media, you don't get to control the narrative or who else they interview.

That said, we see mostly upside in terms of exposure and awareness, and this really is a milestone to celebrate! :) I am very proud of Jack's hard work to get this done, and I am hugely grateful to Gaute for having the courage to go public about his tinnitus.

Hopefully, the Norwegian public will see that doctor for what he is (I think he runs his own CBT clinic, so hardly an objective voice).
 
That said, we see mostly upside in terms of exposure and awareness, and this really is a milestone to celebrate! :) I am very proud of Jack's hard work to get this done, and I am hugely grateful to Gaute for having the courage to go public about his tinnitus.

Hopefully, the Norwegian public will see that doctor for what he is (I think he runs his own CBT clinic, so hardly an objective voice).
Great work by Jack and Tinnitus Quest 👏👏

Awareness is the first step towards a brighter future for everyone in regards to tinnitus/hyperacusis.
 
Thank you, Jack, Hazel, and everyone at Tinnitus Quest.

I just recorded my interview for Tinnitus Quest with Jack today. He was so compassionate and encouraging. I wanted to "come out" and share my story.

I have been telling everyone I meet about the bold and promising work of Tinnitus Quest, including my Uber driver last week, who told me he had tinnitus after I asked him to turn down the music in the car and explained my tinnitus and hyperacusis.

If you are reading this, the best thing you can do is start talking about Tinnitus Quest and donating to support its work.

We all need to share our stories and spread the word about Tinnitus Quest to anyone who will listen. Tell your ENTs and audiologists. Help Tinnitus Quest raise money for research.
 
Once I find a new line of work for myself (got laid off recently), I'm going to be donating as frequently as I can to Tinnitus Quest. The work being done and its potential is well worth it in my opinion.
Yeah, the doctor is hugely disappointing. Unfortunately, when it comes to media, you don't get to control the narrative or who else they interview.

That said, we see mostly upside in terms of exposure and awareness, and this really is a milestone to celebrate! :) I am very proud of Jack's hard work to get this done, and I am hugely grateful to Gaute for having the courage to go public about his tinnitus.

Hopefully, the Norwegian public will see that doctor for what he is (I think he runs his own CBT clinic, so hardly an objective voice).
That's so unfortunate. I see no reason why someone should try to stand in the way of progress. Then again, it's always about lining their own pockets with these people.

Still glad to see you guys getting more publicity in the media. Big win!
 
I was wondering if there are any updates regarding future plans for this year, funding status, etc. :)

Every now and then, it pops into my head that a social media strategy could really help boost awareness and funding.

For now, I have noticed that the Facebook and YouTube accounts have a very limited amount of content and subscribers. For example, the latest updates regarding the Q&A cannot be found on the Facebook page. Something as simple as a monthly update across different social media platforms could make a small but meaningful difference. When current subscribers like or share posts, it can potentially generate new visibility among their own friends. I am not sure if there is a content creator or social media expert around who could look into this, but I think it would be worth exploring.

Another idea, though I am not sure if it is feasible, is that people tend to donate more willingly when they feel they have already received value from the organization. This is the principle behind platforms like Patreon. I know there are already podcasts hosted on Tinnitus Talk, but I wonder if similar content, such as discussions about tinnitus theories and research avenues, could be shared on the YouTube channel. The goal would be to educate and engage people while also increasing visibility. However, I realize this could become a lot of work, and for it to be sustainable without distracting from the main goal of advancing research, it would likely require additional volunteers who are passionate about contributing.

I hope I do not sound too pushy. I truly just want this initiative to succeed and gain as much momentum as possible. I am a bit concerned about the feasibility of everything if there is not a coordinated effort to spread the word. The more visibility and funding this receives, the stronger the message it sends: "This is important. This is something we want." That message could reach not only the broader community but also major pharmaceutical companies that might see an opportunity to invest in a solution. A strong funding and awareness push could create a snowball effect, leading to real progress.

Thank you again for launching this initiative in the first place!
 
I was wondering if there are any updates regarding future plans for this year, funding status, etc. :)

Every now and then, it pops into my head that a social media strategy could really help boost awareness and funding.

For now, I have noticed that the Facebook and YouTube accounts have a very limited amount of content and subscribers. For example, the latest updates regarding the Q&A cannot be found on the Facebook page. Something as simple as a monthly update across different social media platforms could make a small but meaningful difference. When current subscribers like or share posts, it can potentially generate new visibility among their own friends. I am not sure if there is a content creator or social media expert around who could look into this, but I think it would be worth exploring.

Another idea, though I am not sure if it is feasible, is that people tend to donate more willingly when they feel they have already received value from the organization. This is the principle behind platforms like Patreon. I know there are already podcasts hosted on Tinnitus Talk, but I wonder if similar content, such as discussions about tinnitus theories and research avenues, could be shared on the YouTube channel. The goal would be to educate and engage people while also increasing visibility. However, I realize this could become a lot of work, and for it to be sustainable without distracting from the main goal of advancing research, it would likely require additional volunteers who are passionate about contributing.

I hope I do not sound too pushy. I truly just want this initiative to succeed and gain as much momentum as possible. I am a bit concerned about the feasibility of everything if there is not a coordinated effort to spread the word. The more visibility and funding this receives, the stronger the message it sends: "This is important. This is something we want." That message could reach not only the broader community but also major pharmaceutical companies that might see an opportunity to invest in a solution. A strong funding and awareness push could create a snowball effect, leading to real progress.

Thank you again for launching this initiative in the first place!
Thanks for caring and wanting us to succeed! Yes, we are keenly aware of the importance of social media. We have posted quite a few shorts on Instagram, and some of them have gotten up to 300,000 views. I'd say that's a pretty stellar result for a non-profit run mostly on volunteer power that has existed for less than a year :)

But one must also take into account that tinnitus is a VERY difficult topic to raise awareness for. You're literally competing with cute puppies and kittens, flashy influences, and all kinds of other stuff that tends to excite people a lot more than tinnitus research. And we have hard evidence (happy to tell you more if you want, but basically, this is data from campaigns we've done) that for every 1000 tinnitus sufferers you reach, less than 1 of them will like, share, donate, etc., if you're lucky. People are jaded, don't trust anyone, don't want to be reminded of their tinnitus, or they just expect someone else to come up with the solution, without any effort from their side. That might sound harsh, but it's the reality when it comes to tinnitus.

It takes time to build an audience. It takes time to build trust. We cannot focus on all social media channels at once (Instagram, YouTube, Twitter, LinkedIn, Facebook, TikTok, etc.) because it takes time to get to get acquainted with any specific channel, as each has its own video format, algorithm, style, etc. So, our approach has been, for now, to focus on Instagram and add more and more channels over time while we build our experience and expertise. We are taking a very considered approach, it just takes time, and that's normal for a tiny organization like ours. Patience and persistence are key, and it's not realistic to expect immense social media success in such a short time with such limited resources.

Our main challenge is the lack of manpower. We have a small core team of 4-5 people working on this, in addition to other jobs and responsibilities. No one is full-time. Social media responsibilities are shared between myself, Markku, and Jack. But we each have other responsibilities as well (I, for instance, do admin, finance, responding to incoming mail, project management, donor communication, researcher communication, events organization, coordination of the grants program, and more).

We simply don't have the budget to pay for a full-time social media expert, which is what it would take to very quickly generate the kind of exposure you are talking about. If you know anyone -- and I mean someone really good, who also understands tinnitus, research, and the non-profit world -- who would help out for free or at a vastly reduced rate, we'd be much obliged. But, of course, finding someone like that is a needle in a haystack.

But again, I would say we're actually doing really well for such a young organization run on a shoestring budget. We are extremely confident that we're making major progress, and every week is better than the last. We have some very exciting news coming up on various fronts soon, including something that could make a huge blast on social media.

And regarding your idea to share discussions about research avenues and tinnitus theories, this is exactly what we've been doing with the Q&A events we're organized; there were 6 so far, and we'll have more this year. We're also discussing a potential video project with Dan Polley to cover the basics of tinnitus science. But as you point out, all these things cost a lot of time. I think often people don't realize that a one-hour Q&A video represents over 50 hours of work behind the scenes. There's a lot of back-and-forth with researchers/guests around scheduling, helping them prepare both technically and content-wise, event registration, marketing, video editing, writing video descriptions, creating thumbnails, uploading... you get the idea.

By the way, one thing that has become abundantly clear already is that no matter how good your social media is, the REAL donations will come from high-net-worth individuals. And finding them -- while it could theoretically happen through social media -- in practice we have experienced success in this area through other networking techniques that have nothing to do with social media. So far, over 90% of our donations have come from very wealthy individuals, and we believe this will continue to be the case. So, while we very much recognize the importance of social media, it's not the only aspect of a successful fundraising strategy, nor arguably even the most important.

This feels like perhaps an unnecessarily long reply, but I wanted to take this opportunity to make a few things clear, because we do get this type of comment a lot. Just like we get a message or email every other day asking, "Why don't you just get celebrity X to support the cause?". It's obviously not that simple, as A-list celebrities get a million emails per day and can basically only be reached through personal connections. That's why we've been working hard on getting some lesser-known but still very well-respected artists on camera. You can see these videos on the Stories page of our website. By approaching it this way, we build recognition and respect, so that if and when we do get a direct line to an A-lister, they'll be much more likely to say yes.

It's a game of patience, persistence, and professionalism that we're trying to play. We're probably not doing it perfectly, but I'm extremely proud of how much we've been able to achieve with limited time and resources, and I'm very confident that we will be successful in our endeavour to improve the lives of all tinnitus sufferers.

By the way, if you really want to help out, you're always welcome to volunteer, depending of course on what skills you have to offer. We're constantly looking for committed volunteers. We've been thinking for instance of creating a 'digital street team' of people who will share our content all around the internet.
 
@Hazel, thank you for your reply. I do not think your response was unnecessarily long, quite the opposite.

It really helps to better understand the whole process, how things come together, and why they are often more complicated than they seem. I found the information about the challenges of engaging tinnitus sufferers particularly insightful, especially since one of the cornerstones of today's management approach is to avoid giving it attention. That is part of why I have been reflecting on the social media aspect, as I can only imagine how much extra effort a tinnitus campaign requires compared to other causes. Regardless, it is great to learn about things like exposure on Instagram, which is one of the most important platforms these days.

Honestly, it is reassuring to see this level of determination in your response, and reading it instantly boosts confidence. I am a bit sorry for pressing the issue, I did not intend my initial post as criticism, but I understand if it came across that way. From what I have seen so far, Tinnitus Quest is definitely on the right track, and you have every reason to highlight its progress.

If online or event based volunteering opportunities could benefit Tinnitus Quest in the future, that is definitely something I would consider.
 
Hi!

I'm jumping into this thread to share a few ideas after donating to Tinnitus Quest. I apologize if any of them are redundant or unnecessary. I am sure the Tinnitus Quest team has already done a lot of brainstorming. :)

I am French, and there are quite a few French tinnitus sufferers online. For example, there is a dedicated French forum for tinnitus. However, one of the biggest obstacles to sharing information and research is the language barrier. French people are not exactly known for being the best English speakers 😅 (myself included, so I apologize if my posts contain mistakes).

I may have missed this information, but are you planning to translate any Tinnitus Quest content into languages other than English? Even just translating the website welcome page could help reach a broader audience and possibly bring in more donations. I completely understand if this does not fit within your current strategy since it would require a lot of work. But if that is the case, and if my modest English skills can help, feel free to reach out. I would be happy to assist with translations.

Also, regarding celebrities or artists to reach out to, it might be worth looking at the EDM scene. Unfortunately, many artists in that space suffer from tinnitus. I know contacting major celebrities is difficult, but DJs like Alesso and Martin Garrix openly spoke about their severe tinnitus for the first time in February.

Thank you so much for this great initiative that Tinnitus Quest is!
 

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