Tinnitus Research Initiative (TRI) 2023 Conference

Well done guys. I've just followed @ZFire's lead with another donation and tapped the ball into the net.

 

Stinks of "what's an easy way to get funding without having to actually produce any results at the end of the term."

 

I had formerly posted this in regard to another ludicrous CBT study:

"The Impact of Tinnitus on Working Memory Capacity" from the International Journal of Audiology:

Perhaps a study should be done on "The Impact of Having a Pit Bull With His Fangs Imbedded in Your Neck When You Are Trying To Write Complicated Calculus Equations."

The sheer idiocy of so much highly vaunted scientific research.

 

Every one of you who donated are legends. ♥

 

Lmao...

For the record, I’m not loaded with money over here, far from it. But I like being charitable for a good cause. This conference is really important.


Great job everyone. Big shout out to @UKBloke especially for finishing it off. Mission accomplished!

 

And $26 left over for one of Dr. De Ridder's 'cocktails'

 

'kin 'ell imagine that lol. Mine's a Low Dose Naltrexone on the rocks

 

I wonder if you might slip in a word about sub-types of tinnitus, per the conversation with Dr. Michael Golenhofen. After listening to his very thoughtful comments, it seems pretty clear that clinicians are just about clueless when it comes to having an informed and informative discussion with a tinnitus sufferer about tinnitus sub-types.

Those of us who started out with life-altering tinnitus and hyperacusis are left to piece this together ourselves and navigate various medical systems -- allopathic, Chinese, Ayurvedic. For me, this included sound therapy/maskers, Bluetooth use TinnitusPlay app sounds, Ayurveda, craniosacral treatment, TRT 2+ times, off-label drugs such as Klonopin and Gabapentin, acupuncture, Feldenkreis, rolfing, neurologist, counselor, and more.

EACH of those approaches may have taken 1 to 8 tries with different practitioners before finding one who could help. So, let's say 25 to 30 practitioners to put together a complete treatment plan that showed results. Not to mention over $125,000 spent (including much from retirement accounts -- and I realize how fortunate I was to have that as a resource), particularly during the first four years, but that continues to this day as acupuncture, Ayurveda, craniosacral therapy, and even hearing aids are not covered by American health care.

Thank you so much for presenting at the conference! You have incorporated powerful points. I wonder how the professionals, and I use the term advisedly, will respond.

 

A genuine sincere well done and appreciation for those of you who have donated, there were a fair few and you let it be known and rightly so!

In regards to this comment, from what I’ve seen post wise from @Damocles, I believe he means no malicious intent.

However, it did strike a bit of a chord as I am one of those who is unable to donate and my displease around the lack of ability to do so was amplified after reading the comment.

I’ve not worked for months, my business is destined to collapse very shortly. I’m not even sure if I can pay the staff I have left this month. Let alone all the bills and house payments I have to pay for myself. Just another burden created by tinnitus leading to the spiralling anxiety and depression.

 

@Hazel, this makes me so angry. It shows what is important for these people. Money. Their grants, research papers, fame, recognition, having a good time at the conference, etc. Sufferers? Meh, they come last. You should be given a prominent and an exclusive slot - so everyone can and should attend.

This is so dehumanizing, demoralizing, demotivating, devastating. Maybe it is not too late - plead with the organizers to swap slots, you never know.

And thank you for your work and time.

P.S. The content of the conference does not inspire a lot of hope. Sessions 1, 3, 5 and 9 have something of interest. The rest, especially the CBT parts, looks a waste of time. But maybe I missed something.

I can't help but notice zero presence from folks from Boston's Harvard/Massachusetts General Hospital. So much for cutting edge tinnitus research.

 

Thank you! I have seen improvement since those first catastrophic months. And at least I now have a sense of what is helpful, as well as some very helpful practitioners.

Oh my, I figured that the conference would (mis)schedule the exemplary patient advocate who has the personal experience and feedback from this community.

I hope people do attend. Your presentation goes a long way towards helping scientists and clinicians understand the weaknesses of research conducted within an academic echo chamber. Likewise, the presentation shows the possible benefits of a cooperative path where tinnitus sufferers are not merely the patient to be trundled off into the corner but have valuable insight!

Thank you again for attending and presenting - and happy networking!

So sorry to hear what you are going through. I hope you have a support community of friends and family who can lighten the burden. And Tinnitus Talk folks may be able to offer advice, ideas or at least empathy as I imagine many of us have gone on disability/dealt with inability to work given tinnitus.

 

Would be interesting to know the researchers who DO STAY for @Hazel's talk.

Could you take photos of the posters and upload @Hazel?

 

@Hazel, your comment about wanting to see the speakers of these conferences debate rather than just present their own research is right on the mark. Debate creates synergy and that would benefit everyone.

 

Yes, it needs someone or a group to sit down, plan and delegate further research. Otherwise they all go off and do their own thing.

 

You’re a star. Thank you for calling out these charlatans.

 

Me laughing at the psychologists because Jastreboff's shit is finally being challenged:

 

Hazel, you're a star. Thank you for representing us and for liaising with these researchers directly.

That conversation with the senior psychologists is so indicative of senior academics. They have a vested interest and are frightened of having their comfortable positions challenged. Thank you for making them uncomfortable; they and their clinical colleagues certainly need the wake-up call.

 

SAY WHAT - RIDDLE ME THAT, as Robin would say to Batman.

Much kudos regarding your courage in confronting what, to me, was an all-too-common, classic instance of gobbledygook masquerading as Legitimate Academic Discourse.

Did they mean that transferring the funds earmarked for these pointless and frankly stupid psychological Clinical Trials (like trying to determine precisely to what extent this brought people to dangerous suicidal ideation) to Real Research would somehow deprive sufferers of the wider availability of CBT?

Their scarcely comprehensible high dudgeon is such an obvious manifestation of their threatened awareness that the gathering momentum of Real Research will eventually render them superannuated and jobless. Jastreboff has on a number of occasions unwittingly indicated as much. Perhaps they should jump ship now and find another focus, such as the "counseling" of Incels (like that guy in Idaho who stabbed those three college women.)

You should feel tremendously proud of what you have achieved. This reminds me of that insight that the great American historian Howard Zinn had, that all of the Noble American Causes and Movements (Women's Right to Vote, The Labor Movement, The Civil Rights Movement, AA's Universal Twelve Step Program) were all started by unknown grass-roots citizens who were finally fed up with their situations, and not from any Governmental Initiatives.

 

What an uplifting story. Props to @Joeseph Stope!

 

Well done @Hazel!

Thank you for once again being our cumulative voice, and giving us the glimmer and chance of hope we all need.

 

I've got no problem funding CBT practitioners for tinnitus. I have a MAJOR problem funding CBT research into tinnitus. IT IS DEAD. Move the fu*k on and throw your useless app in the bin.

 

I know Canada is small fry, but charitable status here might make a difference. I'm not sure if I'm the only regular monthly donor from Canada, I hope not, but I wouldn't be surprised.

US is a lot bigger, and US military tinnitus is extreme, from what I understand.

 

So they officially found a way to track tinnitus.

 

Hello @Hazel,

What did you think of this 2023 conference compared with previous years?

Compared with previous years, do you feel that doctors/researchers are close to finding effective solutions?

Do you feel that doctors have a better understanding of tinnitus and especially pain hyperacusis?

If we compare 2023 with 2019 (Taipei), has there been a great deal of progress?