Dirk De Ridder: Dreams Can Unlock Ways to Cure

Nail right on the head, Tracy. That's just the one. But as this thread is the research one, I was homing in on the theories of the causation of tinnitus. Pipeline Therapeutics, Frequency Therapeutics and Otonomy are (seemingly perhaps) going on the assumption that deafness and tinnitus are related to damaged inner hair cells, outer hair cells or damaged synapses.

And, so the assumption is extended to the idea that the loss of these and the resultant loss of stimulation in the hearing nerve causes the brain to have something akin to phantom pains just like when you lose a limb.

The great hope is that restoring the hair cells and synapses will restore hearing and remove the corresponding tinnitus.

One other theory is based on an experiment from back in the 1950s where a sample of people were put in an absolute silent room for a time interval. Nearly all of them when they got out reported having heard some sort of noise.
So it was theorised that tinnitus may be due to some filter that got damaged which the healthy, non-tinnitus brain has to get rid of the unnecessary noise.

It's not that far removed from De Ridder's theory of dreams being connected with your tinnitus.

Well I know that this sounds mighty complicated. But I was only trying to keep it simple...

 

For me it is like 3 stages:

1) Not aware of tinnitus
2) Aware of tinnitus but no negative reactions at all (could not care less)
3) Aware of tinnitus and it creates negative emotions

When I have my tinnitus under control it's like:

-30% not aware of tinnitus
-65% aware of tinnitus but no negative reactions at all (could not care less)
-5% aware of tinnitus and it creates negative emotions

Now it's more like:

-5% not aware of tinnitus
-60% aware of tinnitus but no negative reactions at all (could not care less)
-35% aware of tinnitus and it creates negative emotions

The goal for me would be something like:

50% not aware of tinnitus
50% aware of tinnitus but no negative reactions at all (could not care less)

SSRI helps me a lot with the emotional part.

 

Do you feel that the sound of crickets etc. in both ears are connected, synchronized?

To me it´s not. Even if they have similar pitch and rhythm, they are totally 2 different sources. Therefore I suspect the inner ear for that.

 

Pretty similar for me. The not aware of tinnitus part is just being too distracted to engage with after 2 years of constant noise, but it is still clearly there just as much as a knife in the leg would be.

Maybe. I don’t know. I really don’t try to listen intently at my noise but listening to it now I guess it is similar cricketing/mobile noises in both ears but I think the sounds aren’t synchronized. It is hard to tell because there are so many sounds.

I know that my original damage included outer hair cells as you could see the hearing loss on the audiogram, but much of the hearing recovered so I don’t know if that means my tinnitus is due to synaptic damage or what. It does change throughout the day, typically worse as the day goes on so I don’t know if that means that neuroinflammation is part of the story.

 

Hi @David S,

Just curious but did you have any OAE testing? The tinnitus sounds you describe fit my pattern (centralized head tinnitus with high frequency (14-15 kHz) oscillating continual tinnitus) but my OAE is normal at least up to what they can test in the 8 kHz range along with all other tests I have had (Tympanometry, Acoustic Reflex, ABR, two regular audiograms showing normal & one HF Audiogram with loss at 16 kHz).

Also is your tinnitus reactive like mine?

 

@IntotheBlue03, my OAE come back normal. My tinnitus is also very reactive even if it varies a lot over time. I believe my damage is related to outer hair cells, malfunction in the spontaneous activity or damaged nerve ends. I do not think the brain or any somatic cause is involved. It is said that the cause of tinnitus only stays cochlea based for around 6 months. I do not agree with that. It can be much longer.

Sometimes I have an intense sound followed by a few seconds of silence. I have a feeling that this is my body’s way to try to reset thing but it constantly fails. Just hoping that this will start to heal over time but for now I am not too optimistic.

I am trying to change diet and periodic fasting.

 

Wonder where Dr. Ridder is on his research.

 

He's dreaming about it. That's where the cure is.

"Is a dream a lie if it don't come true?"

Bruce Springsteen I think.

Ten years old thread makes you wander how much more time is needed.

No, but I know this is complex stuff and I think and hope Dr. Ridder is doing his best to find a cure for this insane condition.

 

He’s in a K-hole.

 

Yeah who knows. I think Thanos is making some progress? Dr. Ridder is afk. I did speak with somebody who met Dr. Ridder a few weeks ago. She said he was amazing and was testing pain receptors in her brain. She has bad noxacusis.

 

I e-mailed Dr. Thanos a few days ago and he didn't specify exactly when clinical trials are going to start... He just said "soon"...

 

Hahaha the "soon" we get from everybody.

 

Everyone thinks De Ridder is ‘amazing’ yet all he offers is Clonezapam and Deanxit.

Yea... amazing stuff buddy.

 

Lol better than most ENTs that say "ahhh sucks, live with it. Get out of my office."

 

Is it really?

A highly addictive benzo and a drug banned in most countries.

Disgraceful ‘doctoring’ if you ask me and if that is the best De Ridder can come up with after so much time investigating tinnitus then he is defo a ‘catch me if you can’ situation with Frank Agnables charm. It was embarrassing to see @Hazel gushing over him whilst he spouted some amount of horse manure in the Tinnitus Talk Podcast episode.

Just to add I think @Hazel and @Markku are amazing and appreciate their work but this charmer has been pulling the wool over many people’s eyes for years with his theories.

None of which are proven.

 

@Hazel,

To address your first point. Yes, he is prescribing these like candy. 15 minutes into my consultation he had recommended discontinuing ALL my existing medication and going on Clonazepam and Deanxit. Let's take Clonazepam first. It is the 13th highest drug linked to triggering tinnitus according to FDA database records, and has not proven any efficacy in treating most tinnitus apart from Middle Ear Myoclonus, which is an extremely rare type of tinnitus affecting less than 1% of tinnitus sufferers. Deanxit is a hybrid anti-psychotic that has been banned for good reasons (Tardive Dyskinesia) in most countries. Do you not see from an objective point of view that this is terrible medicine. There is no evidence on the community that this combination works. I have not seen one post where it has worked for any member. He mentions committing to a lifetime of Clonazepam if necessary, whilst stating there is a cure coming. He does not have a clue in MY opinion. To recommend discontinuing all existing medication without mentioning 'tapering' is crazy. What a mad man. DYOR on this guy.

As for you taking offence, that is fair enough, but it is what I saw with my two eyes. I am not weak enough to not say it despite it being unpopular. This guy is a charmer, even I was initially taken in by his charm after watching his interviews and presentations on YouTube, etc hence why I arranged a consultation. He is held in esteem as the 'world's leading tinnitus researcher', but what the hell has he contributed? Nothing, zilch, only a bunch of theories. Many of which that have already been proven wrong. He has a brain zapping clinic in Belgium, that offers nothing of benefit to tinnitus sufferers. It states it can help depression, but I have not yet seen any solid evidence. Nothing along the likes of the Stanford Research on TMS this month, which is revolutionary.

I appreciate all your efforts, as does everyone else on here, but my messages are not designed to attack you in the slightest so no need to go on the defensive. I have 100% respect for you, but was a bit sad to see you listen to the utter nonsense this man was spouting and putting him on a bit of a pedestal. I just mean Dr. Ridder says "everyone works together and share data" and then says "should have a competition, with prize money" which is the exact opposite of collaboration. I just could not believe what I was hearing and he should have been taken to task on stuff like this, but hey no one is perfect and in 99.99% of the Tinnitus Talk Podcast interviews the content is excellent and the questions are too. My attack is on Dr. Ridder. He is a charmer, a catch me if you can (2002) film character, and we are all taken in by him. Even Debbie Featherstone who is the CBT expert for the BTA, and as hard nosed/experienced/pragmatic a lady as you will ever meet was overcome by him. "What a man Dirk De Ridder is". Yes what a man, BUT what has he done for the tinnitus community in reality. Nothing, zilch, not a sausage.

I repeat Clonazepam and Deanxit. Jesus... Take an objective look at this and say that's it? Two crappy meds combined. God help us.

Maybe I will be wrong and he will crack tinnitus, but I highly doubt it.

Finally, thank you for all the work. I mean that from the bottom of my heart. If you took offence then I apologise, but it was more directed at the snake charmer himself, than you. I was charmed by him too, as are most others.

I really think this guy is not all that but was built up to be a super tinnitus researcher in the interview. That is just my opinion. When/if he delivers I will be glad to be proved totally wrong.

In the meantime someone should stop him prescribing Deanxit and Clonazepam with such little thought. 15 minutes into a first consultation. That is crazy. I presume I am not the only one.

Thanks again. I truly mean that. I think you are amazing and appreciate your work. Dirk on the other hand needs to up his game.

 

Get off your high horse, 99% of tinnitus researchers are worse than Dr. Ridder and do much less. I'm a big fan of him prescribing Clonazepam when needed, most doctors are scared of prescribing it even when a patient desperately needs it or another benzo. There are many on this community who do well on Clonazepam including @linearb.

I'm very excited about Dr. Ridder's latest trial for one:

Dirk De Ridder Explores Ketamine and HD Transcranial Infraslow Pink Noise Stimulation (HD-tIPNS)

We would be MUCH WORSE OFF without Dr. Ridder.

 

How are we better off? Clonazepam? That’s it. What a contribution! Wow. No mention of Deanxit? Do your research. Clonazepam is the 13th most tinnitus inducing med! Do a bit reading about Deanxit whilst you are at it. No high horse here. Just facts.

Yes his trial. When will we hear about that. It is minuscule compared to Susan Shore’s well designed trial yet he openly questioned neuromodulation but offers nothing himself.

Nothing yet apart from Clonazepam and Deanxit. That is a fact! Nothing apart from that. Absolutely nothing.

I’m signing off from the debate. The FACT is he has produced no treatment for tinnitus and the treatment he recommends in my opinion is highly dangerous and bad medicine.

That is my opinion and I am entitled to it and I am not going to argue anymore about it. Facts speak for themselves.

 

@Padraigh Griffin, I have taken 0.5 mg of Clonazepam for about two years at night before I go to bed. I don’t know why it has such a stigma. It helps me a lot.

 

This is not acceptable. You said you have a day job, but have you ever thought about putting a few night shifts in for the Tinnitus Talk community? Working all day is no excuse when you still have the early morning hours available to you.

Why should anyone else become involved or help out? It’s much easier to judge from the sidelines, and this kind of criticism is much more important. Haven’t you learned this already?

I’m going to watch a movie now, and by the time I’ve finished, I’m expecting you to have posted a few more blog entries or something. Don’t let us down as the fate of this cause is now resting squarely upon your shoulders.