Tinnitus Documentaries (The Noise, The Loud Silence, Devil's Symphony, etc.)
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MemberMy Tinnitus Sounds Like... - Devil's Symphony (part 1)
It's Called Tinnitus? - Devil's Symphony (part 2)
Strange Tinnitus Remedies - Devil's Symphony (part 3)
Solving the Tinnitus Riddle - Devil's Symphony (part 4)
Hope in Tinnitus - Devil's Symphony (part 5)
It's Called Tinnitus? - Devil's Symphony (part 2)
Strange Tinnitus Remedies - Devil's Symphony (part 3)
Solving the Tinnitus Riddle - Devil's Symphony (part 4)
Hope in Tinnitus - Devil's Symphony (part 5)
Calin --- Great find! I just watched Part 1 and Part 5 of "The Devil's Symphony". Part 5 echoes what I believe, about putting one foot in front of the other, and just concentrating on getting through one day at a time. After all, each of us has only one life, and we should not let tinnitus keep us from reaching our life goals.
I enjoyed watching this, and hope others will watch this profound, and ultimately uplifting, film about tinnitus.
I enjoyed watching this, and hope others will watch this profound, and ultimately uplifting, film about tinnitus.
Yes... one day at a time! Less suffering!
Glad you enjoyed it.
It is also nice to know that we are not alone with this and people are speaking out!
- Nov 10, 2013
- 464
- 41
- Tinnitus Since
- 2005
- Cause of Tinnitus
- Bad luck and bad genes
Just want to bump this up for newbies, please watch and share, it's a great insight into this madness.
- Nov 10, 2013
- 464
- 41
- Tinnitus Since
- 2005
- Cause of Tinnitus
- Bad luck and bad genes
Just want to bump it again, also just to add some content, here's another video about action heroes:
- Jun 19, 2013
- 177
- 43
- Tinnitus Since
- 06/2009
- Cause of Tinnitus
- Acoustic trauma
I thought the beeping at the end was my T acting up, scared the hell out of me. I have friends that have ringing on their ears, and don't give a f... With 1 in 10 in the UK, the government should really publish some warning on the telly as he says.
Well, I post this on a few threads already, LOL. But this is the thread for tinnitus video and with a video of William Shatner. So I will post this again of Shatner and David Letterman talking about their T. When I first watched this video, I had a good laugh (though my T was still very distressing for me back then).
This is a tinnitus short film made by a young European lady Zoe Cartwright. She went to the Yuku forum many years ago to introduce her film when I was new with T. She made the film as a university project. She is an inspiration to me in my struggle with tinnitus, prompting me to accept my T regardless.
She told us her story that she turned completely deaf at young 15. Her T is unmaskable due to her deafness. How tough is it to handle the scream without any ability to mask? Tough indeed. I admire her courage and stamina. What impresses me most is her decision to accept T, however loud and %(#%*^! unbearable. She said it is either acceptance or utter misery for the rest of her life. So she chooses to accept T and move on with her young life. She said she loves the beauty of the visible world and she loves diving. That is probably why she has scenes of underwater shots. She also moved on to achieve her goal to attend university where she made her film. You may have a tough time understanding what she narrates in the film due to her accent. But in this site, Zoe came to explain herself in the comment: http://www.grumpyoldeafies.com/2008/05/film_experience_of_tinnitus.html
Here is her film:
She told us her story that she turned completely deaf at young 15. Her T is unmaskable due to her deafness. How tough is it to handle the scream without any ability to mask? Tough indeed. I admire her courage and stamina. What impresses me most is her decision to accept T, however loud and %(#%*^! unbearable. She said it is either acceptance or utter misery for the rest of her life. So she chooses to accept T and move on with her young life. She said she loves the beauty of the visible world and she loves diving. That is probably why she has scenes of underwater shots. She also moved on to achieve her goal to attend university where she made her film. You may have a tough time understanding what she narrates in the film due to her accent. But in this site, Zoe came to explain herself in the comment: http://www.grumpyoldeafies.com/2008/05/film_experience_of_tinnitus.html
Here is her film:
Not exactly a full-blown documentary, but just wanted to post this Sounds of Tinnitus video we did for our fundraising campaign earlier this year.
Featuring some of our members!
Featuring some of our members!
I am the fellow to the left on the DS Part 2 scene above. I've had T since 1972 as a result of artillery and the use of pneumatic tools while serving as a US Navy sailor. For this disability, I receive a whopping $129 monthly compensation. Forty-two years with it and I still hear it, but react to it much less than at the beginning.
I've not had a talk with Mike Cohen in years, although we will for all our lives remain good friends. The ex-railroad worker on the documentary, Ron Harner, lives about an hour from my house. We talk on occasion still, after perhaps ten years following the filming of "The Devil's Symphony".
You become a kind of family with others who understand your plight, which is a good thing. They're great people who are there anytime I might need a word of encouragement, or they need from me. And that's what we're all here for, really, to share and listen.
I'm always open to anyone who would like to write to me, to write of their day or moment. My best aid has been to learn what it is to relax, to continue with sound therapy and to take on a kind of acceptance of the things I cannot change, all of which has brought me to near habituation. I'm certainly a lot better off than I was during the filming of DS.
God be with us all,
David
I've not had a talk with Mike Cohen in years, although we will for all our lives remain good friends. The ex-railroad worker on the documentary, Ron Harner, lives about an hour from my house. We talk on occasion still, after perhaps ten years following the filming of "The Devil's Symphony".
You become a kind of family with others who understand your plight, which is a good thing. They're great people who are there anytime I might need a word of encouragement, or they need from me. And that's what we're all here for, really, to share and listen.
I'm always open to anyone who would like to write to me, to write of their day or moment. My best aid has been to learn what it is to relax, to continue with sound therapy and to take on a kind of acceptance of the things I cannot change, all of which has brought me to near habituation. I'm certainly a lot better off than I was during the filming of DS.
God be with us all,
David
Once again I like to post the tinnitus short film by a young European lady Zoe Cartwright. She was completely deaf at 15 and has loud unmaskable tinnitus. While it would be nice to have silence (as she said so in the film), she nevertheless decides to accept the reality of her T and moves on with pursuing her life's goals one of which was to attend university. Against all odds, she made it to university and there she made this short film.
You may have a tough time understanding what she narrates in the film due to her accent as she is from some northern European country. But in this site, Zoe came to explain herself in the comment section and you can understand her narration better:
http://www.grumpyoldeafies.com/2008/05/film_experience_of_tinnitus.html
How does she view her life in face of deafness and loud unmaskable T? Here in one of the replies she made in the comment section of the above link summarizes it (just incredible positivity & stamina which is so touching to witness):
Dear Dj, Laurence, Chris and Eddie,
Cheers for your lovely comments guys, it really makes me smile
I'm intrigued about Eddie's message regarding "looking at it in the wrong perspective" - the film was not designed to bring out the violin strings or moan about tinnitus. It was simply about showing a different perspective walking around with a noise that can be dominating - which therefore feels surreal. I love my life, and I can honestly say I am happy - Tinnitus is just a slice of my life.
Thanks again.
Zoe.
Here is her film and I hope you come out realizing her courage and positivity to climb this incredibly tough mountain in her young life. She has been a guiding light for me and I hope you can be inspired by her story too. I think she is a film director now:
(by the way, the film title of 24.7.52.10 means she has had her loud, unmaskable tinnitus 7/24 & 52 weeks a year for 10 years at the time of making this film)
You may have a tough time understanding what she narrates in the film due to her accent as she is from some northern European country. But in this site, Zoe came to explain herself in the comment section and you can understand her narration better:
http://www.grumpyoldeafies.com/2008/05/film_experience_of_tinnitus.html
How does she view her life in face of deafness and loud unmaskable T? Here in one of the replies she made in the comment section of the above link summarizes it (just incredible positivity & stamina which is so touching to witness):
Dear Dj, Laurence, Chris and Eddie,
Cheers for your lovely comments guys, it really makes me smile
I'm intrigued about Eddie's message regarding "looking at it in the wrong perspective" - the film was not designed to bring out the violin strings or moan about tinnitus. It was simply about showing a different perspective walking around with a noise that can be dominating - which therefore feels surreal. I love my life, and I can honestly say I am happy - Tinnitus is just a slice of my life.
Thanks again.
Zoe.
Here is her film and I hope you come out realizing her courage and positivity to climb this incredibly tough mountain in her young life. She has been a guiding light for me and I hope you can be inspired by her story too. I think she is a film director now:
(by the way, the film title of 24.7.52.10 means she has had her loud, unmaskable tinnitus 7/24 & 52 weeks a year for 10 years at the time of making this film)
Yes, Billie, an excellent video. Very revealing to the outsider as well as the sufferer. Thanks for bringing it up. I watched it when it first came out and was astonished to find what this woman is able to endure.
David
David
Hi David, ya, she has been a guiding light for me as well as a few others. Simply amazing for a young pretty girl to have the stamina to face up to loud unmaskable T for the rest of her life and yet she triumphs over it.
I greatly admire this young woman, no human being should have to endure what she does, or what anyone with obtrusive tinnitus endures... I think one thing that needs to be stressed is that while life quality (the meaning you make from loving others, work, etc) can be better than before with intrusive tinnitus, quality of life cannot--- it is worse, pure and simple... I think that distinctions needs to be made loud and clear so that tinnitus doesn't get even marginalized more by the medical profession
Hi,
Not sure where to post this but will try here.
My radio feature on tinnitus just aired in Australia on ABC Radio National and it may be of interest for those in the early stages of tinnitus (as I was last year when I started researching) - it's principally about what is tinnitus, how to habituate and manage it etc and everyone I interviewed including the audiologists had tinnitus.
I developed tinnitus early last year when I had surgery for an acoustic neuroma (translab) - SS deafness was expected, tinnitus and its impact a shock. It took me around 18 months to habituate and given my job relies on my ears it was a stressful time.
If you do listen please note there are tinnitus sounds in it so don't play it loud - there is also a written online feature if you prefer to read but the radio version has more information.
I hope this is of help to someone whether it's someone dealing with tinnitus or their loved one, that was my goal in making it.
online written feature: http://www.abc.net.au/radionational/programs/bodysphere/the-ringing-that-has-no-answer/5733350
radio feature: http://www.abc.net.au/radionational/programs/bodysphere/tinnitus/5710154
There are also a lot of comments on both pages that may be of interest.
Maria Tickle
Not sure where to post this but will try here.
My radio feature on tinnitus just aired in Australia on ABC Radio National and it may be of interest for those in the early stages of tinnitus (as I was last year when I started researching) - it's principally about what is tinnitus, how to habituate and manage it etc and everyone I interviewed including the audiologists had tinnitus.
I developed tinnitus early last year when I had surgery for an acoustic neuroma (translab) - SS deafness was expected, tinnitus and its impact a shock. It took me around 18 months to habituate and given my job relies on my ears it was a stressful time.
If you do listen please note there are tinnitus sounds in it so don't play it loud - there is also a written online feature if you prefer to read but the radio version has more information.
I hope this is of help to someone whether it's someone dealing with tinnitus or their loved one, that was my goal in making it.
online written feature: http://www.abc.net.au/radionational/programs/bodysphere/the-ringing-that-has-no-answer/5733350
radio feature: http://www.abc.net.au/radionational/programs/bodysphere/tinnitus/5710154
There are also a lot of comments on both pages that may be of interest.
Maria Tickle
Not necessarily a documentary (I'm not sure), but a short movie about tinnitus.
Very good, I must say.
Very good, I must say.
What an informative video. I dont sleep with fans but with a sound machine as well. My T is so loud that it covers the sound machine, his is more high pitched than mine is.
What a poor soul. This is truly a horrific disorder. I pray to god that we have a cure for this.
I have genuine sympathy for people that live with severe tinnitus. My own is variable and ranges from: complete silence, mild, moderate severe and can reach very severe levels, requiring me to take clonazepam to help reduce the noise. In addition to this, I have counselled people with tinnitus and know how much this condition can affect a person's quality of life and their emotional wellbeing. Some people have it so severe they are unable to work and are on medication to help cope with it and wear devices called white noise generators.
There is no doubt that Mr Berardi has tinnitus like millions of other people around the world. However, if he thinks compiling a ten minute video and hoping to convey to the viewer, how tinnitus is seriously affecting the quality of his daily life then it hasn't impressed me. Nor do I take kindly to him walking around his bedroom, switching on three electric fans and a sound machine placed by the bedside to drown/masked the tinnitus, which is one of the worst things that you can do.
There is no mention of any treatment that he has had under the care of a Hearing Therapist or Audiologist for tinnitus management, or whether he is taking medication to help cope with the condition including a sleeping draft, since he doesn't sleep well. Or that he wears white noise generators during the day. I say this because of the elaborate array of "sound generation" that he uses to get off to sleep each night. Three fans and a sound machine. Through the video the viewer has to endure listening to a high pitched "amplified" noise that is supposed to resemble what he is hearing 24/7. Sorry I am not buying it.
All we see in this video is a man walking around his lovely home, which I have no qualms about for I have a nice one too. Located here in Brighton, England.
In my opinion, people that have tinnitus that affects their life to the degree this gentleman, would like us to believe he is enduring, would relay to the viewer information that I have mentioned above and treatments he has tried to improve the quality of his life and there are many.
Michael
There is no doubt that Mr Berardi has tinnitus like millions of other people around the world. However, if he thinks compiling a ten minute video and hoping to convey to the viewer, how tinnitus is seriously affecting the quality of his daily life then it hasn't impressed me. Nor do I take kindly to him walking around his bedroom, switching on three electric fans and a sound machine placed by the bedside to drown/masked the tinnitus, which is one of the worst things that you can do.
There is no mention of any treatment that he has had under the care of a Hearing Therapist or Audiologist for tinnitus management, or whether he is taking medication to help cope with the condition including a sleeping draft, since he doesn't sleep well. Or that he wears white noise generators during the day. I say this because of the elaborate array of "sound generation" that he uses to get off to sleep each night. Three fans and a sound machine. Through the video the viewer has to endure listening to a high pitched "amplified" noise that is supposed to resemble what he is hearing 24/7. Sorry I am not buying it.
All we see in this video is a man walking around his lovely home, which I have no qualms about for I have a nice one too. Located here in Brighton, England.
In my opinion, people that have tinnitus that affects their life to the degree this gentleman, would like us to believe he is enduring, would relay to the viewer information that I have mentioned above and treatments he has tried to improve the quality of his life and there are many.
Michael
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