https://www.borderline-personality-...lity-disorder-research/new-insights-into-the-
borderline-personality-brain/
I have borderline personality disorder a mental disorder with extremely unstable emotions and clingy personality
as well autism and ADHD. Life was crap before tinnitus but good music gave me the motivation to move on. Until I thought it would be a good idea to indulge in moronic internet memes characterized by " extremely loud noises" as the joke and gutting my hearing in a month's period not even noticing it like a complete moron until my ears starting ringing. Now I have permanent damage in my inner ear and am constantly reminding of my stupid mistake creating this PTSD effect everytime I hear my tinnitus or get a spike.
Before my tinnitus I had a part time job for the past four years and had plans to start classes in 2018 and took test to prove I have normal intelligence, my life was picking up for the FIRST time in five years. It was an escape from my depression! I was finally going to fit in with society and have a real life and good friends.
Then hearing loss, tinnitus and hyperacusis pretty much just killed my desire to be a functioning member of society because no amount of hard work will bring back my favorite music, or give me the peace of silence or stop ear pain.
There is no longer any reward to to being a functioning member of society with vile noises in my head 24/7. Basically I was on thin ice mental health wise before tinnitus but I had a very positive personality to fight it, but my mental toughness collapsed once I realized there was no cure.
From what I observe most people here have tinnitus much louder then I do, Even though my tinnitus is fluxuating from 20-35 decibel range at it's worst. So feel free to criticize me for having "mild tinnitus" and "mild hearing loss" and being a complete oversensitive about it.
The four years of working, successful test and applying for classes is now making it very difficult for me to apply for SS or any government benefits.
Pretty much I still want to go to school and hold a part time job if I can but the Government has a unfavorable system in place where it rewards disabled people for doing absolutely nothing and takes away disability if you are in school or working a small part time job. So I guess I'm still holding onto visions for the future but without disability I'm pretty much screwed and won't bother fighting a losing battle.
Let's move on to my thoughts and criticism's of Tinnitus Retraining Therapy and Pawel Jasterboff himself
Jasterboffs (the creator of tinnitus retraining therapy)'s entire model is based on retraining the limbic system to regulate emotions, yet people with borderline have a broken limbic system to begin with. Plus non mentally disabled people should also be very upset knowing this con is given higher priority in the field of tinnitus and hearing loss research then actual research for a cure. It's self hypnosis essentially. The Limbic system is designed to respond in fear to these unholy head/ear noises. Desensitizing the limbic system is the same thing as constantly exposing yourself to shocking images on the internet to the point where they no longer bother you, Or growing up in a war torn 3rd world nation where violence is so common people are desensitizing too it! It's self deceit by the very definition.
Jasterboff model
Jasterboff also assumes everyone with tinnitus can self hypnotize themselve, he also assumes everyone has a function happy go lucky limbic system, non autistic, non borderline, non adhd ridden brain such as myself.
Basically TRT advice is discrimination towards mentally ill people and self hypnozation for non disabled.
We live in a society where showing emotions is frowned upon and that mental toughness is a virtue instead of a choice
If someone is mentally tough and can cope with tinnitus that's awesome but not everyone has the same ability. Everyone's brain is different and i'm totally okay with being an over sensitive crybaby about it. Pretty much complaining
for a cure for hearing loss and tinnitus will get better attention then praising Jasterboff.
Borderline brain changes in the limbic system
We'll I'm kind of hopeless bound to live off disability for the rest of my life unless there is real breakthroughs for hearing loss and inner ear conditions.
in the mean time I'm going to do the things I love and lose touch with reality
Things I enjoy like making memes, graphic art, using Linux, watching cartoons and going outside to see really cool animals and help protect my states natural resources because nature rules. I also enjoy martial arts a lot but haven't done that in a while but that ruled too! Also MPP (but that falls into the memes category) Those things make me happy and I don't think tinnitus or my mental health issues should keep me from trying to enjoy the things I love. I'm still aiming to going to school and getting a part time job hopefully because I do have some hope for treatment in the future via Frequency Therapeutics and Susan Shores device. To conclude my rant I'd like to say tinnitus and hearing loss sufferers should show extreme appreciate towards the men and women of science racing to solve our problems. That's honestly the only reason I am still a live.
if you actually took the time to read all of this and I welcome disagreement
borderline-personality-brain/
I have borderline personality disorder a mental disorder with extremely unstable emotions and clingy personality
as well autism and ADHD. Life was crap before tinnitus but good music gave me the motivation to move on. Until I thought it would be a good idea to indulge in moronic internet memes characterized by " extremely loud noises" as the joke and gutting my hearing in a month's period not even noticing it like a complete moron until my ears starting ringing. Now I have permanent damage in my inner ear and am constantly reminding of my stupid mistake creating this PTSD effect everytime I hear my tinnitus or get a spike.
Before my tinnitus I had a part time job for the past four years and had plans to start classes in 2018 and took test to prove I have normal intelligence, my life was picking up for the FIRST time in five years. It was an escape from my depression! I was finally going to fit in with society and have a real life and good friends.
Then hearing loss, tinnitus and hyperacusis pretty much just killed my desire to be a functioning member of society because no amount of hard work will bring back my favorite music, or give me the peace of silence or stop ear pain.
There is no longer any reward to to being a functioning member of society with vile noises in my head 24/7. Basically I was on thin ice mental health wise before tinnitus but I had a very positive personality to fight it, but my mental toughness collapsed once I realized there was no cure.
From what I observe most people here have tinnitus much louder then I do, Even though my tinnitus is fluxuating from 20-35 decibel range at it's worst. So feel free to criticize me for having "mild tinnitus" and "mild hearing loss" and being a complete oversensitive about it.
The four years of working, successful test and applying for classes is now making it very difficult for me to apply for SS or any government benefits.
Pretty much I still want to go to school and hold a part time job if I can but the Government has a unfavorable system in place where it rewards disabled people for doing absolutely nothing and takes away disability if you are in school or working a small part time job. So I guess I'm still holding onto visions for the future but without disability I'm pretty much screwed and won't bother fighting a losing battle.
Let's move on to my thoughts and criticism's of Tinnitus Retraining Therapy and Pawel Jasterboff himself
Jasterboffs (the creator of tinnitus retraining therapy)'s entire model is based on retraining the limbic system to regulate emotions, yet people with borderline have a broken limbic system to begin with. Plus non mentally disabled people should also be very upset knowing this con is given higher priority in the field of tinnitus and hearing loss research then actual research for a cure. It's self hypnosis essentially. The Limbic system is designed to respond in fear to these unholy head/ear noises. Desensitizing the limbic system is the same thing as constantly exposing yourself to shocking images on the internet to the point where they no longer bother you, Or growing up in a war torn 3rd world nation where violence is so common people are desensitizing too it! It's self deceit by the very definition.
Jasterboff model
Jasterboff also assumes everyone with tinnitus can self hypnotize themselve, he also assumes everyone has a function happy go lucky limbic system, non autistic, non borderline, non adhd ridden brain such as myself.
Basically TRT advice is discrimination towards mentally ill people and self hypnozation for non disabled.
We live in a society where showing emotions is frowned upon and that mental toughness is a virtue instead of a choice
If someone is mentally tough and can cope with tinnitus that's awesome but not everyone has the same ability. Everyone's brain is different and i'm totally okay with being an over sensitive crybaby about it. Pretty much complaining
for a cure for hearing loss and tinnitus will get better attention then praising Jasterboff.
Borderline brain changes in the limbic system
We'll I'm kind of hopeless bound to live off disability for the rest of my life unless there is real breakthroughs for hearing loss and inner ear conditions.
in the mean time I'm going to do the things I love and lose touch with reality
Things I enjoy like making memes, graphic art, using Linux, watching cartoons and going outside to see really cool animals and help protect my states natural resources because nature rules. I also enjoy martial arts a lot but haven't done that in a while but that ruled too! Also MPP (but that falls into the memes category) Those things make me happy and I don't think tinnitus or my mental health issues should keep me from trying to enjoy the things I love. I'm still aiming to going to school and getting a part time job hopefully because I do have some hope for treatment in the future via Frequency Therapeutics and Susan Shores device. To conclude my rant I'd like to say tinnitus and hearing loss sufferers should show extreme appreciate towards the men and women of science racing to solve our problems. That's honestly the only reason I am still a live.
if you actually took the time to read all of this and I welcome disagreement
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