Tag: Information Access
The Power of CSD: Managing Information in Deaf Community
The information must free itself from the old known. To the Deaf community and the media everywhere in the world through social media—the only freedom lies in the unknown because whatever is known cannot be ignored from the past. Whatever the media learns the facts from Communications Service for the Deaf (CSD) about whoever the Deaf-owned organization were bounded, as soon as it put words around Deaf people’s experiences, it might affect them as state of being Deaf getting lost.
The month of May is Mental Health Awareness is an important learning experience for adequate mental health services in Deaf community. Deaf Counseling Center (DCC)–the first-Deaf owned counseling by Deaf women since 2001 has been the pioneers of mental health services with web-based platforms through Videophone (VP), FaceTime, Zoom, all the available platforms as long as I can remember back to year 2010 when I first learned about DCC through my Deaf friends from several states in America whom themselves been helpful thanks to web-based platforms.
It is the strongest proof that DCC had been the first-ever counseling organization to stay ahead even in technological wonders. It is a marvel invention!
Mental health awareness, may be challenging to slip what little remains of the Deaf community that limits Deaf people seek for help, and DCC takes a bold step, justifies empowerment whatever it takes to help Deaf people since year 2001 in a growing movement in both human interaction and web-based platforms to address a variety of social and life skills.
Sure, there are many Deaf communities around the world, for so long Deaf people have defined themselves in opposition to how the general society has viewed Deaf people, and they have defined themselves, and been defined, by that which seemed to be in them as most different, but their struggles alone in Deaf community with lack of access to mental health, not its difference from the society defining who Deaf people are, and the access to mental health services makes them better.
CSD’s website: Challenging Misconceptions Since 1975.
“For over 40 years, Communications Service for the Deaf has been working hard to create opportunities that allows each Deaf person to discover their gift that they bring to the world.”
For almost 20 years, Deaf Counseling Center has been working hard to create healthy mental health services that allow each Deaf people to empower their well being that they can make all the difference available in Deaf community. It is no easy feat, and they deserve all the hard work.
However, the pioneer by Deaf counseling through web-based platforms who been labeled on the wrong side had been approved by CSD not to recognize DCC as the first Deaf women owned counseling to offer web-based platforms is biggest mistake. DCC is the primary source for its first ideas in American Sign Language (ASL), and nowhere else are intense intellectual debates in ASL a common part of DCC’s mission values. When DCC is silenced, Deaf community is silenced.
It is not the first time CSD had neglected pioneers in Deaf community claiming that they have the right information because of the enumerated powers forging their homework done by CSD researchers or decision makers–yet, 18 years later, CSD said that DCC is not the first Deaf women owned counseling organization to offer web-based platforms is a flagrantly neglected, to CSD’s advantage and give National Deaf Therapy (NDT) the honours that they claim they were the first Deaf women owned therapy organization to offer web-based platforms whom just created baby steps just a year ago (2018)–It is something CSD needs to challenge its own misconceptions.
-JT
Copyright © 2019 Jason Tozier
This text may be freely copied in its entirely only, including this copyright message.
ACLU Conference 2018: Share Your Story
My Experience With ACLU National Conference
Social Media vs. My Personhood
Me and My Father (2011)
“We tell the public which way the cat is jumping. The public will take care of the cat”– Arthur Hays Sulzberger
Being Deaf is personal for me and I believe that it is like my right to believe in any way. The problem is when the media and politics got into my father’s mind.
I did not know about Milan Resolution 1880 banning sign language until three years ago and it took me to realize that from the time we all were being indoctrinated with Oralism as well as Cochlear Implant (CI) today when we did not know why they imposed the Milan 1880 resolution.
Eight years ago, for example, my father asked me during our lunch outing at famous Carol’s Café, and we were about to order our food from the menu when my father said to me in some of “home” sign language that he had found some good news. He heard from other people as well as saw the television advertisement that cochlear implants (CI) is the best tool for me to hear. He thought that if I get CI it would make me happy, get a job, and even to hear all the things I could ever imagine. He thought it was great.
By looking at my father’s face with high hopes, I realized that my being Deaf is not good enough for him. I was 30 years old that time. I had been Deaf all my life since I was a baby. I was devastated and decided to walk away from the table and unlocked my bicycle so I could go home alone. It was raining that day.
My father was puzzled why I left all of sudden. He tried to call me several times that day but I did not pick it up. I did not talk to him for a couple of days. I realized that it was one of my earliest stages of understanding the dynamics of Deafhood.
We need to bring stronger ethics and philosophy back into our Deaf minds and, especially at an early age. We the Deaf need to stop negative media. Do not let negative media degrade us by offering us the Deaf those Cochlear Implants (CI) because they are filled with the false hopes.
Perhaps we should re-frame the question: How can society protect Deaf children from being implanted?
This dangerous “CI myth” is what nearly all the media are selling false hopes. The CI myth is also pushed by media sources that has fed my father into thinking that CI is equated to “happiness,” “job” and “information access.” I did not blame my father for it. I am blaming the social media that exploited my father into believing so.
It has concerned me that the media continues to IGNORE the facts and follow our emotions when it comes to public policy. We the Deaf are people, too, for two things: the state of being Deaf is human right and using American Sign Language (ASL) is our legal right, too. We have the hard facts because we are the breeds of Deaf blood. Why should the public policy by getting cochlear implant be based on? Should it be based on anecdotal experiences?
When Deaf children are being persecuted as in those caught up in Alexander Graham Bell Association of the Deaf (AGBAD)’s stupid policy, which is the first thing that they want to do by eliminating being Deaf right off the face of the Earth, making sure Deaf children are breeding and acting like hearing people. Deaf people do have human rights and basic legal rights, but AGBAD breeds the myths and fictions which had driven my father to think that CI will bring me happiness. It is a legal train wreck.
We the Deaf need to challenge those AGBAD politicians who have only their careers to watch out not for the public good.
Dad, it is not your fault! The media took our love away! They want you to love CI. You might be a turd, but damn it, I do love you, Dad!
-JT
Copyright © 2013 Jason Tozier
This text may be freely copied in its entirely only, including this copyright message.
...And the Truth Shall Set You Free. 
You must be logged in to post a comment.