Showing posts with label Pride. Show all posts
Showing posts with label Pride. Show all posts

Thursday, November 7, 2013

Pride - an ASL Version

Hello everyone,

This is an ASL version of the English poem "Pride" from my eBook "Shadow Boxer & Other Poems". It's a look at a real relationship between a CODA and his deceased father. Please do not look at this ASL version as poetry. It really didn't come out that way at all. It's more like the ASL/Deaf version of spoken word or prose, and quite honestly, I'm not 100% sure how to define it myself. With that said, let's just say "it is what it is". If after viewing this you would like to read the English version, please refer to the 'My eBooks' tab at the top of the page. You can find the link to the book from there, and it is a free download. I hope you enjoy the video, and forgive my near 2 month absence from this blog (assuming any of you still check in, haha).







Until next time,

R. M.

Friday, June 29, 2012

Help Stop Audism Right Now!

Hello to everyone,

I want to point out the recently added widget that you should see to the right on this page. It is a link to sign a petition against author Kristin Henson and the involved publishing companies for publishing the book "Super Smutty Sign Language". What sounds like having fun with ASL has turned out to be a really bad idea for Henson.

This was something I had read about on Facebook through several people in the Deaf community. Apparently, Henson is a hearing person who has only taken a couple of beginner ASL courses, and is now suddenly ready to publish this book. How would you like it if you were Chinese and some random American who took a beginning Chinese language course decided to make a book about teaching Super Smutty Chinese, as if they had any credentials to do so? This is right there as another example of Audism. Let me explain;

We define Audism as "The notion that one is superior based on one's ability to hear or to behave in the manner of one who hears."(Thank you Tom Humphries) If you ask me, only knowing some very basic, and I mean VERY basic ASL does not grant you the right to go ahead and make money off of your limited knowledge. It's a bug snub to Deaf people, and many that I know are not happy about this. It's a hearing person with no real tie to the Deaf community or no identity within the community (by that, I mean CODAs and some ASL interpreters, etc) making money off of something very central to it. Earning a profit for this is absolutely waving the flag of Audism in all of our faces.

Many Deaf people began to respond with their own comments on this website, http://truebizme.com/2012/06/28/action-alert-hearing-person-exploiting-asl-for-profit/ . You can click the link and go see for yourselves if you'd like. In fact, I encourage you to do just that. Here is one comment that I find explains this far better than I ever could;

    
dagrushkin said:
Thank you for the contact info, Octavian. This is what I sent:
Dear Editors:
I am an Associate Professor of American Sign Language (ASL) and Deaf Studies at the California State University – Sacramento.  I am Deaf and have been an ASL speaker for more than 30 years.  
I was appalled to find out today that not only is Kristen Henson doing her “sign language” instructional videos on You Tube, she is now in the process of having a book published of her highly dubious work through your publishing company.  I urge you strongly to discontinue any plans to publish this book, which the Deaf community finds extremely demeaning, for a number of reasons, which I will enumerate below:
First, Kristen is NOT a fluent, competent signer.  In watching her videos, it is immediately evident that she not only produces a number of formational/articulatory errors, but she is also often grammatically incorrect as well.  As anyone knows, if you are going to teach a language, it should be taught correctly, and preferably by native models, which Kristen is not, by any definition. 
Second, the “sign language” that she is teaching has no practical use for any sort of regular contact with Deaf people. Random sentences of a sexual or stereotypical nature are not how one typically initiates contact with a Deaf person.  Moreover, were someone to use these phrases with a new acquaintance, if they were not immediately slapped or punched, they would not understand anything that was signed back to them, since they obviously would not have learned any form of normal discourse. 
Third, ASL has had a long history of being banned, dismissed, diminished and in general, disrespected by professionals and lay people alike.  To produce a series of ungrammatical and articulatorily incorrect videos (let alone a book filled with the same) perpetuates the notion that ASL is not a language deserving of respect and that where ASL is concerned, any sort of movement of the hands means that one  is using “ASL”, when this is clearly not the case. 
Moreover, the Deaf community has had a long history of Hearing people profiting off not only our bodies, but also our language.  Kristen Henson is just the latest of such profiteers, and it is doubly insulting that there are many highly qualified, competent, Deaf people who are not being offered any sort of lucrative publishing deals, while a person like Kristen, without any training or cultural understanding, is being endorsed by your company.  
I am sure that there are some who may think that Kristen Henson’s work is intended in a humorous vein.  However, given the history of disparagement of ASL, any such humor is immediately lost and instead it becomes yet another example of belittlement  of a culture, people, and language.  I am sure that many other cultural and linguistic groups would also find it insulting to have a non-native speaker publish work in their language consisting solely of sexual, racial and stereotypical concepts. 
I could go on, but I think you get the basic idea here.  Kristen Henson’s work is highly offensive, inappropriate, and should not be financially or otherwise rewarded by your company or anyone else.  So once again, I urge you to immediately take action and discontinue any plans to publish this (or any similar) work. 
Donald A. Grushkin, Ph.D.

Here is a dialogue between two people in the comments section. I think it's important to show this as well so you can all see differing points of view;

    
I was born deaf – i think youre all over reacting. If you dont like it….write your own stupid book. Some of these long winded and asinine comments about culture and blah blah blah just makes you look ignorant. You dont like a book…shut up and get another one. I quit using sign language because youre all too obsessed on controlling how its used in your “culture”. You wont use it like a language but more like abbreviated yoda…which NO ONE talks like in real life, books, or tv. Youre all just LAZY not to use complete sentences. But you will raise a stink over what is free speech farce comedy.
  • You are entitled to your opinion. You might want to take some time to educate yourself on the real issues at hand: cultural appropriation, exploitation, systems of power and privilege, oppression, and the content which is racist and sexist. Along with linguistic research in ASL.
  • oh, how did i “quit” sign language…i got a cochlear implant…wow oh wow how awesome it works…and the so called “community” is offended and determines that i couldnt accept myself or some stupid thing like that. The fact is…no one should be blind, deaf, or anything…but a lot of deaf people i meet are so anti technology or enhancement but its ok to use their pda, chatbox, videobox, or any of that…but God forbid i try to hear things, speak orally, and not use sign language.I thought i should clear that comment up.
    • JJ,
      I have no problem with Cochlear Implants. I understand your decision to get one and respect your right to get one. It is unfortunate that you feel you cannot remain a member of the deaf community despite having a CI. Attitudes are changing. I wrote a blog post about my feelings about Cochlear Implants last year and got a lot of positive feedback. The general sense is the real problem is language and education deprivation that accompanies the decision to give a child a CI at an early age without a guarantee that it works and without a guarantee that the child will learn language, become independent, and economically self-sufficient.
Tavian, Educate myself? Are you FKN kidding me? – This whole setup of how the deaf community believes it should function in terms of how to react to polarized issues is so elitist its stupid. Ive been trying to “educate” deaf people to quit pigeonholing themselves into being the victim and change their approach to ASL linguistics. Why have a signed language thats so abbreviated that half of the comments deaf people post online display poor grammar because they write the same way they sign. If they werent so hung up on their “internal” idea of how “deafies” should function maybe their “culture” can start addressing how it can be easier to function in society with a few changes in attitude. And because arguments with deaf people always never get resolved…I am outta here…and good luck wasting more time over a stupid free speech item.
JJ,
No I am not kidding you. The issues I listed for you are issues of concern to all minority populations including African-Americans, Native- Americans, Asian-Pacific Islanders, the overall disabled community, and so on forth. I agree that we should stop seeing ourselves as victims. That is WHY we are objecting. Because we choose not to be victims and to demand equal, appropriate treatment which includes respect of our culture, our language, and our personhood. Best, Tavian



To me, it seems clear that JJ, despite being born deaf, has come to the conclusion that ASL is not a real language. It's a shame. He compares it to English grammar and structure, and since they aren't the same, he says that ASL is stupid. His last words mention this whole thing as being a "...stupid free speech item." Here's what I need to say about that -

Freedom of speech is a right for everyone. The U.S. Constitution grants it. That is why people can say whatever degrading racist, sexist, etc etc, anything they want and not be penalized under law for it. That much is true. That same principle applies here, I suppose as well. However, anyone has a right to respond and stand up for themselves as well. It's nice to see so many in the Deaf community doing just that. When I was younger I saw a lot of Deaf people just sit back and be passive regardless of how offended or hurt they were. Historically for Deaf people, that's how it's always been. What's worse is that most of the hearing world has little to no idea about these things, and therefore, any one of them who could show their support don't even know it's needed.

It's my goal with this post to let those of you who would otherwise never know of this become aware and informed. Granted I can't give you every detail about this issue in a blog post, and that is why I encourage all of you to look into this for yourselves. If you feel strongly enough that St. Martin's press should not go through with this, and that Kristin Henson should not be able to profit from this venture, then share your thoughts in the court of public opinion. Click on the Change.org's petition widget on the right hand side of this page so we can let those people know what they are doing is morally wrong, and while you're at it, show those in the Deaf community that even though you are a hearing person and know little about them, you support their rights. Deaf people need to see this from hearing people now more than ever. It's a good time to start, and if you take that time, I thank you from the bottom of my half-Deaf (CODA) heart.

Until next time,

R. M.

Saturday, June 23, 2012

A Look at a CODA's Deaf Family - Update

Hello to all,

A while back I wrote a post entitled "A Look at a CODA's Deaf Family". In it, I had talked about a Deaf man that I know who was coming to the end of his time with us on Earth. Sadly, I have to say that his time came about two weeks ago. Earlier today was his memorial service, held at the school for the deaf (or one "i" hand tapped twice on top of the other, if you will) where he attended and later worked.

In my previous post I had mentioned what he meant to me as a member of my Deaf family. I won't get into that again, but I do want to talk about the service today. I had the privilege of meeting his Deaf family.

I have to mention first about my own father's passing four years ago. My sister and I had decided to split up the responsibilities of that came along with the process of funeral/ceremonial decisions, notifying everyone, writing the obituary, and seeing our mother was ok, etc etc. I had asked to handle speaking with the funeral director to make the service a little more "Deaf" friendly. One of the things to be done was to have no aisles of chairs in the middle of the viewing room. I did not want my father's Deaf friends to have to look at the back of each others' heads. In an attempt to allow everyone to see what everyone else was signing, we arranged the chairs in a large "U" around the room. It was good for about 40 or 50 people. When people began to arrive, we quickly ended up with far more people than anticipated. Friends came from all over and we had to put chairs in the middle of the room in rows/aisles, anyways. At least we tried, right? What we ended up with was upwards of close to 100 people. Some had to view the service from the other room because we ran out of space!

I say this because at the time, it really impressed upon me what "Deaf family" means. I remembered so many faces of the people I used to see at Deaf Club meetings and get-togethers from my childhood and they were all so wonderful. I also saw many faces of people I had never met before, but whom were great friends with my father at one point in time or another. It really helped me see how much Deaf people cherish each other and how close they all were. That is what a Deaf family is.

With that said let me move onto today. This service was at least twice the size of my father's and held in the school gymnasium. Friends and family gave some touching and personal speeches. There was also a closing prayer conducted by a Deaf Father. That is something I had never seen before. It was such a cool thing to witness. The reception was held in the cafeteria, a slideshow in the meeting room, and the school's museum, something this man had the largest hand in creating, was open for all to view. There was also a video camera setup for people to give their goodbye wishes, share stories, and anything else anyone felt had merit to mention. I saw former teachers and students come today, too. He had reached a lot of people in his time.

And just like any typical get-together in the Deaf Community (with hearing people involved), the Deaf will stay until they are told to leave. The crowd was over half out by the time myself and ELF had left, and nearly all of them were either Deaf, CODAs, or other members of the man's family. And here they all were, his Deaf family. It amazed me to see it yet again, and I cannot explain in any decent amount of words how much it touched me to know that even though most of the Deaf people there were not a part of my Deaf family, the man's wife went out of her way to make me feel like I was part of their's, no matter how small a part it really is.

I guess this is the only way I can explain it. Compared to probably just about everyone else there, I was little more than an acquaintance to this man and his wife. Most of their blood family I had never met or seen until today. I think it's that connection a CODA has or can have with other Deaf people, without even having spent a great deal of time with them, that makes it a Deaf family for each other.

With so little, in relative terms, his life had a significant impact on me. For everyone else there who was much more a part of his Deaf family, I can only imagine how his life impacted them. I have to believe that its value is exponential. Everyone who attended, and everyone who could not but did so in spirit, is a better person because of his impact in our lives. That's the power of Deaf family, and I am honored to have felt its impact again. I love you, man.

Until next time,

R. M.

Thursday, May 31, 2012

Deaf Pride and Audism; One CODA's Take

Hello again to all of you out there. A lot less time has passed since my last post, which is a good thing, I think. Anyways, if you can wrap your head around it, this is going to be another post about Deaf people. I know. You're shocked, aren't you, Pepper?

Well, this one relates to a topic that has always been a big one in the Deaf community for as long as I can remember. This may take a roundabout path for me to explain this, and hopefully clearly, so here goes.

I often come to the conclusion that there are Deaf people who do not view themselves as disabled, and do everything they can to not portray themselves that way to the larger, hearing world. In my opinion, Deaf people are not what I consider to be disabled. A hearing loss has no effect on intelligence and therefore there is nothing that cannot be overcome. We can do this, we have the technology. Please do not mistake technology to mean hearing aids and cochlear implants. I mean things like video phones and flashing light doorbells, etc. These Deaf people are proud, hold down jobs, and fully provide for themselves. They show the outer world what they can do.

I also find that there are Deaf people who do not carry that same sense of pride. They willingly collect disability checks. Not for having a heart condition or broken limbs or anything, but for being deaf. This is the way that federal law looks at deaf people. These Deaf people feel no shame in taking the money and doing nothing for it.

There are also those who collect it even though they would rather be independent. The unemployment rate amond Deaf people is exponentially higher than the U.S. average for the entire populace. Audism has a large hand in that. There are also Deaf people who may have real disabilities and cannot work for those reasons, but are listed as disabled by the federal government in relation to their deafness.

I get to have the wonderful experience of seeing different sides of this. My father was almost never without a job. He held only two, in fact. One was at a woodmill for 20+ years. With that money, he was able to provide my family with a house, a decent vehicle, and enough money to be relatively stable. We definitely were not living paycheck to paycheck. Unfortunately, the mill burned to the ground and everyone was laid off. My father was out of work temporarily, and had to go through the humiliating experience of being turned down by other local mills becasue he was deaf and couldn't hear the machines, so how would he know if he was in danger? Ridiculous. He had all that previous experience and no accidents/injuries, no sick time used, and so on and so on. Even more embarrassing to him was having to swallow his pride to turn to a state program that found a job for him. So he became a butcher at a meat plant. The pay was ridiculously low, and we were barely above the poverty line. Never once did he complain about it in front of us. He just kept on working because he had to. We never complained either. It was a commendable sacrifice to make.

On the other hand, there is my mother. Here you have a woman whose experience as a Deaf person was far different. Society and family oppressed her so much that she believes herself to be incapable. She was lucky to have a handful of jobs over a short span of years, but overall those same issues got in the way everytime and she was let go from every position. She didn't want to be 'disabled', but she accepted it as her lot in life just the same. Let it be known that she has collected disability checks for most of her life and does so to get by, even now. To me, the real 'disability' is not her deafness. It's how Audism has affected her over the years, and possibly other issues as well not related to being deaf. In short, she is not willingly taking advantage of the system.

Those Deaf people who do take advantage of the system are my focus for this post. It's not even taking advantage of the system, it's being ok with showing the world that Deaf people are disabled and can't do this or that. For example, have you ever met a deaf person who pan-handled for money in the streets by offering hearing people a business sized card with the manual alphabet on one side, and a sob story on the other asking for a donation? It's a sore subject for Deaf people who are proud of themselves. This behavior of portraying oneself as disabled makes the rest of the community look bad. Especially when many of these Deaf people are doing so when they have everything they need, and are just doing so to make a few extra bucks. It's bad enough to play the welfare/disability system of the federal government, but at least i can see the logic for many of those Deaf people who make such a decision. I see it as a misdirected middle finger to the government for considering them disabled. However, begging for money on the streets isn't a middle finger at all. It's a flat-out admission that one believes themselves to be helpless. It hurts Deaf people for this to occur, and those who are proud generally stand firmly against it.

What's worse is that there are Deaf people who do this without any financial need at all. They just want some extra money. They have their own homes, jobs, vehicles, etc. If there are outstanding circumstances that force a person to need a few extra bucks, does it have to come to panhandling? You can't find a more affordable car? Perhaps sell your house and rent? Lower your monthly bills through credit counseling services? These are all things the rest of us do. There are so many other options out there.

There are those who believe that pride is a sin. Well, I'm not a religious person, and I believe that pride among Deaf people is necessary in the fight against Audism. If you have no pride, you tell your oppressors that they've won. It's unacceptable for that reason alone. Don't let Audism win.

I did not write this to offend Deaf people, though I know that some who read this probably will be. My concern is that some Deaf people make the struggle for the rest of the Deaf community harder than it has to be. Pride is not always bad. Sometimes you just have to show it.

Until next time,

R. M.