The Michigan School of the Deaf Fiasco

January 29, 2008 at 6:41 pm (Deaf Civil Rights, Deafness, Education, Michigan)

There’s been some accusations/attacks over on Fookem and Bug’s blog towards me about the Ryan Commerson/MSD situation. I find it incredulous for people to accuse me and my mother of destroying deaf education in Michigan. Furthermore, I did not email parents/others telling them to not support him. I did nothing during the protests except write a few emails to The Tactile Mind Weekly. Then long after the protests ended, I had brief dust-ups on DeafDC. That is the extent of my involvement.

My mother on the other hand, as an advocate for deaf/hh children here in Michigan was extensively involved with this situation. With her permission, I’ve decided to post portions of my mother’s letter to the state superintendent about the MSD protests.

——-

March 16, 2006

Michael Flanagan
Superintendent of Public Instruction
Michigan Department of Education
608 W. Allegan Street
P.O. Box 30008
Lansing, MI 48909-7508

Dear Mr. Flanagan:

(snip)

I state my point bluntly: I am very distressed that in general, the Department has chosen to legitimize Ryan Commerson’s tactics, and in particular that it has chosen to commit our tax dollars to appeasing this one individual and his cohorts. I therefore wish to know how much of the public’s money will be spent placating these protesters, the leaders of whom are, by their own description, radicals.

This has been one of the most difficult things I have ever undertaken to write. I am torn between knowing how very important it is for parents and educators to listen to the Deaf Community with respect to the education of Deaf and Hard of Hearing [DHH] students, and my very strong conviction that Ryan Commerson and his co-agitators are less interested in the best interests of the students than they are in exploiting them, their parents and members of the Deaf Community, to further their own ends; that they are not always honest; that they are fueled by personal anger and perhaps hatred, rather than by love for DHH students; that they deliberately employ tactics that I consider to be unethical, some of which are purposefully designed to manipulate others.

I am further torn knowing that the Department is well past overdue in terms of listening to what the Deaf Community has to say about the education of DHH students. However, what the Department takes from anyone must be tempered by the knowledge, expertise and motivation of each individual. I remain torn knowing that many DHH persons are legitimately angry and that we should validate their anger, while also knowing that we cannot allow anger to guide policy and practice. While we must improve the educational outcomes for DHH students, we cannot overlook the needs and rights of each unique DHH student, and we cannot sacrifice the rights of the parents of current and future students in perceived compensation for past failures.

Above all else, I hope that the message I convey to you today, essentially a request to rethink the Department’s treatment of Ryan Commerson and his supporting agitators, which would hopefully result in a rejection of him and his cohorts, their methods and demands, will not be construed as a request to dismiss in general, the concerns of the Deaf Community. Toward this end, I make my case.

While Commerson is certainly the central figure in the “protest” of the alleged policies and practices at the Michigan School for the Deaf, he is certainly not the sole leading agent. Commerson has frequently contributed articles to The Tactile Mind Weekly (http://www.thetactilemind.com/), commonly referred to as TTMW, which is an e-zine that was intended to be a literary journal for Deaf writers.

Alison Aubrecht, Deaf and formerly an employee at MSD, is a featured writer, whose column appears in TTMW.

John Lee Clark, who is Deaf Blind, is the publisher of TTMW; his wife Adrean, who is Deaf, is the creative director of TTMW; Christopher Jon Heuer is the marketing director of TTMW.

Some, if not all of these people were undergraduate students together at Gallaudet University. All of these persons are quite literate. They have college degrees. None were educated using the BiBi approach. By her own report (http://www.michdhh.org/profiles/aubrecht_alison.html) Aubrecht uses signed English, rather than ASL.

It has been noted that when Heuer visited MSD at Commerson’s invitation, he communicated simultaneously using spoken English and signed English. Regardless of their own histories and habits, these protesters condemn simultaneous communication [Sim-Com] and the use of any variety of sign other than American Sign Language [ASL].

They began the attack against MSD in unison, following a pre-determined plan. I come to these conclusions based on the words of these people, themselves, as they appear in the TTMW, the “Starving for Access” blog (http://starvingforaccess.blog.com/) [SFA blog] and the MSD Students blog (http://michsd.blog.com).

Well before Commerson’s hunger strike, he was writing personal attacks against Ms. Winkler and Ms. Steenwyk in the TTMW. Some of the things he wrote are blatantly vicious and betray a personal agenda against them. Ms. Winkler is particularly targeted, with Commerson attacking her on a personal as well as a professional level, evincing a campaign to portray her as inept and an oppressor of DHH persons.

Commerson has accused Cecelia Winkler of flatly refusing to consider adopting a Bilingual-Bicultural [BiBi] philosophy of education at MSD, and of stating that Deaf persons are disabled. Commerson’s cohorts, many of the MSD students, and many of the readers of the SFA blog have accepted these accusations as gospel truth, simply because Commerson has said so. Of course, it is relatively easy to twist the truth and make false accusations when one knows one has nothing to lose. Having no money and no assets provides significant protection from civil suits. Even those who are slandered and libeled cannot wring blood from a turnip.

I know Commerson’s claims to be false, because I know Cecelia Winkler, having worked with her over the course of many years. So, approximately two years ago, when these attacks upon Ms. Winkler first surfaced in the TTMW, I directly asked her about Commerson’s accusations. She was naturally distressed by the false accusations and the personal attacks, and she unequivocally denied their veracity.

She informed me that what both she and Ms. Steenwyk conveyed to Commerson was that MSD would not adopt a BiBi philosophy as defined by Ryan Commerson. This is entirely different from a blanket refusal to consider a BiBi philosophy of education for MSD. Ms. Winkler expressed great regard for the BiBi philosophy, but not for many of the demands that Commerson characterized as part and parcel of a BiBi program.

She also was very mindful of the rights of parents and was particularly concerned about employing ASL as the sole through-the-air language with students who enter MSD with little, if any, mastery of American Sign Language [ASL], and in particular for those students who have disabilities in addition to Deafness, for whom use of any form of communication is a challenge. While MSD must and rightly serves all DHH students who need to be in a signing environment, Ms. Winkler is a wise and experienced enough educator to know that one approach cannot serve the needs of all students. There must be sufficient flexibility in MSD’s communication policy, to allow for meeting the diverse language needs of the MSD students. Commerson’s version of BiBi lacks that flexibility, and was properly rejected.

(snip)

Well before Commerson began his protest and hunger strike, MSD officials, led by Ms. Winkler, were already undertaking the task of revising MSD’s communication policy. This was commonly known, as reported by Freida Morrison, president of the MSD Alumni Association [MSDAA] in her letter that was re-printed on the SFA blog at http://starvingforaccess.blog.com/432085/#cmts. In part, she states:

The protest is unnecessary and inappropriate at this time. First of all, Starving for Access supporters never approached or attended general meetings to open up the discussion about ASL or BI/BI issues. We had general meeting recently, November 19, 2005, and shared new information regarding the plan to work on implementing BI/BI philosophy. Starving for Access supporters never made the effort to attend any meetings or contact us. We did not know about the protest beforehand and were surprised to hear about it on the morning of November 21, 2005.

MSDAA has been working with Strategic Plan Committee developing a proposal, specifically using BI/BI (ASL/English) methods. We just started dialogue with the State Board of Education (Beth Steenwyk and Jacque Thompson). The State finally agreed to hear about using BI/BI in MSD. This is a long process and will not happen in few days. Cece Winkler, the Principal of MSD, has been willing to open up and work with us.

(snip)

So why does Commerson and his cohorts persist in promoting these falsehoods? Such accusations are sure to inflame the Deaf Community and turn many against the MSD administration. I believe that at least some of the answers are to be found in the SFA blog. In this blog both Commerson and Heuer reference Saul Alinsky, and his book, Rules for Radicals. It is this book that sets forth the general plan that Commerson and his cohorts follow. While I, personally, refuse to spend money on that book, there are several references on the Web that suffice in providing a good idea of what Alinsky advocates, and what Commerson, et. al., are implementing.

(snip)

That Commerson and his cohorts would use Alinsky’s tactics in order to achieve some nebulous victory (the goals of the protest are ever-changing, as evidenced in the SFA blog) while dismaying, is not shocking. What is shocking is Commerson’s indoctrination of MSD students in Alinsky’s techniques. At http://starvingforaccess.blog.com/2005/12/, Commerson, himself reports in an interview with Aubrecht:

I want it on the record that I have never denied having contact with the students.

I have been in touch with several students over the past few months, students who have expressed they feel frustrated and oppressed at MSD. Many of those students were looking for ideas on how to effect change. I discussed Saul Alinsky’s “Rules for Radicals” with those students and encouraged them to think of non-violent, legal ways they could protest without breaking rules.

This is hardly the work that Commerson was hired at MSD to do. It is also inconsistent that if, as Commerson claims, language deprivation is rampant at MSD, the students would be able to express their feelings of oppression and frustration to Commerson, much less understand Alinsky’s teachings or Martin Luther King’s “Letter from Birmingham Jail” that Aubrecht posted in its entirety on the MSD student blog, for the edification of the students.

(snip)

Since writing to Dr. Hughes, I learned that in furtherance of his agenda, Commerson assisted MSD students in setting up a student blog, (http://michsd.blog.com/) that is open for contribution by anyone, and for all to read. Taurean Burt, one of the student who manages the blog, wrote, “Thank you RC and Kid for participent [sic] this, this is also reason why I am start to set up and let have our MSD student’s rights to set up their own opintion [sic] down here and get us some of idea how to improve MSD.” (http://michsd.blog.com/393643/#cmts ).

In the student blog, MSD students are encouraged to read the Starving for Access blog, “Check out: http://starvingforaccess.blog.com Written by: alison at 2005/11/21 – 13:37:22.”

Commerson, Aubrecht and Heuer also use the student blog to engender anger and rebellion as well as to turn the students against Ms. Winkler and other MSD staff. Given the writings of Commerson, Aubrecht and Heuer, perhaps it is also their goal to turn the students against hearing persons, in general, and hearing parents of DHH students, in particular. When the Department legitimizes Commerson’s efforts, it also legitimizes his indoctrination of minor MSD students. I am horrified.

(snip)

If one reads the SFA blog and TTMW, one finds Commerson, Aubrecht and Heuer filled with deep and abiding anger toward hearing persons. While some of the personal stories told by members of the Deaf Community are filled with anguish that is palpable, Commerson’s and his cohorts’ brim with anger that arguably spills into hatred. Remember that the MSD students have been encouraged to read the SFA blog. This blog is dominated by Heuer. Even knowing that minor students read the blog, Heuer has written there, “Have you thought about organizing? Seriously organizing with every intention of packing an ugly punch?”

(snip)

Commerson has published on the SFA blog all correspondence between himself and/or Aubrecht and John Austin, Jeremy Hughes and Cecelia Winkler. Anyone who cares to read it can witness Commerson’s demands, not just of Ms. Winkler and the community in general, but also to the Department. His arrogance, his insolence, his disrespect and his threats are exhibited for all to read. His insulting questioning of Dr. Jacquelyn Thompson’s judgement, abilities and suitability is counterpoint to his excoriation of Cecelia Winkler as a leader of the referent group.

All who read the blog are similarly witness to the Department’s acquiescence to this uncredentialed, petulant agitator, as it legitimizes and honors not only his demands, but also his tactics and methods. This is a strong lesson not only for MSD students, but for all students in Michigan’s public schools. It is of great interest to parents and advocates.

Will the Department so honor every person’s demands? Will the Department commit similar funds to all those who take their grievances to the street or who otherwise rebel against an LEA, ISD or the Department, in spectacular fashion? Will the Department accept responsibility for the health and welfare of every person who is disgruntled with any public education agency in Michigan, who takes potentially harmful action in order to force submission to his or her demands? Will it similarly appease groups of parents who take public and sensational action to secure, for example, ABA programs for their autistic children, or Orton-Gillingham programs for their learning disabled children? Will the Department be as accommodating to all others who insult and demand, as it has been to Ryan Commerson? Or will the Department discriminate against all others?

The SFA blog is a peek into the souls of the chief actors in the MSD protest: Commerson, Aubrecht and Heuer. One would have to read the entire blog in order to fully appreciate what MSD is really facing, and what the Department is legitimizing. I can only list just a few of the things that are revealed there:

  • Commerson and his cohorts have purposefully introduced “Outside Agitators” into the protest. Posted by the “moderator,” OA [Outside Agitator] #3 explains:

    Thus begins the group: Outside Agitators. The primary goal of this group is to teach different tactics for self-advocacy, group advocacy, and for challenging the system of Haves. The goal of this group is to offer ideas and feedback, ranging from the expected “move up the political ladder” to more radical tactics that may be employed should they be deemed necessary.

    • The SFA blog, though dominated by Heuer, is rife with postings from anonymous persons, including those who use the pseudonyms OA#3, OA#14, OA#6, among others. These anonymous messages include those from the Outside Agitators, who pursue their stated purpose, employing the tactics prescribed in Alinsky’s Rules for Radicals. Heuer tries to justify the anonymity, claiming that it protects them from retaliation. Their anonymity protects them, too from being held accountable for their words, and from being sued for libel.
        • The SFA blog in general, and the messages of Heuer, in particular, are filled with misinformation not only about the staff and administration of MSD, but also about the achievement levels of Deaf students who have Deaf parents, the MEAP, and the provisions of NCLBA, among other things. Neither Commerson nor his Agitators have the honesty to correct the references by others to Commerson being a teacher. Commerson, in fact, taught at MSD on a substitute’s certificate. He is not a certified teacher endorsed to teach HI students; he does not have an education degree; he does have a BFA degree in film making.
        • Initially, Commerson and his cohorts attempted to assure parents that they respect their rights, and that it is not their intention to tell hearing parents how to raise their children or to dictate what kind of communication mode to use. The authors of Letter to parents, http://starvingforaccess.blog.com/2005/11/, are apparently ignorant of how condescending their letter is. The placating tenor of the letter, however, soon gives way to deep-rooted resentment and disrespect, if not outright hatred, toward hearing parents of DHH students. Unwittingly, their words will drive parents of young DHH children to oralism, rather than to American Sign Language.
        • Heuer preaches that unless changes are made now, the window of opportunity for learning to read will close before the students can achieve literacy. Heuer consistently claims that the “neural pathways” shut down at about age 12, or perhaps sooner. He makes claims about learning to read that the literature actually documents relative to language acquisition, based on neuro-biological studies of neuronal plasticity. Heuer uses his inaccurate claims to engender fear in parents, and inspire them to act quickly as he instructs. He predicts dire consequences if parents do not follow his instructions, not only because it will soon be to late for their children to learn to read, but also predicting, “Your school is going to be a dumping ground for 13 year old illiterates every other school can’t handle AFTER they’ve sucked him dry for all the propoganda [sic] energy he has to offer their programs.”
        • Disclosing his ignorance of placement procedures and truancy laws, Heuer instructs the bloggers, particularly parents of MSD students, that the way to break the union’s refusal to terminate poor quality teaching staff is for the parents to withdraw their children from MSD en masse. He writes:

        …the one thing that would send these institutions into a state of widespread panic, the one thing that would open them up 100% to new ideas and make them a thousand times more willing to pursue new options…is if we all withdrew our children from that institution AT THE SAME TIME.

        A few more issues bear in-depth consideration. A great deal is discussed about the poor record of academic achievement record of DHH students. Many writers to the blog point out that these are national statistics and no one seems to have any data that is specific to MSD students. Even Heuer admits that the issues of teachers who have poor sign skills and the dismal literacy level of the average deaf student are national problems, not unique to MSD or even to Michigan.

        Yet, Heuer expresses outrage at the suggestion that the referent group promised to Commerson by Jeremy Hughes, focus on the education of all DHH students in Michigan, rather than exclusively on MSD. Given the acknowledgment that the education of DHH students is a national issue, and Heuer’s claim that it is a crisis situation, why would anyone oppose making the focus of the referent group education for all Michigan DHH students?

        (snip)

        In sum, Commerson and his agitators would not be able to control such a referent group. That such control is sought was voiced by Heuer, when he wrote to the SFA blog:

        I would think that Dr. Hughes or any MSD administrator would infinitely prefer to talk to a rep for all of you than all of you together. It will help facilitate things, especially if you start moving outside of the area of just Bi-Bi-related concerns. Some of you seem to have listed other concerns as well, and you don’t sound like you’re just going to discuss these things in your meetings and not eventually approach MSD admin on them. So when you eventually do make that approach, a rep could be helpful. . . Plus this would put us all a step ahead of whatever Referent Group that gets formed. [Emphasis added.]

        There is no escaping the fact that education for DHH students in this country is dismal. Michigan must improve its efforts in the delivery of education to all DHH students in this state, not just to those attending MSD. MSD, as an institution whose constituency is the entire State, has unique problems and characteristics.

        Nonetheless, I believe that it is wrong and wholly unwise to establish a referent group to scrutinize MSD, alone. I am utterly aghast that the Department has kowtowed to Ryan Commerson and his demands and threats. I am horrified that much of our scarce public money will be dedicated to appeasing the Agitators. I want to know exactly how much money that will be.

        I do not want the children of Michigan to learn the lessons that Commerson and his ilk wish to teach them. I do not believe that anyone other than Ryan Commerson, himself, bears any responsibility for what Commerson may do to his health if his demands are not met.

        (snip)

        The Department should never reward methods and tactics such as those Commerson and his cohorts employ. If Ryan Commerson chooses to resume his hunger strike, that is his personal choice, made as an autonomous adult; he, and he alone, must accept the consequences of his behavior. He should not be allowed to hold the taxpayers of Michigan hostage to his demands and threats.

        Thank you for your time and attention.

        Sincerely,

        Celeste D. Johnson, M.A.

        Permalink 18 Comments

        Worst Parents Of The Century Award

        January 28, 2008 at 8:35 pm (Deaf Civil Rights, Deafness)

        The worst parents of the century award goes to the parents who returned their deaf adoptee like a piece of suitcase. The kid wasn’t eligible for a cochlear implant and the family was learning American Sign Language, but upon discovery that the mother was pregnant, the deaf child went back to the adoption agency.

        What kind of person are they? “Hey, I’m preggers! Let’s get rid of this kid so I don’t need to learn American Sign Language anymore!”

        That’s the message they’re sending to the world. They’re screaming to the world that they’re not willing to make sacrifices for a child that deserves to be loved and cared for. They’re also screaming that they’re not up to the task of being a parent. Any decent human being would know that you make sacrifices for your child and not the other way around.

        It’s bad enough that the Deaf Community is already full of wounded adults fuming over their parents’ and the larger society’s tacit rejection of them. Now we have this? I thought things like this only happened in the Dark Ages. It’s terrifying to think in 2008, something like this could happen and there’s only silence in answer to this outrage.

        That kid’s going to have an emotional scar for the rest of his/her life. I’m not one to pray, but I pray in this case that the deaf child finds a loving home – preferably a Deaf couple who signs and is capable of healing that child’s wounds.

        I also have to pity the unborn child the “parents” are going to have. What if that unborn child isn’t “perfect”? What are the “parents” going to do then? Give the baby back to God?

        Hat tip to DeafMom3 and MishkaZena.

        Permalink 20 Comments

        Coming of Age

        January 27, 2008 at 6:57 pm (Blogging, Deafness, Musings)

        After reading the blogs slamming DeafRead, I think I can say DeafRead has come of age. I do find it interesting that there are two factions who disagree with each other over everything except for one thing: there’s censorship, DeafRead is not neutral and the guidelines are not clear.

        To me as a moderate, it shows me that for the most part, DeafRead is doing its job. Aside from some bugs and human errors, DeafRead is posting blogs and vlogs that neither factions are happy with. There’s talk about setting up another aggregator to suit the desires of those factions, which is fine with me. If people can pull that off, then great! I’ll register my blog with that aggregator too if my blog fits their criteria.

        But in all honesty, I don’t think people realize how difficult it is to code one from scratch. Look at DeafPulse for instance. It’s buggy and spams v/blogs with pingbacks and I ended up blacklisting DeafPulse pingbacks from my blog.

        Coding is very difficult. During my teenage years, I played a free online game that was all text. People who knew C and C++ would create those games and people from all over would play it. At its inception, like DeafRead, the users were small in numbers. It also was volunteer run. But as it grew, the more complaints there were.

        There were conflicts amongst the players themselves and with the administration. So when those conflicts played out, there were quite a few who stood up and left, shouting that they would set up their own game and attract the rest of the players to their game.

        Invariably, those games would fail because they didn’t know how to code well enough and often also were tyrannical toward their own players. So those complainers would come back to the game they originally left. They never stopped griping though and the administration was stupid to ignore all of the criticism leveled against them which came back to haunt them. Some of the criticism happened to be valid.

        I for one though, don’t see the DeafRead team ignoring all of the criticism that’s aimed towards them. One criticism to me that I think is valid is the conflict of interest situation with the DeafRead Awards.

        If DeafRead wants to present a professional and impartial image, the editors should be exempt from receiving the v/blog awards. The DeafRead team deserves its own special recognition, separate from the awards ceremony and hopefully that will happen sometime from us v/bloggers. There will always be a perceived bias if they are eligible for the awards, whether true or not. It’s a human nature thing.

        So, if there is a v/blog award ceremony next year, I hope the DeafRead team does recuse themselves from being eligible for the awards. I don’t think it’s fair for the editors to recuse themselves right now for this year’s awards, because that would throw off everything. For things to be fair for this year’s, we would have to re-nominate and re-vote then be ready for this Saturday.

        It’s impossible to please everyone and I definitely see DeafRead going through a growth spurt. Some things may not have caught up with this growth spurt and I hope DeafRead takes action to remedy those things in a timely manner. This is truly on an unprecedented level – so many v/blogs sharing their thoughts and ideas and there are more on the way. It is my sincere opinion that the Deaf Community is not used to the freedom of speech aspect. We’ve been ignored and oppressed for so long that this whole thing is so new to us.

        Here’s to hoping that we come to age without too much pain. The world deserves to see our voices – all of them and thanks to DeafRead, more and more of us are being seen and heard.

        Permalink 24 Comments

        Technorati

        January 24, 2008 at 8:16 pm (Deafness)

        Permalink Comments Off

        Show Your Love for DR by Voting!

        January 22, 2008 at 2:37 pm (Blogging, Deafness)

        As most of you know, DeafRead is holding voting for the DeafRead awards on February 2, 2008. You can either click on the top of the DeafRead website, or go to DeafRead’s official blog to vote.

        Remember, you need to check your email for the confirmation from DeafRead, or your vote won’t count!

        Now for the self-promotion part! ;)

        Since I was nominated for three categories, and there are a lot of newbies here on DeafRead now, feel free to check out my blog review of 2007 posts. It has been updated to show all of the December 2007 posts.

        Enjoy.

        EDIT: I realized I didn’t put in the url. Whoops. It’s now there.

        Permalink 2 Comments

        Diversity in DeafRead

        January 20, 2008 at 2:46 pm (Blogging, Deafness)

        Normally I don’t post more than once a day, but I was surfing DeafRead and I saw people blogging for the CI blogs to stop. I feel compelled to say something on this matter.

        Has everyone forgotten the Deficit Thinkers fiasco already? Nobody owns DeafRead. Not the CI users. Not the DeafHooders. This is a place where we can exchange our thoughts, feelings, ideas then debate and refine those things.

        The cochlear implant situation is a very much part of our community. It’s here to stay. Instead of brushing it aside and refusing to talk about it, I think the best thing for us to do is educate ourselves on the technological advancements and continue to debate the pros and cons of it. Otherwise, how will we be able to share or debate with parents our feelings on it without looking ignorant?

        I have to also say that Rachel, whose blog caused such angst, is part of the Deaf Community. Rachel may not use American Sign Language and have misconceptions about many things about us, but she’s still one of us. Castigating her for who she is, isn’t going to help her feel welcome and be open to learning more about us. Rachel does not know the complexity of those issues because she doesn’t really see the need to. She is happy with who she is and considers herself to be very successful. Why are we angry about that?

        I can understand being angry when lies and misconceptions are being spread about ASL and the Deaf culture, but we haven’t exactly made ourselves very endearing to people like Rachel. When someone goes off at her, it only intensifies her and others’ beliefs and misconceptions about us.

        In my previous blog post, CI Militants, I was furious at Susanna and I now realize I may have given the wrong impression. I was furious at Susanna because she was very dismissive of us, our experiences and ASL. She’s the one who I considered to be a CI militant. She should know better because after all, she is an adult and should be open-minded enough to explore all angles to this issue. But she blatantly dismissed us and that’s wrong.

        But it’s also wrong when Deaf people dismiss people like Rachel and her experiences. It’s the reality for her and others like her.

        And I feel I need to clarify this part: while I dislike CIs in general and will not choose it for myself, I do think it’s important for us to respect other people’s decisions when it comes to CIs. It does work for some people.

        We need to continue emphasizing that the CI industry, the doctors and audiologists need to be transparent with their data, numbers and research so the parents then are able to make a fully informed decision.

        Through our v/blogs, we can be part of that. If you don’t want to discuss CIs on your v/blog, then don’t. Your v/blog is your internet home/cafe/whatever you like to call it. Your v/blog is your place. It’s your right to post about whatever you want and if it’s any good, readers will come and discuss that topic that you enjoy discussing about.

        You also have the choice of not reading v/blogs that you don’t like or agree with. Nobody is forcing you to go to a particular v/blog and watch or read that post. Nobody’s forcing you to discuss those issues that was on a particular site.

        It’s all about freedom of speech and choices. I’ve yet to find someone who 100% agrees with me and other v/bloggers on every single thing that’s been posted. So if we want to boot CI blogs off DeafRead, then someone’s going to want to boot DeafHood blogs off. Then pretty soon there’ll be no v/blogs left on DeafRead.

        Is that what we want?

        Permalink 82 Comments

        Too Many Words!

        January 20, 2008 at 12:52 pm (Deafness, Education)

        I thought I would take the liberty to recommend a few books for the newbies to our Deaf Community. The blogs and vlogs can be quite overwhelming and doesn’t always give an accurate picture on all of the issues within the Deaf Community. So I will be listing the top five books that I think all newbies should read so they can enjoy their stay in the Deaf Community more and gain a better insight into us.

        1. What’s that Pig Outdoors?: A Memoir of Deafness – An auto-biography of a man who turned deaf at age three and his subsequent life experiences.
        2. A Journey into the Deaf-World - This is an excellent book co-written by a hearing person, a hearing CODA (child of deaf adults) and a Deaf person, explaining about Deaf culture, American Sign Language, and how deaf children in general are educated and raised. It covers the broad experiences of the Deaf Community. This shows both sides of our culture and community.
        3. Deaf in America: Voices from a Culture – Co-written by two Deaf professionals, this gives an extremely detailed insight of the beauty and positivity in our culture and community.
        4. The Silent Garden: Raising Your Deaf ChildSelf-explanatory. I have not read this book personally, but it is highly recommended by those who have read it.
        5. The Mask of Benevolence: Disabling the Deaf Community – This is quite a scholarly book, written by Dr. Harlan Lane, a hearing psychology and linguistic professor at Northeastern University. This book explains a bit about the history of the DC and explores the misconceptions the hearing have about us. The scholarly aspect may cause it to be a bit difficult for some, but reading this book is truly worth it.

        Enjoy reading!

        Permalink 17 Comments

        CI Militants

        January 17, 2008 at 9:20 pm (Deafness, Rants)

        MishkaZena is doing a CI blog series, and I’ve gotten so furious at Susanna, a CI mom who’s commenting over there, that I told her I’m done with her. And I am done with her. MishkaZena is done with her as well and Susanna has been booted out of her blog.

        But you know what? I’m not done debating this. Susanna over there wrote, “Mishka, I think it’s possibly beneficial for the deaf community for you to post these blogs. But it may be entirely detrimental to parents who come across them in the early stages if they even consider choosing against a CI for an infant. That is my personal opinion. I am not neutral, I am speaking in favor of the choice which allows deaf infants to avoid such painful situations as Aaron described in his childhood.”

        So is that what it takes? Only partial information about CIs? In other words, Susanna is here to promote CIs with only partial information. She is denying and arguing against the very notion that CI users could have and do have adverse side effects, such as headaches. Susanna is also telling us that she is not here for a dialogue like other parents are. And hearing parents wonder why the Deaf Community is so angry?

        This is exactly why we are angry. Because we get brushed aside like we know absolutely nothing about this issue. Hello? We live this life. We live with the failed consequences.

        Is that what it takes to convince parents to have their deaf children implanted – the subversion of the truth?

        I also find it interesting that there’s no statistics tracking on the success/failure rates of the CIs. The CI companies do keep track of the mechanical failures, but why is it that there’s no tracking of the audiological failures? I don’t know about you, but it sure looks like hell to me that some people have something to hide.Not only is that enraging me, but when I read Rachel’s blog, about how the CIs were so successful for her. That part didn’t bother me, but what bothered me was her claim that ASL impedes speech. Tell me…. Where’s your evidence that one sense impedes the other sense? Where is your evidence that American Sign Language does impede learning of speech? WHERE IS IT?

        We walk around everyday, using all of our senses. Hearing people walk around, singing to the music they’re listening. Does singing and listening impede their walking?

        Our bodies was not physiologically designed to separate usage of one sense from the other. So when people like those two continue to whisper lies about American Sign Language impeding speech amongst themselves, other parents and to us in private… That’s when I and others get angry.

        They wouldn’t dare say that lie in public, because then it would become far too inconvenient for them to explain why baby signs are booming, and why research paper after paper after paper, starting over fifteen years ago from the Salk Institute, showing that if you know American Sign Language as a baby, it increases your language acquisition abilities!

        That’s when dialogue between the two worlds shuts down, and more and more deaf people become militant in response. That’s when the Deaf Community’s anger spills over in public, and all of the rest are stunned, wondering what the hell is going on. Well, I’m here to tell you right here and now in public: This is what is going on, and this is why we’re so angry.

        It’s bad enough that so many of us have horror stories of parents who were so fanatical about the AVT method that there were threats to their own children, like that parent who stood up during a parents’ meeting and said, “If I ever see my son signing, I am going to hang him high up at Calder Plaza by his thumbs at high noon!”

        What kind of message does that send us when there’s no wide-spread public condemnation from the hearing over those kind of comments? It’s only done in private. Never in public. Nobody is willing to stand up in public and say, “I’m sorry those things happened. What can I do to help to ensure this kind of thing will never happen again?”

        I’ll tell you what it tells us when nobody is willing to do that. It tells us that people think we are second-class citizens. That people think we are a people to be subjugated, because English and speaking is superior to anything else, and we’re not intelligent enough to recognize that.

        It also tells us that people think we don’t deserve equal communication access if we don’t speak or hear and don’t conform to their idea of what a human being should be like.

        Permalink 27 Comments

        Bilingualism Equals No Deaf Identity?

        January 16, 2008 at 9:25 pm (Deafness, Musings, Rants)

        On Jodi’s blog about deaf attacking deaf, an anonymous person wrote, “She isn’t willing to experience the emotions in her deaf feeling as she doesn’t feel a deaf identify. That is, she can speak in ASL fluently and write well. So, I don’t blame her.

        That anonymous person left a second comment, clarifying that the comment was referring to me.

        So, is that true only for me, or is that true for all other deaf who write well? Does that also mean any deaf person who is bilingual has no deaf identity? How about MJ Bienvenu, the chair of ASL and Deaf Studies department at Gallaudet University? She has a B.A. in English, and writes extremely well. Does she not have a deaf identity? Or how about Ella Mae Lentz? If I remember right, she also has a B.A. in English. Does that mean Ella doesn’t have a deaf identity?

        Let’s widen the implications of that comment and put aside bilingualism. How about people who identify themselves as more than just a deaf person, but also a gay person? A Latino? A bisexual Asian woman? The list can go on ad infinitum.

        I’m also left wondering what ‘deaf feelings’ meant in that comment. I’ve always thought that feelings were a human thing. What exactly are ‘deaf feelings’?

        I’ve experienced oppression that is unique to the deaf, like the readers of my blog serial know. Does that mean I have to hold onto my anger over that experience, or any other experience of oppression to be considered as a person who has a deaf identity? Is that part of the deaf identity – being forever angry and bitter at the hearing world and letting them know at every opportunity possible?

        I would like to think that having a deaf identity is more than just being angry at the hearing. I for one enjoy Peter Cook’s gorgeous ASL poetry. I advocate on behalf of the Deaf Community, so we can get equal communication access. Almost all of my friends are Deaf, and those who are not, know ASL. I laugh at Deaf jokes, and deeply appreciate stories that are unique to us Deaf. I celebrate our diversity, deafness and American Sign Language.

        But to that commenter and to some others probably, I don’t have a deaf identity. In other words – I’m Not Deaf Enough.

        Permalink 20 Comments

        My Ideal Deaf Community

        January 1, 2008 at 9:28 pm (Deafness, Musings)

        My ideal Deaf Community by 2020 is:

        • A Deaf Community that has taken initiative in working with the hospitals to ensure impartial, accurate and statistically sound information are provided to parents of deaf children about all options available, such as American Sign Language, Deaf Culture, Cochlear Implants, Cued Speech, and so on.
        • A Deaf Community where Cochlear Implant users are free to use their implants, and whom may or may not know American Sign Language, but fully respect ASL as a true, viable language perfectly acceptable for many deaf children.
        • A Deaf Community where ASL users or anyone else do not view CI users as cyborgs or as having deficit thinking.
        • A Deaf Community that is visible and thriving, so all parents that have deaf children know who to turn to, instead of turning to the doctors and educators.
        • A Deaf Community where the mass media (internet, movies, plays, sporting events, etc) is fully and immediately accessible via captioning and other avenues.
        • A Deaf Community that truly embraces diversity of thought and be able to debate rationally without resorting to labels.
        • A Deaf Community where the emergency notification system is fully accessible to the Deaf.
        • A Deaf Community that is strong and united enough to break through the glass ceiling of job discrimination such as having a culturally Deaf who is an United States senator, a Hall of Fame NFL player, a Fortune 500 CEO managing hearing employees, a Nobel Prize winner, an Ivy-League university president, or a Supreme Court Justice.
        • A Deaf Community where qualified, certified and college educated interpreters are fluent in American Sign Language and who are provided everywhere 24/7 without any battles being needed to be fought.
        • A Deaf Community where the transit system is fully accessible to the Deaf, like it is for the hearing.
        • A Deaf Community where there is no need to point back to the Milan Conference of 1880 and AG Bell as the source of all of our problems, but instead identify the immediate problem, and present reasonable, realistic solutions to them, then act on those with fellow community members and hearing allies.
        • A Deaf Community that is recognized by the United Nations as a viable cultural and linguistic minority group.
        • A Deaf Community where the educational system no longer produces an average of an eighteen year old Deaf person having a fourth grade reading level.
        • A Deaf Community where advocacy has reached the level of success that police officers no longer are ignorant on how to deal with the Deaf.
        • A Deaf Community where the educational system recognizes the fact that no one size fits all.
        • A Deaf Community where everyone is free and comfortable enough to use vlogs to express and exchange thoughts in American Sign Language.

        Permalink 16 Comments