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#361 (permalink) |
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Registered User
Join Date: Feb 2005
Location: Norway
Posts: 4,706
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In another thread, there was mentioning about bridging the gap between "deaf" and "hearing"....
I started off with a wish to get into Deaf culture and hold on to that while Lotte grows up. But there is also reality. Deaf culture has to be around in order to be part of it. Hearing parents cannot always just do that, since sign is foreign to them as well. Still, I read Harlan Lane, learned sign, Lotte to a deaf school etc. Choosing CI does not reduce the wish to engage with Deaf culture, and learn sign language. What does reduce that wish is the attitude and ignorance at times from the Deaf. Calling parents names, saying that they don't love their child, that they don't accept their child. I have been around in order to show a different side compared to the assumptions that are around. But is does not help most of the time. The ignorance is still there. Also with people to whom I explained time and time again how CI works. The insults are still there, The assumption are still there. THAT is what nowadays turns me off about Deaf culture. And when the decsion is made for CI, no matter how much one would like to continue sign, it will become obvious that the child will lead the way. It will show when to use speech, when to use sign. The parents will notice what works and what does not. So, bridging the gap has to come from both sides, and one of the main thngs in doing so, is accepting that hearing parents handle with the best interest for their child. They DO know what they are doing. My focus on Lotte, who is doing great with Ci, is because of the huge focus on children that do not do well. And that is not strange... in this (Deaf) culture, the focus is on how CI doesn't work, how children fail, how parents refuse to learn sign. And with that tunnelvision, it is only that what is seen. Because think of it... how many parents will spend time on being abused, and misinterpreted. Not many, and since I have been here, I have seen quite some parents of which Deaf culture could have learned a lot go away. And I have to say... I also have the feeling sometimes that there is nothing to say here. Actually, that's not the case. There's lots to say, but there is so much denial that there's no listning. There's so much focus on failure that no-one listens to succes. But fortunately, there are people that do listen, think freely, look beyond their lack of hearing. And these people are happy for children that benefit from CI. Because the focus sometimes seems to be on how Deaf culture should be perserved... not how deaf children can be helped. And they can be helped in different ways. It can be by raising the child in a Deaf culture, with sign, whatever. It can be by raising the child with the ability to hear.. In the end, it's all about the child. And THAT is what is often forgotten...
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. The limits of my language mean the limits of my world. . . . Ludwig Wittgenstein (1889 - 1951) ![]() Information about . . . . . . . . . Lotte Sofie . . . . . . . . . How the ear works . . . . . . . . . Parents info . . . . . . . . . Nonsense/ Myths about CI here or here. |
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#362 (permalink) | |
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Prayers for my dad.
![]() Join Date: Nov 2003
Location: Ohio
Posts: 22,819
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Quote:
It's a disappointment. You're not being fair not at all, not one bit. I'm just so fed up with hearing parents who decide to have their child implanted because they believe it will help the child in listening and speaking and these skills will help their child fit better with their family and the hearing world, again it's all about them, not the child. You see my point? Where's sign language in this, where's the deaf community in this? I don't see any of that coming from you Cloggy, You decide to wait until the child decide which world she prefer, when she would have no knowledge of sign language, no knowledge of the deaf community because of that you blind her out of the other side of the deaf world. As you said, You no longer signs to her because she reply on speech, does that give you a right to cut that out of her life now just because she no longer uses signs? That just pissed me off even more, I'm outta here.
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Avoid being a victim of a stroke, a stroke can happen to anyone at anytime. You will never know how devastating this could be until you had live through it. It affects everybody. So Support Stroke Awareness to find a cure and hope.
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#363 (permalink) |
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Registered User
Join Date: Feb 2005
Location: Norway
Posts: 4,706
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Sure Cheri
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. The limits of my language mean the limits of my world. . . . Ludwig Wittgenstein (1889 - 1951) ![]() Information about . . . . . . . . . Lotte Sofie . . . . . . . . . How the ear works . . . . . . . . . Parents info . . . . . . . . . Nonsense/ Myths about CI here or here. |
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#364 (permalink) |
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Sussi *7.7.86 - 18.6.09*
![]() Join Date: Jan 2004
Location: Germany
Posts: 31,038
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Cloggy, Did you expose Lottie to mix with deaf and HOH children or meet the parents of deaf or HOH children? (no matter deaf or hearing parents)... Example first step is at kindergarten..., family club, or whatever then later deaf community to know the parents of deaf and HOH children better?
I think itīs important for Lottie to recongize who really she is and can make friends with deaf & HOH children... she will feel comfortable to know that she is not only one... She would feel uncomfortable when she know she is different as hearing people, thatīs why I suggest you to expose her with deaf or HOH children then she will know who she is. If you let her then she will know which she prefer to... and feel comfortable... All what I want to say that Lottie is lucky to have great parent who come to register Deaf forums to learn anything which our parents doesnīt at our old times. |
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#365 (permalink) | |
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Registered User
Join Date: Feb 2005
Location: Norway
Posts: 4,706
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Quote:
Why does she need to be forced to make friends with other deaf children. Don't worry - she will meet them.. in time. Thanks.... but don't hold the late arrival of internet against your parents...
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. The limits of my language mean the limits of my world. . . . Ludwig Wittgenstein (1889 - 1951) ![]() Information about . . . . . . . . . Lotte Sofie . . . . . . . . . How the ear works . . . . . . . . . Parents info . . . . . . . . . Nonsense/ Myths about CI here or here. |
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#366 (permalink) |
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Registered User
Join Date: Apr 2007
Location: Ohio
Posts: 1,153
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Cloggy,
I dont think Liebling meant that you should force her to be with other deaf kids. But she is young enough that she could be exposed to both worlds and that would give a choice later on in life. Am I right Liebling? However, some of you need to realize that not all countries are like the US. In the US it is easy *usually* to go from an area like mine *no deaf* to an area like Columbus *alot deaf* in a very short drive. Maybe, Im not saying Im right about this. But MAYBE it isnt easy for all parents to be able to join deaf events or deaf clubs because of the distance. I would say it highly depends on the area that a person lives in, and what source of income they have to judge how often you could be around the deaf community. Before I got a computer, I pretty much had no contact with the deaf community. Mostly due to not knowing where to go. But also, the deaf community does have its negatives. And because of those negatives, I chose to have minimal contact with it. Doesnt mean I cut off all contact, its just not something I wanna expose myself to on a daily or even weekly basis. Try to consider when making these statements, location and income. |
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#367 (permalink) |
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Prayers for my dad.
![]() Join Date: Nov 2003
Location: Ohio
Posts: 22,819
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I owe you an apology Cloggy for what I said recently on this thread after reading your post on another thread, I have second thoughts about you, Your aren't too bad as I thought u were.
I hope you accept my apologies.
__________________
Avoid being a victim of a stroke, a stroke can happen to anyone at anytime. You will never know how devastating this could be until you had live through it. It affects everybody. So Support Stroke Awareness to find a cure and hope.
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#368 (permalink) | |
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happily engaged
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Location: the heart of my love
Posts: 4,306
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Quote:
and what can we say if parents of a deaf child are poor and live in an area where other deafs are rare.. what could they do ? Would signing be a better choice or CIs in this case ? depends on each individuals life conditions,IMO |
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#369 (permalink) | |
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Registered User
Join Date: Feb 2005
Location: Norway
Posts: 4,706
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Quote:
__________________
. The limits of my language mean the limits of my world. . . . Ludwig Wittgenstein (1889 - 1951) ![]() Information about . . . . . . . . . Lotte Sofie . . . . . . . . . How the ear works . . . . . . . . . Parents info . . . . . . . . . Nonsense/ Myths about CI here or here. |
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#371 (permalink) | |||
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Sussi *7.7.86 - 18.6.09*
![]() Join Date: Jan 2004
Location: Germany
Posts: 31,038
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[QUOTE]
Quote:
Quote:
Force? I thought I offer you my friendly suggestion/advice. Quote:
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#372 (permalink) | |
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Registered User
Join Date: Jun 2005
Posts: 3,384
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Quote:
Cloggy mean- why force LOTTE to make friends. Fuzzy
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. A 'No' uttered from the deepest conviction is better than a 'Yes' merely uttered to please, or worse, to avoid trouble. Mohandas Gandhi . |
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#373 (permalink) |
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Sussi *7.7.86 - 18.6.09*
![]() Join Date: Jan 2004
Location: Germany
Posts: 31,038
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Excuse me, I do read Cloggy's post... I know that he did NOT POINT his finger on me or accused me for force him ...but stated his post in general way ... I would say something different if he point his finger on me and accused me but he didn't.
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#375 (permalink) | |
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Registered User
Join Date: Feb 2005
Location: Norway
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Quote:
My hands - the are holding the cards when I play cards with Lotte. She also holds the cards in her hand. Then she asks me if I have a certain card, I ask her.... We couldn't sign if we had wanted to. ![]()
__________________
. The limits of my language mean the limits of my world. . . . Ludwig Wittgenstein (1889 - 1951) ![]() Information about . . . . . . . . . Lotte Sofie . . . . . . . . . How the ear works . . . . . . . . . Parents info . . . . . . . . . Nonsense/ Myths about CI here or here. |
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#376 (permalink) | |
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Banned
Join Date: Jun 2006
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#377 (permalink) | |
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Registered User
Join Date: May 2005
Posts: 1,645
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Cloggy - Nice pic! Gotta love card games! Sounds kinda like "Go Fish?"
Do you have a ........?
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#378 (permalink) |
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Registered User
Join Date: Mar 2006
Location: Beautiful British Columbia
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Even as an adult with better eye-hand coordination as a child, I found it extremely difficult to play cards AND sign! Let alone for a child with little hands, having to hold them all up AND sign "do you have a....."
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#379 (permalink) | |
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♥"Concrete Angel"♥
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Quote:
Are you serious?...my son signs with one hand while hes holding the cards on the other hand and so does my husband and I.... Nothing is impossible, people can do it if they try... Cute little girl....*smiling*
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"When we do the best we can, we never know what miracle is brought in our life, OR in the life of another." ~ Helen Keller |
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#381 (permalink) | |
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♥"Concrete Angel"♥
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Quote:
Hello? did you forget Im not native ASLer either are my children....
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"When we do the best we can, we never know what miracle is brought in our life, OR in the life of another." ~ Helen Keller |
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#382 (permalink) |
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Registered User
Join Date: Apr 2003
Posts: 15,730
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You know, Angel, as much as I hate having to tip-toe lest I offend someone, if you would re-read, you would see that I was actually supporting what you were saying except it's on an incrementally higher plane of skill.
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#383 (permalink) | |
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♥"Concrete Angel"♥
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Posts: 19,089
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Quote:
I did read your post I thought you were replying this to Neecy and I had to remind you that I'm not a native ASLer either are my children , I'm sorry you thought I was being offend which I wasn't...
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"When we do the best we can, we never know what miracle is brought in our life, OR in the life of another." ~ Helen Keller |
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#384 (permalink) |
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Join Date: Mar 2006
Location: Beautiful British Columbia
Posts: 1,409
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Okay so some can and some can't. If somebody can't (like me) I can only hope it won't be used to bring up a case of bad parenting ( like almost everything else in this forum is ) and yet another example of how a parent of a CI-implantee is suppressing their children's "deaf identity"....I could immediately see where this was heading.
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Friends are angels that lift us to our feet when our wings have trouble remembering how to fly. |
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#385 (permalink) | |
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♥"Concrete Angel"♥
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Posts: 19,089
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Quote:
And about the "deaf identity" well, what can I say, I admit I was upset about that yeah....
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"When we do the best we can, we never know what miracle is brought in our life, OR in the life of another." ~ Helen Keller |
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#387 (permalink) | |
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Banned
Join Date: Jun 2006
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#388 (permalink) | |
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Let It Snow!!!!
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There are Deaf poker tourneys and stuff like that. Cards are not an obstacle to our communication needs.
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"Wine improves with age. The older I get, the better I like it." --- Anonymous |
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#389 (permalink) |
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Registered User
Join Date: Feb 2005
Location: Norway
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Lotte was 4 at the time... your son is ????
__________________
. The limits of my language mean the limits of my world. . . . Ludwig Wittgenstein (1889 - 1951) ![]() Information about . . . . . . . . . Lotte Sofie . . . . . . . . . How the ear works . . . . . . . . . Parents info . . . . . . . . . Nonsense/ Myths about CI here or here. |
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#390 (permalink) | |
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Sussi *7.7.86 - 18.6.09*
![]() Join Date: Jan 2004
Location: Germany
Posts: 31,038
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Quote:
It's really not hard what some people thought. Cloggy, Lottie grow big now... she look cute ... |
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