![]() |
|
|||||
|
|
#241 (permalink) | |
|
Registered User
Join Date: Jun 2006
Posts: 18,979
|
Quote:
|
|
|
|
|
|
|
|
__________________
This advertising will not be shown in this way to registered members. Register your free account today and become a member on AllDeaf.com |
|
|
|
#244 (permalink) | ||||||||||||
|
Registered User
Join Date: Jun 2005
Posts: 1,968
|
Quote:
Quote:
They are absolutely capable of understanding psychosocial implication of deafness. They are not afraid of their children's deafness - they give them gift of hearing and speaking, and neither is excluding ASL. The mere fact that both of them participate here shows their interest in the deaf culture. What you and other fail to understand, though, is this -almost everyone who replies to Cloggy's and Rick's posts is too often missing the point. Hence their focus on maintaning clear and comprehensive information about CI, and returning and sticking to the SUBJECT. Quote:
However I must clear up one thing - I am progressive sensori -neural loss, brought up as "hearing" hence HoH but my audio showed (and shows) clearly early severe to profound hearing loss. I have no CI implanted. I have applied, but was denied as I was borderline with too good oral and listening skills. Before I applied for CI I educated myself on the subject. Big help was Beverly Biderman book "Wired for Sound". A few years passed since I applied, though, and I am sure now I would qualify. But my migraine complicate the matter - the noise is a strong trigger for me. So, I am hesistant. MARIA: I asked you a question, please reply: Maria: """That HAs worked and soo much better than CI since""" Fuzzy: Better? how can you know? You have no way of knowing how CI would work for you unless you were implanted? also, Quote:
Cloggy asked you how do you know some other child wouldn't be sorry their parents didn't implanted him. You can not answer for OTHER CHILD. you don't know how the other child might feel. It may feel different than you. That is the point. You don't mind, but other child might mind very much. Quote:
The problem is the child will grow up and learn about CI. Then the child will ask - ""I found out about CI - WHY DIDN'T YOU GAVE ME A CHANCE ?! I hate it!! now is too late!!"" Rick48 Thanks, Rick. I could see thru her right away. She IS transparent. SHEL: Quote:
Quote:
Shel, it proves how little you know about CI. I would suggest to read more on the subject, then you will understand why it is once come "the earlier the better" and sometimes "the late implantees get excellent results". there is a very good reason for this, and easy answers. you just must WANT TO know them. btw this is why I am so against you making statements like "I just see CI doesn't work". It's underinformed, manipulative, and misleading statement. and the last thing the deaf community needs is more confusion. Liebling: Quote:
Quote:
Being happy and accepting one's deafness has nothing to do with wanting to hear better. CI is just a technology that is available, the only problem is that for children born deaf it's crucial to be implanted asap, and sadly there is too many misinformed and underinformed parents who lose forerver the best chances of their child hearing. Quote:
your data is correct in one aspect - that in order to reap benefits of either HA or CI one must work hard toward understanding sounds. But no matter how hard you work, if you have certain hearing loss HA will NOT work as well as CI. Quote:
Ci or HA has nothing to do with "we deaf have no problems with accepting the word". The world we are in is still HEARING. with people who don't want to sign or write. Just the fact that hearing people have problem dealing with the deaf indicates the usefulness of such technology as CI, HA and oral skills. Same way as visually impaired people use visual technology to their benefits. Quote:
What about TTY interpreters, ASL interpreters, closed captions, various devices for the deaf etc. Things are done for us too. Granted the deaf had to fight for it but so had any other handicapped for theirs - for wheelchair ramps, elevators in every building, extra wide entries, job protection, you name it. But that is what happens in real world - when you are MINORITY you are easy to overlook, and unfortunately yes YOU have to try harder than the majority. Fuzzy |
||||||||||||
|
|
|
|
#245 (permalink) | |||||
|
*slotting*
|
Quote:
Quote:
Quote:
Quote:
Quote:
__________________
Finally found Ruby, my puppy ![]() See this thread for more info. http://www.alldeaf.com/our-pets/5515...ml#post1049543 *NOTE* I will be gone on September 10 to 21 working on my temporary job @ out of the town, so just let everyone know
|
|||||
|
|
|
|
#246 (permalink) | |||
|
Registered User
Join Date: Jun 2005
Posts: 1,968
|
Quote:
Quote:
perhaps if you were truly dedicated to learn how to use CI then after a year or two of HARD WORK you would aprecciate it better. btw - what were you thinking when you wanted to be implanted? you thought it's like you wake up and bingo bango you hear? also, were you born deaf, or...? Quote:
That might be so, but that has nothing to do with how both of these work (differently) Having ASL interpreters, closed captions typers, etc. was the gift from us the Deafies to the hearing people to support themselve for their living. They should rather be thankful to us. Not everybody want to be an interpreter etc, though. Fuzzy |
|||
|
|
|
|
#247 (permalink) | ||||
|
*slotting*
|
Quote:
What's more, I can see your ignorant attitude while I was being so honestly. Quote:
I was born pro-founded deaf, my parents haven't found out till I was about 1 and half years old. So my parents and I was learning the sign language and done it very wonderful and very happy without surgery, struggling to get used, headaches, inconvience metal inside my head, whining about the CI, etc that I am having the experience right now. When I was about 5 or 6 years old, my parents was thinking about getting the CI for me, but my parents heard other little girl was having lot of problem with the CI surgical on her head, her head was growing, she got headaches every night, she crying all the times, etc. It scare my parents away from the CI. I do remember look at the brown machine thingy and I thought it was cool just because it was label as "FM" like my mom workplace Fred Meyers Marketplace and I wanted it. While I look back there from now, what was surprised me is that my parents NEVER tell me what it is for or about the surgical or anything, which pissed me off but was very thankfully to my parents to let me decide whatever I want when I get older. Anyway, I wore the hearing aid instead from my age of 3 to 12, and always arguing with my parents because I don't want to wear it and there is no point for me to wear it, till I took the speech class at my 9th age, and oddly I read lipping better compare to listening from my hearing aids. So I decide to stop wearing the hearing aids at my 12th age, and continue taking the speech class till my 13th age, the speech teacher told me that I am good at read lip and are comfortable with that than wearing anything on my ear. Thus, I should've really keep what my speech teacher said to me in my mind before I undergo the surgery for the CI. Anyway, from 13th to 19th age, I always signing, never have problem with being deaf, even I was good student equalized with other hearing people during my high school. I DID fight with the staff who works with deaf students because I don't want to go to special education, somehow my fight was a failure, but lucky the teacher at special education let me go to the library as study hall instead, I want to go to the same as hearing students went, I did very hard work, till I ended up graduated very normal as other hearing people graduated without anything that I need to done before I receive a diploma. During those times, I never think about CI, not even once. Till I became 19 and went to the Japanese class, I was really into it. I thought maybe if I can get the CI so I can learn how to speak Japanese language, so I went got CI and it was terrible for me, most of things I got CI is regret. Reason why I regret to have the CI: *Giving me headaches just like the hearing aids even though I turn it very down. *Sounds kept coming out inside the area between my nose and mouth which are hurtful that make me feel like want to get it off. The audiologist said it's because my brain don't know where to put the sounds. *The metal on my head is not convience AT ALL. Everytime I itch my head, I barely feel my skin, my ear rings all the times if I itch or shake my head or brushing my hair or whatever which are very annoying. *Change my relationship to my family members because some of them kept begging me to wear the CI makes me feel like don't want to see them again. I feel like they have no respect for "me", but only desiring for me to just "hear". *Believe those lies what the audiologist said about the CI such like can talk and hear through the phone, radio, music, etc. which does not work for me. Finally only thing that I actually benefit from the CI is: *Playing with it just for fun, it's just a toy. Quote:
Quote:
Other than that, I read one of your post, you don't have the CI. While you don't have CI, it shouldn't be your business and you have no reason to get involve into the CI situations, but taking it up to make the drama.
__________________
Finally found Ruby, my puppy ![]() See this thread for more info. http://www.alldeaf.com/our-pets/5515...ml#post1049543 *NOTE* I will be gone on September 10 to 21 working on my temporary job @ out of the town, so just let everyone know
|
||||
|
|
|
|
#248 (permalink) | |
|
Sun Whorshipper
![]() Join Date: Sep 2006
Location: A Desert Rat that has found herself in Maryland
Posts: 14,718
Blog Entries: 1
|
Quote:
__________________
~Shel~
|
|
|
|
|
|
#249 (permalink) | |
|
Premium Member
![]() |
Quote:
|
|
|
|
|
|
#251 (permalink) | ||||||
|
Hiiiiiii it's meeeeee
![]() Join Date: Jan 2004
Location: Germany
Posts: 25,540
|
[quote]
Quote:
Quote:
I know, I know... I had been repeat the same thing as you as well... Our posts are being ignored and think we are closed minded and wrong or whatever Quote:
Quote:
Quote:
*nodding agreement* I have seen the same as you as well. Quote:
|
||||||
|
|
|
|
#252 (permalink) | |||||
|
*slotting*
|
[quote=Liebling:-)));838616]
Quote:
Quote:
![]() Quote:
Quote:
Yeah I know some of my friends who are unsafisy(sp?) with the CI, some of them said that sounds are like too robotic.Quote:
![]() Thank you for the reply
__________________
Finally found Ruby, my puppy ![]() See this thread for more info. http://www.alldeaf.com/our-pets/5515...ml#post1049543 *NOTE* I will be gone on September 10 to 21 working on my temporary job @ out of the town, so just let everyone know
|
|||||
|
|
|
|
#253 (permalink) | ||||||||||||||||||||
|
Hiiiiiii it's meeeeee
![]() Join Date: Jan 2004
Location: Germany
Posts: 25,540
|
[quote] Quote:
Quote:
Quote:
Quote:
Quote:
Quote:
Quote:
*Repeat sigh* CI & HA users CAN speak and hear with their OWN WILLING. They would have no mood to learn anything when you FORCE them to do... Mainly important is positive them why you beleive in and why you think best and support them... Quote:
Quote:
![]() Quote:
If they don't want to learn to speak or hear then is their decision... If they want to wear HA and learn to speak and hear then is their decision. If they want to have CI out of curious then is their decision. If they want to have CI and learn to speak/hear then is their decision. It's mean is that they are happy and accept what they are... that's what I am trying to explain. Please don't twist it. Quote:
Quote:
I have met many late deaf in spa last year. They decided for HA (special HA - mould inside their ears). They are happy with their decision... Some decide for CI because they are happy. It's about their own willing with no force from anyone. You think CI are only who can help children to hear and speak which I respectfully disagree. Let me share the example: Computer do nothing because you can't do anything to add something in the computer. Computer do something only if you add something to create in the computer. It's an exact same with HA or CI... The HA or CI children will do NOTHING without parent's support/education. The parents feed their HA or CI children with speak/hear development. It depend on different child who is willing to learn anything or lazy to learn anything... It's same with hearing people as well... Without their own willing, HA or CI will not works. That's why I leave my child's choice. I will support if he/she has strong willing to learn anything. Quote:
Quote:
Quote:
Quote:
Quote:
Quote:
I remember few of closed minded and ingorant co-workers complaint to my boss that they lose their waste time to walk to me or email to me because I can't phone. I asked him a question front of my boss: Do you have problem to use email, walk to computer room to use fax or walk to my office? and then look at my boss - then question him "Did you see me complaint that I walk to his or anyone's office for discuss about work issues or for not have fax machine in my office but just email"? I rather to walk because it's good execise for me than email to them. All what I see is that they complaint that I can't phone... Now they know what I am - we get on well with no problem for over 15 years now... ![]() Quote:
Quote:
|