CSign
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That's something but it's not enough. Kids shouldn't be sitting in classroom not learning. Any percentage of the time.
I agree with you 100%.
That's something but it's not enough. Kids shouldn't be sitting in classroom not learning. Any percentage of the time.
Often times if a DHH child is mainstreamed they will have the support of an Itinerant Teacher of the Deaf to ensure that the student is receiving proper accommodations, and that their needs are being met. Another example is that they will work 1:1 with the student to pre-load concepts, or to work on areas where the student has goals. The itinerant teacher carries the same weight as the other IEP team members, including the parents.
That's something but it's not enough. Kids shouldn't be sitting in classroom not learning. Any percentage of the time.
The teachers have so many kids with different needs in the classroom that none of them get met. I don't blame the teachers. The administration puts them in an impossible situation. Most teachers are doing the very best that they can.
Generally, large regular classrooms are best for "average" students. If the child is very bright or needs additional instruction, she/he tends to get lost in the crowd. It's all about the money and it's getting worse with the latest budget cuts.
Did you know that school teachers send their kids to private schools at twice the of non-teachers? At least that's what I read. I was one of those parents.
Absolutely. Preloading and post teaching would not even be necessary if they could just access the material in the classroom! Our deaf kids don't need freaking itinerant, glorified tutors. They need qulified, bilingual TODs. For the entire time they are in a classroom.
Plus my Internant teacher worked at different schools so if a situation came up when I needed her support, it would have been out of the question because she was out in the field giving "support" to other deaf kids who were also lost. I am best friends with one of them. Her mainstreaming experience is identicial to mine. She is now a fluent ASL user and hangs out with other ASL users.
In no way am I saying that mainstreaming is ideal or perfect. However; there is a difference between putting a DHH student in the mainstream environment without support beyond an FM system, and putting a student in a mainstream environment with an interpreter. The interpreter enables the student to benefit from their education, as it makes it accessible for them.
Again, if there is an option I am not advocating for putting a DHH child in a mainstream environment. I realize it's not perfect, nor is it ideal.
An interpreter in the mainstream is better than nothing, but it is still a very, very restricting accommodation and increasingly becomes loaded with negatives as the child gets older.
In no way am I saying that mainstreaming is ideal or perfect. However; there is a difference between putting a DHH student in the mainstream environment without support beyond an FM system, and putting a student in a mainstream environment with an interpreter. The interpreter enables the student to benefit from their education, as it makes it accessible for them.
Again, if there is an option I am not advocating for putting a DHH child in a mainstream environment. I realize it's not perfect, nor is it ideal.
Yes, an interpreter is better than nothing but if the parents had the option to send their child to a deaf school nearby, it would be better for the child. However, if there is no deaf school nearby, then I would recommend looking for a deaf/hoh program that uses ASL and English in a public school. If no luck, then better to mainstream with a terp instead of oral only.
I am profoundly deaf. I grew up in a foster home and I am glad that the welfare dept found a right school for me in the first place. I went to the deaf school from kindergarten to high school. All teachers use signs which is the best method for deaf students to understand and learn, IMO. I had speech therapy there for the first 5 years but I despised it. During my time, there were at least 500 deaf kids on campus.
When I was 16, I found out that I have a deaf brother who is 5 years older than me. I was so shocked to learn that my real mom sent him to a mental hospital where he stayed most of his life instead of a foster home and I still feel bad for him because she did the wrong thing to him.
BTW, my wife went to a deaf program at a public school. There were only 8 deaf students in her class. She wished she went to a deaf school because the teacher who signed in her class didn't teach well and the hearing students didn't talk with her socially.
One of my deaf co-workers told me about her experience at her mainstream school. She was not happy with it because since her teachers talked too fast, the interpreter had to sign very fast so it was hard for her to understand what the teachers said, therefore she didn't learn much.
I'm sorry about your brother. My mom was a rec director at a mental hospital and somehow she found out that there were two patients whose only diagnosis at the time of placement was deafness. My mom was like, wth...?!! But it had been years since they were first placed...so sad. It pissed me off whenever I think about it. But yeah, the deaf school is often the best placement because of ongoing access to language.
Okay, I'm confused. That is what I said.
I know that it can happen to anyone. Some parents just dump their children who are deformed, deaf, blind or mentally retarded away from home. My real parents was one of them. However, I thank God for putting me into the right place when they got rid of me at the age of 3.
Mom of the deaf child, I am really glad that you asked for our inputs and show your thoughtfulness about your child's future. I am proud of you and God bless you.
CrazyPaul, on the other hand sometimes it might be a good idea for the kid not to live at home. I mean I do agree with you that it is super sad that a parent can't accept that their kid is deaf blind or mentally handicapped.....Some of the grieving stories I've heard about from parents are just so.....you almost want to say " Look sweetie...you have a very healthy and normal kid who just happens to be deaf or blind. ...They can do anything a hearing kid or a sighted kid can do. Mentally handicapped thou....that's a wee bit more complciated......
WOW.. The qualifications one needs to write a post.... Even father of a deaf daughter is not enough any more...Good to think ahead. Best thing to do is to find out how much she can hear.. With moderate hearing loss and HA's she will develop speech and get around as any other kid in the neighbourhood. Totally deaf when she's an adult sounds as if the rate of losing her hearing is very slow. slow enough to be able to hear and speak..
But communication with your child Is the main thing. And sign and speech go very well together.. It's an excellent combination..
You guys are very lucky to have found out that she needs help to hear now.. And she's lucky to have her parents realise that..
Why must you persist in making predictions based on things you know virtually nothing about? You are spreading audist, oralist mythology. Parents need the truth, not some fairy story. The last I checked, you were a fisherman, not a Deaf adult, deaf ed specialist, a neurologist, a clinical psychologist, a speech pathologiist, or an expert in child development.:roll: