Your early intervention services may be provided at home, but what exactly is preventing you from contacting other parents in your area to arrange play dates, activities, and get togethers? It just doesn't make sense that you have no contact with other parents of deaf children, particularly since the area you are in has not only Clarke School, but a School for the Deaf, as well. We found out only 3 months ago about her hearing loss. I have not yet (through Clarke or anyone else met anyone with a hearing loss or child with hearing loss. I have seen children with hearing aids in the audiologists office but that's about it. When Natalie begins the toddler program at Clarke I will be in contact with other parents because each room has another room attached with a 3 way mirror where the parents sit. That has not happened yet so I have no contact. I don't know why you're so against me reaching out to people here?
It helps if you use another font color so your replies can be distinquished from the questions. I'm not against it, but it certainly is not the most effective way to expose your child to other deaf children or to socialize with other hearing parents. I raised a deaf kid. I never had any problem finding other deaf kids for my son to play with or deaf adults for me to socialize with.
You'll prove us wrong? There is another red flag. Why is it so important to you to prove a bunch of strangers that you claim have been nothing but rude and nasty to you wrong. If you believe you have been treated so unfairly, the logical and reasonable thing to do would be to leave. You have no committments to anyone here. You didn't pay for your membership here, so it can't be a matter of getting your money's worth out of a membership fee. We are strangers to you, and have no effect on you one way or the other. So why this need to prove us wrong? I've already answered this question in a previous post.
So why do you keep doing it if you don't know why it is so important to you? It might be worthwhile for you to examine some of your own issues.
Funny, last night you stated that you might consider ASL at some future point if her hearing got worse, but didn't see it as something she needed now. That is certainly a huge change in philosophy in less than 24 hours. So what changed your mind so quickly? I've never heard any of the reason why to learn ASL. I've only been told why for Natalie, it's not needed. I had no idea there could be social effects if ASL is not learning until a previous post. I was also told with her age and hearing aids spoken language would be natural and easy for her which seems to be contradicted by many of the comments here.
Are you in the habit of just accepting people's word without doing any investigation of your own? You just accepted what they told you without question?
And you found no others? Particularly the ones that are focused toward hearing parents? No, I found this and stopped looking.
Are you in the habit of just taking the first thing that comes along without looking at other options? That seems to be a pattern.
Where did you call? Answered in a previous post, yet none of your business.
Yeah, I didn't expect you to be able to actually name a place you had called. Another one of those predictable things.
What do you see as the benefits of adding ASL to the environment? Less social effects, easier communication, ability to express herself with a language that may feel more natural to her, not having to rely on her weakest sense to communicate with others, and obviously it would help her fit in better with the deaf/HOH community.
Wow! You figured all that out in less than 24 hours all on your own? No one here has told you that. Odd that it didn't occur to you earlier if you were able to figure it out all on your own. Yet, you just accepted the oral /aural environment without quesion.
You changed your mind regarding ASL very quickly. What happened to create such a drastic change in philosophy in such a short period of time?
I was presented with information that I knew nothing about in relation to the emotional and social effects of NOT knowing ASL for a person who is HOH.
Where did you get presented with all this information? There have only been 1 or 2 posts even mentioning ASL, and none with that extensive information.
Now they are all in one convenient place. Should be easy for you to answer them.