windz23
08-21-2007, 11:42 AM
Hi everyone, I thought I would post here because I am getting very nervous about the upcomming meeting. It is for tomorrow. My daughter is 10. When she was 8 she lost her hearing. Up until that point she was a normal hearing child. She could speak and hear and read and write. After her hearing went, we got jossled from doctor to doctor. They are still unclear exactly what happened. She was going to public school and because they were unable to give her the help she needed, they sent her to CID in St. Louis. This is a really good school for the deaf, but unfortantly only teach verbal skills. When I asked if they could get an interpreter in at her public school, I was told that they could, but first she would have to be fluent in ASL. I decided to send Abby to CID and got her the implant. She was at CID for about a year and a half. School has just started, and she is back at public school. I asked for this IEP meeting to ask again for an interpreter. This time I am asking that they teach her ASL so she can become fluent.
The people at the school are very nice. I have already met with her teacher, the nurse, the speach teacher, and the special ed teacher for reading and math. I explained everything they need to do in the class setting to help Abby succeed. We are also in the process of getting Abby a FM system to help her hear in the class setting.
Here lies the problem. From what I understand, the school doesn't have to supply Abby with a teacher to teach her sign if they decide they don't want to. They can say that she has the implant and that she can read and write, so therefore has a mode of communication that is "good enough". (by law) I am nervous that this is what they will say, even though I have the support from the teachers and the nurse I have met with. They were very well informed and understand my fustrations when people assume that the implant is the cure all. It is a tool, but not the answer to deafness. My daughter does very well with her implant. She went to hearing nothing to understanding speach about 75% of the time. I am worried about that missing 25%. I am worried about what will happen when parts need to be replaced, or when there are times when she can't wear her earpiece. Is she expected to spend those times out of school? Is she expected to read lips and written notes in class and try to keep up?
When Abby first lost her hearing, I had no idea what the best thing was for her was. I know now that signing is the answer. That using all the tools available will guild her to a full and promising future. Now I just have to convince the school of this.
Fustrated and Worried in IL.
Mandy mother of Sebastian 12 (hearing)
Abigail 10 (deaf w/CI)
Xavier 6 (hearing)
The people at the school are very nice. I have already met with her teacher, the nurse, the speach teacher, and the special ed teacher for reading and math. I explained everything they need to do in the class setting to help Abby succeed. We are also in the process of getting Abby a FM system to help her hear in the class setting.
Here lies the problem. From what I understand, the school doesn't have to supply Abby with a teacher to teach her sign if they decide they don't want to. They can say that she has the implant and that she can read and write, so therefore has a mode of communication that is "good enough". (by law) I am nervous that this is what they will say, even though I have the support from the teachers and the nurse I have met with. They were very well informed and understand my fustrations when people assume that the implant is the cure all. It is a tool, but not the answer to deafness. My daughter does very well with her implant. She went to hearing nothing to understanding speach about 75% of the time. I am worried about that missing 25%. I am worried about what will happen when parts need to be replaced, or when there are times when she can't wear her earpiece. Is she expected to spend those times out of school? Is she expected to read lips and written notes in class and try to keep up?
When Abby first lost her hearing, I had no idea what the best thing was for her was. I know now that signing is the answer. That using all the tools available will guild her to a full and promising future. Now I just have to convince the school of this.
Fustrated and Worried in IL.
Mandy mother of Sebastian 12 (hearing)
Abigail 10 (deaf w/CI)
Xavier 6 (hearing)