Today was my son's IEP. Every year we sit at a big table and dig through the many details of his education. Today for two hours we preformed this well rehearsed task. I am really tired.
The cool thing is the district is awesome. There are a couple of issues regarding team interpreting for lectures but really given the red tape it takes to get approval I am impressed with the services and attention to detail the special education folks provide. They have years of experience with deaf education and listen to me when I have an opinion. For the first time I really feel like everyone at the table really wants my son to get exactly what he needs and has the power to make it happen. There was even a general education teacher at the table who is very dedicated to my son. She has done independent research and is determined to do the best she can to make sure my son's experience is on par with the other kids. Amazing. I walked away knowing everyone is learning but that I can trust the learning is happening, even with me.
It has been years of figuring out how to communicate my opinions that got me to this table. This is why I am tired tonight. I have researched for years. I have learned the law and jargon. This is a component of raising a deaf kid that only a parent really at the end of the day understands. It goes beyond your child's development and progress into a whole new academic world. A world that is foreign, off your radar.
While deciding on how you will raise your child you are also called on to protect that decision before you even get a real understanding of what that decision is. You are left to figure out how to negotiate, how to get to yes. You have to develop tools to ascertain who is really knowledgeable and who is intrenched in personal bias. You have to wiggle around "privacy" issues to get to the heart of why things happen. You have to hope you can create a team and not adversarial chaos. The most important thing is you have to do is
Leave your emotions at home.
So I am tired tonight after a good IEP. I walked away with a sigh of relief and grateful hope. My son skipped his meeting for the first time. He had a twelve hour day today and he was stuck in rehearsals. He was a bit ticked about missing it but the law has requirements and his birthday is sneaking up. On that night his show will be interpreted for the community.
Showing posts with label IEP. Show all posts
Showing posts with label IEP. Show all posts
Tuesday, November 2, 2010
Wednesday, April 28, 2010
Part Two- The Pediatrician
The parents called the pediatrician who was very supportive and wanted to have them come to her office for an appointment. The tone I got when the conversation was relayed to me was she wasn't sure there was an issue but would help the parents any way she could. There was about a week waiting for this appointment.
They took her for the appointment and the news back I received was my student had a really bad infection in both ears and failed the hearing test administered in the office by the pediatrician. The parents were told they needed to treat the infection before they moved forward. They put her on antibiotics for two weeks and scheduled a return appointment.
Meanwhile they were referred to an ENT who felt the who issue was related to the infection and fluid and if needed they could give her tubes. They were told to wait for the infection to clear before worrying about a hearing lose. They were told that if this was the issue she should be just fine once the ears clear up. They see it all the time.
An SLP friend told me that is not always an effective course of action.
I am a parent who remembers the waiting. I continued to document my observations and teach her ASL. It was interesting to me that she never showed signs of pain in her ears. It was a surprise that the language delay was not a factor. Her delay was severe in my opinion and it may be an indicator that this has been an ongoing infection, hearing lose, processing disorder, motor control or something else hindering her language acquisition over an extended period. At this point it is all medical focused on the infection. The duration of the infection didn't seem to be a concern. I was thinking about the whole child. Regardless of the source of her delay she needs to catch up with her language if she is going to experience productive brain development. She needs language for typical social emotional development. She needs language for typical abstract critical thinking skills. At this point her expressive language hindered that.
So my strategy was to provide a natural language while we wait. ASL is very natural for her. It allowed her to participate. I was also worried that if there was a hearing lose that would benefit from hearing aides the sooner we know that the better. Of course we would have to wait to fit them given the current condition of her ears but that information would be so helpful. At this point I am not sure if she has any lose since she responds most of the time to conversation and environment. I want an accurate hearing test. I suggest they ask for an ABR.
I was also working on her social strategies and verbal confidence.
At the second appointment the parents were told the infection had not responded to the antibiotics and a stronger one was prescribed. The pediatrician washed her ears out which was very uncomfortable. She tells them it would be wrong to put her though more tests right now so no ABR.
When I talk about "breaking the fourth wall" I imagine life trying it out. Let the audience interact an become part of the play. Let the professional see the audience and really interact on a humane level.
Weeks have gone by. In a child's life it is more like dog years.
Next stop..... the audiologist
Labels:
asl,
deaf,
early intervention,
IEP,
kid,
school,
special education
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