Guest guest Posted February 16, 2008 Report Share Posted February 16, 2008 Hello, I am new to the group. I was homeless until now, meaning I do not know what group I belong to, since I had been given several diagnoses, we rule in, then we rule out or better put, in the process of ruling in and/or ruling out. the doctors are not done yet, my 7 y/o daughter and me are waiting for another " official " diagnosis. ....But yes, Chelsea did not speak until age 4 and some, yet recognized words and clicked the right objects and right letters that correspond to each other. This was when she barely sat up straight in front of a computer. She was echolalic. Was frustrated. We changed MDs 4x, until one was smart enough to recommend a neurologist. Positive for Subependymal grey matter heterotopia in the lateral ventricles of the brain, via MRI. She had other Dx, ASD, PDD, MULTIPLE MIXED DEVELOPMENTAL DELAY, RECEPTIVE AND EXPRESSIVE LANGUAGE PROBLEM, lately, Central Auditory Processing disorder. I am facing another IEP, to be scheduled yet. What should I tell them as far as the doctors changing her Dx, because now, they are trying to rule out autism, that one definitely thinks its CAPP, and one is not sure it but would consider it. Should I stick to what ever it is on record in the school, or change it everytime the docs make a change? How would one diagnosis affect my daughter's IEP? thanks emayhlmee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2008 Report Share Posted February 17, 2008 With the exception of autism, I'm not sure how the dx affects your IEP. We never had to provide a dx to get services, and when we voluntarily said that our private SLP said it was apraxia, the school SLP disagreed and they gave us a lesser level of services anyway. They should be basing your services on their own evaluation of your daughter. They should be able to identify the deficits that need remediation, separate from the dx. If you feel that the level of services is inadequate, a doctor's letter can help you get more sometimes, but it is still no guarantee. in NJ > > Hello, I am new to the group. I was homeless until now, meaning I do > not know what group I belong to, since I had been given several > diagnoses, we rule in, then we rule out or better put, in the process > of ruling in and/or ruling out. the doctors are not done yet, my 7 y/o > daughter and me are waiting for another " official " diagnosis. > > ...But yes, Chelsea did not speak until age 4 and some, yet recognized > words and clicked the right objects and right letters that correspond > to each other. This was when she barely sat up straight in front of a > computer. She was echolalic. Was frustrated. We changed MDs 4x, until > one was smart enough to recommend a neurologist. Positive for > Subependymal grey matter heterotopia in the lateral ventricles of the > brain, via MRI. She had other Dx, ASD, PDD, MULTIPLE MIXED > DEVELOPMENTAL DELAY, RECEPTIVE AND EXPRESSIVE LANGUAGE PROBLEM, lately, > Central Auditory Processing disorder. > > I am facing another IEP, to be scheduled yet. What should I tell them > as far as the doctors changing her Dx, because now, they are trying to > rule out autism, that one definitely thinks its CAPP, and one is not > sure it but would consider it. Should I stick to what ever it is on > record in the school, or change it everytime the docs make a change? > How would one diagnosis affect my daughter's IEP? > > thanks > emayhlmee > Quote Link to comment Share on other sites More sharing options...
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