Home General Discussion Special Ed and CAPD Going to add a Special Ed section to site
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Mom2Boys
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Going to add a Special Ed section to site

Based on the discussions I've seen in the message board, I think it would be very useful to add a Special Ed link in the main menu and provide some information about special ed with regards to CAPD. I was wondering what everybody would like to see in this section. I'll research and compile as much info as I can find. If you can provide any resources please do pass them along as well.

Thanks!
Bonnie



Edited By:  Mom2Boys
Sep-21-09 18:16:53

Mom of 2 boys: James (6 & CAPD) and Michael (3)

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duranie
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Re: Going to add a Special Ed section to site

Would this be an area where we discuss the process of dealing with the school system?  I've been contacted today by our son's school about a "screening meeting", which means they want to get together, figure out what testing THEY want him to do in order to justify having an IEP or not.  Needless to say, I'm not happy about it, it seems like a reason to waste time instead of getting the therapy started NOW.


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Re: Going to add a Special Ed section to site

Hi Diana,
I'm so sorry to hear the school is using their tactics to keep things in limbo. We went through the same merry-go-round with our school. The fact is, if you have outside tests, they MUST consider those when making a decision. They do not have to make their decision based on them (as we found out the hard way), but they must at least review and take them into consideration. If you have an audiologist who says he has CAPD, and the school's audiologist says differently, you may have to go out and get another assessment done by a third audiologist. Or hire a lawyer. You might consider bringing an advocate to the screening meeting. Do you have funds to afford one? They often charge $75-$150 per hour. But having one right off the bat is a great idea because then you're showing schools you're serious.

You can definitely talk about all these issues in this section (Special Ed and CAPD) on this chat board. The area of the site I'm talking about is an informational area, like the Therapies or Diagnosis sections in the blue bar at the top. Seems to me that special ed is a particular challenge for CAPD, so I wanted to put together some resources to help parents make their case. One of the problems with CAPD is it's not specifically delineated as a learning disability. There is ambiguity over where it lies in the IDEA, or if it lies there or not.

I would just love to hear the concerns parents have faced, or the solutions they have found, in getting special ed services for their child. I know we have had an uphill battle, and I would love to shortcut anybody else's attempts to get their child help. My mom asked me the other day why I built this site if I don't make any money out of it. And that is why... to save somebody else time and heartache in their search for an answer and get help. I cannot tell you the adversity I faced in order to get my son diagnosed. We all need to band together and education the school systems. Our children are faced with a serious learning disability, and somebody has to recognize it, $%$*#!

Thanks,
Bonnie


Mom of 2 boys: James (6 & CAPD) and Michael (3)

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duranie
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Re: Going to add a Special Ed section to site

The thing is Bonnie, this audiologist IS the school's audiologist.  The reason they want to do more testing, from what they say, is that they want to see if they think he's significally impacted enough with this condition to need this treatment.  I can tell you right now our son makes mostly B's, a couple of A's and a C.  This year, the progress reports for 3 of his 4 classes say he's making A's.  But the reason for that is because I am so involved with his schoolwork.  I call the school, or email the teachers, when Matthew has no idea how to do something he brings home.  I have to contact the teachers to find out why he missed a problem or question so I can make sure he knows why he missed it, and explain it to him so he won't miss it again.  There is no way he'd be making the grades that he does right now if I didn't do so much to keep up on it.  I look at his homework every night, questioning him to make sure he's doing it the way it was intended.  I make sure he keeps his binder organized and neat so he can find things.  I ask him every day to make sure he's got his homework written in his agenda book.  Do they really think all parents do that?  I can guarantee you they don't. Most parents say "how was school?" and that's about as far as they care. 

Now, we have this "screening meeting" next Tuesday.  I have paperwork on Matthew's past testings, including his PPVT, his Wechsler Intelligence Scale for Children test, and his Woodcock Johnson Test of Achievement.  I need to get paperwork on his 2005 diagnosis of Cluttering.  All I can find on that is copies of the IEP paperwork, and none of those have any copies of the testing they did.  The more I read about CAPD, the more I am convinced it does tie somehow with cluttering and other learning disorders.  I am also going to ask his English teacher who has CAPD to be involved in this meeting. 

From what I understand of this meeting, this will be a meeting where one of his main teachers will be there, a special education teacher, and some other person for the school.  I want to make sure I have all the paperwork I can get with me, to show the past diagnosis he had, and the ways he has been affected with the treatments.  I'm hoping this will show a pattern of learning issues, and I also want to find as much information about what could happen with his education if he gets NO treatment for this.  I am so afraid of what could happen that way.  I know the older he gets, the more verbal the school instruction is, and the less likely teachers will be willing to accommodate him with extra help.  He will need whatever he can get to do well in school and not feel singled out with his peers.  My husband will be there (mostly because he knows my temper, and knows if someone tries to tell me that therapy won't help, I'd punch them!) so I'll let him do the majority of the talking.  He's an executive, and in management, so he's good with negotiating.  They are suppose to "recommend" further testing to see if therapy would benefit him.  I know what that means... do they think I'm stupid?  What if I don't think he needs 3-4 hours of testing again, he just had these psychological tests in early 2007!  I'll try to be open minded and hear what they have to say.  I am trying not to get angry about this, but it's almost impossible not to.  You all understand how I feel, but some nitwit with a Master's degree that says "I've got a Master's in special education, I know what they deal with" has no freaking clue what it's like for my son!  To think that someone like her could decide what course of action needs to be taken is ridiculous.  Just because you have a piece of paper with a school's name on it, doesn't mean you know what these kids go through. 

I'll work with the system, for now.  If I don't like what they tell me, I know I can appeal to the school board directly.  I'll do whatever it takes, even if that means homeschooling him to make sure he gets the right education.  I won't let them tell me what my son needs, I know what he needs. 

*trying to breathe and not strangle anyone*


Diana


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Re: Going to add a Special Ed section to site

NOTE FROM ADMINISTRATOR:
I moved a copy of Laurie's post to the Introduction Board so everybody would see it. I've left a copy here so everybody could reply within this thread as well.


Hi, I'm new on this board, and would just love to say how THRILLED I am to find a support group for Auditory Processing (FINALLY!).  My 10 year old son is a 5th grader at a very good elementary school in Atlanta.  After struggling through several years of mediocre grades and report card comments such as "lacks focus", "doesn't participate", "lazy", "has trouble grasping the subject matter", "disorganized" etc., we finally got the school involved.  Long story short, we wasted a lot of time sitting in meetings with no guidance toward where to go or what to do.  There seems to only be one pathway, and that is to call it ADHD.  After a consult with his physician (who was SHOCKED that I hadn't already set up a ritilin assessment appointment with him), I knew there had to be something else going on.  He actually told me that I'd waste a lot of time & money on testing when we could be solving the problem right away with medication.

We now have a new pediatrian.

We finally had a full battery of tests performed and discovered it was Auditory Processing (with working memory defecits) and dysgraphia (difficulty performing handwriting neatly).  Despite getting an IEP in 4th grade, the accommodations were lacking, and the support we received in the co-teaching situation was, lets just say, disinterested.  They decided that he was just lazy.  After spending the summer educating myself on everything I could find on CAPD (which is precious little), I realized that I needed to become his biggest advocate ever.  I'm very happy with the co-teaching arrangement this year, and have gone to great lengths to make them understand the world that he lives in.  Just yesterday, we had our 4th meeting of the school year to continue to tweak strategies and IEP goals.  I plan to touch base with his teachers approx every 2 weeks just for an update.   I've also made it very clear that bullying tactics not only do not help the situation, but are creating a self-esteem problem that makes it impossible for the child to succeed.

I just finished reading the book "Don't you Get It?" and found it to be energizing.  I'd love to hear other people's experiences, and how to approach this subject when the school becomes skeptical.  I'm especially interested in any classroom accommodations and strategies that work for other people, and looking for ideas to help teachers, students, and parents guide their child toward self-advocacy.   

Thanks for a great site!
Laurie


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