Saturday, October 04, 2014

3rd Times the Charm - Navigating the Special Education System

When we left off, I was complaining about the VA special needs system. Well, I'm sorry to say that our experience this time around has pretty much mirrored our first experience if not exceeded it in terms of crappiness. After our two years in Manila at a wonderful school that provided him excellent support,* which was supplemented with regular Skype ST sessions with our therapist in the US, we were hopeful that A could continue to make regular gains. We also came back with IEP in hand, so they had no choice but to continue offering him ST. This time around we entered the Fairfax County Public School (FCPS) system. FCPS is regularly ranked as one of the best school systems in the country. I repeat: in the whole damn country. Our experience has been that that reputation is vastly undeserved. While the school had no choice but to continue his ST - I still had to fight to get regular updates or any information about the type of therapy that was being used. At our first meeting with the school I noted that Husband and I were concerned because A was not reading yet and he was already 1/2 way through 1st grade. I was told that it was too early for them to be able to judge since he had just entered the school system. Fair enough, but I wanted our concerns noted in his IEP meeting notes so that they would be there for future reference. His classroom teacher - who I want to note was FABULOUS(!!)** - also noted that she had some concerns about his academic performance and suggested that he be enrolled in a before-school reading intervention program, which we agreed to. Unfortunately the before-school program did not seem to help, and A was still not reading. I called to school to voice my concern and was told we could discuss it at the end of year IEP meeting.

Fast forward to May when I came back from Manila, and we again convened for the end of year IEP meeting to discuss progress, goals, etc. At this point A was still not reading, although he was beginning to learn better, savvier strategies for hiding it. So I again raised my great concern that here we were at the end of the school year and A was no closer to reading than he had been at the beginning of the year. In spite of a whole academic year and the before-school program, A entered FCPS reading at a DRA level 3 and ended the school year at the exact same level. Literally no progress had been made. His teacher stressed that this was really not within the normal bounds of elementary learning, and she was concerned that there might be some other reason that was keeping A from making progress. The committee, however, told me that since the school year was about to end there was no way to start the testing process for anything new this late in the game. We would have to wait until next school year, at which point we would have to request an evaluation which would require having him monitored by his new classroom teacher (who would need at least a month or two to get to know A and determine whether or not he/she thought there was a need for intervention). Then, if the teacher thought there was a need, they would try some in-class interventions to see if that helped (another 2-3 months), if that didn't help then they would conduct a battery of psycho-educational tests to determine if there was a delay or disorder. All that is to say, we'd be long gone for Hong Kong before the school system ever determined whether or not there was anything actually wrong with my son much less have figured out any way to help him. Fucking ridiculousness. I pointed out that the process would take more than half a year, and by the time they actually did anything A would be an illiterate 3rd grader. At this point I did get some sheepish looks, as if they themselves realized how fucked up and slow the process was, but, I was told, nothing could be done. You have to follow the process.

At this point I was so frustrated and fed up, and, frankly, I didn't trust FCPS to follow through on anything anyway. So I went ahead and plunked down $3,000 for private testing and came out with the exact diagnosis we expected (dyslexia and dysgraphia)*** and one we didn't (ADHD).**** With evaluation in hand, I went back to FCPS hopeful that we could open up a new IEP and start helping my son at the beginning of the year. Oh, how foolishly hopeful of me. I did find out, however, that FCPS has something called a summer session meant to test kids that have possible needs identified when regular school is out of session. Which would have been great knowledge to have when the idiots at the elementary school told me IT WASN'T POSSIBLE to have him tested until the next school year and then I shelled out $3,000 to have it done because I was so desperate to start helping my son. F.u.c.k.i.n.g. ridiculousness. How is it possible that the IEP team at my children's school was not aware of this? After I got over being angry, I charged ahead because in the end all I care about is helping my child. So we ended up meeting over the summer during the FCPS summer session where all of the IEP team members (different than the ones at my local school, although the VP did attend as the school's representative) agreed that the testing we had done was incredibly thorough and they saw no reason not to re-open the IEP. They did note that there was no social worker report, something that is required by the school system, so we scheduled that. I signed all the paperwork and went off about my way happy and excited that my son might actually start the year with some new assistive measures in place. Me and my silly hope.

In spite of the fact that I met with the social worked in August, and A met with the school system's psychologist at the same time, we started the school year with nary a peep from the school. After a couple of weeks, I became concerned that I hadn't received anything regarding his new IEP. After 3 weeks, I started contacting the school. After 4 weeks I finally got a response in which I was informed that the school was re-conducting all of the tests to come up with their own diagnosis. The fuck????!!!! Apparently, despite the fact that everyone at the summer session meeting agreed that the private testing we had done was above and beyond anything the school needed they still somehow thought they needed to conduct their own tests to, what, ensure that we spent our $3K wisely? I really have no freaking clue, and the school rep couldn't really explain it to me either beyond the fact that it was necessary to complete the testing (and then the analysis of the testing, which, oh by the way, is the really lengthy part). All that is to say that they finally asked if we could schedule a meeting to discuss A's eligibility on Oct 17th. Eligibility, people. Do you know what that means? That means it is a meeting to discuss his test results wherein they will (if they have any decency at all) say, why, yes, we agree that A has some issues that need to be addressed. That's it! The eligibility meeting is solely to discuss whether or not your child may qualify for services. No talk about any actual service or accommodation that might be forthcoming. You have to set up a totally different meeting for that! And who knows when that will happen. I mean it will be six weeks into the school year before the school will even agree that there is a problem, 10 months after we originally identified it! And that elevated timeline is solely due to the fact that I was able to spend $3K and countless hours to get a diagnosis for my son. My heart bleeds for the many, many families who could not possibly afford to get outside help.

So, I gave up on the school system. After all of this, I started doing some digging to try and figure out what I could do. What I unearthed just made me feel even more desperate. FCPS does not even recognize dyslexia. Much less have a coherent strategy to help affected children. His reading assistance will likely be with whatever reading specialist is already assigned to the school who probably does not have any specialized training for kids with special needs. There are several well known, peer tested and reviewed therapeutic systems for helping kids with dyslexia. FCPS uses none of these, which I guess isn't surprising since they refuse to acknowledge it exists anyway. After feeling even more depressed, I put on my big girl pants and started strategizing on what I could do. I scoured the web for resources and found a tutor who specializes in the Wilson Program (based on the Orton-Gillingham system) at a cost of $75/45 minutes. Ouch. For kids with dyslexia it is recommended that they have at least 1hr/day additional 1-1 reading support using a system like Wilson. Double ouch. Well, since we could never afford that, and we have other obligations during the week, we settled on 2x/week. As much as we can't afford this right now, at least I will know that we are doing everything we can to help A get started with reading.

*I cannot rave enough about International School Manila. We always say that it was the best part of our tour in Manila. 

**Our experience with FCPS has been that the individual teachers are amazing, but the system itself is a bureaucratic mess. 

***Actually, FCPS doesn't even recognize the term dyslexia (please don't ask me why), so it is termed "Specified Disorder in the Area of Reading." 

****Although, now having received this diagnosis and learned more about what it actually is, it really helps explain a lot!

3 comments:

alexis said...

sigh. what a freaking nightmare!

Michael Podolny said...

I wish I could say that there was any hope that his will change. But I remember the issues our kids had in the Howard County MD schools system that was also supposed to be excellent and it mirrored yours. And that was 20 years ago. There is a reason why charter schools are taking off. Because the US education system is broken beyond repair.

Bernice said...

As a parent wanting the best for A, that has to be extremely frustrating.