Showing posts with label IEP. Show all posts
Showing posts with label IEP. Show all posts

Tuesday, March 2, 2010

A Perfect Storm

Sometimes, when your kid has a bad day you can go back and analyze it and figure out all the places things went wrong that cause the problem.

Well, yesterday we experienced a perfect storm, Jason-style.

Because Micah is sick and Hannah is recovering, I made arrangements for Jason to walk home with the daughters of our friends. Jason has walked with them in the past on occasion and while it isn't the best situation, it works most of the time. In fact, we walked friday of last week without a single problem.

Although yesterday the fourth grade celebrated Ohio's birthday by eating lots and lots of Ohio made food. All of it contained processed sugars and chemicals. Stuff we don't feed Jason. Stuff his brain reacts, um, poorly too. In my defense, I misread the sheet and thought the party was Friday. Still, it was not a good thing for Jason.

Add to the food, changing Jason's routine. Although he is a normally flexible enough guy to handle this, routine changes do increase his anxiety.

And then, as they walked away from the school, someone hit him with a snowball. A kid who has been unkind to Jason in the past. A kid Jason who bullies him.

Jason yelled in anger and went after the kid. His friend tried to stop him by grabbing his coat, thus causing Jason to feel like he was choking. This was bad. Unbeknownst to the girl, this is a HUGE PTSD trigger for Jason. What followed was not pretty.

For the remainder of the 25 minute walk home, Jason yelled, pushed, tackled and threw snow at every kid he felt was bullying him or had in the past. The boys also yelled, pushed, tackled and threw snow at him. It appears that while Jason was the first to make thing physical, the other boys certainly played their part. It was not a good thing.

Also, remember how I talked about Jason's Autism and his inability to read situations or respond to them. Jason was yelling things that didn't even make sense, things he had heard on TV, making it funnier for the kids going after him.

When Jason did get home, I could tell something was up, but it took quite a while to decode it and get to the bottom of everything. His PTSD reaction means he only has vague images and recollections of what occurred after the coat was pulled. Of course, we were upset because he knows not to fight like that. But once we pieced everything together, we began to see things in a bit differently. In fact, it was this morning when clarity set in, that I realized while my son's response was wrong, the situation with the school has reached ridiculous proportions.

So, I started making phone calls and writing emails. I became Super Activist Mom and spent the majority of the day with a phone on my ear and a keyboard under my fingers.

I heard back from the school we are considering to learn that Jason made it to the final phase of the selection process and we should have a decision after they complete some testing and meet with the committee.

I spoke with two more Autism specific programs in town and have appointments made to tour their schools and meet with the administration.

I requested a revision on his ETR to qualify him under Autism instead of OHI so we can access more services.

I am asking that transportation be added to his IEP because he cannot travel to and from school safely like his peers.

There is a lot still pending and a lot of decisions to be made in the coming month, but at least now we have a plan.

Friday, February 5, 2010

Educational Insanity

Last night I had a meeting at the school to write a new IEP and discuss the results of the latest testing.  We also spent a great deal of time brain storming how to deal with the bullying situations.  The staff at the school really likes him and find him a joy to work with.  Overall, I am happy with the results, but still have some questions.

Because at the time we started testing, Autism was not in question, they did not do any educational autism assessments.  Now, they do believe he is on the spectrum and have written a portion of his IEP to deal with pragmatic language and social skills.  In fact, this social group that he is now a part of actually meets in the specialized Autism classroom once a week.  However, because they didn't do their assessment, they couldn't take his doctor's letter at face value and qualify him under Autism for his IEP.  My concern is that he will need this qualification to get the Autism Scholarship to cover the new school if he gets in, but the school psychologist says that is not the case.  That I just need to call the district office and they will help me through the steps in getting the scholarship.  Still, I'm going to be making some phone calls today to confirm this.

In addition to being stressed and in a meeting most of yesterday evening, this morning I am taking Jason over to visit the new school.  We are still very hopeful that this will work out, but don't know anything yet. They mentioned concerns about his language scores and the "underlying cause" of his LD.  We're still hopeful though and appreciate any and all prayers as we work towards this.

Wednesday, February 3, 2010

Lots and lots and lots of stuff...

We have so much going on right now, my head is spinning.

First, we have been invaded by illness.  Micah and Hannah have strep throat and Andy has tonsillitis, bronchitis and pink-eye.  Jason and I are so far healthy, but I think our days are numbered.  I think I might take my friend Nancy's advice and build us a bubble.

Jason's observation by the new school admissions department went well and they are "interviewing" him on Friday morning.  So far, we have no indication of how things are going, but they do have some concerns about the underlying causes of his LD as well as his language issues.  Still, we're praying that they will at least give him a chance.

Jason's present school situation is continuing to chug along.  We have his new MFE/IEP meeting tomorrow.  He's making great progress on his goals so I don't know what he will still qualify in.  For special education parents, this can be a good and a bad thing.  We don't want to see them lose there assistance, but we also want to see them make progress.  For example, Jason is doing great in math, but it's because of how the math is being taught to him.  Put him in a regular math class and he will fall behind again.  It's a bit of a catch-22.

Jason's also still struggling socially as school.  We've had a few more incidents of bullying behavior and I have a feeling a portion of tomorrow's meeting will be devoted to talking about it.  Honestly, we are doing everything we can to work with Jason on his social skills and he is making progress.  He's in individual and small group therapy as well as participating ins social groups at school.  Yet, the game of frustrating and bating Jason continues.  I've honestly reached the end of my patience, so tomorrow's meeting should be an interesting one.

We also started doing Dave Ramsey's Financial Peace University at church.  It's a great class and we are really learning a lot.  Still, it also means that we have tightened our budget and there are no more Starbucks Fraps in my near future.  On the bright side though is we'll gain financial peace and all this eating in will make me a better cook and healthier person.

Which leads up to our final bit of news...

Andy and I are praying about adopting again.  There is still a long way for us to go on research and prayer, but it's in the open now.  The kids think it's great and Hannah is begging for a baby sister.  Right now, we're thinking it will like be a waiting child from the foster care system.  We have a lot of questions, but know that God can answer them as He has in the past.

Monday, October 26, 2009

Not What We Expected

I'm back from the meeting.  It was good, but turned out differently than we thought.

The meeting went fairly well.   I started by talking about what we started this process and the events that led our principal to arrange for me to visit the classroom.  I spoke about the classroom and how it appeared to be exactly what I would want in a class for Jason.  Then his teacher and intervention specialist each spoke about the progress he is making and concerns they have.  As it turns out, things are settling down for him a bit.  He's maintaining very well in Science and Social Studies and he has been making progress in reading.  Math, spelling and writing continue to be his weakest areas.

Finally, Mrs. Fox, our principal, asked the teacher of the learning center how she felt Jason would fit in her class academically.  She had concerns because transitions are difficult for Jason and her students still have them. Then she noted that Jason is very advanced compared to her students in language arts.  Basically, Jason is working at a second grade level and her students at a kindergarten level.  She was concerned that with the disparity in Jason's learning and her students that it would not be a good fit.

This would be where I cried.

Mrs. Fox asked me what I thought and it was so very apparent at this point that the option I thought was perfect, wasn't.  I didn't sob, but I did choke up and get teary while explaining that I agreed that the learning center wasn't likely the best place for him, but I knew he needed more and had maxed out on his intervention minutes.  Jason's a unique kid as far as special education.  I was concerned because while I understood the learning center was not a good fit, I didn't like that he spent time in the class lost, confused and not really doing anything.

Then Mrs. Fox noted that she spoke with the Director of Special Education about Jason.  She wanted to explore all options before the meeting today.  Apparently, the 90 minutes is more of a guideline instead of a rule to prevent schools from creating learning centers instead of using those already  in district.  Basically, we can give Jason more time with intervention and make things work where we are.

Basically, we looked through Jason's entire day and noted times when he was in the class and the class was doing something he wasn't  We added 15 minutes of time to his math goals and he'll be taking part in a reading program for intervention level kids called Project M.O.R.E. for about 30 minutes a day.  This may take a few weeks to get everyone trained and schedule, so in the meantime he will stay with his intervention specialist for an extra 15 minutes doing independent work before returning to the class to  work on his keyboarding until lunch.

The only other time he is lost in class is during the reading aloud time and that is because he has his speech and occupational therapy interventions then.  We came up with a plan that we would read the book his teacher is reading in class at night before bed.  This was he would still hear the story and know the characters so he could join in the discussion despite missing parts of the time for his therapies.

Socially, Jason still struggles, but he in involved in a couple of lunchtime social groups.  Also, I know the staff at the school are aware of his challenges in this area and keep a close eye on him during lunch and recess.  I'm trying to make things happen on my end with that and Mrs. Fox is looking into a buddy for him from the 6th grade.

In all it was a very positive meeting.  Not having the massive transition will be a good thing and if we can make things work, I think Jason will be happier.  Also, I love his team and that he has people there who KNOW him so well and want whats best for him.