I am going t get a bit serious, and maybe even a bit controversial, for a minute. I know what your thinking..."YOU...Serious?!...HA!". But even I can get serious sometimes. Especially when it comes to my children. More specifically...my special needs child. Zachary has had a really rough week that began last Wednesday. He has been even more impulsive, agitated and aggressive than normal. He has an overload of energy and spends his evenings running around, jumping on furniture and making loud firetruck noises. He has begun biting at himself, chewing on his clothes, swatting at his teacher and aid at school. He is experiencing more difficulty during transistions and disrupting class with his loud vocalizations. His medications haven't changed and, as far as I know, neither has anything else. He has told me that he doesn't love me, he has thrown things at me and even grabbed my legs with both hands in an attempt to pinch me. He goes up and then down. One minute he is drawing a photo of he and I holding hands and smiling with the words, "I love you mommy and I miss you when you are far" written above them. The next minute he has drawn a big x through it and rewritten, "I don't love you mommy, you're mean!". It hurts my heart so bad that I spent Friday morning at work, crying my eyes out. He is so angry and so upset but I can't figure out why. I have tried everything to comfort him and calm him down, but it only seems to make things worse. I checked with the school and they verified that the behaviors are happening there too.
So I made him an appointment with his Neurologist. I just wanted to make sure that something else wasn't going on. After all, they told me that his chances of developing epilepsy are extremely high according to his EEG. Maybe he is on the verge of his first seizure. I am grasping at straws probably, but I just can't understand why he changed so drastically and so suddenly. After talking to his doctor, I had more understanding of what was going on. He said, "imagine that he is a car and he is having issue after issue. You know he needs a major overhaul but you keep taking him to local mechanics to fix this or that. Knowing the entire time that the dealership is the only place that can truly fix it with a major overhaul." He says it is due to the fact that Zachy is getting older and stronger and he has never had the much needed behavioral training he needs. He concluded that without this training from a trained Autism provider, it is only going to get worse. He said, "taking him to a regular teacher in a mainstream class is a bit like taking your car to 7-11 for repair in hopes that the cashier knows something about cars". WOW! I never really thought about it like that.
So now I am on a mission to get my son what he truly needs. Not that I haven't been on that mission all along. I was just not as well equipped prior to my conversation with the Neurologist. See, he hooked me up with a paper that contained this statement...
Education is the fostering of acquisition of skills or knowledge...including not only academic learning, but also socialization, adaptive skills, language and communication, and reduction of behavior problems - to assist a child to develop independence and personal responsibility.
At the beginning of the year, I attempted to get Zach placed into a special classroom taught by teachers with experience in dealing with special needs kids. This school does not have an Autism class and the County I live in is in great need of Autism teachers. So they convinced me that since he is doing great academically, we could just place him in a mainstream class with the assistance of a full time aide. I admit, he is doing great academically, with lots of prompting and constant reminders to stay on task. However, he is not doing great in all other areas. He has made attempts at socialization but is incredibly awkward in his socializing. Eventually, this will lead to teasing and being shunned by classmates. I was always led to believe that the school was only responsible for his academics. Now that I know they are responsible for more, I am pushing it forward. I have already been in touch with an advocate to speak on our behalf at the IEP meetings and I sent an email to the school letting them know what I want for my son. They stated that we will have an eligibility meeting next week to see what he qualifies for and what label to put on his IEP. After all, he has "outgrown" the developmentally delayed label they previously gave him. Even though my son has the diagnosis of Autism from 2 very highly respected child developmental doctors, the school feels they need to test him. They apparently think they know more than these professionals. I say they just don't want to have to provide the therapies required by the Autism label. No Child Left Behind has no funding behind it and therefore the schools are scrambling to care for these children. But this is not Zachy's fault. He deserves what he needs in order to lead a "normal" life someday. So I begin my fight! I WILL win! For my son, I will do what it takes to see him get what he needs. My child will not be left behind!
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14 comments:
I hope everything works out and you can get him into a class that will be better for him with a teacher that knows what she is doing .
Reading your post looks like you want what is best for your son, around here no child left behind means everyone is mainstreamed and basically brought down to the lowest common denominator which is where I have a problem with the whole no child left behind thing- I *think* you are saying you want what I do, what is best for each individual child so they can excel, not all lumped together as if they need and learn the same ways.
While my kids are on the opposite end of the spectrum (the ap and pre-ap classes) I don't think taking away the funding from one for another is fair or right either, then you are left with a bunch of cookie- cutter carbon copies and no-one is allowed or encouraged to excel.
I hope your son gets what he needs that will be best for him. :)
This gave me chills!
Now that my stepson is coming back to live with us, I'll most likely be battling again. I did it when he was with us before and I have no problem fighting for him again. He has ADHD and, I believe, other yet-undiagnosed issues. I'm not going to let him fall through the cracks. You go mama!!
Your son is so lucky to have you as his advocate. I know you'll prevail and get him the education, care and specific attention he needs.
Hang in there with the process - I'm sending my best wishes!
:^) Anna
As a teacher, I have to tell you that this post warms my heart in many ways. It is so great to see a Mother stand up for her child and do anything and everything to make sure that he can have the best life possible. I have had way to much experience with families in denial, who just can't understand that needing something different from the "norm" doesn't make your child defective...just different.
It pains me that it is so difficult for you to get the services your son needs to thrive. Please continue to share your journey with us, and let us all know what we can do to help in the effort.
Big hugs to you!
A friend of mine has been having issues with the jr high she was zoned for, she knew it was a "rougher" school and her son would not thrive there, with all of his issues (still undergoing testing for full diagnosis). Come to find out, the reason they would not release him was due to how much money the school made off of his special needs!!! That infuriates me! What is best for the child sorta goes out the window when the dollar signs are flashing!
Best of luck to you. I'm sorry there isn't any good resources around you. Each child is different and I believe their education should be tailored to fit each child. My daughter Mercede is having a horrible year. This is her first year of high school. For the last four years she has had one main teacher and now she is being shuffled alot. She is rebelling. She does well at the work sites they have her at because it is organized. At this time, I'm struggling to find what is right for her.
YOU GO GIRL! You're son is so lucky to have such a great mom and a great doctor. Praying for the best for you all.
Over from SITS - go get them! Make them do that IEP right!
I apologize if I step on toes here, but the issue of no school left behind infuriates me. It does not meet the needs of the students. It forces teachers and adminstrators to cover their backs and feed the budget anyway they can. Instead of putting more money into early childhood education (which has been proven not to work), it should be going in to pay for programs which your son needs. Too many families are encountering this with not enough support.
Ok, sorry, this stranger is off their soap box now, :) hehe
Have a great day and congrats on being the feature blogger!
As a mom with four kids, two of mine hold "labels". I have a medically diagnosed ADHD 12yo, and a developmentaly delayed 5yo. Before we moved to our current location I was and ABA therapist and worked in the autism classrooms. I know what you want for your son, and your doctor is right--it is what he needs. I'll keep you in my thoughts. I know that there are a lot of schools districts who can't afford their special needs children, and it breaks my heart. I believe that schools should go out of their way to provide anything, and everything, that a child needs to be successful no matter what it is -- be it advanced classes, or an autism teacher. Good luck!
You go sister--your are exactly what he needs and with you in his corner, I know he will get everything he is entitled to!
The properly-focused teacher will make a world of difference
Hiya...I'm visiting from SITS and was perusing your blog. Wow, your little Zachy IS so lucky to have you in his corner. Don't give up! There is help out there! Hopefully, you and the school district will be able to work as partners to get him what he needs. Best of luck to you! I'm off to read more of your lovely blog! =)
Hi, I found you on SITS. My friend has a now 6 year old son with autism who was acting a lot like how your son is now. He would hit and yell and throw horrible tantrums. Turns out he wasn't getting proper sleep. I took a class on pyschology and they had mentioned something about the meletonin that your body produces tells you when your tired and its ready for bed. A lot of kids with Autism don't produce enough or some none at all of this and without proper sleep they will start acting out during the day. I advised my friend and she started giving her son 1/2 a pill 1 hour before his bedtime and since then he has been sleeping properly and hasnt been throwing tantrums like he used to. It's a thought. Maybe it will help. Good luck
Happy SITS day! This post caught my eye because I am a Special Education Teacher. : ) I think it is great that you are fighting for your son, more students need a mother like you. The evaluation should take in account the diagnosis of Autism. It sounds like they are doing a psycho-educational report which must be done with any new questions about diagnosis. It is also reviewed every three years. It sounds like your son is not meeting his goals. Keep fighting for that classroom or teacher. They have to provide it if he is not showing adequate progress. Review your procedural safeguards and become familiar with IDEA (the SPED law if you are not already familiar with it.)Good luck! My thoughts are with you!!!
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