Showing posts with label teachers. Show all posts
Showing posts with label teachers. Show all posts

Thursday, April 30, 2015

The Transition to Public Special Education

Tate is having wonderful experiences at school. He likes school and that is so important. But that has not always been the case. Once upon a time, he cried almost every morning before school. School was very stressful for him. He had a lot of needs that were not being met. He could not communicate his needs. Anxiety ruled him. It was hard on him and it was hard on our whole family. Because when Tate is unhappy, we are all unhappy.

When Tate began kindergarten he had come straight out of early intervention. He began Applied Behavior Analysis (ABA therapy) before his third birthday and we aimed for forty hours a week of discrete trial. Incidental teaching was used throughout every waking minute, trying to turn his whole day into one learning experience after another. We were trying to “catch him up” to his peers and get him kindergarten ready. We did the ABA with experts in the field of autism and the price tag was huge.

I knew there might be some issues with the public school immediately. One reason being-- I had called the public school and inquired about their preschool program. I also asked about the district’s ability to provide Tate with some services for our in-home ABA therapy program. The voice on the other end of the phone told me if I had determined ABA therapy was best, I had been reading all the wrong books. I knew ABA therapy was the ONLY research-based therapy at the time. So my first impression of the special education director and the program was not good. I did not contact the school district again regarding Tate’s education until he was ready to start kindergarten. We had an IEP meeting so Tate would begin school with paraprofessional support. It was evident from our first meetings the special education providers and I were not going to agree on what an appropriate education for Tate would look like. It did not get better for a long time. I had set my expectations high and I was sorely disappointed. I was also shocked. Tate has five older siblings and I had NEVER had any complaints in the past about our children’s education. I had a lot to learn about the difference between general education and special education.

Tate at his early intervention program
I had a lot to learn about the difference between private early intervention and the public school’s special education program too. There were few similarities. When I had questions about autism or challenging behaviors while Tate was in early intervention the staff had answers. Those first few years of public education I saw little evidence the ones providing Tate’s services understood autism.

We had some unforgettable experiences those first few years of public education. When Tate was six, one day he used his pencil to pretend. He pointed it at his paraprofessional and said “pow pow.” The para mentioned this to her supervisor. That teacher took Tate to the principal’s office. She asked if the incident should be reported to the police as the school had a zero tolerance for threats. Tate was six. He has autism. He was holding a pencil. And he was made to feel like he had done something bad. In his early intervention program it would have been celebrated. Pretending! Object Substitution while pretending! This was huge! The autism expert from Tate’s early intervention program would have written me a note or called me to tell me the great news. In the public school setting he was taken to the principal. Luckily the principal was a very reasonable man. When he told me about the incident he was smiling and assured me he never even considered making that call to the police.

Tate at Kindergarten
One phrase I heard often when I made a request for a service was, “We’ve never done that before.” Social skills coaching on the playground was one of those things they’d never done before. The argument against it was that Tate needed free time on the playground to do whatever he wanted. He would have paced and stimmed. I did not want those precious teaching opportunities wasted. The consultant / advocate I brought with me to our meetings argued for the coaching. In an effort to convince me Tate did not need coaching on the playground, the school district brought in their own autism consultant. The plan was for her to observe Tate for a few hours and then give some recommendations. (My own consultant had worked with Tate for years and knew him well but they wanted someone to observe him for a few hours and make recommendations.) I asked if I could be present to hear the consultant give her recommendations when she was through with her observations. Even that was a point of contention, as some did not seem to want me present. Thankfully, the principal called me and told me when the meeting was about to convene and I lived one mile from the school so I was able to get there and hear firsthand what was said. I will never forget what I heard or the looks on faces that day. That consultant agreed Tate needed playground coaching. AND she recommended even MORE social skills coaching than I had asked for be incorporated into his school day. I smiled all the way home that day. The suggestions made by the district’s consultant were not implemented in full but I am quite certain they would have gone with her advice had she said Tate needed LESS services. No one argued with me about the playground coaching much after that. For every battle I won though, I lost two.

We fought many other battles as well. I asked for Tate to receive a warning before he was to have a substitute teacher. I understood it would not always be possible and I know sometimes people become ill right before school begins. However, if a teacher had scheduled an absence and I could give Tate a warning before he walked into a room with a stranger in charge, it made a world of difference to us at home. Tate’s anxiety level after having a substitute was often high. I asked. I begged. I demanded. This became a real problem and no matter how many times I explained the need it did not seem to matter. General education teachers would willingly tell me when they were going to be absent. But the special education staff rarely seemed to be able to get me that information. The time that mattered the most was once when Tate had a gift to give a special education teacher before the holiday break. He took it to school two days before the break only to find a substitute. The secretary told me the teacher had scheduled time to be off long before that date. He was so hurt. If the goal was to show me who was “in control” then I was shown. Often. There was nothing I could do. I saw over and over that one person could ruin Tate’s day and ruin our evening. One person.

Para professionals and I often had to communicate in secret if we had information we wanted to exchange because I was not allowed to talk to my child’s paraprofessional without their supervisor present. I know what you are thinking. It was a ridiculous rule. It was a hindrance to everyone involved, especially my kids. I was told I could not even say, “There is a Chapstick in Tate’s pocket” to the paraprofessional. The special education director could not be moved no matter how many times I appealed to her. Despite the rule, the paras and I found ways to communicate when it was in Tate’s best interest. On two separate occasions I received phone calls at home in the evening from two different substitute teachers I’d never met. Both had been subs for Tate’s para. Both wanted to tell me something that had gone on at school they felt I should know about. Both had been told they were not to talk to me. They did anyway. Not that I was able to do anything about the problems they discussed with me though.

I came away from that first experience with my district’s special education department disheartened. It has taken me years to recover and be able to fully trust my children’s IEP teams. We have wonderful teams now and are very satisfied. The differences are amazing. My faith has truly been restored.

I learned some really valuable lessons and made some valuable observations those first years.

1.     One person can make or break a child’s education. One person.
2.   When your special needs child is miserable at school, the whole family is affected.
3.   The words “Promote independence” are spoken with a smile by educators, but those words are code for “reduce services” and a parent should not be fooled. Of course everyone’s goal is for a student to become independent, parents included. But not prematurely and not to save the district money.
4.   If the school wants to amend the IEP to “promote independence” and promises the services being reduced “can always be added back in later,” it will take an act of Congress to get those services back. Parents should not allow themselves to be coerced or pressured into signing anything amending their child’s IEP to reduce services.
5.   The law says a child’s needs must be met. So, in theory if there are ten children who need XX for one hour a day and only one person who can deliver XX, working eight hours each day, the district is obligated by law to hire another XX provider. In reality what I believe happens is the children who needs the XX the most get the XX and the children who need XX the least do not get it, OR the eight hours is split between the ten children. But an additional provider of XX is probably not going to be hired. The law is often ignored but dollars carry a lot of weight.
6.   Privacy policies can be a real detriment to a child’s education and safety. Privacy policies keep substitute teachers and many others from knowing about a child’s disability, needs, behaviors, treatments…
7.   Not every educator is good at his / her job.

8.   Tenure protects bad teachers.

Friday, March 6, 2015

12 Things I'd Like My Son's Teachers to Know About Autism

This is the kind of list I would have handed my son's teacher in elementary school. It is pretty general. Stay tuned for a part two that is more Tate specific. 

Autism is a huge spectrum. If you have taught children with autism  before you may have a good general idea of what autism looks like. My son will still be different than the others. If you have questions about how autism affects him, ask me. Nothing will impress me more about you than your willingness to learn about my son's needs.

A routine and transition warnings are helpful for a child with autism. While we know that flexibility is an important life skill and one we need to work on, my son does not handle surprises or big changes in his routine well. Things like a substitute teacher, a fire drill, or a field trip are all going to cause anxiety for my son. A warning and clear instructions will help. A visual schedule would be a helpful tool for my son. Before transitioning to a new activity (especially when going from a preferred activity to a non preferred  activity) a five-minute warning, a two-minute warning, and patience will be needed. 

A child with autism needs extra time to process language. Use simple language and short sentences. Give no more than two-step instructions. Give my son at least three full seconds after you make a statement or ask a question to respond. If you choose to repeat, do not rephrase, as then he will have to start processing over again. Trying to hurry my son will only slow him down further.

Receptive language and expressive language are two different things. My son may understand much more than you think he does. He may not be able to put into words all the things he wants to say. On the other hand he may be able to quote long complicated phrases or passages without understanding any of the meaning of the words. It is difficult to know exactly what my child really knows and what he still needs to learn sometimes.

Children with autism are literal. Figurative language and abstract ideas are a mystery to a child with autism. So, when you say things like, “Pick up the pace” and your other students know you want them to walk faster, my son will be looking for something called “pace” that he should be lifting from the floor. These things happen all day long.

A child with autism can get stuck on one subject. My son obsesses about things that do not matter to you or I. He might want to talk about Disney movie characters or Muppets for a long period of time and there will be little you can do to distract him. He gets stuck in a continuous loop. Occasionally these topics of interest can be incorporated into his learning but mostly they distract him from learning.

A child with autism may need help with social interactions. My son will probably appear disinterested in his peers and he may actually be disinterested but he will never learn social skills unless we keep trying. You have him in a perfect setting for teaching social skills. It is an environment I cannot recreate at home. It would be so helpful if you would use every opportunity available there to teach and reteach social skills.

Sensory issues are a distraction for many children with autism. Sounds that are barely noticeable to you may distract my child and keep him from learning. Textures may cause my son to recoil in disgust. Smells may cause him to gag. Please be considerate of this. Over stimulation can sometimes overwhelm him and cause a meltdown. A meltdown looks similar to a temper tantrum but it is not the same at all.

Children with autism use stereotypic behaviors or repetitive behaviors when they are excited, bored, or stressed. My son will need redirection throughout the day. The behaviors will cause him to appear odd to his peers. Please consider giving the class an age appropriate definition of autism to help his peers understand.

Positive Reinforcement will be helpful but punishments will not. Punishments or threats of punishment will probably result in anxiety and impede progress. He will work toward a reward but will shut down if he fears a punishment.


People with autism tell the truth as they see it. My son may let you know you need to lose weight, you need a shave, or your breath smells bad. Do not take it personally. A sense of humor is a must when working with children with autism.


Kids with autism are not scary or unlovable. They are just different. Sometimes different is intimidating but educating yourself about autism and about my son will help. I’m can help with that! I will willingly answer any questions you have.

BONUS TIP: NOTHING IS MORE IMPORTANT IN MY SON'S EDUCATION THAN COMMUNICATION BETWEEN HOME AND SCHOOL. 

Wednesday, April 2, 2014

Why I Wore Blue Today

What did the color blue ever do for me? Actually, my family would laugh at this because blue is my favorite color. I wear mostly blue and decorate almost exclusively in blue. Once, my older sister had an intervention of sorts for me.  I asked her opinion on the counter top I was looking at when remodeling my kitchen. I was leaning toward blue. She looked around and said, “No more blue! Your carpet is blue. Your walls are blue. Choose a different color for your counter top.” Ha! I chose a light green with a splash of blue in it.

Why do mothers of children with autism ask their friends and family to wear blue one day a year? It has nothing to do with the color itself. What can the color blue do for us? The answer is fairly simple for me. The color blue cannot perform some kind of therapy for our children. It cannot help with their social skills, their communication skills, or their motor skills. It cannot calm them, lessen their quirkiness, or ease their anxieties. By wearing the color blue on World Autism Awareness Day, you let me know you care. You let me know you are “aware” of our walk. My family does not want your pity or your condolences. We would like your empathy though. We would like to know that you know that we are struggling and that you understand just a little bit. THAT is what the color blue did for me today. When I knew that Tate’s school had made an announcement yesterday to let the students know that today was Autism Awareness Day and people were wearing blue in support of awareness, it let me know that the administrators care.
          Tate with his two amazing teachers
On a much bigger scale, the campaign to wear blue for autism awareness is exactly what it sounds like. It is about educating the public. People today know so much more about what autism is than just a few years ago. It is partially because of campaigns like this. The Centers for Disease Control announced last week that the numbers are now 1:68. You would have to live virtually in isolation to avoid knowing people with autism in this day and age. The education and consciousness takes away the fear of the unknown. It diminishes the bullying of people with autism. Our education about autism causes people with autism to become so much more approachable. Awareness makes it easier for them to attend school, easier for them to find employment, easier for them to fit-in in their communities, and easier for their peers to befriend them. Even the word itself, “autism,” is becoming a word used in everyday conversations. Raising awareness if very important to us in the autism community. Awareness of what autism is will keep our children safer and cause their futures to be so much brighter.


Educating the public also means that children with autism may receive a diagnosis earlier and receive the early intervention they need. I am confident that every dollar spent on early intervention saves many dollars in the long run. So many of the children who receive intensive early intervention become successful in ways they could not have otherwise. They may need a lot less support as adults. The younger the intervention, the better the results. The brain is much more malleable when it is young. Education and awareness are so important. So next year, on April 2, “light it up blue” for autism awareness.