Preschool and Discovering SPD

September 14, 2012 by in SPD with 6 Comments

Over the past year I have been on an incredible journey learning about SPD and helping my almost four year old son transition to a school environment. Until O was 2.5, he was cared for at home by a nanny for 30 hours a week. When I became  pregnant with our second child, we wanted O to start a preschool. We found one by our house that was highly recommended and was actually a private elementary school. They valued diversity and acceptance and had a gorgeous campus. Before starting there we needed coverage for a few weeks, so started at a local YMCA daycare. O was not happy about being at school at first, but it only took a week for him to stop crying at drop off. The teachers were really nice, and he was the youngest in the class by a year.

One day his teacher laughed and said “he likes to hit the other kids. We tell him to be nice to friends.” O had been saying “don’t hit friends” over and over, so I finally knew why. I was concerned because he had hit my nephew during a visit back home just before starting school. My brother assured me it was normal two-year old behavior, but of course it really bothered me. After hearing about his Y experience I was worried about the next school, but I also felt like the next school was more professional and would have ways to redirect and handle the behavior other than laughing.

We started the new school, and I was so excited because it had a yoga class, music class, and a Spanish class. The classrooms had gardens, and I was so excited for O. On the first day, my husband and I picked O up, and O left a circle time and doubled back to hit a friend before reaching us. It looked random, but I was already sensing it was a reaction to our leaving him at school all day. O started during the summer program, and we kept hearing this was a great way to introduce him to school since it was more relaxed. Within weeks we had a meeting with his teacher that she called asking us about his strengths and weaknesses. She assured us we weren’t even her first meeting of the day. We chatted and then she asked about O repeating sentences and saying things like “Don’t let S get it” during snack time. S is our dog, and of course the dog wasn’t there. He would also say “cars coming” when the teacher took his hand. His teacher was concerned that he had trouble during transitions and always wanted to play with sensory items. We didn’t know what any of that meant and just nodded.

I wasn’t too concerned about his language because at home he wasn’t doing that. We were shocked to learn that he only communicated at school with these few sentences. The teachers said they were working on gentle hands and teaching O to communicate when he wanted to play with his friends. My instincts were telling me something about the class was creating stress for him. A resource coordinator watched him, and I had a meeting days later with a sheet full of resources. The teacher and coordinator starting casually talking about how I’d want to do this assessment and that assessment. And they talked to each other about how difficult it is to find out something is wrong with your kid. I just sat there in shock not understanding what they were saying, and I assumed they thought he might be autistic.

They were telling me he wasn’t connecting with the teacher at circle time and that he didn’t understand where his body ended and the next person’s began. They gave him a squishy mat that seemed to help. It was a lot to take in, and in hind sight should not have been delivered in the way it was.  The school had a two week break, and I took O to our pediatrician who said “He’s not even three. Relax.” Still, I wanted the school to see we were on board, so we made an appointment with a pediatric development specialist. The appointment was for the end of the school semester, so we had months to survive.

During the break we went to story times at the library and for the first time O sat still through them. I thought school had made this difference in him. School started again with the same teachers, and O started off great. He found his circle spot, followed directions, and was ahead of the kids who were just beginning. Then my daughter was born, and we started getting reports that O was head bunting people, pulling hair, licking the walls, putting everything in his mouth, and at times being physically aggressive. The teachers told us he wasn’t aggressive but that he seemed to be trying to play with others.

By now I had read enough about SPD to see him as a sensory seeker. At the same time, he had gross motor delays and was slow to climb stairs or be confident with movement in general. At his school assessment they recommended one-on-one attention if his physical and vocal outbursts did not decrease in six weeks. He had also been screaming at random times. My husband and I decided to start the one-on-one sooner, and my husband began in the classroom. We hired someone else when he couldn’t attend. Orion seemed to thrive with the attention, and it became clear that he had some problems with sitting in circle for twenty minutes at a time in one exact position. He also had trouble transitioning because of a loud bell the teacher would ring and the chaos that ensued. My husband felt like the school day was too structured for a 2s and 3s class. I dismissed him until I sat through a morning and saw that O was not having fun except at very specific times. The pace was frenetic, and the kids were constantly getting into trouble. The school uses Love and Logic, and we attempted to adopt that at home with poor results. It just didn’t mesh with our parenting style.

O’s assessment with the development team told us nothing except that he probably wasn’t autistic. We could do occupational therapy or speech if we wanted, but that process was easier said than done. We decided that funding a third teacher for his class was not sustainable, so we left the school mid-year and started at a daycare center that was also watching our infant. In part we left because the school refused to make any changes that would have made the day easier for O such as letting him always be at the front or back of the line, stop ringing the hand bell, and other transition ideas my husband had after weeks in the classroom that would have helped all of the kids be more successful. At the new center, O cleaned up without a problem because the lights were turned off and the kids all cleaned. I am not sure why there were always kids screaming in the more structured classroom but the new school was calmer, at least during times of transition. O became potty trained (the other school didn’t potty train), started putting his shoes on by himself, stopped using a pacifier, and started thriving in various other ways. After a few months he moved to an older classroom, and he did well at first. But then the class size grew, and we received reports of hitting and eating crafts. I told the teachers about SPD, and they implemented sensory activities for O. I also bought him chew toys. They treated it seriously, but they didn’t make us or O feel bad.

After months of working with him outside and inside the classroom O’s days have gotten much better. We met with a SPD center that offers Sensory Integration Therapy, but the owner said O had a mild case, and since our insurance was not going to cover the treatment, we could wait a year to see how he does. He had outgrown so many of his more severe symptoms (hitting himself, head bunting others), so we were willing to give it more time. At this stage we are starting another structured preschool that provided services if needed, because a spot opened. Looking back at this past year, it has become clear that the style of preschool and teacher really matter. In fact, we will always look for teachers that connect with O and who are willing to work with him. The teacher connection is so important, especially in the preschool years, and we were too blinded by the idea of a “good school” to recognize that it might not have been a good fit for our son.

We spent all of our energy trying to make O fit into the school rather than helping the school make him more comfortable. I have stopped feeling guilty and helpless, and I have (mostly) stopped resenting the school. I am still sad that O loved the school and had to deal with yet another major transition, but I feel like he has become so much stronger through these transitions and has learned to cope in amazing ways.  As we start the new school, I will be looking for ways to help O continue his positive growth and become a better advocate for my children.

It is difficult having a child who would hit other children.  I love my son so much and think he is amazing and creative, and I could only imagine that his teachers didn’t see those things.  They saw him as an impediment to their highly ambitious curriculum. I spent so much energy feeling ashamed and embarrassed, and it was others who helped me realize that O was hurting and stressed.  I still do not have any answers for what we went through or what is ahead for us, but I know reading other people’s stories gave me the most comfort, and I am putting our story out there in case it resonates with someone.

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  • Michele


    This is an excellent and very important post. My daughter has cerebral palsy and I have experienced and learned very similar lessons as you have even though her challenges are different. It’s amazing what we see once we have come through the other side of experiences such as this.

    A wonderful contribution here…..

  • Mary


    Sing it, Sister!! My seeker-boy is five now and just started kindergarten. So much of this is what we went through, though mine actually bit(!) until he was past three (and my son was advanced in his gross motor development, which sounds good, but anyone who isn’t raising a seeker has *no* idea what they can get up to and into!! He sure caught the daycare off guard a few times). Last year in pre-school and this year in kindergarten have just been amazing, though. Not perfect, mind you, but amazing. As you say, the biggest plus has been that his most recent teachers *get* him. He isn’t “bad” or a trouble-maker, but he is different from other kids. They’ve encouraged him to be proud of the things he can do better than many of his peers (his climbing skills, his zest for life!), and worked with him on the things that he has trouble with (impulse control, sitting still for long periods). We have years to go and miles still to walk, and some days are still much harder than others, but having professional and academic support by people who think my kid is great — it’s just so much better than it was.

  • Heather Finnegan


    HUGS! It’s a hard road to walk! I was a teacher and I truly believe that not every school is good for every child! Keep fighting the good fight, and adapt when needed!

  • Home School Mom


    Thank you so much for sharing your story!! My son does not have sensory issues, but a friend sent me your blog. She knows our story and read your’s and saw us in this blog. My son is allergic to gluten and dairy. We had MAJOR battles last year w his preschool. One teacher messed up his food every week. We tried talk to the lead teacher and the director. No one wanted to make any changes. It was so stressful. I took him out for a month in the summer and it was amazing how happy we all were! That’s when my husband and I said, we are done! We tried to get him into another school, but it was at the last minute so it didn’t work. We are home schooling him this year and his behavior is amazingly different. Your struggle, your guilt, fear, anger, etc…. I know it all first hand. It’s good to know we aren’t the only ones!!! Thank you!

  • JJ


    Thanks,everyone! It has helped putting the story out there. And it really helps hearing that other people understand!

  • EHCMom


    I truly appreciate your story. You and your husband should be proud of the proactive ways you’ve used to meet your child’s needs. My 5 y.o. daughter was in a special ed preschool for two years prior to starting kindergarten this year. She enjoyed attending preschool, and she progressed and learned new things happily, so it was quite surprising at the first school conference when we were told she was scaring other children in class by hugging them too hard and speaking in a booming voice at inappropriate times. Why would they wait over two months to tell us this? No one mentioned sensory issues or recommended an evaluation, so we assumed she was just getting overexcited and had trouble controlling her excitement. Along came the second year of preschool (same school). Again she progressed and learned and her speech continued to improve. Two school conferences came and went with good reports. Then came the annual team meeting at the end of the year to set up a plan for whether she would continue to need speech services in kindergarten. Imagine my surprise when I hear the teacher saying, “she has self-regulation problems, is inappropriately loud, she knows how to spell her name but makes it different every time,” etc. etc. This is at the end of the school year when it’s too late for me to seek any assistance to address these problems. Finally, the speech therapist recommended I read the Out of Sync Child. Eureka! I still struggle with anger and disappointment that she spent two years with teachers that are supposed to be trained in working with special needs children, and no one ever mentioned SPD, even in passing, until after she was leaving the school. Two important years that she could have been getting OT and learning to adapt to meet her needs, gone. Why? I’m still asking myself that. Was it ignorance, fear of confrontation, apathy? I’m so thankful we have the diagnosis now and can meet her needs. Already, only three weeks into kindergarten, she’s doing well, and I’m getting nearly daily reports. This time I took on the role of informing them what her unique needs are, how to meet them, and that I expected reports immediately if an issue came up. This year I’m wiser and educated, and at conferences I’ll come prepared with a list of questions to ask the teacher, not wait for her to fill me in.

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