The Other Side of the Table

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I am no stranger to the IEP process that’s for sure.

I just finished my 12th year as a special education teacher in a small town in the thumb of Michigan and I absolutely love my job.

I’ve known I wanted to be a special education teacher since my junior year of high school and I pride myself in always trying my absolute best to put the students first and try to create great relationships with my students’ parents.

I can’t tell you how many IEP meetings I have run in the last 12 years but it is a pretty high number. But none of this prepared me to be on the other side of the table, as the parent attending the IEP meeting.

My 4 year old son was recently diagnosed with autism and now the tables were turned and I was going to be the parent at the IEP meetings.

I thought my wealth of knowledge on the IEP process was going to make this so much easier; but I was wrong.

I’ve sat through many meetings about my son already and he is only 4 years old, but the other day at meeting to do a possible amendment to my son’s IEP was the first one that I cried.

We were meeting to discuss his integration into a regular education preschool program and the possibility of an aide to help with this transition.

As the meeting began, I noticed that it didn’t seem that the people sitting around the table felt this was a good transition and words like “amount of hand over hand prompting” and “his ability levels range from 3 months to 2 years old” started to hit me like a ton of bricks.

These are all things that I already know about my sweet, energetic little boy but to hear them like that in a meeting was on a whole different level.

I guess you could say this was one of those moments when autism hits you hard.

I have had many of them and I’m sure I have many more to come.

I think this one is especially hard because of my profession and the moment I realized that my knowledge of the special education world couldn’t and didn’t save me here.

This journey I have gone on with my son has made me a better special education teacher. I am so much more aware of parents and the journey they have been on with their children.

I ask myself this question with each and everyone of my students, “What if this were Franklin, what would I want for him?”

And although I tried to do this with my students before my journey with autism began, I know that I did not in the way I am doing it now.

I know it’s difficult sometimes to sympathize or empathize with something you don’t have experience with, but I ask my fellow special education teachers to please be aware of this…

Although you may think you know what it is like to have a child with special needs because you work with them everyday, ultimately unless you have a child with special needs I would argue that you do not.

I am only saying this with the greatest of love and respect for special educators because I was that person until 4 years ago when an amazing little boy with autism came into my life.

Written by, Jessica Bluhm

My name is Jessica Bluhm and I am a 6-12th grade special education teacher and mom of a 4 year old son with autism and a 2 year old typical daughter. I am married to my best friend, Tyler and we enjoy spending time with friends and family.

Finding Cooper’s Voice is a safe, humorous, caring and honest place where you can celebrate the unique challenges of parenting a special needs child. Because you’re never alone in the struggles you face. And once you find your people, your allies, your village….all the challenges and struggles will seem just a little bit easier. Welcome to our journey. You can also follow us on Facebook, subscribe for exclusive videos, and subscribe to our newsletter.

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Kate Swenson

Kate Swenson lives in Minnesota with her husband Jamie, and four children, Cooper, Sawyer, Harbor and Wynnie. Kate launched Finding Cooper's Voice from her couch while her now 11-year-old son Cooper was being diagnosed with autism. Back then it was a place to write. Today it is a living, thriving community of people who want to not only advocate for autism, but also make the world a better place for individuals with disabilities and their families. Her first book, Forever Boy, will be released, April 5, 2022.

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