And the Oscar Goes To…

Some days you just gotta congratulate yourself because no one is going to do it for you! As a sensory parent, no one is hosting some grand dinner for you to honor your Outstanding Dedication and Perseverance.

My big win was this weekend at a birthday party. We arrived a little bit late and the place was in full swing. My 5yo took one sweeping glance at the “dance party” birthday and instantly insisted I sit with him for a while.

Initially I was thinking, why can’t my kid just join in for once without any drama? But then the drama didn’t come. He sat quietly and asked me to scratch his back. This from a tactile defensive kid. So he was trying to find a way to acclimate to the loud music and commotion. Hugging or cuddling would have been too much. But today the back scratching was just right.

Then he began to get into the groove. He didn’t jump into the group but stayed off to the side, having a great time doing what looked like a Jane Fonda aerobic workout.

He excused himself from the room twice, saying it was just getting too loud in there. And this was when I had my Aha moment. He’s finally starting to get when he needs a sensory break and acting on what his body tells him. Yes, this is where you break out into applause!

This is the moment we all work so hard for. When our child, even though he may still have sensory issues, is able to identify what he needs and then does what he needs to do to self regulate himself.

Now I’m not kidding myself. This child cried and cried and cried and cried when I picked him up from school last week before he had time to finish looking at a book. He was so upset he couldn’t respond to what I was saying or probably even hear it. So I drove the car with a sobbing child to OT. It’s what we have to do sometimes.

But then there are times like this weekend. When I can see into the future and know that even though I may not be able to fix my child’s sensory challenges, I’m able to grasp onto the very real hope that in the end he’s going to be okay.

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About The Jenny Evolution

As the mom of two children with Sensory Processing Disorder (SPD), I’ve discovered there are so many parents out there on the sensory spectrum that have suffered in silence. I have been one for quite some time, and it’s time to stop. Over the past year, I’ve worked hard toward becoming authentic with myself, and now it’s time to rediscover myself as a whole person while balancing the ever-demanding needs of my sensational kids. My first step was finding an outlet for all of the information I’ve amassed over the past years. I was initially exhausted trying to learn about SPD and keep up with the latest info. After almost two years of occupational therapy, I was ready to “pay it forward” for other parents facing this disorder and created The Sensory Spectrum (www.thesensoryspectrum.com), a communal page for parents who have children with SPD to find information without having to scour the Internet. The next step is to start sharing the personal side of sensory disorders, which define SPD but are also components of Aspergers and Autism. So I welcome you to The Jenny Evolution (www.thejennyevolution.com), my own personal journey, insights, knowledge, messes and triumphs. Most people call me Jennifer. But we’re going to become intimate friends, so call me Jenny.

    Comments

  • Dorothy Stronglove


    Thank you for this post, it is Au-Some! Our Autistic girl is 3.5,and has huge sensory issues. She is a fluctuator, but most days is a seeker. She recently started to make her own sensory breaks (getting on her trampoline, bringing me fer vest, asking to swing, etc…) Every time I see her do it, I am amazed and proud. She has come so far in the past year, and although we still have a long way to go, I am filled with pride and hope. Reading your story brought tears to my eyes, because it is beyond wonderful. Sending you HUGS!

  • Sybil


    Congratulations to you and your son! It’s good to celebrate those days when progress is evident. Keep that day in your mind, so you can remember it when the day isn’t so good. Your post was very encouraging…thanks!

  • Susan S.


    Congratulations! Yes, my SPD kiddo is 9 now, and is very good with satisfying his sensory needs when he is outside of school- where he’s in an environment that he can do what he needs, when he needs to do it. School is a whole new challenge that we’re still working on.

  • Heather


    Hear the clapping coming through the screen! AWESOME!!!

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