The scary thing about an Autism Evaluation is the fact that it’s an Autism Evaluation.
The morning of the appointment I felt unsure. I was nervous. A small part of me was convinced that maybe this would be the diagnosis that put all of the thoughts floating around to rest.
Instead it seems as if all of those thoughts were simply poured into a glass jar and shaken.
It reminds me of when I was younger and my brothers and I would play in my grandmothers backyard at night. We would always beg her for a jar to catch lighting bugs in. I remember running around the yard on warm summer nights with my brothers catching bugs. My brothers would smush the bugs against their skin until all that was left was the whisper of a faint neon glow. I remember how much I hated this. I kept my bugs safe in their jar, took them inside, and poked holes in the top. I remember falling asleep tucked under the thin sheets watching the little bellies of these precious bugs illuminate. My mind has been like a jar jam-packed with lighting bugs. Swarming and swarming round and round.
It turns out Wyatt passed his evaluation with flying colors. “He doesn’t have Autism,” the doctor said.
I wish I could say that after that statement William and I stood up to kiss each other, grabbed Wyatt and left that building. But that’s not what happened. The doctor followed up that statement with the dreaded “But…..” and my heart sank. Of course. Of course this wasn’t over.
She said that during the evaluation when she was examining Wyatt’s legs she noticed that he had some extra muscle mass. She said this is a common finding in kinds with neurological delays. She then said that she wanted Wyatt to have blood testing and and MRI.
My mind immediately flashed to an old episode of Grey’s Anatomy and I had to stop myself before I let my thoughts spiral. The doctor said that sometimes when a fetus doesn’t get enough oxygen to certain parts of their brain certain things can happen. So we’re looking at Wyatt’s brain to see if this is simply a speech delay, or if there is something more to it. But the extra muscle mass in his legs leads her to assume that there may be more.
We left her office feeling incredibly beaten-down. I held it together until we got to the car. I tried my best not to cry in front of Wyatt. I tried. But it was merely minutes before I felt the warmth and wetness dripping off my chin – and before I knew it – I was sobbing into my hands.
My baby. My baby is going to have an MRI.
To make matters worse – after the appointment we took Wyatt to the lab to get his blood drawn. There were two ladies poking him with needles in his arm and hand – and they couldn’t get anything. It was like they had never drawn a toddlers blood before. Wyatt’s body was shaking and shifting on the table under the weight of William and I attempting to hold him down. I softly sang the ABC’s in his ear but it did nothing to help. He looked up at me with tear-filled eyes and screamed. After they poked and wiggled in his arm, they poked and wiggled in his hand. Wyatt was drenched in sweat and hysterically crying. 15 minutes into it – I picked my baby up from the table and told them we were done.
So, that’s it folks.
I wish I had something happier to report.
But this is it – the genuine and raw truth.
I pray right now for Wyatt. I pray God holds him extra close in His hands & I pray as he is guiding the doctors & nurses through the MRI- they see what they need to see. I pray for his future growth development. Sweetie- this is not your fault. God simply has a plan for little Wyatt & he’s going to guide his way. I love you and will continue to pray for him. I wish I could hug you right now.
Praying for you guys!
Aww mama. You are so strong! Hugs and prayers for you and Wyatt. This is not your fault and your little man has a special plan for him no matter what it is! 🙂 I can’t imagine having to watch your baby go through that but you are doing amazing!
Wishing Wyatt and all of you the best outcome possible – kia kaha!
Praying for you and Wyatt. It’s tough, I have been there. I am still there. Every few months we have an IEP meeting with Matthew’s teachers. His last appt. of the school year to determine where he goes to school next year, is next week. Matthew is 5 1/2. He is Book smart, he plays with other kids like a 4 year old. He can read, write, add, subtract, and he’s only in a kindergarten transition class. He will go to kindergarten in August, but the issue is, where? Will they let me keep him for one more year at the great school that he is currently attending in which the teachers are used to dealing with kids with special needs and behavioral issues? Or are they going to make me put him at the school near my house with a teacher who not understand him and be patient with him, and understand that it’s going to take him longer than the other kids to do his work? Will his teacher understand that keeping him from recess to make him do his class work, probably won’t work for Matthew? And that it will probably result in a tantrum and meltdown in front of all of his friends? Will the kids in his class tease him? I hate the unknown.
First, know that you are not alone in your fears for your son. I hope that the doctor will have answers for your soon. Our minds tend to imagine the worse which is totally normal. Wishing you quick and reassuring answers!