autism, anxiety, and lost time

One of the most unreasonable, exhausting, and heartbreaking sides of my son’s autism is his battle with anxiety.  Sometimes anxiety falls under the ever-broadening umbrella that is Autism Spectrum Disorders, and sometimes you face anxiety as one of many comorbid diagnoses.

In our world, anxiety is the fierce sidekick to autism. It’s the root of things like self-injury, aggression, and property destruction.

It is also the thief of time.

Anxiety is the reason you will not find our family in line for a ride at Disneyland, a photo with Santa, or even a burger and fries.  No line, anywhere. Waiting is hard and waiting in unfamiliar environments is when anxiety seizes the opportunity to creep in and serve up an emotional and physical beating until my sweet boy is missing from behind those bright blue eyes.

What I would give to crawl in there too, to fend off this awful intruder for him. To remove all the pain and confusion and just leave behind the unique, beautiful wonder.

We have found some alternatives, like Sensory-Friendly Santa appointments.  You learn to adapt.  I have accepted that some places in the world are just not for us.

At least not for right now.

But I would be lying if I didn’t say that I sometimes wish we had a perfectly curated family photo at the local pumpkin patch.  We went the other day, my two kids and I, and after disrupting all the other families there with my boy’s bloodcurdling screaming (he really has found a new pitch), my attempt to carry him out looked more like a curated kidnapping was underway.

Here’s the thing: a kicking, screaming, fight-or-flight meltdown looks a lot different in a seven-year-old than it does in your typical toddler I-want-a-candy-bar scenario.

When Wilson was five, we both sat in the middle of a busy hospital lobby, sobbing. I could not move him. I had given up until a guardian angel in the form of a nurse offered to help us.

Sometimes we spend hours on meltdown and recovery over something as simple as clothing or food. These are moments, hours, and days that we will never get back.

The thief of time, you see.

These kinds of days can take it out of you in every way imaginable. You boil down the goals to giving him space and keeping him safe.  Sometimes you just want the day to end so that tomorrow can be new, and hopefully different. And just maybe the world won’t be too much for him then.

Here’s the part of our picture I want to paint very clearly: my boy is happy.  He is kind, gentle, finds joy in the simplest things and then radiates that happiness throughout the room. He is also fearless, brave and works hard every single day on regulation and communication.

A little contradictory? I know, I am confused too.

We cannot control when anxiety will show up, how long it will stay and what it will leave in its wake.

We try, but this is just one of the many unpredictable parts of this autism journey.

What we can do is continue practicing coping and regulation skills, even if sometimes that means getting out of our comfort zone, so that one day, you will see us waiting patiently in a line somewhere.  

We can also soak up the happy moments and continue to celebrate all the small victories, because really, they are all big ones to us.

never give up

There is much going on inside of this sweet boy right now.

We’ve had a rough week. One full of behaviors so unpredictable they leave you quietly planning ways to never leave the house again. The world is just too overwhelming for him sometimes.

Today is a new day though. Wilson felt calm and regulated, so I felt brave.  We ventured out to the bakery. This little man did amazing, he even kept his mask on the whole time.

Thanks to nevergiveup.org for the important reminder.  It’s always worth trying again, when the time is right.

The TikTok Autism Challenge – Parents: We Can Do Better

Bullies are bored. 

In the recent “Autism Challenge” videos on TikTok, users are shown mocking people with disabilities, specifically using sounds and gestures to mimic those with autism. These people are making fun of kids like my six-year-old son, and I am not okay with it.

What is funny about someone struggling to get their basic wants, needs and feelings across? Someone who cannot say when their stomach hurts, or that they feel hungry, tired, or sad?

ASD longsleeves

The people shown in these disgusting “Autism Challenge” videos take simple things like communication for granted. They are at home making videos about how people like my son move, jump, flap, bounce and dance to express themselves. We are supposed to laugh and be entertained? Well, we are not.

And let me tell you, we are not bored.

We are struggling. The safety of routine in my boy’s world was ripped away by quarantine, something we have found impossible to explain to him via visuals or a social story.

We are here, listening to the piercing screaming, working on food therapy, language development, self-care, co-regulation, and self-calming skills.  We continue to work on safety in our home with hopes to get back to working on safety out in the community soon.

writing work 2

We are here, painfully watching a six-year-old battle anxiety.  We are his calm in the storm of aggression, self-injury, and fear.

This kid is not bored.

He puts in work, all day, every day. He is resilient. He is tough. He is smart, curious, brave, gentle, kind and he understands much more than he can say. He has more heart than these mindless TikTok “Autism Challengers” probably ever will.  

new haircut

Thankfully, for now, these videos break my heart, not his. 

It completely devasts me that he will eventually cross paths with ignorant people like this.

We need to do better.

I am talking to my fellow parents. The most appalling part of this video challenge was the parent’s involvement. Some were behind the camera and some were even participating in the mockery.

We need to teach our children that their words and actions carry weight. They affect people, they can hurt people.

We need to show our children how to stand up and use their voice when they see people mistreated.

Inaction is easy. When we advocate together, change will happen. 

born rad

 

 

Autism on Paper

0FE1DD52-BD93-407E-9F1A-1C53BBC3068D

Seeing it on paper has been one of the more difficult parts of this autism journey.

The first developmental pediatrician we took our son to gave us an “Active Problem List” that was a mile long:

Global Developmental Delay

Mixed Expressive/Receptive Language Disorder

Childhood Apraxia of Speech

Impaired Social Interaction

Hyperactive Behavior

Anxiety

Toilet Training Resistance

Sensory Processing Difficulty

He was three years old. I didn’t know where to start but I knew we could work on all of it.

Autism Spectrum Disorder

The first time I saw his autism diagnosis on a piece of paper, I sobbed uncontrollably while sitting at a conference table, mostly full of strangers.  You hear about mother’s intuition and “gut feelings” and people will ask you if you saw this coming.  None of that made a difference.

That experience is something I have struggled to put into words for years. Fear, sadness, grief… these don’t even come close to encompassing it. Truthfully, I don’t even want to put it into words.

This was only the beginning. Over the years, evaluators, doctors, therapists, while all well-intentioned, are constantly rating, judging, and assessing my child.  Some things feel wrong, “they don’t know him” we think to ourselves. Some sting, they cut my breath short or keep me up at night. The end-product never feeling like a summation of my boy.

On a few occasions now, I have had to fill out a 30+ page questionnaire covering everything from “Can he use a spoon without spilling?” to “Does he want to kill himself?”

These words get tucked away in file cabinets everywhere: school, the county, therapy, a few pediatrician’s offices. But the weight of them never leaves us.

Anxiety

Self-injurious Behaviors

Aggression

We continue to carry them.

How do you ever get used to these words?  For their sting to become dull?

Medical Incident Reports

Property destruction

Elopement

For special needs parents, the line between acceptance and determination is a blurry one.  We maintain an ironclad grip on these heavy words, these “problem lists”, until we decide in which category they are going to land.

Over time, we loosen our grip and let some words go.

Public school

Organized sports

Music lessons

Sometimes, when we let go, we make room for something better to come along.  Adaptive sports, music therapy, and amazing interventionists who help your child practice sitting in a restaurant and safety in the community.

The heaviest ones, we continue to carry those. We make it our mission to send those words into the fire one day, for them to cease to exist in our children’s lives.

Anxiety

Self-injurious Behaviors

Aggression

We, along with our children, will continue to carry the weight.

8221F061-EF3B-4BC2-AE7D-52591B90B174