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Maddie Saves the Day

Time to Elevate.

Time to Elevate.

People tell me, “you make jokes about your kids but I bet you can’t imagine your life without them.” Uh, try me. Sometimes that is all I can hang onto. –from my standup act

I’m not very proud to say this, but sometimes I resent my own 5 year-old twins. I know this statement sounds horrible, but hear me out. This problem of mine comes from my childhood. Considering how young my parents were when they had me (20 and 18), it’s remarkable how much they did provide for me, but as I’ve outlined before, it was a very dysfunctional situation. In comparison, my twins are growing up in a great suburb, on a cul-de-sac, with a life of pretty much anything they want–they get. They can’t help it, but I sense the entitlement they have to their nature, which triggers the resentment I feel towards them.

It’s nice to hear from so many people that my twins are well-behaved, but my wife and I are constantly working to improve upon them as little human beings, as they are definitely still a major work in progress. As parents the goal should be for your children to have a better childhood than your own. I know my Mom tried hard to do that for me, but life kept overruling her dreams. The most important thing to me is creating a great life for my children, but there is a nagging doubt about how good always creeping in.  The nagging doubt is wondering if I’m not making my twins too soft.

My guess is this thought-process comes from growing up with a bi-polar father who often had views that reflected his split-nature. He would come home from working in the factory and tell me he would never let me follow him into that place. You can do better than that. (Closest thing to a pep talk he ever gave me.) On the other hand, he would constantly tell yell (at) me that I had no idea what hard work was and I needed to toughen up. Listen Papa Roach, you can’t have it both ways. You can’t tell me that I will never do that job, but belittle me for not having done that job. Well, come to think of it, I guess you can if you are a really big man with an explosive temper. No such thing as double jeopardy being illegal in the house I grew up with.

As an adult I sometimes have guilt for living such a soft life. Don’t get me wrong, I put more hours into my job per week than my Dad ever did into his, but comparing the level of manliness between working on a Maytag assembly line and coming up with a clever tweet are miles apart. Evolution has brought us to a point now where physical size will become less important as technology has taken us out of the industrial revolution. Even nerds have less reasons to be strong considering the advances in computers. The 2013 moder of nerd doesn’t have much chance of pulling out their back lifting an iPad, unlike the 2003 model who had to clean and jerk up a Dell monitor and tower.

I know I have wandered from my main point. It comes down to this. I’m not sure it’s that important to toughen up your kids, as it’s not as much of a hard-scrabble existence. My instincts, though, fight this potential reality. This is where Maddie is my great helper.

No matter how great my 5 year-old twins lives are, they will always have a sister with developmental disabilities. Her special needs often trump the attention they get from their parents. Susan and I feel some guilt about this, but ultimately, you just do the best you can. They might not like it, but that’s what it’s like at our house.

There are a lot of challenges that Maddie’s autism brings to their lives. Now at the age of 5, they don’t feel embarrassed by their big sister’s quirky behavior and public meltdowns, but this will change soon. It will be hard for them to recognize in the moment, but I’m confident that growing up with Maddie will inform their lives making them deeper, more caring people. It will also make them tougher, as they have went through things most of us never did as children.

For those of you that grew up with sibling(s) think for a minute about the things that pissed you off the most about your childhood. My guess is that them getting away with things you didn’t feel you were allowed to would be right towards the top of the list. I can tell you that there are things my brother did that I would’ve never thought of doing that still piss the living shit out of me. (Which I will admit is much better than pissing the dead shit of me. That really is an icky phrase, isn’t it?) Well try to contemplate what it would be like to have an older sister who is held to a completely different standard than you are. A sister who is coddled during a meltdown, while you are chastised for just talking too loudly. I’m sure it chaps their little 5 year-old rumps, but that is the way life works at our house. Total double standard as Maddie’s autism usually gives her a get out of jail free card that they can’t pull out on their way to buying the Boardwalk.

So ultimately, I need to get past my own problems about my twins not being as tough as I think they should be. They are a lot tougher than I give them credit for, as life with a sister on the autism spectrum has brought them a different view of life that they could never get from a TV show or even a great story like the one you just read:)

I’m predicting that when my twins get older they won’t agree with everything I write, but I’m betting they will buy into this one. Considering how much better of a person Maddie has made me, I can’t imagine how they could have any other view.

Fundraiser Comedy Show for Special Olympics in Louisville

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Really looking forward to the event we have coming up this Saturday, July 27th at the Comedy Caravan in Louisville. Showtime is 5pm. The ticket sale proceeds go to the Special Olympics of Kentucky. Tickets are 20 dollars at the door or 15 if bought in advance. Click on the event brite link to purchase them.

This show will be feature my It’s An Autism Thing: Let Me Help You Understand performance, which outlines the journey I have undergone from in-vitro fertilization to having a child on the autism spectrum. Oh and did I mention having twin babies, too? It’s a Real Reality Show. Opening the show will be Louisville’s own, Cody Clark, an illusionist who considers himself magically autistic. (Cody is on the autism spectrum) 

I hope you can be part of this event which will be raising money for a great cause! Don’t forget to get the discounted ticket price at this link. Email me at insidescott@hotmail.com if you have any questions.

Clips from the show

Shorter Clip

Longer Clip

Happy Monday with Maddie: July 22, 2013 Edition

Madeline has really come to love doing these videos. Since I was traveling all day she didn’t get a chance to do her video until after dinner. She was a little stressed about this but she is a pro and came through as usual when the iPad camera was focused her way.

What To Say to a Person with a Special Needs Child?

Maddie at 6 years old.

Maddie at 6 years old.

Beats me.

Tune into tomorrow for a more lengthy post on a different topic.

Ok, maybe I can try a little harder to answer this question. I mean I did name this site It’s an Autism Thing: LET ME HELP YOU UNDERSTAND. The problem is that I have a child on the autism spectrum and even I often don’t know what to say to another parent with a child with a similar disability. Hey, fellow parent of a child with special needs, some days really suck and some days are pretty good.

So I don’t really know what to tell you for an answer to this question. What I can speak to with total clarity is what I don’t want to hear. Here are a few examples of things people have said to me and how I’d like to respond them.

  • Wow man, I don’t know how you do it Scott.

Guess what, neither do I. Here’s the deal, though. No one else is going to show up to fill-in for me if I don’t. There is no Kelly Girl or Manpower Temporary Services  we can call to give us a break. Woody Allen said that 80 percent of life is showing up. Sounds about right, though I’m a little uneasy about the part of using a Woody Allen quote in regards to something that has to do with my daughter.

  • Well you’re a better man than me.

You are totally right. I’m a way better man than you. You see, you are what I call a selfish prick. Considering you’ve consistently run away from anything in life that was difficult, you would’ve hit the next Greyhound out of town if this type of responsibility was thrust your way. Hey, but thanks for the compliment.

  • Well she looks so normal.

Uh, thank you? (I look towards my daughter) Maddie, hold still for Daddy. (Looking her over from head to toe and then turn back to the person.) Huh. Well you know something, you just might be right. She does look pretty “Normal”. Not really sure what normal is, but I guess by the standards society has set, she does fit the criteria. Hey Maddie, guess what, you look normal. You got that going for you!

  • You just never know in life. Some day she could grow out of it and become the next Bill Gates.

That would be alright, especially since I don’t have enough money to get someone to fix our shitty Windows based Desktop. Truth be told, though, I would prefer her to become the next Steve Jobs, as I’d love to get a new iPad, but that shit is way expensive.

  • I love kids that have special needs.

Well isn’t that wonderful. I’ve got an idea to test out your love. I’m going to leave my girl with you for a month. You will get to be on call 24-7 worrying about whatever issue that can pop up at any minute. Act now and you get the extra bonus of experiencing the crippling financial burden of spending *91% more than you would on a typically developing child! You finish this task and I will believe you. It will also be good training for being picked as a participant on the show Survivor.

(*(91% figure comes from a Washington University study published in Pediatrics Magazine.)

  • I think we are all a little autistic.

Damn, someone has finally figured out why autism rates are exploding. Who would’ve thought that a woman running a Bedazzler kiosk at the Mall would be the one to accomplish it? And to think that the rates of 1 out of 50 people born with autism is actually way too small. According to your accredited research done at the Fashion Institute of Fort Wayne, it is actually 1 out of 1, since we are all a little autistic. Thank you so very much. You are a modern day Louis Pasteur, if his main skill had been bedazzling pill boxes and armpits.

I want to add that I never try to pretend here that I’m speaking for every parent of a child with special needs, but I do know a lot of parents in my shoes that are shaking their heads yes to my full-flavored snark. I know that people say these things because they believe they are kind comments. I also realize that by publishing these I’m making some people even more uncomfortable of dealing with me, as I put your words under a magnifying glass.

I’m sorry about that, but remember this site is about helping you understand the way things hit me–a parent of a child on the spectrum. I don’t think I’m talking out of my ass when I say that we walk around like Mama panthers trying to protect our kids who are wounded cubs. The world is not designed for our kids so we are ultra-sensitive.

Let me try to leave you with some positive things you can offer up when you meet with someone who has a child with a mental or physical disability. Begin with a smile. Then just do the basic talk you would do with a parent of a typically developing child. How old are you? What grade are you going to be in? What kind of music do you like? Oh and here’s the most fail-safe one you can offer up.

Your Child is Beautiful.

No parent ever hates hearing that one. You want to tame a Panther with a wounded cub? Throw that beautiful compliment out. Remember that many parents of kids with special needs don’t hear that often. They are used to the uncomfortable behavior that people have when they come in contact with their child. A smile and a your child is beautiful will always get you off to a good start.

 

Mallory Long (Maddie’s Sister) Weighs in on Autism

Sisters Mallory at 3 and Maddie at 7

I have noticed as my 5 year-old twins get older, their lives become more impacted by their older sister on the spectrum. Don’t let the looks fool you, Mallory can be a handful, but she also fills the family roll of helping Maddie when we (her parents) are busy doing something else. I like a lot of who she is becoming…most of the time. :)

I thought it would be interesting to get the perspective of a 5 year-old who has a sister on the autism spectrum.

Meet My Little Photo Wrecker

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Unlike anyone else I know, I live in a world of very conflicting points of view.

The comedian side of me knows how hard it is to make an audience laugh. If you want to kill the humor, try to make comedians behave like politicians–going over every word they say to the point where nothing ever feels off-the-cuff. My standup idols were always the most shocking, in your face comics. People like George Carlin, Richard Pryor, Bill Hicks, and Sam Kinison.

The father of a child with special needs side of me, on the other hand,  knows how hurtful words can be. Yeah, I know that some of you think they are just words and people need to get past them, but it just doesn’t work that way for many of us.

So what is a person like me, who lives in both these worlds supposed to do? It took me awhile but here is where I came down on the subject.

My style is not to tell someone not to say something I might not like. Go ahead, I’m not the comedy police. What I am going to do is to be as in your face and be just as irreverent as I have always been, but sell my viewpoints while I’m doing it. Most people in the special needs community have to be careful about how they go pushing their agenda, as they could lose their jobs in the politically correct world they work in. I’m a comedian. You know, the last place, supposedly, where true freedom of speech generally lives. It’s a bit of a tightrope, but I want to bring both of these worlds together in all the creative endeavors I attempt.

Ok, enough with the context, let’s get into why I offered all this up today. It saddens me how many phrases are out there that are demeaning to people with special needs. The newest one I’ve heard over the past year is Photo Wrecker. The idea behind this gem is that a person with some type of disability would ruin your family photo. Hilarious, right?

To me this is people at their most superficial. Let’s make a joke at the one group that can’t defend itself.  I started doing the Happy Monday videos with Maddie so people who have little to no contact with someone like my daughter could feel some of the charm that emanates from her. I wanted people to realized that sure she does carry herself differently than most, but that doesn’t mean she doesn’t experience all the same emotions that you do. It’s not an easy life for her, but on a few levels she surpasses most of us typically developed people.

What inspired me to write this piece today was something I read in USA Today. In the article by Liz Scabo, this was the part that most blew me away.

Nearly 99 percent of people with Down syndrome say they’re happy with their lives, and 96 percent they like how they look, the survey found. Just think about that.

In that same survey, 88 percent of siblings say their brother or sister has made them better people.

 

I’m guessing that my readers here are not at that same level of satisfaction with their lives and their personal appearance. I know I don’t feel close to that level.  It does my heart a lot of good to read the stats about how siblings feel. I can share that Madeline has made me a better person–by a 100 percent. (This wasn’t totally difficult considering I’m your typical narcissistic, but insecure standup comedian. Most of us people who do this biz start pretty low on the good person scale. Hey, but self-hatred is the ingredient that makes us fun at parties!)

While the stats of this study are great to read, I’m not going to pretend for a minute that life with a child with special needs isn’t incredibly difficult, also. It’s such a huge rollercoaster of a life.  Just read here for a refresher. 

So here I sit as a comedian.  I will defend your right to say what you want on-stage, as much as I might not like it. I hope you will defend my right to say what I want on-stage as well, like how I see it is as lazy and weak to make fun of people with developmental disabilities. I hope you will defend my right to tell you to your face that don’t you feel like a big-adult making fun of people who can’t defend themselves? I hope you will defend my right to tell you I lose respect for you every time I hear these type of words come out of your mouth.

I think the word standup means more than just being upright, it means to standup to people in society that need taken down a notch. By this I mean the celebrities and politicians who don’t deserve the money and power they inhabit.  I guess I don’t believe making  jokes about people that can’t defend themselves fits that same criteria, but if you are someone who is unable to work a little harder to find a more challenging topic, go ahead and hit the easy target. You know, the target that isn’t capable of coming back at you. I know you think you are being edgy, but the real truth is it’s the safest comedy, as there is little danger anyone is going to put you on the spot.  Well, almost no one. If I happen to be there, I just ask for you not to flinch when I call you out for your laziness and lack of heart.  As I said, I defend your right to say what you want. I just hope you do the same. 

I am not telling you that my daughter needs to be beautiful to you. Beauty is subjective. But if you think for a minute she has ever wrecked a photo in my eyes, you are totally out of your mind.

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Happy Monday July 15th Edition

Our family was having a tough morning, but Maddie demanded to do her Happy Monday video. You might notice she is rocking a little more heavily because of the stress around her, but she will not disappoint her fans by skipping a Monday.

Well Look Who Became a Man

 

Maddie at 2 years old.

Maddie at 2 years old.

Here is something that you might not expect to hear, but my wife Susan and I were not stunned when Maddie was initially diagnosed with autism. After having test after for a very long year trying to get some information on why our little girl was having major developmental delays, we just wanted someone to give us some answers. Also, being diagnosed on the spectrum opens the door to some increased services that are not available without it. So we were not hit that hard by the words your daughter is on the autism spectrum.

It was the next part of the Doctor’s conversation that left me feeling depressed…

You should be aware that there is a good chance Madeline will never marry, never be able to hold down a full-time job, and a good chance she will live with you the rest of her life.

I had done some research about autism, but I guess I hadn’t let myself acknowledge that these were potential outcomes for her. Now I will promise you these words felt like a punch in the gut. I had all these dreams and fantasies about what my little girl was going to do in life and it seemed like most of them were now out of reach. I tried to keep a happy exterior around my wife, but internally I was very depressed for a couple weeks. Then I had an epiphany. These dreams and fantasies weren’t Maddie’s dreams and fantasies, they were mine. My job from now on was to help her live her dreams and fantasies. 

Now I don’t know the definition of what makes a man, but I point to this moment as when I feel it officially happened for me. I became less selfish. Unconditional love needed to take over.

We have been told by lots of therapists/teachers that as parents, we have been ahead of the curve in embracing the reality of Maddie’s autism. I think that has a lot to do with both us being realists who try to take in as much information and advice that we can and then we proceed from there. Maybe this seems a little too cold and calculated for some, but 1 major piece of advice I will give any new parent of a child on the spectrum is that you don’t have time to fuck around. Literally and figuratively. Pretty much the only definition of getting busy you are are going to have to concern yourself with is to make things happen for your child.

What are these things I’m speaking of? Well, unlike when someone is diagnosed with a disease, autism is a disorder so there isn’t a simple medical path you are given to help your child’s development. The best thing you can do is to search online and also contact an autism advocacy group so you will know what therapies are available. Kick it! You gotta fight…for your right…for therapies!

The more time has gone by since the Doctor gave us the real truth about Maddie’s future, the more I appreciate his candor. It greatly helped me understand what was going on and while it took me a couple weeks to really process these statements, but when this epiphany happened, I was then able to get started with what needed to be done to help my girl. I feel a little angry when I hear about a parent of a child who clearly has major developmental issues occurring, but hasn’t had them tested. You can’t just wish away autism.  Keep in mind, the day you have a baby you are no longer the most important person on your radar. Time to take off your skinny jeans and put on your man pants because lots of shit has to get done.

Go Ahead and Stare

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The best moments in my standup career have been since I’ve been sharing my story of having a child on the autism spectrum. So many people that have someone they love with special needs come up to me after the show to tell me how much they appreciate my perspective on the subject. I have been privileged to share some special moments with these fans, as they tell me stories about a person they love. They are part of the same tribe as myself.

Last year following a show in Detroit I had a memorable moment. Some guy comes up to me and says So you have an autistic kid? Let’s begin with that. If I hear someone say something like this, I generally know they have little knowledge on the subject. I’m not saying you are a bad person if you say something like this, as it’s not a prerequisite in life to always say the perfect thing, but I promise you I would never describe my girl that way. My girl is not autistic first. She is my beautiful girl first. It might seem like semantics to most, but the reason I mostly use the phrase “autism spectrum” is because people with autism are so diverse that it seems unfair to label them all with just one word. Spectrum helps me denote the wide range of people that are on it.

As I said, though, I tried to keep an open mind to this guy, despite internally flinching a little at his initial sentence. He then offered this up. My girlfriend has an autistic kid too. Let me tell you, some people annoy the shit out of me. I was at the store the other day and someone was staring at the kid. Well I told them to quit fucking staring and focus on something else. 

At this point, the guy seemed pretty impressed with himself, which is why I’m guessing he wanted to tell me this story. I know what he wanted was for me to slap him on the back and congratulate him for standing up against these staring people. Instead, I just wished him the best of the luck with his girlfriend and told him to treat her well, because she has went through a lot as a mother with child on the spectrum.

Here’s what I took from our conversation. To me this guy was no hero. He was someone embarrassed by his girlfriend’s son and was constantly looking around to see if other people were judging him by being with the boy. I would bet big money that he is no longer with the Mom. As hard as it can be for a single mother of a child with special needs to meet someone, an insecure lout like this guy would have been a bad addition to the already chaotic life they were living.

Here’s a little secret that parents of children with special needs don’t usually share. When we are out in public, we rarely have anytime to notice what other people are doing, as our focus is trying to navigate the bumpy road which our child is trying to navigate. I truthfully couldn’t tell you what other people’s reactions are to Maddie, as my focus is on Maddie first, and then the list I’m trying to get through as fast as I can.  As I’ve discussed before, Commencing Meltdown Engines On can happen as fast as 10, 9, 8…

I will tell you that since I’ve known Maddie was not a typically developing child, I’ve become more apt to look at people that are like her. I feel a strong connection towards these people and whoever is taking care of them. In a world where we as parents of children with special needs often feel alone, I wish these parents could read my mind and understand that I know many of the challenges they live with on a day to day basis. Now when I’m not with Maddie, though, I’m like most everyone else, concerned that these people might take my looking at them in the wrong way. So I know how difficult it can be to choose the right reaction. It’s human nature to want to look at people that don’t fit the norm. That is why the reaction this lout had created the opposite reaction he was hoping for from me.

So what should you do when you see a person with special needs? Start by not turning away. That is the most hurtful thing you can do. Even though society has always treated people with special needs like social lepers, they are not. A smile would be a good place to start. If you have an empathetic heart, that will serve you well. I promise you that Maddie has never complained about someone smiling at her. As I said, it’s a WIDE spectrum, so the social skills of each INDIVIDUAL will run the gamut–which when you think about it, is not much different than typically developing people.

I realize it’s not easy to know how to react around someone with special needs. I have a child who can be hard to predict–even for me. Most cliches are bullshit to me, but the patience is a virtue one is a great place to start. I have no problem with you staring as long as you show my child some mix of patience, empathy, and especially if you add a smile. Come to think of it, that’s a pretty good formula to treat everyone with. I know I would be better served if I treated others that way. Well, except hecklers.

Happy Monday: July 8th (Patriotic Edition)

Maddie decided she wanted to start with the pledge of allegiance, but then it diverges into a metaphysical break about God. (Note: Ron is the name of her bus driver last year who passed away. He is still an important person in Maddie’s thoughts.)

Happy Monday: July 1, 2013

Maddie becomes completely infatuated with someone every few months. It’s like puppy love to her whenever she thinks of that person or mentions there name. These people fit 3 categories; teaching aide, bus helper, or during the summer, camp counselor. Her current crush is a counselor at Easter Seals Crossroads’ Camp Abilities.  Like a typical almost 10 year old girl she gets these crushes, but unlike most girls who focus on a Justin Bieber-type, Maddie goes for someone who shows her attention and love back.  Kind of evolved when you think about it.

A Friendly Smile in Every Aisle

Sisters

Sisters

When you have a child with special needs you try to make as few trips out in public as possible. You try to plot these excursions out like there is a zombie war happening outside your window, with dangers lurking around every corner. Since your home is the most controlled place you have to keep your child from having a meltdown, you end up holing up as much as humanly possible.  We are not agoraphobic. We actually would love to get out of the house, but the negatives often out-weigh the positives for doing so. Going to the grocery store, though, is a necessity that can’t be put off.

Continuing with the theme of trying to keep many of my single male readers interested here, my next analogy following zombies will be superheroes! (Scott tip: Pandering is good if it helps get people to what you really want them to read.) When you leave the house with a kid on the spectrum, you sometimes feel like you need to have a utility belt. A belt with all type of weapons that can slay the demons that are liable to pop up when you are outside the Hall of Justice. For Maddie this would begin with a pair of headphones to keep any loud noises away. Make sure to have tissues handy, too, as my girl tends to be a projectile sneezer, producing runny hangers that will sway down to her neck. For quite a long time the belt also needed a chewy tube, which is a rubbery tube that helped her get sensory input when biting on it. Besides helping calm her, these tubes kept her from chewing her own clothing or many things worse, which were damaging her teeth.  All of these items are/were part of Team Maddie’s mechanisms to help keep her from losing it at the local A&P.

Maddie likes to pack a few things with her when she goes out.  Maddie brings a backpack almost wherever she goes. It kind of serves as her purse. The more weight she puts in it, the better. This need for heavy weighted things is called proprioception. (Please don’t leave me now, I realize looking at that word hurts your brain, but I promise there are some good stories below the technical understanding section.) The best definition of proprioception I have found comes from an article by Jeannie Davide-Rivera. She writes a blog called Aspie Writer. Jeannie has first-hand knowledge of proprioception as she grew up as undiagnosed person who as she describes was stumbling through life with a form of Autism called Asperger’s Syndrome. It took her 38 years to be properly diagnosed. 

Proprioception refers to one’s own perceptions. It’s an unconscious perception of movement and spatial orientation controlled by nerves within the body.

Our proprioceptive system allows us to locate our bodies in space, to be aware of where our arms and legs are in relation to one another, as well as, where they begin and where they end. Proprioception helps us perceive the outside world, telling us whether our bodies are moving or sitting still.

This system helps us perceive the amount of force needed to complete a task, and then allows us to apply it appropriately. It helps us measure and perceive distances, allowing us to move through our world without crashing into everything around us.

Child and adults with autism often have difficulty with proprioception and very well may just be the thing that goes bump in the night … and the day, and at work, and in the streets. Poor proprioception may likely be responsible for those many bruises, skinned knees, and torn stockings that plague our days.

 

While a “normal” person unconsciously perceives and is aware of each step they take, an autistic person must think about and focus consciously to perceive what comes naturally to others.

Not long ago people with special needs used to be referred to as simpletons. How completely asinine was that? I can guarantee you that Maddie is way more complicated than any other person I’ve ever met. Life for her can seemingly be like one big-ass obstacle course and she’s not exactly Kyle Rote Jr. or Renaldo Nehemiah finding her way through it.**

**Reference to Superstars competition that used to air on ABC. I could’ve gone with a young Scott Baio if I was referencing the Battle of the Network Stars version . Younger readers might remember the obstacle course talents of Herschel Walker or Jason Seahorn. Yes, I know I’m strange.

So lets get to the contents in Maddie’s backpack. She has never watched more than a minute of the Mickey Mouse Club, but for some reason Minnie resonates with her. We went to Disney World last summer and I can’t remember Maddie once being interested in wanting to see the real-deal Costume Character. It’s her security blanket. It’s not about the voice or the personality that bonds her to Minnie, she just likes how it looks and feels. It’s a Maddie thing.

She also likes to jam in old school homework papers and pencils, as pretending she is going to school makes her happy. Oh and she must bring a basketball. She loves basketballs and our agreement is that she can bring it with her in the car, as long as she doesn’t bring it in the store. While this is the agreement, every other time we go to the store she nonchalantly gets out of the car with the ball and begins to bounce it in the parking lot. If I let her bring it in with her I’m afraid she’d be dribbling down the aisles running a fast break like Chris Paul.  Well maybe more like Cliff Paul. I promise you she has been told it stays in the car and it’s not like while we’re driving there I’m playing Sweet Georgia Brown on the stereo, but she still pushes me. This leads to a frustrated parent yelling Come on Maddie, you know you can’t bring the ball in the store! Much of the time in public I know that I appear to be a crazy person. At this point, appearances could be correct.

For most parents of young kids, the cereal aisle is the toughest one. That was never a big issue with Maddie, but the frozen food aisle was a different story. For a couple of years whenever we got to this aisle, Maddie would make a break for the doors, open them up and put her tongue on the inside cool glass. It wasn’t like it was so cold that she was going to reenact the recess scene from a Christmas Story, but you really aren’t that wild about your child tasting the germs of every grimy grocery customer. When she first started doing this I will admit this was one of the few times where I was a little embarrassed by one of her strange behaviors, but eventually I got past it. I’m glad to say that she eventually got past it to, as this compulsion ended a couple of years ago.

The best way to keep Maddie from acting up at the store used to be putting her in the cart. If you have seen the great HBO biopic about Temple Grandin, you would know that many people on the spectrum love to find confined spaces. Grandin designed a thing she calls the Hug Machine that would help calm her down from the deep tissue stimulation it would provide. While a shopping cart doesn’t give the same exact stimulation, I’m guessing the tight confined space of it helps her with all the over-stimulation she feels from the bright lights and sounds that a grocery offers up. Now putting a child in a cart is not that big of a deal early on, but that really starts to change by the age of 5, especially when you take into consideration that Maddie has always been in the 90 percentile for height and weight. Still, you do what you have to do to get groceries, so even at the age of 8, I would hoist my 80 pound girl into the cart, if it was needed.

I’m happy to say over the past year she hasn’t been demanding to be put in the cart, but the meltdowns continue. A number of times she has thrown herself to the floor and yelled NO! when told to stand back up. These are the worst because you can’t reason with her and she gets louder if you try. You can’t physically lift her up anymore because besides her now weighing in at 85 pounds she also goes into dead weight mode like a Vietnam sit-in protester. A big reason I workout is to be able to handle situations like this, but when she does the dead weight, I start wishing I could afford to get on the juice or at least HGH.*  What ends up happening, as people try to steer around us, is me squatting down by her and promising a special treat if she will rise to her feet again. This works, but you feel like the worst parent in the world. Talk about encouraging bad behavior. Don’t think just because a child has developmental disabilities they aren’t capable of some clever hi-jinx to get what they desire.

One of the major side effects with using steroids/HGH is your balls shrivel up. Considering I drive a minivan already, can’t see how much more damage I would suffer. 

Now a logical answer after reading so far would be hey Scott, leave her at home. Here’s the problem with this point. Maddie loves to take car rides and she hates being bored at home. She will promise that there will be no outbursts from her. If you don’t take her she will spend most of the time you are gone melting down at home. Over the past couple of months she has made things a little easier as instead of melting down in the store, when we park she will start to yell and scream about how she doesn’t want to go. Ok, calm down Madeline. We will go back home. Often her passionate response when you start driving away is I want to go to the store! I will be good! While this is new when it comes to being in the parking lot of the store, this type of manic decision-making has happened with Maddie for a long time. She is so distressed when this occurs. It breaks my heart sometimes how tough life can be for my girl.

As much as you try to be 3 steps ahead there are always landmines that you never see, though. Recently I was grabbing a couple of things and turned around to see Maddie chewing on a chicken wing. They had recently put in a chicken wing stand that I hadn’t accounted for. Now open bar seems to be universally good, but not when it has chicken wings in it and Maddie is on the loose. Where most people would realize it’s intent, Maddie saw it as just one big-ass sample display. Channeling a seasoned TV cop, I calmly told her to step away from the cart and drop the wing. She responded by taking one more bite and then tossing the half-eaten buffalo appendage like a drug courier throwing the evidence out the window during a car chase. I watched in slow-motion hoping it would land helplessly to the floor. Nope. Right back into the display of undamaged poultry. I promise you I really wanted to do a hit and run and flee the scene of the crime, but instead I told the manager and they cleared out the bin.

The toughest moment is following next. Parental Discretion is advised.

I can remember being at a grocery store, by myself, with my daughter on the spectrum and her twin 2 yr old siblings (at the time.) This was not something I had ever attempted to do before, but I’d been overcharged over 5 bucks for some Mexican chip dip and and had come back to get the refund. Normally I would have just let it go, but the only reason I had bought this dip was it was a last day for the sell-by date, so I threw caution to the wind and purchased it. I don’t know who these 7 dollar paying Mexican dip people are, but our budget doesn’t allow us to enjoy an extreme luxury like that.

Now I knew I probably had about a minute before things would escalate, so I was focused on the task at hand. I spoke to everyone in the van on the way, plotting out the details of this like a bank robbery. Considering that developmentally I was talking to a trio of 2 year-olds, I’m doubtful they understood the magnitude of my plan, but as I mentioned, my sanity was questionable at best during this period. I can’t say we were striding in like the dudes from Reservoir Dogs, but we did went anywhere we were guaranteed to make quite an entrance.

Strolling up to the return desk the woman manning its counter was busy gossiping to another employee. We waited. The minute went by. I wished it was a situation like when you are at the park and a ball gets away–so I could just hold my hands up and say a little help, but despite what you might think, I’m actually a very polite person who always waits my turn. So my anxiety reaches 10 as I could feel the ticking time bomb behind me about to reach detonation. Maddie was manically rocking back and forth, as patience is not a facet of life she has ever mastered. Inside I was feeling just as manic, as patience is not something I’ve ever mastered, either. At this point, my youngest (Princess Pistol) started screaming, which set off Maddie, since loud noises usually create an instant volcanic eruption. Oh and I don’t want to forget that while this was going on, my son had realized this was the diversion he’d been looking for and he wandered off to check out the candy bars.  I had 2 girls crying their lungs out and an escaped convict. (My boy was looking to eat and run.)

Now if you want to get a store employee’s attention, bring my crew with you.  This did force the woman behind the desk’s hand and she finally asked what I needed? (Top-notch customer service!) I put the item up on the counter and showed the receipt, while multi-tasking like a mo-fo to try to somehow put out the 5-alarm fire. Well the woman rang the item through and said that this wasn’t the right item. I grabbed the receipt and showed her again. She explained that even though it was the same product, I had bought 2 and only 1 had rang up wrong. I had brought the wrong one. I tried to explain over the cacophony of screams that were going on in the background that they were the same product. Sorry sir, she responded, but there was no sorry in her voice. I walked away pushing 3 screaming young children. (It had went up in number by this time, as I yelled at the shoplifting toddler that we don’t run off from Daddy!)

I got everybody in the van and shut the doors. As the hysterical crying continued, I just sat there stunned. I was broken. It wasn’t the first time and it wouldn’t be the last. I had spent 2 years on the verge, but this moment put me into a full-on nervous breakdown. It felt like the last ounce of my vitality had been drained. Total desperation overcame me. The only thing I had to push me forward was knowing in a few hours Susan would be coming back home from work. I started up the van and cranked my White Stripes CD to try to Icky Thump myself out of this nightmare. We headed home. I can imagine what it’s like to face these challenges as a single parent and I wonder how some days these people are able to manage. I tip my kangol to the incredibly strong human beings that are on their own and pushing on.

These are just a few of many incidents I could discuss at the store. I will tell you that as I wrote this I struggled with how much I wanted to share. My number 1 concern is about protecting Maddie, but I also feel a responsibility to helping others have a better understanding of the challenges people on the spectrum, (and their families) face. Sometimes I am asked what can I do if I see a parent struggling with their child at the store?  My recommendation would be for you to feel a little empathy and try to clear out of the way until the fireworks end. Oh and definitely make sure to shove a crisp $20 dollar bill in the back of my pocket as I make my way out. Thanks again for your patronage!