A Granny Smith Breakthrough: Success with A New Food!

A Granny Smith Breakthrough

Bright green, shiny apples. They must have been speaking pretty loudly in order to get Stevie’s attention amidst the cluttered kitchen.

Stevie doesn’t eat fruit. Or vegetables... or protein for that matter.  He’s a crackers and cereal kind of kid with his super restrictive and self-imposed diet on top of a few food allergies that restricts him even more.

Stevie has autism, which includes a heavy dose of Sensory Processing Disorder.  He stopped eating all but a handful (literally) of foods between 18 months and 2 years of age. Restrictive eating is a very common symptom of autism spectrum disorder.

But the other day as I was picking up some toys my 3 year old had strung across the floor, I happened to glance over at Stevie.

He looks at me with that look that says, “I’m doing something and I might get in trouble for it so I’ll hide it.”

“What are you doing, Stevie?”  His look begged the question.

“Eat the apple?”

“Are you really going to eat it? As in, put it in your mouth and sink your teeth into it kind of eat it?”

He puts it up to his mouth and bites just enough to make an indentation as he continues to look at me.

I watch a tiny drop of juice dribble down the side of the Kermit-colored apple. I see him sneak a taste and I wonder what he thinks of it.

“Eat it.  Goodbye Mommy!” (This is his tactic to get rid of us when he wants to do something he isn't supposed to.)

I honestly didn’t think he would eat the apple. Usually, if he has a piece of fruit, he plays with it until it is destroyed into looking like a decomposed bruised and mushy mess.

But this apple must have been begging to be tasted, so Granny-Smith green and tart. And that one enchanting droplet of juice just sealed the deal for him.

I leave him alone for a minute and return to spy him biting all the way through the crisp green skin, chewing, swallowing and biting again as he contemplates this new experience.

The tart.

The sweet.

The crunchy.

The irresistible!

Not only did he eat the one apple, but he asked for another one and ate that too!

And not only did he eat an apple for the first time in years, but he ate it whole!  In the past, it had to be cored and cut in thin slices and he’d eat just the middles.  But this time? He sat at the table like the 10 year old that he is, and ate the apple whole. One big teeth sinking sensory bite after another.

It was a beautiful sight.

I always thought he’d eat new foods (eventually) in the same accidental way that the chocolate fell into the jar of peanut butter to create the concept of the first Reese’s Peanut-butter Cup (or so the commercial led us to believe) and he’d realize that other foods really do taste good (and that maybe it is ok if foods touch)!

Maybe this is the start of a sensory turn-around in the food department. Stevie started this life as extreme sensory aversive and defensive, but in the last few years he's been experimenting with more things in a sensory seeking style.  So maybe this next couple years will bring some experimenting with food!

Now It's Your Story Sharing Turn:

For those of you who have a restrictive eater, how do you introduce new food or encourage him or her to taste something new?

What was the turning point in your child's eating behavior if they have successfully expanded their diet?

For everyone else:  Don't you just want to go eat an apple? Remember to send up a toast to Stevie when you take that first bite!

SensoryBlogHop


Autism And Discipline: Why I Don’t Spank

Autism And Discipline

This may be the most controversial post I've written. Never the less,  this is our story....

I recently posted a question on Facebook asking for ideas on how to get Stevie to stop throwing things down the stairs.  Amidst several creative, problem solving ideas, were some more traditional suggestions that I "just spank him". After all, it is a direct disobedience of the rules, right?

So, let me just "go there" for a minute.

The assumption is that spanking works, and that it is a reasonable punishment for direct disobedience.

While that may be true (although not publicly acceptable anymore)  for some typically developing kids, it is not true for all kids, especially those on the spectrum.

For any punishment to work, there are 3 things that must be understood by the child, according to Bill Nason, MS, LLP:  They must know that what they did was wrong, they must know what to do that is right in that situation, and they chose the wrong thing (which assumes they were able to choose the right thing, but didn't.).

Now that seems like a nice, neat formula for whether you should punish or not, but nothing is straight forward with autism. When you add the confounding factors of sensory disorders, language barriers, cognitive abilities and medical issues, it isn't so neat and tidy any more.

Here are a few examples of stories from our journey:

Let's flash back to the year 2005, when my twins were 2 1/2 years old, and we did not yet know that Sage has autism.  We had just put the twins upstairs in their toddler beds, and were trying to get them to sleep in them. Hope did so happily, loving the idea of a big-girl bed. But Sage? Not so much. He wanted to sleep in his pack-n-play, which he had recently destroyed and was no longer an option.  So to the bed we required.

He wouldn't stay.

No matter what we did.

Friends said to be more consistent, and he would figure it out.  Not.

Friends said to spank him every time he gets out of bed. Didn't work. He'd look up and laugh, and then run to bed so he could get right back up again and have the scenario repeat. He thought it was a game.

Nothing anyone told us would "work". The child would not sleep.

Completely flabbergasted, I called Focus on the Family and set up a time to talk to them about what to do. The counselor was great (especially considering I mistakenly thought of them as "the spanking people") and advised that if spanking doesn't work, then don't do it.  She said that not all kids respond to spanking as a discipline and to find other ways. She suggested we pray about him and what to do, and she sent us some books to read in the mail.

Looking back, I know she suspected SOMETHING was up with Sage, the one who couldn't talk except to say numbers, letters and colors. The one who repeated his steps over and over.  But, she didn't know it was autism. We wouldn't figure that out for a little while longer.

So, we started sticker charts and positive reinforcement. Didn't work. Now we know that he couldn't connect the dots between an action and it's consequence (good or bad).

I honestly don't remember all the things we DID try, but we pretty much tried everything we found to try.

And then I went to the bookstore and decided to find a book on toddlers and behavior. The first book I opened, described Sage to a T:  doesn't like to color, doesn't play with other kids, doesn't point, delayed speech, great with puzzles, doesn't eat snack with a group, etc.  That kid had autism.

And then, we knew: Sage has autism.

We spied on him at church to verify our suspicions.  We knew what to look for, and we saw it.

And we found out after reading THAT literature, that kids with autism are KNOWN to not produce enough naturally occurring melatonin and therefore have a hard time falling asleep, or staying asleep.

It turns out that what looked like a direct disobedience (not going to bed) was instead a medical problem--he just didn't have the language skills to tell us that he couldn't sleep.  

Once he was given Melatonin, he fell asleep within 30-45 minutes!  He had been staying awake until 2am running himself until he literally collapsed.

Another time when we thought Sage was being "stubborn" and just refusing to do what we asked, it turned out he had no idea what we were asking of him.  We used to tell the twins to put their shoes in the shoe basket, and Hope would trot over happily and put them away. Sage would go off and do his own thing. He would only do it if we took him over and made him do it.

It was the same way with spilling cheerios.  We would tell him to clean them up. He'd ignore us. It was infuriating because we did not know he did not understand the English language. If we took him by the hand and had him pick up the cheerio and put it in the bowl, he would complete the task 100% with no problem.

What looked like direct disobedience, was actually a lack of understanding what we wanted him to do.  Punishment will not help that.

Even at age 8, he didn't get it.  I remember one day he was doing something he was asked not to do, over and over again. I can't remember what it was exactly, but basically he was told if he did it, he'd have to go to his room. He'd do it, and be sent to his room. Over and over this happened until like the 6th time he came downstairs, did it again, and was told to go to his room and he says, exasperated, "Why do you keep sending me to my room!"

He didn't get it!  I would have sworn he understood but he he did not.  No spanking would teach him that.

When Stevie was 3 years old, he had already greatly restricted his diet. We had found out he was allergic to eggs and dust, and so we were trying to enhance his diet and offer him foods he could eat and see if he'd try it.  Some people gave us advice to offer him food and when he is hungry, he will eat it.  Not true for Stevie, he'd rather starve himself.  

Anyway, I remember one terrible experience with an OT we had coming to our house. She was trying to "make" Stevie eat peanut butter (a food he used to love but then refused to eat) by giving him a cracker (that he loved) and then telling him if he wants another cracker, he has to taste the cracker with peanut butter on it first. (For those of you who know how much we dislike ABA therapy, this is one of the reasons why!).  So of course, Stevie refused to eat the cracker with peanut butter and the OT did not give him any more crackers, so he threw a massive temper tantrum that lasted hours.  (We ended up refusing to let that OT back in the house!) Then a while later, I made Stevie some toast with peanut butter on it, and offered it to him. He gave me the most pitiful "no" and he almost looked like he may vomit if I didn't move it quickly. Like even the smell was making him queasy.

It turns out, that Stevie had developed an allergy to peanuts and tree nuts. No amount of punishment would make him eat it. Eating it was a worse punishment than anything external that could be inflicted upon him. He didn't (and still doesn't) have the ability to tell me the peanut butter makes him sick.  He could not tell me that food made him feel bad.

I cannot tell you how badly I felt for trying to help Stevie eat more foods, just to find out he was allergic to them and could not tell me that.  What looked like stubbornness at worst, or sensory difficulties at best, turned out to be self-preservation.  He now carries an epi-pen everywhere he goes.

All this to say: we don't always know what is really going on.  The child that hits and kicks and jumps and stomps may feel completely unattached to his body because of his sense of proprioception being under active.  Instead of punishment, this child needs some Sensory Integration OT to give him the input his body craves in a safe way.  The child that spins and runs and bolts off and runs on top of the furniture instead of on the floor may need some OT targeting the vestibular sense.  The one that processes motion.  

We won't know what the true problem is, if we just demand immediate compliance, and discipline and punish instead of taking the time to listen (and research) to what the childs behavior is telling us. It isn't always easy to determine, and sometimes we may never know.

Yesterday morning (the morning after I posted my question on facebook), when Stevie got up from bed he looked like this: 

 

photo 1 photo 2

How might you behave if you itched insanely and couldn't escape your own skin?

*I do want to make it clear though that we are not anti-discipline!  Not at all. We do discipline our children and teach them what is the right way to behave.  Sometimes it is more straight forward than others. We do used calm-down times (or "breaks") to decompress and for safety of everyone, and time-outs for bad behavior. We use reward charts and positive reinforcement and social stories--lots of social stories--to teach the boys and help them understand what we are saying, in their language!*