Sensory Integration

Picky Eaters

If you have a picky eater, you’ve probably heard comments such as “Don’t worry, she’ll eat when she’s hungry” or “All young children are picky eaters.”  While these statements may be true of most typically-developing children, some kids take picky eating to the extreme and mealtimes are miserable for all involved.  There are some children who can refuse foods indefinitely, long past the point when most would respond to hunger signals.  Others eat such a limited number of food items that their diet is extremely restricted to just a few accepted foods. Some children insist on using the same plate and cup each time they eat.  Many children with feeding aversions often resist even a change in the brand of foods they will eat.  Is picky eating just a normal part of childhood?  For some, it is far more than a developmental stage and can become a serious concern for the family.

A friend of mine went into a panic when she learned that the only brand of frozen waffles that her son would eat was being discontinued by the manufacturer.  In desperation, she went to several stores to stock up on that particular brand of waffles while feeling anxious about what her son would eat when one of his regular, accepted foods was no longer available.  This little guy had multiple allergies and would only eat a few different foods.  His parents were obviously very worried about his nutrition, and the more they pushed their son to eat, the stronger the resistance they encountered.  Mealtimes, which his parents had hoped would be an enjoyable time of togetherness, instead became a battleground fraught with stressful interactions.

Feeding aversions and extreme picky eating can have a number of underlying physical causes.  A child who has been on a feeding tube may not have developed the muscle coordination needed for eating.  They may have to be taught how to bite and chew foods.  Without adequate feeding skills, children may resist foods that seem too challenging to them.  Some children stuff their mouths with food or just mash food using the tongue instead of moving the food to the molars to chew.  These children may experience gagging and choking, which can lead to avoidance of foods in the future.  Swallowing large pieces of food can also lead to physical discomfort after meals.

Prematurity, allergies, aspiration, reflux, and other physical issues can all contribute to extreme food selectivity in children.  Many children, such as those with autism spectrum disorders (ASD) or attention deficit hyperactivity disorder (ADHD), have difficulties processing and regulating input, including the taste and textures of a variety of foods. Sensory processing dysfunction (SPD) can cause a child to become squeamish just at the sight or smell of certain foods.  Some children will only tolerate foods with specific textures. Children with feeding aversions may eat chicken nuggets from a certain fast food restaurant but refuse chicken nuggets prepared at home.  It is puzzling and frustrating when children refuse to eat or have strong reactions just at the mere sight of a food that they don’t typically consume.

One mother told me that her son’s feeding aversions made it difficult to go out to a restaurant or another family’s home for a meal.  His limited repertoire of accepted foods left his devoted mother trying to explain to others about her son’s strong reactions to smells and textures of foods.  She worried about his nutrition and was baffled by his refusal to try new foods.  She tried strategies that worked with other children, but her son seemed impervious to them all.

When is it time to seek help for a picky eater?  One indication is when a child consistently refuses food or only eats a limited number of foods. For example, a child who eats no fruits or vegetables is missing entire food groups and may have difficulty getting adequate nutrition.  Some children do not drink enough fluids and are poorly hydrated.  A child with repeated respiratory infections may be at risk for aspiration, with food or liquid entering the lungs.  Over time, a child with feeding challenges may develop behavior problems related to eating such as crying and gagging when offered a meal or snack.  When eating problems are interfering with a child’s health and family activities, it can be helpful to consult with a feeding specialist or feeding team.

A feeding team consists of a group of professionals with expertise in the various aspects of feeding and nutrition.  It may include some or all of the following:   primary care physician, dietitian, gastroenterologist, psychologist, speech/language pathologist, and occupational therapist.  At a feeding clinic, the initial evaluation will gather information through parent interview and observation of the child when presented with a variety of foods and drinks.  These professionals work with the child and family to determine ways to meet nutritional needs and expand the child’s diet to include a greater variety of foods.

Feeding aversions and extreme picky eating are far more complicated than mere childhood whimsy.  Feeding problems can interfere with a child’s health and affects the entire family.  When every meal becomes an ordeal, there’s a problem.  Treatment usually progresses slowly, but over time feeding aversions can be lessened, diet expanded, and health improved.

Easy Materials You Make Yourself




I like to give my children a lot of different ways to learn. My two kids with AD/HD are strong visual learners, and their sensory processing challenges lead them to seek out hands-on experiences. So, besides offering them fidget items when the lesson doesn’t have manipulatives, I try to find ways that they can see and touch objects as they learn. I also know that my children are externally motivated (not unusual for those who have weak executive functions) and they need frequent reinforcement or reminders to stick with a task. In case I haven’t mentioned it before (though I think maybe I have either here or during my workshops) I am also reluctant to spend a lot of money on things I can make myself. Of course I always think I will go to craft shows and then make whatever has grabbed my fancy once I get back home, but I never seem to do that. But with school materials, I sometimes manage to get inspiration from my recycling bin. The picture above shows a simple set of materials that are readily available and can be used for a number of things. It took me about 15 minutes from start to finish to make it.
First, get a cardboard egg carton. Make sure it’s clean and no eggs have cracked and leaked in it. I spray mine with Clorox Anywhere Spray to kill any germs. (Disclaimer: Melinda cannot be held responsible for any icky things you pick up from your egg carton. I am not a doctor…blah, blah…) My egg carton had a little circle indented on the bottom of each cup, and I cut around them to make the holes in the middle of each cup. If your carton does not include these handy, preformed circles, you can just cut your own. The circles need to be large enough for a clothespin to fit through but small enough to hold the clothespin in place. Leave the lid on the carton so you can store small materials inside and to provide a base for the clothespin to stand on. There are many ways you can use your newly recycled materials, so I’ll just get you started with a few ideas. I’m sure you will be able to come up with more ideas, and I’d love to hear about them.

  • Use the clothespins to practice counting.
  • Practice fine motor skills by having the child place and remove the clothespins
  • Use as reinforcement by putting one clothespin in place for each completed task
  • Use as a motivator by placing clothespins in the carton for each task that needs completed. Remove a clothespin as the work gets done, visually depicting for your child that progress is being made.
  • Paint the clothespins (or use colored popsicle sticks or tongue depressors) to match colors

Making this is easy to make, easy on the budget, and easy on the environment. A winner all around!

Child Discipline

Let me start with a disclaimer. I am not a child expert, nor a parenting expert. The things that I share on this blog are intended to be helpful and the reader has the responsibility to apply what they find useful and ignore the rest. With that said, I want to share with you an experience I had years ago with my AD/HD daughter. Beckie was a very active girl with a lot of energy. With her sensory processing issues, she exhibited low body awareness and regulation was a challenge for her. My exuberant, active, and sensory seeking child had trouble sitting through a meal. She wasn’t a picky eater, so food aversions were not to blame. She just had a need to move around. A lot. And it didn’t matter if we were doing school during the homeschooling day, or if we were having a meal together. That girl had to move. Having been down this path previously with her older brother, I had learned to be more flexible and accommodating. Even so, it’s distracting to have a distractible child and it can be disruptive even when that is not the child’s intent. I honestly don’t believe that Beckie was trying to cause problems, and in fact I don’t think she was even aware of her movements sometimes. I would remind her to sit down, and she would look down at her legs with a surprised expression on her face as if to say, “What? I’m up again? How did that happen?” One night during dinner, my sweet Beckie was having more difficulty than usual sitting still. Her father, Scott, decided it was high time Beckie learn to remain seated during the meal. Beckie would promptly sit down as soon as she was reminded, but Scott was getting tired of having to repeatedly request that she return to her chair. After several reminders, Scott decided to kick it up a notch and be firmer with Beckie. The next time Beckie popped up out of her chair, Scott leaned over the table and pointed an index finger at Beckie. Then he used her full name, which every child knows is a serious warning sign. “Rebecca Michelle, you need to SIT DOWN!” At this point, Beckie became very still as she stared at the finger in front of her face. It was so close to her that she went cross eyed. She then looked up at her Father, eyes still crossed, and with amazement in her voice pronounced “Two Daddies!” Totally missing the point, Beckie happily discovered that crossing her eyes made things look interesting and incredibly she was now seeing double with two Daddies in place of one. I was trying so hard not to laugh that I had to leave the room. My husband wasn’t far behind me. We looked at each other and Scott said, “Well THAT didn’t work!” We continued to work with Beckie on sitting still when it was called for, with the understanding that she needed to mature and eventually would. I was crazy about Beckie, even when her zest for life couldn’t be contained. She grew, and was able to sit still when she needed to. Maturation takes time, and refuses to be rushed. We do what we can to promote and facilitate it, and then we get to practice patience. It’s so important to keep your sense of humor when you are a teacher and/or parent. Your kids will give you a plethora of opportunities to see the humor even in challenging circumstances.

Dressing Up A Sensory Guy

People with sensory issues often have strong clothing preferences. I don’t know if this is generally true, but in my experience most men do not enjoy dressing up. The men I know prefer comfortable clothing. They call their attractive dressier outfits “monkey suits” and yank their ties loose at the first opportunity as if their oxygen has been reduced and they need to gasp for air. Now add together “man who prefers comfortable clothes” with “sensory guy” and you’ll see the issues faced by my son. A few weeks ago we were getting ready to attend a wedding reception. I informed Josh that he would need to dress up for the event. To Josh, “dress nicely” means wearing jeans without holes. Josh doesn’t own a lot of dress clothes for the obvious reasons that he doesn’t typically need them and he doesn’t like to wear them. I asked my husband, Scott, to help Josh find something nice to wear. They are close to the same size, so sometimes they can share clothing in a pinch. This was a pinch, all right. Scott, who like Josh has AD/HD, didn’t spend a lot of time selecting an outfit. He found something that matched and tossed it to Josh to put on. Then Scott was off to do something else. A few minutes later, I found a distressed Josh in my room. He looked truly miserable, although quite handsome. When asked what the problem was, he started describing how uncomfortable his clothes were. The shirt needed to be tucked in, but then wasn’t comfortable. The cuffs around the wrist felt odd, but were tolerable. The shirt material was a little scratchy. I tried to tell Josh that it was necessary to dress up for special occasions and he quickly explained that it wasn’t dressing up that bothered him. It was being dressed up by someone else. His Dad has made the choices for him, and because Dad doesn’t have sensory issues he selected what would work for most men. Josh is the only one who knows how his body feels and responds to clothing, though, so we needed to make some adjustments. A change of pants for a looser fit made tucking in the shirt more comfortable. A belt held things comfortably in place – not too tight, not too loose, but just right. A plain cotton, tagless t-shirt under the dress shirt made Josh much more comfortable. Having the tie a wee bit looser but barely noticeable rounded out the outfit. Josh didn’t own any dress shoes and his feet are bigger than Scott’s, so he wore his nicest boots and it didn’t look too bad. Tomorrow we are going to a wedding, and sensory guy Josh will be dressing himself up again. We bought a pair of dressier shoes (Rockports) that are slip-ons, with a little elastic around the tongue of the shoe for flexibility and comfort. Josh tried on several slip-on style shoes and found that some of the styles bothered him because they did not come up high enough on the back of his heel and he could feel them slipping around. The shoes Josh picked were high enough on his heel and comfortable, so hopefully the sensory guy will be able to relax and enjoy his time at the wedding and reception even though he is in a “monkey suit”.