Showing posts with label food. Show all posts
Showing posts with label food. Show all posts

Thursday, December 13, 2018

Interoception, Autism, and Food


I am sure you are asking yourself what the heck is interoception? I had not heard of it either until recently. Interoception, as we will be discussing today, did not really come about until the start of the 21st century. The overall definition has various interpretations; however, in this discussion, we will talk about inclusive interoception as an umbrella term to mean all experiences of sensation and consciousness that are the result of information to the brain by the central nervous system.

Interoception plays a role in so many systems in the body such as: pain, medically unexplained symptoms, anxiety, emotions in general, emotional regulation, decision -making, time perception, food and water intake, eating disorders, self-awareness, consciousness, addiction, sexual functioning, empathy, meditation, and hypnosis.

Children with interoception can have issues with food intake. A child may have a high desire for food to the point of eating when they are no longer hungry or the opposite problem, they do not want to eat and rarely, if ever, experience the sensation of hunger. Interestingly, I had one of each in this category.


Margaret Eating Fries
Margaret Eating Fries
Margaret had many issues when she was young, and I knew they were odd, but I did not know what to make of her quirky behaviors. One of her quirky behaviors was her LOVE of french fries! That girl did not eat much. Heck, she was on the 3rd percentile for a long time in height and weight, but when it came to french fries (or a few other preferred foods) she would eat them until she vomited.

I am not sure how many times I had to apologize to parents and staff at the McDonald's restaurant near us when Margaret ate too many fries and vomited in the Playplace. The parents would look at me and think Margaret had a stomach flu or something and the poor staff at the McDonald's were disgusted. I get it. I was too but I did not realize what was going on at the time. It would be another 6 months before I realized Margaret had MAJOR sensory processing issues and would be diagnosed with autism. Margaret's issues with overeating were due to interoception. When the pleasure center of her brain is turned on eating HIGHLY preferred foods, she would not receive internal signals saying she was full so she would keep eating until she vomited.


Joseph FINALLY eating Stage 2 baby food @ 20 months
Joseph FINALLY eating Stage 2 baby food at 18 months

Joseph was a complete opposite of Margaret. Where she would eat until she would vomit, Joseph would not eat. He was orally VERY defensive. Again, I know this now, but I had NO idea why he would not eat baby food! He would ONLY open his mouth for the nipple of a bottle. It wasn't until Joseph had OT to desensitize his mouth (again, no one explained about sensory processing disorder to me at that time) and work with a feeding therapist did Joseph get to a point where he could eat Stage 2 baby food without refusal or choking. He was 18 months before he started to eat any sort of food. I had no idea his sensory issues would be so profound.

It was, and to some extent still is a CHORE to get him to eat! He would button his lips SHUT if you came at him with a spoon. He would even do that with the nipple of a bottle until he could feel the texture of the nipple and then he would open his mouth. He NEVER seemed to have an internal sense of hunger. Even now, he is about to be 11 years old, an though he is the size of a 6 year old in height, he weights only 45 pounds. He has seen a nutritionist since he was a year old and has supplements to add to his food to increase the calorie content of the food, yet he never appears to gain weight. Internally, he is rarely hungry. He has gotten up in the morning and would not request to eat anything until dinner (I experimented one day to see if there was ANY internal drive to eat; thankfully there is, barely). Joseph struggles to eat because he body and his brain do not tell him he NEEDS to eat nor does his body seem to light up the reward center of his brain by eating. Again, this is an issue with interoception.

The concept of interoception has been around for awhile but the "new" science on interoception is taking the concept in interesting directions. New medical journal articles are coming out fairly regularly. I feel like we will be hearing more and more about our "8th sense" and how it impacts children with disabilities.

All research for this article is embedded into the article's links. You are welcome to join us for more discussion on ADHD at our FB group, IEP/504 Assistance for parents of public school students from all over the United States, or at our homeschool group, Homeschooling Special (Needs) Kids. We also have a group for all parents and caregivers of special needs children called Special Needs Parenting Advice and Support where we discuss ALL things related to special needs care.

Tuesday, May 15, 2012

It's a PITA!

I have not posted in awhile and I think part of it has to do with I am not sure what to say. Its not that I don't have a lot I could say but I feel like most of it is not good news.

On a personal note my marriage is hanging by a thread. I mean it literally. I am expecting John to file for divorce at any moment. If he does I am not sure what I will do. I am close to finishing my MS degree. I am in my last class now and then I have a two month break (June and July) before I can start my capstone project. I should finish that class at the end of December and should graduate then. I have been looking for a job but so far I have not been able to find anything.

John did say he would stick around longer if I went to therapy so I have tried calling a few therapists. So far I have called seven of them over the last two weeks. I have been doing research on the internet of the therapists in the area and no one yet had called me back. A couple of the instances were funny because I would call and one said, the therapist had a six week waiting list and the second one said they were closed for the next three weeks. Just today did one of them call back. I will have to cancel another appointment to make it but I plan to go. John thinks I have a lot of problems. I think I have some problems and the problems I think I have I am pretty sure is different than what he thinks I have.

This past week the homebound teacher for the school has been here. I got a bit upset with her because she was getting pretty cross with James. At one point she told him, "Do we need to get your mom in here?" What kind of threat is that to an autistic four-year-old and all I could think is what would she have done if she know I was not going to be there to witness what was going on. It scares me for my children.

We went to two appointments last week around all the homebound stuff. One day for me as to get the children up, clean the house some, have the homebound teacher arrive, have the OT person arrive, have them both leave, feed the kids lunch, put stuff away and gather what I need to leave, get shoes on everyone, pick up Joseph and herd the other two out the door and into the car, buckle everyone in and head out. I get to my destination and take everyone out. Joseph goes in a stroller while I keep and eye on Margaret and James making sure they do not run off, we go to the appointment and wait. We see the doctor and then get to leave. I take everyone out and make sure they do not wander off as we head to the car. I get everyone into the car and buckle them all back in and then collapse down the stroller and put it into the car. We drive back home and typically 3 to 4 hours have passed since we first left the house. So I arrive home about 4pm to 4:30pm. I have to feed the children again and get them settled. Then I have a bit of time, maybe, to make some phone calls before 5pm.

Alternate scenario is homebound teacher leaves at 11:30am. Then I feed the children lunch and we have maybe 90 minutes before the speech therapist arrives to work with the children. She works with the children for the next hour. She packs up and leaves and I take the children outside for about 30 minutes. By then it is 4pm-ish. I bring them inside and give them a bath. Then it is time for me to start dinner. I fix food for them and feed them again. By then it is about 6pm. That gives them 2 hours before bedtime to do as they wish. Overall we have pretty packed days.

My days often fly by. Lately I have been struggling with keeping up with school. I am towards the end of my last class. I will then be on a two month break and in August I will be starting my capstone project. Once that is completed in December then I will graduate. I will be SO excited!

Right now my life is a PITA (Pain In The Ass) but I think things will be getting better soon. I hope...lol.