What a challenging prospect in times of a pandemic. It’s a tough decision in terms of how to educate your child whenever schools open up. Both kids and parents will have feelings. Nobody seems to be considering that, in my opinion. There are novel CDC guidelines. In case you missed them, here is a link CDC Guidelines Other thoughts are outlined by the American Academy of Pediatrics.
For starters: How do you explain coronavirus? In very simple terms
Your child is entitled to additional services in terms of having lost much therapy time if they have an Individualized Education Plan (IEP)? Check with the school special education supervisor and/or the principal.
and finally, how do you deal with the emotions that kids may experience when potentially planning for the first day back if that is your decision? There are some ideas below:
We have all been preoccupied with the coronavirus pandemic, but how can we not be. It still is a month during which we acknowledge and bring awareness to the nature of Autism. For those with families where you have a child with this diagnosis, there are indeed ways in which we can more effectively cope in day-to-day life. So many have told me that it is just too hard to schedule appointments, or that they are overwhelmed and having trouble working. Temple Grandin https://en.wikipedia.org/wiki/Temple_Grandin has some thoughts that I felt might help others. I hope that it does and welcome your comments about what enables you to get through this challenging time. Please share…
Continuing from the theme of earlier this week in terms of preparing for the holidays, part of doing so is to think about meals and what will be served, how many people are coming, what ingredients you will need and then cooking. If you have a child who can’t tolerate eating different foods then YOU have an additional layer that is so emotionally ridden. If you have a child who cannot tolerate the smell of foods cooking or the site of those which you have on the counter how will you prepare them? Food is such a basic thing that we need for every day. Working with parents each week with children who have feeding challenges reminds me of the emotional influence that problems in this area pose to families. Having taken Dr. Toomey’s training this past fall, I became aware of information that might be able to help you and I have already found its benefit during my daily practice. It is known as a sensory-based feeding therapy approach, building on each of them. http://autism.sesamestreet.org/daily-routine-cards/?fbclid=IwAR0VKcWb_ZAHzheWdgT7ekqhwG_NuW8JLOMtCHZyT4PnolRXeyq6oeXxLSw
“The SOS Approach to Feeding program was developed by and copyrighted by Dr. Kay Toomey. Please note, all materials, documents and forms taken from the SOS Approach to Feeding program are copyrighted and cannot be reproduced in any form without the written permission of Dr. Kay Toomey. For more information on the SOS Approach to Feeding program, please visit http://www.sosapproach.com.”
The SOS Feeding approach is appropriate for children that are “problem feeders” and not “picky eaters”, which can sometimes be difficult to distinguish between. Picky eaters are those that have a limited variety of foods and will not easily eat, but they often will reluctantly touch or taste new food. Picky eaters do not need SOS feeding therapy. A problem feeder, however, has an even more restricted variety of foods with more severe reactions to interacting with non-preferred foods and is a candidate for SOS feeding therapy. Here are some questions to consider if you are concerned about your child’s eating:
Does your child have a decreased range or variety of foods (less than 20)?
If your child gets “burned out” on food and takes a break from it, will they refuse that food still, after the break?
Does your child refuse entire categories of food groups (proteins, vegetables, etc.) or texture groups (hard foods, soft cubes, puree textures)?
Does your child almost always eat different foods at a meal than the rest of the family?
Have you reported concerns about your child’s feeding across multiple well-child check-ups?
If you answered “yes” to several of the above questions, talk to your child’s pediatrician about a referral for an evaluation to determine if feeding therapy would be warranted for your child.
Please note, the term “problem feeder” is used by the SOS Feeding approach program to delineate children who are outside the normal range of age-appropriate feeding behaviors, i.e. only being a “picky eater”.
Is your child a red flag for a referral? Know that in this season of giving that you can be given the hope of improved ability to help your child enjoy eating!
I personally have a dislike of labels being put on people, but on some level, they do enable us to understand what we see or experience ourselves. The area of Sensory Processing Disorder is not that commonplace of a condition and not as familiar as the “flu” or “stomach virus” for example. So the importance of understanding and then conveying to others that which you know about the condition has meaning. It allows for the potential of gaining the understanding of others around you and empowers others to be more empathic of the needs of those with SPD.
The below five systems are typically those that we learned about in school… keep reading – there are additional ones:
In a visual manner, we can take a look at the neuroanatomy of the disorder which adds greater understanding of the fact that there is a REAL reason for why the behaviors exist and what may cause disturbances in self-regulation.