Friday, 15 November 2013

Plateau

Lately I don't feel as though there has been much healing going on in our home. There are rollercoasters, and dietary plateaus. I have found some reading material to help me out with planning meals around being broke and needing to eat healthy. what to eat when you are broke!


We have been talking a lot about how the body works, we are homeschooling so this gives us plenty of opportunity to focus on what matters most to us at the moment.


Everyone can use inspiration in their day-to-day life, so here are a few videos we have watched this week to keep up the positive energy with the kids.

This week's episode of Dragon's Den Canada on CBC had a series of very young entrepreneurs, wow!

Last week's finale of the first Masterchef US Junior, was encouraging to say the least!

Masterchef US Junior Finale 2013

This weekend we kick off a sensory intervention for 'D' who is sensitive to any and all foods. He has been waitlisted for referrals for support but I've been offered some awesome strategies I intend to do at home. Wait for it in next week's blog!

Friday, 8 November 2013

Relationship Development

I am certainly not an expert, but here is what I know about children on the spectrum, and friendships.


It is very important to ensure the person has typical friends to spend time with, not just people the parents are comfortable with, not just kids from the same therapy programs or classrooms, but kids of different backgrounds. It is important for autistic kids to adapt to change in relationships, yet engage and connect with others over and over again, without fear.


We try to make sure that our boys get at least two social activities with people outside the family every week. This could be anything from a playdate, to respite, a field trip or social skills at the grocery store. There is no reason for me, to consider the possibility that they may not be able to make friends. Why? quite simply, they have been making friends since they were toddlers. The only things that seem to get in the way of that is discrimination, excessive amounts of social trauma, controlling guardians, or not enough advocacy.

As a parent, I find that tolerance without enlightenment, or acceptance without understanding, can be as much of a challenge within the special needs community as it would be assumed to be in society. My experience has been something else; The more proactive the parent is, the more the kiddie will see success, and it will rub off on them.


No matter what type of mom you are, you have probably experienced being told your child has a handicap. I challenge you to see past that handicap and get to know your child, I doubly challenge you to acknowledge that handicaps are fluid, and can be molded into any shape desired. The only real challenge you face from your child is to know when they are really sick, and when you have given up. The thing with giving up, is that it is a relationship dynamic with yourself, and just like the friends your children make, they can come and go. That's just what I think.. because instead of fighting the service providers, instead of fighting the school, instead of fighting an ambiguous label which will take years further for proper social acceptance and understanding to take place.. I focus on the desire for change and growth.


I can't ask for society to move 'faster' to its inevitable conclusions, and I think its wrong to find personal fault with those who operate at the whim of the instruments that fill their day-to-day lives. I truly don't think that fighting the good fight against the world is part of my duties as a mother, but I am pretty certain that my kids are not that different than others, but maybe just maybe it is the ethics of the individual parents that insist on finding individuality in this mass perception of one label fits all.

Tuesday, 5 November 2013

Proud to have Autism

I wake up in the morning, turn on the educational cartoons, and the boys decide to keep it on, turn it off, or change the subject. We eat breakfasts, sometimes together, often as we go on with our individual wake up routines and grounding strategies. By mid morning we are either in a social activity with people outside of our family, or running through our retention drills.. math charts and spelling manipulatives with 'D', math manipulatives and language charts with 'A'. Then we often play outside, or indoor games before lunch. After we gorge, we usually are looking for more social opportunities, or quiet learning activities (usually the latter). Then we are looking at science activities and environment investigations (home, outside, or personal interests). By late afternoon we are looking for games, ipads, computers, whatnot.. errands or outdoor play. we often eat dinner in two sittings which may be a problem, I don't know but it can be an inconvenience, bath time and hygiene routines occur here.. then they horse around and play together before we listen to music and watch some calm and pleasant cartoons. Slowly, rooms are then tidied up and linen changed while they come up with all these needs that must be taken care of before bed. Sometimes there are late bedtimes, often for one of the reasons above, usually to do with picky eating, missed routine, or wellness consideration.. but its not a big problem. If they can't sleep right then, they will eventually.. usually after catching that missed routine they will sleep...


To be autistic is said to be 'more' .. more happy! more sad :( .. more easily frightened, and often quite shy. When autism parents are faced with typical challenges, they usually get advice that intends to 'maintain-control', or manipulation strategies that encourage more adult-friendly and socially-tolerable behaviours. Rarely is there support that addresses the issue of a child being 'more'. When we look at a child who is feeling more intensely than we expect, it triggers shock, anxiety, and other distressful reactions in the people around them, it often seems unprecipitated, overreactive, or spirited. If you think about the reality that this happens in our lives anyway, perhaps less often, but we do know how to overcome our own stresses as adults, you become more capable of handling autism. When we get past the label, it is easier to see the child.


'Auties' or people with a sensory disorder usually experience their 5 senses in a different way than people sometimes referred to as 'neurotypical'. Imagine a person who has blindness, in many cases their other senses are compensated, and thereby heightened. If I were a neurologist.. I'm sure this would be easier to explain or describe, but as a parent and person with similar experiences in this area, I will say it like this: when one area is triggered, the others may overreact to the environment or in a way to correct itself. Sometimes it is hard or impossible to say which way it will go, often behaviours can be different depending on the senses, and the responses of the rest of the body. Over time and through getting to know an individual, being with a person who has a sensory disorder becomes predictable and manageable. Two terms fall under this part of the autism lifestyle: Sensory diet and sensory profile.


Whether its with professional support, or informally done at home, each child with a sensory challenge has sensory accommodations.. a sensory diet is designed to address the child's specific needs effectively, so he can be less impacted by frequent disruptions to daily routines by his/her nervous system. A sensory profile is a checklist that is then calculated to determine the child's true needs through behaviours they exhibit on a regular basis.


The key to understanding autism (I think) is to realize that our nervous system can send similar messages to the brain, from overwhelming sensory input, as it would physical pain. This is why a child can seem like they are reacting to something as though it is causing them pain, some may be able to demonstrate more specifically than others, in more generally understandable communication strategies, and others react as profoundly as a young child having a temper tantrum. Part of the therapies these children receive, is to help them adapt, communicate, and develop tolerance to these stimuli. Triggers, as briefly referenced to above, can be sights, smells, sounds, sensations, or from internally by digestive issues, lack of sleep, headaches, stress, anything that bothers the average person, can be traumatic to a person who has an autism spectrum disorder. In many cases children develop, grow, and overcome these challenges as they age, but often times not 'enough' without intervention at pivotal points in their development, these can often be looked at as when the child achieves growth from toddler to preteen, or from tweens to teens, and teens to adults. Usually at these points, there are services available for the most challenging aspects of growing up.


Now you may be wondering, or asking yourself (and probably others at some point!) what can you do to get around this challenge while developing connections, friendships, working relationships, or providing care for a person or family with autism.

  • Don't be afraid to ask questions. 
  • Be yourself.
  • Offer positive reinforcement and encouragement, criticisms, judgments, anything with any sense of finality can often be negative.
  • Acknowledge and Accept that what you see, hear, smell, sense, or notice may not represent their 'normal'. 
  • Know that Autism is a communication and social handicap. Social can mean anything from sorting out 'empathy', anxiety disorders, and stress intolerance. Communication does not mean ability to use language in written, verbal, or electronic means, but to express thoughts, emotions, and ideas. 
  • Many people with autism experience the old-fashioned idea of 'left-brain' tendency.. they tend to process their surroundings differently, desire different outlets for creativity or recreation, or simply have differing learning styles.
  • All children with autism DO grow and develop, but at delayed rates to typical children. (for instance, my youngest was assessed as being developing at 41% of the pace of typical children the same age).
  • NO TWO AUTISTIC CHILDREN ARE THE SAME. There are many interventions and strategies available for kids and adults alike, and they are often tweaked and customized to the individual, and rarely are they (exception being in non-specialized programs such as public school) taught exactly the same. What does occur, is similar symptoms at similar degrees of severity are addressed the same, and this shows the most consistent positive and swift results.