A few autism "fun facts":
(taken from National Autism Association and TACA)
- Autism now affects 1 in 68 children
- Autism is a bio-neurological developmental disability that generally appears before the age of 3
- Autism impacts the normal development of the brain in the areas of social interaction, communication skills, and cognitive function. Individuals with autism typically have difficulties in verbal and non-verbal communication, social interactions, and leisure or play activities
- Boys are four times more likely to have autism than girls
- About 40% of children with autism do not speak. About 25%–30% of children with autism have some words at 12 to 18 months of age and then lose them. Others might speak, but not until later in childhood
- Autism greatly varies from person to person (no two people with autism are alike)
- The rate of autism has steadily grown over the last twenty years
- Comorbid conditions often associated with autism include Fragile X, allergies, asthma, epilepsy, bowel disease, gastrointestinal/digestive disorders, persistent viral infections, PANDAS, feeding disorders, anxiety disorder, bipolar disorder, ADHD, Tourette Syndrome, OCD, sensory integration dysfunction, sleeping disorders, immune disorders, autoimmune disorders, and neuroinflammation.
- Autism is the fastest growing developmental disorder, yet most underfunded.
- Children with autism do progress – early intervention is key
- Autism is treatable, not a hopeless condition
To me, Autism is NOT what defines Chase. It is not a label, it is not who he is, it is not all that he is, is it merely a diagnosis, a road map of sorts, as to how he learns, interacts with and sees the world around him.
In the beginning, the word AUTISM was scary. Before we had the diagnosis I was terrified of it. I thought everything about Chase would change if he got that diagnosis. I was afraid people would only think of him as "autistic" and not see him for who he really is. But in reality, he was already the way he was, and will be, and his diagnosis changed nothing about him. And by the way...I hate the term "autistic". It's too defining. Autism does not define someone, it is simply a SMALL part of who they are and how they learn, that's it.
I grieved the diagnosis when it was given. The dreams I had for Chase, the plans, the "ideals". Nothing was going to be how I had imagined it would be, or had planned it out in my head. But that's when my eyes were opened and my faith restored. Silly me for thinking I was ever in control or could actually plan out the future.
Shortly after Chase's diagnosis I was doing my daily devotional and read this passage...
"I am leading you, step by step, through your life. Hold My hand in trusting dependence, letting Me guide you through this day. Your future looks uncertain and feels flimsy - even precarious. That is how it should be. Secret things belong to the Lord, and future things are secret things. When you try to figure out the future, you are grasping at things that are Mine. This, like all forms of worry, is an act of rebellion: doubting My promises to care for you.
Whenever you find yourself worrying about the future, repent and return to Me. I will show you the next step forward, and the one after that, and the one after that. Relax and enjoy the journey in My presence, trusting Me to open up the way before you as you go."
Deuteronomy 29:29; Psalm 32:8
The things that Chase has taught me...I've elaborated on this before in a previous post, but they are things I would not have learned otherwise. I began to see Autism as something more. Yes, Autism sucks. I wouldn't wish it on anyone. There are a lot of hard days. A lot of money spent. A lot of researching. And a lot of sleepless nights. But in the midst of all the struggles, my eyes were opened to how beautiful Autism can be. The relationships formed. The tears shared. The "club" of supporting moms. Strangers willing to reach out and help because they "get it". There are good people in this world.
I have come to realize that all those "crazy biomedical moms" who chose alternative treatments (in conjunction with or in lieu of traditional therapies) are really on to something. Don't get me wrong, I think the traditional Speech, OT and ABA therapies are key, but Autism is not just a learning or developmental disorder, it is also a disorder of the "gut". My eyes have been opened to the toxic/GMO/processed/unhealthy world of food and drugs that we live in. We have dipped our toes in the water of "biomedical" treatments for Chase, but from what we have seen so far, it has made all the difference in the world in helping his little gut "heal".
The people we have met, the connections we have made, the journey we have taken...it has all been because of something MUCH bigger than ourselves or our sole efforts. God has had a hand in this journey since before Chase was even born. I know without a doubt He has big plans for all of us and I pray daily that He will use our experience to glorify Him and help others in similar situations or struggles.
April is Autism Awareness Month. I challenge everyone to education yourself and others about what Autism actually is. Because with growing statistics like 1 in 68, chances are you or your children will interact with someone with on the spectrum at some point.
April is Autism Awareness Month. I challenge everyone to education yourself and others about what Autism actually is. Because with growing statistics like 1 in 68, chances are you or your children will interact with someone with on the spectrum at some point.
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