
I created This blog in response
to my own struggles and experiences in dealing with my son, Reagan's,
Autism. Like most children diagnosed with Autism, the symptoms were not
so evident during his first year of life. He spoke words - more words
than he speaks today at 6 years of age. At just 6 months old he had
said his first word, "Yes."
A few months before his first birthday Reagan became
very sick with the flu and an ear infection. His congestion was so bad
that Dad would stay up all night monitoring his breathing and removing
his mucus through any means necessary. Reagan was too young to use the
nebulizer machine or take cold/cough medicines, we were told. He was
treated with antibiotics for his ear infection. The cure alas was a
simple Epsom Salt vapor bath. By the time we were advised of this
remedy it was a week into his cold. I wish I had known sooner. And I
wish I had started him on baby probiotics upon finishing his
antibiotics.
A few months after his first birthday, Reagan
discovered finger foods. And not just any type but the oh-so convenient
fast food chicken nuggets and french fries. The once "wonderful eater"
no longer wanted to each from a spoon. Aside from fruit, which
thankfully he loves, his diet significantly degraded. This was another
"I wish I had done things differently" moment.
By the time he was 19 months old, the signs had become
apparent. His speech began to disappear. His eye contact was less
direct. He wouldn't respond to his name and he wouldn't point to ask
for things. It was easy to misinterpret his autism by his happy
disposition. That was around the time that a childhood friend of mine
told me to get him screened with the Early Steps early intervention
program. It is the Federal government's way of taking care of all
children ages 0-3 with development delays.
Our journey since the day I made the appointment with
the Early Steps office has brought my family and my oldest son many challenges
and many blessings. It was really hard to lose all those expectations I
created for my son when he was first born. It was even harder to see
this loss in my oldest son. All he ever wanted was a little brother.
When God finally gave him a little brother – he gave him one that he
could not converse with and has to constantly help watch over. I had
gotten through some very difficult struggles in the past. While
difficult at first, I always persevered and eventually got to a place
where the struggle seemed unrecognizable, as though it had never
happened. With Reagan's Autism, the struggle never disappears - it never
ends. You persevere by getting through each day - one moment at a
time. It's true that I wish I could do more for my son. And I wonder
whether autism could’ve been avoided had I done things differently. But
that is the fire that has been fueled within me. It is this drive to
do more, not just for my son but others like him and others like me, that is the inspiration behind this blog.
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