Getting Back to Basics
Originally, I began this weblog for myself, as my way to look back over time - particularly during times of discouragement - and see just how far we have come in our journey to recover Alec from his autism spectrum disorder.
Over time, I have learned much about the relationship of thimerosal in learning disabilities. Emotionally, I have run the gamut from confusion to anger and acceptance. I still have not allowed myself to think that Alec won't be able to overcome autism.
There are so many things going on in the media right now that recently, I have focused on posting what I am hearing on the autism/thimerosal battlefront. I will continue to do that, but I do remember why I began this journey and I do want to stay focused on the walk; that is, the day-to-day battles and success stories that I along with others face daily now that our lives have been touched by autism.
One thing I realize that I so need to hang on to in this walk is my sense of humor! Alec is a really funny kid, and he knows it. He enjoys making others laugh and I so need a good belly-buster from time to time.
Case in point: Alec has discovered a "savant" skill, or so we call it. He is talented in the gift of hanging a spoon off of his nose. He does it at home, at friends houses, and particularly when we eat out. He will say "Look, I'm a clown!" and laugh and laugh. His laughter is infectious, and before we know it, we are all lauging with him.
Recently, our family was eating at the Big Boy Restaurant in Cherokee, NC when Alec was entertaining us with his spoon trick. Elise, Matt and I couldn't help but laugh at Alec's rolling giggle as he balanced that spoon on his nose. (By the way, we tend to eat out at more casual restaurants. This spoon trick probably wouldn't go over at a refined restaurant!) The waitress came to our table and told us that we were the "happiest people she had had that day". I asked, "Really?". Later, as Matt paid the bill, another gentleman came up to him and said that he was watching our family and was happy to see the interaction that we all enjoyed together.
So, in this story, I want to say that we should not allow the pressure of finding treatments, providing education and paying for all of this steal our laughter and our joy in our children. They are incredibly special and wondrous kids, created by God with a divine purpose for each of them. Even though the battle is hard and long, and maybe especially because of this, we need to take the time to enjoy our kids just as they are today. I am so thrilled to see Alec's progress - progress that I hope and pray other ASD kids will find as well - but sometimes I get so consumed with envisioning Alec as totally recovered that I miss the specialness that Alec offers today.
Once, I heard a saying that "Angels can fly because they take themselves lightly." Let's not forget to stop, breathe and laugh once in awhile. Let's not forget that each day is an opportunity and a gift, and meant to be enjoyed. Not that we should stop seeking the truth - we should! But let's hold onto the joy of our children as well. The journey itself is even a gift. It's all in our outlook.
"I am the door. If anyone enters by me, he will be saved and will go in and out and find pasture. The thief comes only to steal and kill and destroy. I came that they may have life and have it abundantly. "