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My oldest daughter and I took our first vacation away from my wife and my youngest daughter, who is afflicted with PDD-NOS. The separation was toughest on the younger girl, Kaitlyn, because without a doubt her older sister is her “BFF” (Best Friends Forever). Her sad words as we left—“Nicole, I will never see you again”—uttered while tears rolled down her face, still haunt me today.

So, off we went to spend six days in Montauk, New York, visiting with my family and soon to be 99-year-old grandmother, who resides year round in that majestic location. After spending time in Montauk, I always find myself coming home, even after 50 years of visiting there, grounded spiritually and at a much better place then when I left.

Back home, Kaitlyn stayed with her mother and attended a wonderful camp in Westwood, MA. YouthCare Summer Camp, affiliated with Mass General Hospital (MGH), has been an eye-opening experience both for our daughter and us.

Just a week before, when still negotiating an appropriate IEP since our “Stay-put” is going on two years old, the new Sped Director made it a point to explain that buttoning was a very difficult task to master. With the help of the YouthCare camp councilors, our daughter mastered that life skill within a week's time. Go figure!

There is no vacation from autism, but recharging one's batteries is a good thing. As long as 1 out of 150 children are being diagnosed with an ASD, one must never give up fighting for appropriate education, health care services, and, of course, a cure for all families with children afflicted with an ASD.

We are faced with an undeniable epidemic, and how we handle it—or choose not to—will say much about our generation for years to come. So let’s keep recruiting others to join the fight and demand a cure in our lifetime. Anything less, in my opinion, is unacceptable and unconscionable.