Family Fun

When your child first gets diagnosed, it can feel totally overwhelming. Naturally, all of your focus goes to them and trying to figure out a gameplan for how you will help them. But your special needs child is just one member of your family. It is such a simple idea, but one we need to remember: take care of yourself. Continue to have family get-togethers, invite friends over, meet at the park with another parent to have coffee while the kids play. You need that! It is good for your soul and when you are happier and more relaxed, you’re modeling that behavior for your little one. Believe it or not, there are tons of opportunities for learning in these kinds of situations.

On this particular day, my husband’s friend took Michael under his wing and you can see him in one picture shielding Michael’s eyes from water spray while going on the attack in the water gun fight. Michael had a blast!
If you had asked me before that day, would Michael like a water gun fight, I would never have predicted that he would LOVE it. The lesson is to let go a little and try things. Could he have hated it and melted down? Yes, but if he never had the opportunity to try, how would we know? You really can’t know what your child wants, likes and thinks until they can express themselves. If they can’t tell you with words, let them try things (within reason) and watch their reactions. It turns out, Michael loves water guns. What will your child love?
Big ideas:
- Take care of yourself too!
- Let go a little and try new things.
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About the Author
Erica Mauro is a mom to two teenage boys, Will who is neurotypical and Michael with Autism and cognitive delays. She holds a BA in Psychology from Colgate University and a Masters of Psychology in Education from Columbia Teacher’s College. Before staying home with her children, she worked as an elementary school teacher. For five years, she served on the Board of Directors of the Molly Ann Tango Memorial Foundation, a charity dedicated to enriching the lives of children with special needs. In partnership with her husband Dave, she aspires to parent by using daily life as an opportunity for therapeutic intervention, seizing on real experiences as opportunities to build skills and strategies for Michael in a joyful, loving home environment. On the tougher early days, she just tried to get everyone safely to bedtime and start fresh in the morning. *wink*
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