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I may never be able to express just how grateful I am for each little accomplishment my
able-bodied kids are able to do. I can't even express the joy Steve and I feel as parents when we take Jorie and Joshua to the park and they are able to play on the equipment without ANY help from either of us. I watch my two year old son playing with his cars on the floor and I think back to 11 years ago when Ryan was this same age and how little he was able to do. Just playing with his toys was difficult. I remember the guilt I used to feel when I was exhausted with just caring for him and meeting all of his daily needs. And then I also needed to find the energy to
help him play! I remember setting up trays of cornmeal for him to drive his little hotwheel cars through. Or when Steve became more involved in our lives, I can remember him modifying many of his toys so that he would be able to play with them too---flashlights, squirt guns, rubik cubes... I can even remember a very excited Ryan one day when we bought him his own can of silly string..only to get the can home and realize he was not able to spray it himself and no matter how hard Steve tried, he was not able to adapt that button so that Ryan could use it. Those are some of the toughest things to see as a parent to see the disappointment in your child's face. He couldn't even squirt a can of silly string! Ryan is no longer very interested in most toys. He will be 14 in just a few days! But, I will never grow tired of watching Jorie and Joshua play effortlessly with anything they choose. And I will always be grateful for each and every ability that Ryan does have. Even if that means just enough movement to play a video game or turn the pages of a book. SMA has forever changed our lives and perspectives.