When you special needs child pushes her Go Talker and asks for french fries at 7am you run don’t walk to make some.
Once upon a time, many years ago …… Emily ate lots of yummy things.
There’s even a picture of her eating a Happy Meal on our fridge.
She ate ice cream cones,pretzels, chicken nuggets, and the cute Gerber Graduate meals. All that fun kid stuff.
Then….after her flurry of seizures at 1 1/2 it all stopped.
Besides a sensory disorder, I think one of the side effects of seizure medication is loss of food interest. If it isn’t, they should add it.
So here’s to mornings with super hero fries, cheez its, vanilla wafers & milk.