I first suspected I had ADHD as a teenager, but finding the right professional to take me seriously was much harder than I expected. Previous attempts only ended in frustration and tears.
Enjoying the holidays with a food allergy sounds like an oxymoron doesn’t it? After all, eating together is an integral component of the holiday season. I looked forward to making our traditional holiday foods until I was diagnosed with a dairy allergy in 2012. What was to enjoy about the holidays when the foods associated with it were off limits to me?
It was a short, ten-minute drive from the hotel to the residential facility. I maintained composure while I navigated the busy public roads, and then residential streets. I had a whole range of emotions racing through my body, mind and spirit as we pulled into the campus. This was not just a pleasure drive or a routine errand, this was a significant milestone in the life of my son and our family.
While Halloween is a fun time of year for many children, it can be a really difficult time for some, including many children with additional/special needs. For them it can be a confusing, anxiety-inducing, or even utterly terrifying time. But it doesn’t have to be like that. If we stop for a moment to think about the things they might find hard and how to put things in place to help them, children with special needs can safely join in the fun, too. So what are some of the things about Halloween that children with additional needs can find hard?
“While we’ve had many years of travel speaking together on marriage, discipleship, and other topics, we are seldom alone and ‘just us’”Joe & Cindi Ferrini write on the struggle of never truly being along as special needs parents, and the importance of making time “just for us.”
Sometimes we only learn our lessons the hard way. There is truth in consequences. With autism or developmental disability, however, it can be hard to know what is reasonable to expect from our children. How much is too much? How much is too little? When do we make legitimate allowances for a disability and when do we not?
Whether at the doctor’s office, with our child’s therapy team, in the classroom for an IEP meeting, many times we are just not considered experts on our children. We are relegated to being just a bystander while the real “experts” make proclamations over our children. While they may be truthful many times, they still don’t define our children totally. It is in those moments that we must step in and be the voice in the gap between the understanding of the experts and the knowing of our hearts, and speak out the value of our kids that only we can communicate as parents.
My autistic non-verbal son has picked up some interesting habits recently. My son, who I always assumed was demonstrating illogical and repetitive behaviors due to his autism, was possibly copying what I did and trying to do the same things. He was legitimately observing my actions and trying to emulate them in the best ways he possibly could. He was watching me.
