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.”
Every child receiving services in the special education system is required to complete a series of assessments every three years. One question I was asked at least every three years was particularly haunting: Where do you see your daughter working and serving in the community in 5, 10 or 15 years? I have often asked God to give us vision, and I’ve learned that Jesus measures a person’s value and success very differently than the way we do.
How often do we, as parents of kids with disabilities, crown ourselves King or Queen when it seems obvious that no one else can perform the miracles we pull out of the hat on a daily basis? We crown ourselves indispensable, don’t we? But if Jesus didn’t consider himself indispensable, why should we?
