What can you do for parents of a Special Needs child?
1. Babysit or just take the kids out. We tend to trust our SN kids with people who we know understand them. That eliminates alot of cheap and readily available babysitters. Some SN kids would do best with a night at home, but some would do well with an adventure out and about with a trusted friend or relative. And it gives the parents a break, while feeling no guilt from “dumping” their kids with a cold babysitter.
2. Come to visit THEM, on their turf. Its alot of work to pack up any kids and take them on an outing to a relative’s house, but its more work for a SN family. We have to worry about wandering, unfamiliar pets, upset routines, missed bedtimes, chaos that we cannot control because its not our house. So, please, come to see us once in a while, rather than inviting us to your house all the time. We do love to come to your house, but not everytime.
3. Think ahead. If you are in a position to help financially, you might consider it. Raising a SN child costs more, its the simple truth. Therapies, developmental toys, modified equipment and such costs money. These costs do not taper off or end in adolescence/young adulthood. They get bigger. If you are considering buying your grandkids each a go-cart. Ask the parents of the SN child if they think a session of camp or summer tutoring might be more beneficial in the long run. Then let the kids share the other go-cart.
4. Recognize the extra work the parents put in each and every day. Don’t be patronizing or baby them. Just quietly and firmly establish that you know and understand. That goes a long way.
5. Know the family’s goals and strategies for the child. Understand how to use the PECS cards. Know how to ignore undesirable behavior. Understand why there can be NO M&Ms in the Easter baskets (unless someone pees in the potty.)
6. Treat all the children in the family the same.
7. Don’t assume that the parents are actively involved in “Cure this” and “Walk forThis” events. Some of us are just trying to get through the day. We are glad that there are people out there trying to cure and walk. But when you are living your life on the front lines, it is hard to spend time looking for a cure that will help someone else in 30 years. Being on the front lines means you don’t always have time for the long term investment. We would love for you to fight for a cure, because we do think its important, but we do not always have the time or emotional energy to help you.
