“When the past no longer illuminates the future, the spirit walks in darkness.” -Alexis de TocquevilleParents of children with Reactive Attachment Disorder are no different. They have the same dreams for their children. Before they receive a diagnosis there’s no thought that the future might not include everything they are dreaming of. After the diagnosis, and as the reality sets in, the ideas of the future start to take on a very different view. What kind of therapy will my child need? Will my child be able to be in regular classrooms? Will my child be able to continue living at home? Will we have a relationship as our child becomes an adult? Will our child be able to heal? All of these questions and so many more have gone through my head over the years with August. Because of his violent and volatile behavior, I can add some even scarier thoughts. Is this the night the sheriff shows up to tell me he’s been killed? Will he get angry enough to physically harm me? Will I get angry enough to physically harm him? Will time in prison make a difference or make him a better criminal? I know as most parents do that at some point we have to let go and know that we have done all that we can do. What our children become is at some point out of our control. I have been watching on Facebook this week as many of my friends are moving their children to college for their freshman year. August would be a junior this year if things had gone as planned. I can’t even get him to complete his GED. He doesn’t see the point. I continue to ask and prod because that’s what parents do but I also know that it’s not my choice to make and if he doesn’t see the value nothing I say is going to matter. I have been thinking much about the future recently because I am considering the future of this blog. The last few months have been very cathartic. I started writing at a time that I needed to write for me. And if anyone found it helpful that was fine but it really didn’t matter. I needed to write. And it served its purpose. But over the years since August has been diagnosed I have had people tell me I should do this or that I should be a therapist for others who are dealing with similar situations. My experiences with law enforcement and the school system have shown much need for educating about children with RAD and I always imagined finding a way to work with these groups. So here’s the deal. Going forward I will still be telling my stories but I am going to fold this blog into a website designed for other families and anyone who is involved with a child with reactive attachment disorder. My vision is to create a community of resources for parents, teachers, law enforcement, extended families and others. There would be advice from professionals as well as hands-on tools that families can use. I have seen other blogs that are for home-schooled children or children with special needs that are mostly medical but I really want to focus on RAD because it is so very different from medical issues and from any other mental health issue and still so unknown. And that’s my plan for the future. If you’d like to be a part of it here’s how you can help. Please subscribe to my blog if you currently just read it off of Facebook or LinkedIn. I don’t want to bore you with the details but it helps. Please share it! You may not know anyone with a child with RAD but someone you may know might. If you are a praying type, always welcome. I hope you’ll stay tuned to see what my future holds as well as August’s.
Map out your future-but do it in pencil. The road ahead is as long as you make it. Make it worth the trip.
-Jon Bon Jovi