Wrightslaw: From Emotions To Advocacy - The Special Education Survival Guide

Success Story: Plans are My Safety Net

kids faces Laura and Steve have four children. Fifteen-year old Justin is their youngest child. Justin has autism. Laura and Steve have encountered obstacles in their son’s education from the beginning. Today, Justin attends his local high school, takes general education courses, and earns “A’s” in art and wood shop.

Listen to Laura and Steve describe the importance of planning.

Do we have a clear view of what we want for our son? Yes.

We started out, as many parents do, with goals and aspirations for our son. With the diagnosis of autism, we had to modify what we saw as the path for his future. We had to get through the grieving process before we could look forward to a future for our son.

Forming a plan and thinking about possibilities for his future helped us to heal and to adjust our perspective in a positive way. We did not give up our vision; we modified it.

When you have a child with a disability, you battle with insurance companies and schools, negotiate with employers and co-workers for time off, respond to the needs of family members, and deal with the unexpected. As these demands increase, your stress level increases too. It is easy to be sidetracked and forget what is important.

What keeps me sane? Planning! I cannot emphasize this enough for parents.

A master plan helps us stay focused, anticipate problems, and prepare for the future. Our master plan includes goals for our son in academic and non-academic areas – hobbies, interests, sports, play, and friendships. Master plans are clear, focused, concise, and flexible.

We make lists of expectations. We write out our goals. We post outcomes of what we want to see happen.

We have a plan for our son. We also have contingency plans. Plans are my emotional safety net. If things do not go as expected, we have plans to fall back on. We make the best of the present situation or make temporary fixes until we can put changes into place.

We realize that Justin may never be completely independent. We plan for that too. When you have a special needs child, you have to modify your expectations more often. Sometimes there are obstacles you do not see until it is too late.

Our main goal has always been for Justin to have the most fulfilling life possible. We broke this down into several areas. In the beginning, our goals were very basic – like communicating and cleaning his room. During modification times, we add to these goals. Now, some of our goals for himare: