Just wondered if anyone has a view on whether the degree to which their DC with ASD is affected by their sensory, social or other issues varies a lot over time, i.e is much more pronounced at times, and then less so at others?
My DS was diagnosed with AS around 7 months ago and to state the bleedin obvious it has been a difficult time for my DP and me. During this time we started to talk to DS about his diagnosis as we didn?t want it to be a ?big, bad secret?. But at age 8, even though we have tried to be super positive about it, I guess it?s a lot to take in. Anyway, all his sensory issues seem to be so much more dramatic recently, it's starting to really affect his life much more so. Yesterday I took him for a very special day out, something he has wanted to do for years. To cut a long story short it was a disaster, his sensory issues took over, his distress was extreme, and we abandoned it. Hugely upsetting. The thing is, he would have been fine a year ago, I?m convinced of it. So, does this mean his sensory issues are on a trajectory and things are going to look very difficult indeed in a couple of years, or is it that he has had a lot to take in, he?s stressed by it, and if we worked hard to lower his stress levels his sensory issues might abate a little?
Just wondered what people thought and what their experiences were?