My son who has autism was continent of bowel and bladder until he started working. He is 23 and started to work last year. He is not working anymore due to his incontinence. I think it might be a sensory issue because he says he doesn’t realize it’s going to happen until it already has? All his doctors and specialist so far don’t know what to make of it? His gastroenterologist said it may be a behavior issue which his autism physician may need to address? We are going to go see a urologist next week. What should I try next? Any suggestions.
