This collection of posts (below) are my son’s original thoughts and insights of living in his world of invisible disabilities. They provide a rare glimpse and offer a unique voice, and outlook of a child’s life with dyspraxia (DCD), dyscalculia, dyslexia, complex motor stereotypies (CMS), intense imagery movements (IIM), and more. They are taken from conversations my son and I have had over the years. This is his way of helping.