I was diagnosed with dyspraxia while a student in the early noughts, having lived with increasingly unmanageable anxiety and depression from the age of sixteen. Later, after my brain and my first graduate job turned out to be somewhat incompatible, I wrote several articles about dyspraxia for the national press, became involved with the Dyspraxia Foundation, and began giving talks and workshops on dyspraxia across the country, everywhere from City boardrooms to community centres. I made dyspraxia part of my work because I wanted it to be something that would fit comfortably into everyday conversations, and, most importantly, because I wanted my experiences to help others. I’ve met people with dyspraxia from all sorts of backgrounds, through work related and unrelated to dyspraxia. I often receive moving and relatable emails from people wanting to know more about dyspraxia or share their experience of being dyspraxic. I read them all and try to respond to as many as I can. To try to help you, I’ve answered below some of the most common questions people ask about dyspraxia. Many answers to “Where can I get…?” questions will depend on your or your child’s age and where you live, but should give you some idea where to start.
– Maxine Roper, Genuine Copy.
Please note, while I can always empathise with people looking for advice, I can’t diagnose dyspraxia, give detailed individual support, or be responsible for information about dyspraxia on other websites. If you ask further questions or make comments, please be sensitive to the fact that this was written by a real person, with lived experience.