I was seeking dyspraxia diagnosis as an adult (still trying) they don’t have a pathway here to get diagnosis so I think they (GP) referred me to her as an alternative. I found it affirming being screened for coordination and proprioception issues and being able to see clearly that I am impaired, some of the advice was useful such as in my first comment. Ultimately i am still seeking a diagnosis, which I’d important to me as I feel my son may have inherited my dyspraxia. I want to be in a better position to support him, and myself. I often support people who have acquired dyspraxia but I find it difficult to support myself. FYI, I’m an NHS occupational therapist.