Post autism diagnosis and I’m still working through it, trying to get to grips with my symptoms. Below is the autism model that my Consultant says is relevant to me.
Some of the information is based on a copy letter from my Neurologist explaining my particular brain damage, which I gave to my Autism Specialist. From his letter he goes on to explain in more detail my strengths and difficulties that have identified me as being on the Autism Spectrum.
Unusual Sensory Experiences
“More than 9 out of 10 people with Autism are thought to experience their senses differently to those without Autism. These differences usually affect more than one of the senses and include over and/or under sensitivities to hearing, smell, touch, taste and sight.
If too much information is presented, it can overload the senses. This describes a disorder of brain function which affects emotion, learning ability, self-control and memory and which unfolds as the individual grows.
Neuro-developmental Model of Autism
The brain damage in the right frontal lobe at birth has made me becoming autistic more likely, brought about through cerebral palsy.
This model of autism is relevant to me as it outlines that the parietal and temporal lobes part of the brain (that is affected) may process much more information than a person without autism, but processing too much information can lead to delayed sensory processing such as being slow to find objects in a cluttered environment.
In contrast, with people with autism the ability of the frontal lobe to function when stressed is often impaired, leading to problems with short term memory, switching tasks, reorganising oneself in response to sudden changes and understanding others.
It typically modulates emotion and attention preventing emotions getting too high or too low, so that they’re more balanced. This can lead to a pattern of ‘hyper-focusing’ on a particular interest, or difficulties when it comes to concentrating on mundane tasks.”
I am grateful that finally I have managed to bring answers on symptoms I never officially knew I had.