Copied from a comment I left on Facebook. During a discussion regarding how cerebral palsy might or might not be seen socially as an active disability that impacts a person's social or professional life
I am medically disabled.
I'll be medically disabled and socially disabled even when society makes everything accessible and easier to navigate.
My disabilities are part of me forever because of my brain being abnormal and different from the average. I'm cool with that.
I don't want to fight or struggle or handwave against it. Disability is a part of Joanna Me, just like shortness and writerbrain and cat loving an writing paranormal urban fantasy with future elements.
It is one definition of Joanna Me but it is not the biggest. It gives me powerful insight into my world and the world around me. It's like a friend woven into my neurology. However, there are much stronger definitions to show.
Being disabled and having a disability are often unconnected depending on how the person feels. Hence the disconnect between medical model and social model. Cerebral palsy is medical, but social depends on how society is able to make room.
If someone wants to see my disabilities first, that's cool, as long as they see the rest of me too.
I identify as disabled. One of my disabilities is cerebral palsy. It is a result of congenital brain damage. I will always be brain damaged. I will always be disabled. That is fine by me. I embrace being disabled while having a disability.