3 ms·
I have a genetic condition which makes my corpus callosum (the part of the brain that connects the two halves) small(er). This leads (as described by my doctor
by lettergram 11y ago
I have a genetic condition which makes my corpus callosum (the part of the brain that connects the two halves) small(er).
This leads (as described by my doctor) both halves processing data and then having trouble syncing. I don't really know if that's true or not. However, it runs in my family (we have taken genetics tests) and it turns out that's why we are neither right or left handed, and we all have various issues related to spelling, geometry, etc. We also have an increased risk of schizophrenia and alzheimer's, but increased IQ according to studies.
For me it manifests itself mostly dyslexia. My brain gumbles words, and I don't realy left to right directly, I pretty much read a sentence and have to put it together in my head. Spelling is awful, and thank god for spellcheck, I can't remember names randomly or other words for things. The weird part is adjectives and pronouns are fine. I just have an issue with nouns if I cannot see an object.
The other day, I had to describe a toaster to my wife because I couldn't remember the word "toaster". Same goes with countless other things.
My grandfather, mother, and brother all have this issue. However, it did manifest differently for each of us. For my brother he can't think in 3 dimensions very easily. My mother has Dyslexia and my grandfather can't spell....
- thenipper 11y agoI have a similar thing. When i did the battery of SPED tests in elementary school they mentioned something about the two halves not communicating as well. What you talk about not remembering names really strikes a chord with me. Interesting to know what its called. Not that i'm sure I have the same thing but definitely seems similar.
- slg 11y agoIf I ever found the time, it might be interesting to revisit some of those tests as an adult. I haven't really spoken to a professional expert about my Dyslexia since I was diagnosed at 8. I doubt I could really articulate what I was experiencing at the time and nearly everything that was mentioned to me has long been forgotten. I'm sure going through the same process as an adult would offer some interesting insight.