My paternal grandparents were from southern Idaho. Much of my family is still there. Nobody diagnosed with Chiari that I'm aware of.
Hi and welcome to the Chiari forum.
From what I understand it is genetic, not heredity with chiari....CP is a lack of folic acids.....so I would wonder what this could mean...but it sounds like somewhere to start some research.
I also wonder if for some reason the pesticides may just trigger the symptoms that more cases r reported...as some regions the people just do not have a trigger???
Very interesting, thanks for sharing : )
"selma"
i've personally not seen anything like that at all. for that matter, i don't recall having ever seen a demografic study of any kind being done on chiari. interesting concept, though!