I few months ago, I didn’t know Chiari Malformation existed and the I gave across the topic while doing some research on CarePages. Frankly, I feel lucky that I don’t have it and I feel really bad for the people who do. It is a bottom-of-the-skull thing; it is a PAIN thing. As I understand it, you are born with it and it may lie dormant for a long time; then again, it can assert itself in childhood. It’s trademark is PAIN. A lot of it.
Obviously, I do not understand it very well, but I understand these CarePages I have been reading. One of them was featured on the CarePage homepage, along with an invite to read Gabe’s story. Reading it may be difficult, but, hey, living it is . . . Well, that is the stuff of nightmares.