Update on Bone Flap & Ehlers-Danlos Syndrome

Thank you all for your comments in various places about the potentially moving bone flap from my surgery (here, Tumblr, etc.).

My neurologist, physician, and neurosurgeon all think that it's not moving, and seems okay, which puts my mind to ease a bit more, though I'm a little antsy about now even being able to SEE the bumps on my forehead from the clips instead of just being able to feel them.
But... As long as they aren't moving!

And also, I may have Ehlers-Danlos Syndrome, along with my mother, apparently.
The specifics are in my blog entry, since I don't have time to type it out, but apparently it is linked to AVMs. It will be interesting to see what the results will be when I get tested!

Hi Hiro. I did a search for you…http://www.avmsurvivors.org/main/search/search?q=Ehlers-Danlos
It seems there are quite a few members with this syndrome.

So there is! Thank you! It’s such a blessing to be able to find people with such rare diseases on the internet. I am still going to have to be officially diagnosed by a specialist, but I wouldn’t be surprised, with my amount of hyper extension all over my body.