There is very little information about Arnold Chiari Malformation (ACM) and relative chronic illnesses. Do you know why? We go unnoticed, we don't have a face. They say it is rare. How rare is it that we are all here looking at this? How rare is it that most of us know someone with ACM if we don't ourselves already have it? IT"S NOT RARE! It is just going unnoticed. We deserve a voice! We deserve research! We deserve awareness! WE DESERVE A CURE!!!!

By raising awareness we can get noticed. We can get funding. We can get educated professionals.

FIGHT TO GET A CURE!!!
https://www.facebook.com/pages/Two-Faces-of-Chiari/1489182308036754?ref=hl