
Welcome to Opening-Minds to
Arnold Chiari (KEY-R-EE) Malformation
and Related Disorders
This website is not for medical use as I am not a professional doctor.
The website is made for me to share my experiences and knowledge of
Arnold Chiari Malformation with others living with or without Arnold
Chiari Malformation, family members, friends, spouses,
caregivers and other are welcomed to read this website and become a member.
Membership is FREE!
My goal is to someday to open up a not-for-profit organization in my province to raise awareness to many doctors, public service workers, schools, universities, neurosurgeons, neurologists, family doctors and people living in my community.
Feel free to leave a comment in the forum/message board section or kindly sign my guestbook, play a game of Simon for your memory, join us for chat times (Click on "Calendar" in the left margin for times), vocabulary regarding Chiari (short hand) and so much more.
Cheers,
Debra Murphy,
Owner/Founder of (Opening-Minds to Arnold Chiari Malformation)
Canada
Decompressed April 3, 2003
20 mm Herniation. No Syrnx
Craniotomy, Laminectomy of C1, C2 and partial C3
Duraplasty, Bovine Graft. (Lining of a Cow's Heart)
Disclaimer: Debra Murphy and/or Opening - Minds to Arnold Chiari Malformation & Related Disorders are in no way ever responsiable for any action a person may take in life from reading this web site. It is not for medical use. Always go to your nearest emergency room department and always listen to your medical doctor.