I was diagnosed with 1.2 cm left side AN in August, 2008. This forum has been immensely helpful and informative. Having pretty much ruled out surgery at this point, I have spent a tremendous amount of time researching radiosurgery options and spoken to both CK and GK facilities about treatment after they have evaulated of my MRI and medical records. Each has there own set of facts, statistics, and reasons why either CK or GK is the "best" treatment option. I believe my AN is increasing in size due to balance, hearing and facial nerve issues and want to be sure I make the best decision for my circumstances. What was the deciding factor for those who have either completed radiation treatments or have made the decision and are scheduled for treatment? Was it radiation dosage, the specific treatment facility and staff, location of facility, head frame vs. the mesh mask, stats on side effects, insurance issues, etc? I can point and counter point this choice endlessly and every medical staff has differing opinions. How and when did you know that either CK or GK was your treatment choice? I certainly respect everyone's point of view and appreciate everyone sharing their experiences in order to help others through this process.