I am 62 and a Kaiser member in No Cal. They discover my AN in 2004. After 3 MRIs, on the last one there was a spurt of growth that got the doctors attention. I had CK (3 sessions) on 12/05 at Stanford (Dr. Alder) because Dr. Nutik decided I was a poor candidate for surgery (failed back surgery 11/02). I considered myself lucky to be approved so easily for CK in 2005. The treatments went smoothly and was painless. But my last MRI showed my AN has grown another 3mm to 23mm (01/08). If CK has failed then I am a candidate for brain surgery. So we "wait and see" until June, the next MRI.
I am starting to have eye twitches and facial spasms intermittently but advancing at a greater frequency. It happens in times of stress or if I get a deep chill. They don't recommend a second CK treatment (is this true?) so if there is new growth in June, I am facing surgery. I now suffer from extreme fatigue, chronic insomnia, poor concentration and short term memory loss (I'm working on it), constant headaches, punctuated by migraines. About 4 to 5 months ago I started having the most severe headaches behind my left ear (AN side).
If there is new growth, I will be likely be forced to have to have one of Kaiser's neurosurgeons do the work. Considering the experience required for such a procedure, I am curious of Kaiser's doctors expertise in this particular field. The head of neurosurgery at Kaiser (Redwood City, CA) is Dr. Stephen Nutik (
http://www.permanente.net/homepage/doctor/stephennutik/). Anybody hear of him? I know that "doctors practice medicine", I just don't want them to "practice on me".
Has anyone had a failed CK treatment? Has anyone had AN surgery from Kaiser? Any suggestions where to go from here?
Thank you
Timothy Harris