connie1 wrote on Apr 28th, 2004 at 10:43pm:she wrote me back, just as you said, and unfortunately said that it would be an uphill battle getting a referral from kaiser. i'm not sure what i should do. i'm thinking i should at least, after my appointment with the neurologists i can ask about their experiences and ask members here what they think. how else could i pay for services with stanford? any ideas?
its been 2 weeks since my discharge and i have yet to have an appointment scheduled. is that a good sign?
Connie,
Obviously, I don't know all of the details about your insurance and how Kaiser works, but that's an "uphill battle"
I'd fight!
I
do know, however, you are less than 10 miles from someone who's done over 200 surgeries on moyamoya patients, is considered one of the leading moyamoya specialists in the world and deals with moyamoya on a daily basis! I know when I was diagnosed with moyamoya, I wasn't going to let anyone touch me who had to read a "how to" book when they were operating on my brain! I'm not trying to imply the Kaiser doc's don't know what they are doing, but when it comes to something this serious,
I would only settle for the best!
I looked at the Kaiser website tonight and noticed what it said about being referred to a specialist...
"Services of a non-Plan specialist are covered only when authorized in writing by a Plan physician." Maybe you could get one of the "
Plan physcian's" to refer you to someone
in the same zip code who knows as much as
anyone in the world about what's going on and how to treat it?
Again, just my