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Anyone who has fought to go out of network w/HMO in California? From: Stephanie (anonymous@obgyn.net) Sun May 6 13:53:07 2007 Messages sorted by: [ date ][ thread ][ subject ][ author ] Next message: anonymous@obgyn.net: "Re: Who had ultrasounds that didn't see anything?" Previous message: LorettaB: "Re: Lap yesterday!! Please help!" Hello everyone...well as ive said before i was just diagnosed w/endo stage 3. My obgyn burnt some off and said that she didnt touch the endo on my bladder because its avery risky area. So, were trying Lupron for six months. I just want to get a head start and see if i can fight my HMO to send me to a Endo Specialist if the Lupron doesnt help at at. Iv heard horrible stories of Lupron, but i have to give it a try and PRAY that it helps. So my question is if anyone on this forum had succeded at going to a Endo Specialist out of their HMO network here in California? And if so, how did it happen? I greatly appreciate any advice! I cant change to PPO until Feb of next year. Thanks Steph :) Next message: anonymous@obgyn.net: "Re: Who had ultrasounds that didn't see anything?" Previous message: LorettaB: "Re: Lap yesterday!! Please help!"

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