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Hello All,

Well I just returned from Seattle and was very pleased with the

Rheumatologist that I saw there. He wants me to start on Enbrel. Only

problem is that my insurance company is balking that it is an

experimental drug. I had to have the Dr. write a letter of medical

necessity and they said it could be up to 3 weeks before they let me

know. My pharmacist says that is will be approx $1500 per month if I

have to self pay. I need to do something. Because I have tried all of

the other drugs in the past and have already suffered more joint

damage and bone loss than I even realized, he wants me to go directly

to the Enbrel. Unfortunately I contracted Parvovirus(yes there is a

human version of this) this Spring and that is what is causing my

recent awful flare. Those of you with children or involved with

children, be aware of Fifth's Disease. It's a childhood disease that

when kids get it is fairly benign. However if adults, particularly

women get it it can be quite disabling. Fatigue, severe joint pain,

low grade fever and flushing of cheeks. I guess if you already have

RA it's rather like adding insult to injury. At least that explains

why I have felt the worst I have in 15 years.

Have any of you had problems getting insurance companies to cover the

drugs? Has anyone ever gone to Canada to get the drugs? I heard on

NPR that this is becoming a popular approach to out of reach

pharmacutical costs. Wish me luck. Thanks for listenning. Janet

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