Insurance companies are a pain in the rear and make no sense.  Misti has been on injections 3x a week since late summer and they are doing their job, but she keeps having injection site reactions.  We went and saw her neurologist a few weeks ago to talk about a change in meds and decided on a once daily pill.  They put the order for new meds through the insurance company and they denied it and wanted her to try a cheaper drug.  It make no sense because the original drug she was on was $30,000/month and the new one is only $5,000/month, so its saving them a crapton of $$ and is the better option on the few meds we had a choice of.  Now we decided on another drug and they are sending it through insurance again, so hopefully this one gets approved.