Ok I wanted to stay on but got a call from my daughter's insurance company. They informed me they are no longer gonna pay for her seizure medicine in liquid form cost to much. Ok I do agree it is WAY OVER PRICED! 4,000 some odd dollar's for a month. They wanna put her on pill form. I told them my Daughter can't take pills she don't understand she needs to swallow not chew! Her Pediatric neurologist told you when he was seeing her she needs liquid form and now for adult neurologist has told you she needs liquid form. But you wanna take her off? Ok you know what go the hell ahead! Just remember what happened when she didn't have her meds she was in the hospital 3-4 times a week sometimes 2-4 days that what about 10,000+ a day? Not including food. Nor the cost of the ambulance so 20,000-40,000 every week is better cost effective then 4,000 a month? Really? So deprive a disabled adult her meds? Go for it see how fast the media picks it up. They decided to keep her on her meds.
OMFG what is wrong with people!!!!!
OMFG what is wrong with people!!!!!
