<<Disclaimer: Verify this information before applying it to your situation.>> Hi all, I know I've seen bits and pieces of this in previous posts, but I'd like an up-to-date response, and will summarize. My question: We (celiacs) have to be VERY careful with the prescriptions we take - as I'm sure we all have experiences the 'downside' - Our Insurance company has what they call a 'formulary' - Generics cost $10.00 co-pay Formulary cost $25.00 co-pay NON FORMULARY COST $45.00 CO-PAY !!!! These costs are all for a 31 DAY SUPPLY. If I could get the necessary info concerning Gluten content in generics, I would have absolutely no problem using them - but I CAN'T ! We're (myself and my two children) getting hammered by these costs that are unavoidable due to our illness. Does anyone know of a solution ? Our pharmacist said she thought we might be able to have our Doctor write a letter of explanation to the Insurance company stating our specific needs - BUT, Many Doctors are now 'Graded' by the insurance companies on how the adhere to the formulary list. Can others please share their experiences/solutions ??? Thanks, Sandi