<div class="FTQUOTE"><begin quote>And if he has to take more and more with each meal, how will we afford them after he goes off the first three years free program?</end quote></div>
The way the dr. writes the script will give you a month's supply every time, even as his dose changes (i.e. 'X amount with each meal and X amount with each snack' so every time you fill it you should have the same copay regardless of the number of pills are in the bottle. Emily's insurance covers her enzymes now at a dosage of about triple what it was at the time of her dx a year ago and we have no indication that this will change. Oh, and as he grows he will likely also switch from the 4's to the 8's, reducing the number of pills he has to take.
And as seen from the posts here... the amount of enzymes needed is SO variable- especially for babies/young children, I think, since pancreatic insufficiency kicks in at variable ages and it might be a gradual process. A baby might do pretty well for a while without many enzymes, others need a high dose from the start. It's very individual and your baby needs whatever dose is working for him.