J.O.
I'm not exactly sure what kind of information you are looking for but the CFF website is a great place to start.
As far as the baby is concerned, both you AND your husband would have to be carriers of the gene and the baby would have to get one copy from each of you to have the disease. If only one of you has the gene then the baby is only at risk of being a carrier.
So in a nutshell:
If you AND your husband are carriers, the baby has a 50% of just being a carrier, a 25% chance of having the disease and a 25% chance of being clear of the gene altogether.
If only one of you is a carrier, the baby has a 50% chance of being a carrier and a 50% chance of being clear of the gene altogether.
Hope this helps some!