boyfriendofCFer
New member
So I was told by a family friend that goats milk was better for people with CF and cronic asma because it is easier to digest is that true? We went and bought some and Amanda finds it ok I just try not to bring up the fact that it's goats milk. When we used to do physio she would always through up a bit of milk and since we started with the goats milk she hasnt thrown any up so thats been a positive cause it just makes physio easier, but anyways if you have used it I would like to know what you thought about it?