Hey Ashley! I do have CF, and you'll have a good report if you read this post. First, cf affects the lungs and digestive system. We have very thick mucus, and not enough water(that's our lung problem). Our digestive problem is that we don't have enough enzymes(which break down and use food) to digest food. So we take artificial enzymes, and you just swallow them, they don't hurt. Most of our treatments are painless. However, when we go to the hospital, it's a different ball game. Usually we get many shots, all kinds of medications(some painful, some disgusting) until we get better. NOTE: This is just an outline. And as a bonus, many CF patients feel a special bond with each other(at least I do). Hope you do good on your report!
In Christ,
