I don't plan on posting TOO frequently. :) I don't want to become annoying... lol but I do want to share what life is like with this sweet little girl who has a lifelong struggle ahead of her.
To briefly sum it up: Cystic Fibrosis is a genetic disease that affects the lungs and pancreas. Calleigh has to take enzymes to help her digest her food, and she does twice daily sessions with a nebulizer and "pitty pats." Some day we hope that medication will progress so that she can have an easier time but for now we take things a day at a time. :)
Til next time!
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