BiographyAbbey was diagnosed with Cystic Fibrosis two weeks after birth with double delta F508, the most common and most severe. Life expectancy for Abbey is mid 30's. It was clear something wasn't right as she didn't put on any weight and was always lethargic and tasted 'salty'. To help keep Abbey well, she takes antibiotics, vitamins, creon daily and has a high calorie diet and lots of exercise. She also has physio twice a day, 3 when poorly to help move the mucus off her lungs.
This is her life, which also involves regular hospital appts and checks. Monthly swabs are done to check for bugs in the lungs and has been admitted for IV's to help clear these, then 3 months of Nebulisers and additional antibiotics at home. She has had nebulisers at home on a few occasions. Eventually, Abbey's lungs and stomach will become blocked and she may need a lung transplant. Abbey is a vibrant happy little girl and to look at her, you wouldn't know anything was wrong. She certainly is a little CF fighter!
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