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Cystic
Fibrosis
Cystic
Fibrosis is a disease that is inherited through families
and is not passed on through infections.
It
affects approximately one in 2500 people.
This
means that on Wirral it would be diagnosed in approximately
one or two children each year.
Cystic
Fibrosis is a difficult disease to diagnose and it has similar
symptoms to several other minor ailments. Because of this
the majority of children who have a sweat test will turn out
not to have CF.
CF
affects the digestive system and the lungs and the test is
doen when children show some of the following symptoms (Please
note that these symptoms do not mean that a child has
CF):
- Poor
weight gain or slower than normally expected growth.
- Recurring
bouts of diarrhoea or oily motions that are difficult to
flush away.
- Difficulty
in digesting food.
- Frequent
coughs, colds, chest infections
- A
family history of the disease
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