Cystic Fibrosis
What is Cystic Fibrosis?
Cystic Fibrosis is an inherited genetic disorder that mainly affects the following areas:
- Lungs - thick, sticky mucus is produced which can cause difficulty in clearing infections
- Digestive System - the sticky mucus can make it difficult for the digestion of food
- Sweat Glands - people with CF lose a significant amount of salt and potassium when they sweat
What are the characteristics of Cystic Fibrosis?
The most noticeable feature of CF is a persistent cough, which can often lead to repeated chest infections. People with CF are also prone to malnutrition.
Is there a treatment to arrest the progression of Cystic Fibrosis?
At present there is no cure for CF. However, treatment methods have improved over the years. These inlcude:
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- Physiotherapy - physiotherapy sessions are required on a daily basis
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- Medication - in addition to medication, special supplements need to be taken in large quantities
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- Exercise – is important for people with Cystic Fibrosis
Are there any useful teaching and learning strategies for people with this medical condition?
For information on teaching and learning strategies, click
TeachingLearningStrategies
Cystic Fibrosis House
24 Lower Rathmines Road
Dublin 6
Tel: (01) 496 2433
Lo call: 1890 311 211
Fax: 01 496 2201
Email: info@cfireland.ie
Web:
http://www.cfireland.ie/contactus.html∞
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