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An information resource by the Children’s Liver Disease Foundation about cystic fibrosis and liver disease. A number of children and young people with cystic fibrosis develop liver problems later in life.
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12 to 19 year olds with cystic fibrosis should do at least 30 to 60mins of moderate to vigorous exercise daily. Resistance training should be done 2 to 3 times a week, including exercises for your arm, leg and tummy muscles. What counts as moderate activity? When you are working at a moderate...
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Outpatient clinics Clinics are Monday morning, Wednesday afternoon and alternate Friday afternoon (this clinic is for specific organisms). Clinics keep patients who have and do not have bacteria separate to keep everyone safe. Your follow-up clinic appointment will either be sent in the post or...
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Blowing games, or deep breathing games are designed to promote deep breaths and to fill the lungs with air. The extra air can also get behind secretions and help to move them out of the lungs. When should they be done? Blowing games should be done 1 or 2 times per day for around 10… Continue...
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Physical activity is encouraged from birth. Young children aged 1 to 6 should take part in at least 60 minutes of developmentally appropriate activities throughout the day. Children with cystic fibrosis should also do at least 1 session of structured exercise at least 15 minutes each day. This may...
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Children aged 7 to 12 should do at least 60 minutes of moderate to vigorous activity everyday. Activities should involve exercises that help build up muscle and bone strength. What counts as moderate activity? When a child is working at a moderate intensity they should feel that they are breathing...
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What is percussion and postural drainage? Percussion and postural drainage is a chest physiotherapy technique to help clear mucus from the lungs. It includes: Postural drainage, which uses gravity in a few positions to help drain mucus from different areas of lung. Percussion (patting), which is...
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Bone health Childhood is an important time for building strong, healthy bones into adulthood. As adults get older, bones become thinner and weaker and can sometimes be more likely to fracture. In cystic fibrosis, bones are at risk of becoming weaker at an earlier age. This is called cystic fibrosis...
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Flucloxacillin This is an antibiotic which is given to protect your baby’s airway from a bacteria called staphylococcus aureus. This is a common bacteria in young children, so the antibiotic needs to be given 2 times a day for the first 2 years of their life. If this bacteria is found on snot...
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The Cystic Fibrosis Team can be contacted on the below numbers, all 3 phones are in the same office, so if we don’t answer please leave a message. Cystic fibrosis nurses: 0114 305 3366 and 0114 271 7319 (answerphones), and 0114 271 7375. Dietitian: 0114 271 7212 Physiotherapist: 0114 271 7273...
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Nebulisers are used to convert liquid medicines into fine droplets which can be breathed directly into the lungs. Your child has been prescribed DNase (Pulmozyme). DNase is a copy of an enzyme that occurs naturally in the body. It helps to thin down sticky mucus and makes it easier to clear. When...
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What is infection control? Infection control means using ways to prevent or reduce the spread of infection. Infection control can keep your child healthy and is an important part of cystic fibrosis care. Why is infection control important for people with cystic fibrosis? Infections (‘bugs’, or...
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PEP stands for positive expiratory pressure. Bubble PEP is a treatment to help children who have a build-up of mucus in their lungs. Who should complete bubble PEP? Bubble PEP can be used by any child who has difficulty clearing mucus, most commonly those with cystic fibrosis or those who have just...
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What is pseudomonas aeruginosa? Pseudomonas aeruginosa or ‘P. aeruginosa’ is the most common organism causing chronic lung disease in patients with cystic fibrosis. Chronic infection with P. aeruginosa can increase the number of chest infections and in some people, can accelerates the...
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Timetable during inpatient stay Download a PDF of the timetable during inpatient stay What do I need to bring with me? You will need to bring with you: medicines, inhalers, physiotherapy equipment, nebulisers clothes, nightwear, toiletries (toothbrush, hairbrush and so on) nappies or sanitary wear...
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If your child has any of these bacteria they can still go to school or nursery. Children sometimes come to clinic and have a cough but we do not find any bacteria on their swab samples. We will treat these symptoms with a course of antibiotics. Sometimes children may come to clinic and have...
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Nebulisers are used to convert liquid medicines into fine droplets which can be breathed directly into the lungs. Nebulised hypertonic saline is often used for children with cystic fibrosis. Hypertonic saline is a salty solution which can help to clear mucus from your chest. It works by making mucus...
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You should always follow the instruction leaflet provided with the I-neb. You will be taught how to use the I-neb by the physiotherapy team when it is issued. Promixin This is an antibiotic and is a form of Colistin. When using the I-neb you must use the grey chamber. Make up the Promixin as...
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Nebulisers are used to convert liquid medicines into fine droplets which can be breathed directly into the lungs. Your child has been prescribed Bramitob. Bramitob is an antibiotic (Tobramycin) and by nebulising it the medicine gets directly into the lungs to target where bacteria are growing. When...
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Nebulisers are used to convert liquid medicines into fine droplets which can be breathed directly into the lungs. Your child has been prescribed Colomycin. Colomycin is an antibiotic (Colistin) and by nebulising it, the medicine gets directly into the lungs to target where bacteria are growing. How...
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Males with cystic fibrosis can make sperm normally. Potential fertility problems for males with cystic fibrosis The problem in most males (about 98%) with cystic fibrosis is that the tube which carries the sperm is blocked or not there. This does not affect the ability to have erections and sexual...
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A cough can be a problem for people with cystic fibrosis. People with cystic fibrosis have thick, sticky mucus in their lungs which is hard for them to clear. This sticky stuff is a good place for bacteria to grow and a if your child gets a cold or viral infection, it can lead to… Continue...
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When will I join this clinic? You will join the cystic fibrosis young persons clinic you are about 14 years old. When is the young persons clinic? The young persons clinic is very 2 months. There are 3 clinics a year here at Sheffield Children’s Hospital and 2 a year on the adult cystic...
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Why do breathing games? The aim of breathing games is to help deep breaths and fill the lungs with air. The extra air can also get into the airways behind fluids and help to move them. There are a number of different breathing games available. The physiotherapist will tell you which ones are best...
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Western Bank
Sheffield
S10 2TH
United Kingdom
Switchboard: 0114 271 7000
We’ve got a special MRI scanner just for teddies so children can see what it’s like before they have a scan.
Help to transform our extraordinary hospital into something even better.