Aim is to Provide Cystic Fibrosis Patients Enhanced Access to Medications and Expanded Pharmacy Services
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Press Release
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Oct. 2, 2012
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4 min read
Update: On February 3, 2017, the Cystic Fibrosis Foundation divested its remaining ownership stake in CF Services Inc., a specialty pharmacy. The pharmacy is now fully owned by Walgreens.
Press Release
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Feb. 3, 2017
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3 min read
Your CF doctor may prescribe many medications to help keep your lungs clear, prevent or fight infections and, for some people, help correct the underlying cause of the disease. Medications that people need to fight infections for a long time may require additional devices, such as PICCs and ports.
If you have cystic fibrosis, you have sticky mucus in your digestive system. You need to take enzymes to digest food and medications to stay regular. Doing this will help you grow, maintain your weight, and fight lung infections.
Nutritional needs for people with cystic fibrosis are determined by their degree of malabsorption, activity level, and the severity of lung disease. Individuals with CF typically need 1 ½ to 2 times as many calories as people without CF.
People with cystic fibrosis are living longer than ever. As people age, bones get weaker and break more easily. Let's look at different ways that this can be prevented with nutrition and exercise.
Tube feeding can be a great way to get the calories and nutrients that you or your child with cystic fibrosis need to gain and maintain a healthy weight. Explore this as an option with your CF care team.
Good nutrition for children with cystic fibrosis means high-calorie foods, enzymes, vitamins and minerals. It also can mean accepting tube feeding as a way to help your child thrive.
Managing cystic fibrosis can feel overwhelming at times — but we’re here to help. Learn how to navigate life with CF.