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Coping with Cystic Fibrosis
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CF education helps patients and their families face the physical and emotional effects of the disease and encourages CF patients to lead active, fulfilling lives. Educational programs and materials suitable for both patients of various ages and their parents are available from local CF centers and from local chapters of the Cystic Fibrosis Foundation.
Patients and their families and friends should know that:
All information on this web site is for general knowledge only and is not intended to function as, or substitute, professional medical advice, diagnosis or treatment. Never disregard, or delay in seeking, professional medical advice because of something you have read on or through this web site. Use of the CaringParents.org online service is subject to our Disclaimer.
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