Diet And Exercise In Cystic Fibrosis

Diet and Exercise in Cystic Fibrosis, a unique reference edited by distinguished and internationally recognized nutritionist and immunologist Ronald Ross Watson, fills the gap in the current dietary modalities aimed at controlling cystic fibrosis. Using expert evaluation on the latest studies of the role of food and exercise in lifelong management of cystic fibrosis, this valuable resource shows how to maintain intestinal, hepatic, and pulmonary high quality function for improving quality of life for those with cystic fibrosis. A helpful tool for researchers and clinicians alike, this reference helps refine research targets, and provides the beginning of a structured dietary management scheme for those with cystic fibrosis. Provides a detailed resource that reviews the health problems occurring in Cystic Fibrosis relative to dietary, complementary, and alternative therapies Contains expert evaluation on the role of foods and exercise for lifelong management of Cystic Fibrosis to maintain intestinal, hepatic, and pulmonary high quality function for improved quality of life Defines and evaluates various nutritional and dietary approaches to the unique problems of those with Cystic Fibrosis

This one-of-a-kind guide offers clear explanations and real-world advice on cystic fibrosis and its management. Here you'll find practical and reassuring information on day-to-day concerns--school, travel, exercise, nutrition, medication--as well as on physiological effects, long-term issues, and prospects for a cure. Cystic Fibrosis offers straightforward answers to the questions most frequently asked by patients and families--what causes cystic fibrosis; how it affects body systems; what pharmacological, surgical, and physical therapies are most effective; what roles exercise, diet, and nutrition play; what complications can occur and how they can be managed; when and why a lung transplant should be considered; what psychological effect the disease has on the patient's family; and how the special needs and concerns of adult CF patients can be addressed.

Written by Dr. David Orenstein, director of one of the nation's leading CF centers, this one-of-a-kind guide offers clear explanations and real-world advice on cystic fibrosis and its management. Here you'll find practical and reassuring information on day-to-day concerns - school, travel, exercise, nutrition, medication - as well as on physiological effects, long-term issues, and the prospects for a cure. Cystic Fibrosis offers straightforward answers to the questions most frequently asked by patients and families - what causes cystic fibrosis; how it affects body systems; what pharmacological, surgical, and physical therapies are most effective; what roles exercise, diet, and nutrition play; what complications can occur and how they can be managed; when and why a lung transplant should be considered; what psychological effect the disease has on the patient's family; and how the special needs and concerns of adult CF patients can be addressed. Cystic Fibrosis: A Guide for Patient and Family is the only complete answer book for everyone living with the disease. It is an indispensable resource for families of children with CF, adolescent and adult patients, and physicians, nurses, respiratory therapists, and social workers involved in the care of CF patients.

Describes the challenges of living with cystic fibrosis, as well as a description of the illness, and an explanation of procedures for diagnosis and therapy.

Nutritional therapies have been key early interventions, and remain central to the well-being and survival of patients with cystic fibrosis. The nature of the disease causes significant alterations in a patient’s ability to process and assimilate nutrients. Furthermore, many factors contribute to higher metabolic demands throughout a patient’s life. In combination, maldigestion, malabsorption, and increased metabolic demands pose a high hurdle for the patient to overcome in order to maintain optimal nutritional status. Nutrition in Cystic Fibrosis: A Guide for Clinicians is an excellent resource for physicians, nurses and dietitians who deliver care for patients with cystic fibrosis. The book provides an introduction to cystic fibrosis and nutritional assessments. It will also serve as a comprehensive guide to the nutritional monitoring and management of patients with cystic fibrosis including special populations within cystic fibrosis that require additional considerations. The chapters are written by experts in their fields and include the most up to date scientific and clinical information. Nutrition in Cystic Fibrosis: A Guide for Clinicians targets pediatric and adult pulmonologists and gastroenterologists, residents and fellows, internists, pediatricians, nurses, dietitians and general practitioners who treat patients with cystic fibrosis.

This one-of-a-kind guide offers easy-to-understand explanations, advice, and management options for patients or parents of patients with cystic fibrosis. The book explains the disease process, outlines the fundamentals of diagnosing and screening, and addresses the challenges of treatment for those living with CF. As one reviewer said, this book “is the only complete answer book for everyone living with the disease. It is an indispensable resource for families of children with CF, adolescent and adult patients, and physicians, nurses, respiratory therapists, and social workers involved in the care of CF patients.”

This book shares the latest findings on exercise and its benefits in preventing and ameliorating numerous diseases that are of worldwide concern. Addressing the role of exercise training as an effective method for the prevention and treatment of various disease, the book is divided into eleven parts: 1) An Overview of the Beneficial Effects of Exercise on Health and Performance, 2) The Physiological Responses to Exercise, 3) Exercise and Metabolic Diseases, 4) Exercise and Cardiovascular Diseases, 5) Exercise and Musculoskeletal Diseases, 6) Exercise and Neurological and Psychiatric Diseases, 7) Exercise and the Respiration System, 8) Exercise and Immunity, 9) Exercise and HIV/AIDS, 10) Exercise and Neuropsychiatric Disorders, and 11) Future Prospects. Given its scope, the book will be particularly useful for researchers and students in the fields of physical therapy, physiology, medicine, genetics and cell biology, as well as researchers and physicians with a range of medical specialties.

Cystic fibrosis is a lifestyle disease. Very few people on the West are aware that there are many Russians with CF (cystic fibrosis) who are over 50 and even 60 years old due to their adherence to one medical therapy that was developed and practiced by over 150 Soviet and Russian medical doctors. Since 1960s, these MDs have applied the Buteyko breathing therapy to increase body oxygen levels, and these doctors claim that people with CF can have at least normal (or average) life expectancy if their maintain high (or normal) body O2 content. You will not find such information in any other cystic fibrosis books. Cystic fibrosis life expectancy has been steadily growing for many decades. In late 1930s, most babies with CF died before their first birthday. Later, in the 1950s, CF life expectancy was less than 10 years. Soon after, due to use of various therapies, it increased from 14 years (in the 1980s) up to current 35-37 years. Some researchers, in their cystic fibrosis books, predict that babies born with CF during this century can live up to their 50s. But a group of Russian doctors claim that main symptoms of CF can be defeated. My own experience, in successful elimination of major symptoms of CF in my students, also suggests the same conclusions. These breathing methods address lifestyle factors that influence body O2 and use breathing exercises to increase body oxygenation. The book offers a detailed description of main lifestyle modules that increase body O2 naturally and significantly reduce many symptoms of CF (e.g., coughing, too much mucus, wheezing, and various digestive concerns) within days. How and why can these therapies work? CF is considered a genetic disease. So is asthma, or Down syndrome. Not all genetic diseases are the same. Many of them, CF included, are also lifestyle diseases meaning that lifestyle choices have a direct impact on quality of life (and CF life expectancy). Western medical studies clearly proved that tissue hypoxia (low O2 in cells) creates problems in the work of tiny ionic pumps that transport chemicals (sodium, chlorine and water) across the epithelial layers. This negative effect of hypoxia is present even in healthy people, but more expressed in people with CF due to the presence of the defective CFTR gene. Each and every study that measured respiratory parameters in people with CF found too fast and deep breathing (hyperventilation) in comparison with the medical norm (that is tiny). There are two long-term scenarios due to overbreathing. Either we get low CO2 levels in the blood (this causes spasm of blood vessels and reduced body O2) or we destroy our airways and lungs due to injurious effects of hypocapnia. In any scenario (with and without lung involvement), hyperventilation leads to low O2 levels in cells. Low cellular O2 causes formation of too thick and viscous mucus. Cell hypoxia also suppresses the immune system. Both factors promote growth of pathogens in people with CF in the respiratory and digestive systems, while other organs and body parts are also under physiological and biochemical stress due to low O2 in cells. Other factors, such as chronic mouth breathing and chest breathing, also reduce body O2 and make any treatment of CF less effective. Therefore, the suggested medical therapy, in order to increase CF life span, is to slow down automatic breathing back to the medical norm and increase body O2 naturally. Clinical experience of Buteyko breathing MDs in Russia suggests that results of a simple body O2 test predict cystic fibrosis life expectancy. People with moderate degree of CF usually have only about 15-20 seconds or less for their body oxygen test, while the medical norm is 40 seconds. In terminally ill people (with CF and many other disorders) body O2 is less than 10 seconds. With over 40 seconds for the body O2 test, a person with CF can eliminate all symptoms and have an average life expectancy.