Anatomy And Physiology: Cystic Fibrosis

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Cystic Fibrosis Heather Province Southwest Florida College Anatomy & Physiology August 30, 2012 Margaret Forget Cystic Fibrosis What is Cystic Fibrosis and what it means to me personally? This disease is a lethal genetic disease that’s common in the white population. Many patients with this disease live till 37 years old due to better treatment to improve their survival rate. “Average Life Expectancy in Cystic Fibrosis Better Treatment=Improved Survival” (Source: Cystic Fibrosis Foundation). Throughout my research I will explain treatments, therapy options, and prescription drugs offered to patients with this disease. Most treatments of this disease are more focused on both digestive and respiratory…show more content…
Back in the 1970’s newborn screening “was an assessment of the albumin content of meconium by means of a filter paper card.” The type of screening has many benefits including, improved survival, improved nutritional status and growth, prevention of nutritional deficiencies and many more. Cystic Fibrosis patients have a PICC (Peripherally inserted central catheter) that’s a long tube that goes into patients arm through a large vein. It then delivers medication near the patient’s heart and allows the heart to pump frequently. Patients can continue with their most normal activities. “Inserting a PICC Line is a longer and more difficult process than starting a regular IV.” (Lauren B.) A PICC Line can last for weeks or even months, if the patient properly cares for the PICC Line. “The most important part of placing a PICC Line is to verify that the tip rests in the correct position near the heart.” When showering, the patient must cover the PICC Line to avoid moisture to collect in the…show more content…
I never knew all the different types of treatments and therapy that my friend went through before she passed way in 2005, until I read more about it for my paper. While researching all this information I really wish the newer drug Kalydeco was approved while my friend was still alive. Even with some of the common side effects I really believe my friend would be still here today and would have lived passed 37. Overall, I really enjoyed looking up this information and writing this paper I feel I know a little more about this disease and understand the different symptoms as well. References Lauren B. Cystic Fibrosis Community Children’s Health Understanding Cystic Fibrosis: The Basics Wedmd Understanding Cystic Fibrosis—Diagnosis and Treatment Dankert-Roelse,Jeannette E. International Journal of Clinical Reviews Newborn Screening for Cystic Fibrosis: From Experiment to Routine Procedure O’Sullivan, Brian P; Cystic Fibrosis KALYDECO is the first and only FDA-approved CFTR potentiate For patients with cystic fibrosis age 6 years and older who have a G551D

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