Introduction The bio-psychosocial assessment is an important document that develops a plan of action for all the work that follow in the clinical setting. Curtis and Christian (2012) mentions when assessments are conducted effectively, clients gain a better understanding of how they can play a role in their treatment process. Debb and Blitz (2010) noted that to aid patients in positive outcomes, clinicians must formulate a clear conceptualization of how a protracted medical condition affects the
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growth of noncancerous tumors in the nervous system. Unlike Neurofibromatosis type one, this form of the disease does not need an affected family member to be acquired. Neurofibromatosis type two affects only “1 in 25,000 people worldwide,” (“NF2,”) and is much more common in adults, rather than children, which is sadly a relief due to children having less of a pain tolerance than adults. The disease occurs when benign tumors evolve on “the nerve that carries sound and balance information from the inner
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Cancer, the word that everyone in the world is terrified of hearing but everyone has experience with. These days everyone has had a mom, dad, brother, sister, friend, or relative who has been diagnosed with some form of cancer. Some of us have been lucky enough to get to support our survivors while others are left with memories of those loved ones with whom they have lost. Prostate cancer is one of the most common forms of cancer that has led to the heartbreak of millions in the United States because
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Background: Pneumonia is a disease, in which the lungs become inflamed and congested, reducing oxygen exchange and leading to uncomfortable cough and shortness of breathing. It affects individuals of all ages but occurs most frequently in children and the elderly. Pneumonia in children is the most common cause of death around the world. Historically, in developed countries, deaths from pneumonia have been reduced by improvements in living conditions, air quality, and nutrition. In the developing
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inherited condition. The disease I have chosen are cystic fibrosis which is a recessive disease and Huntington’s disease which is a dominant disease. I will assess the relationship between them both and discuss the impact on individuals of genotypes resulting in development delay of normal body functioning. Also, I will evaluate the support available for individuals with the two chosen conditions. The dominant inherited condition I have chosen is Huntington’s disease. This is a disease that damages certain
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suffer from many different types of diseases all around the world. These diseases vary in many different ways such as the part of the body they effect, how serious they are, and how they are obtained. The human body has five vital organs that are needed to survive. These vital organs are the brain, heart, kidneys, liver, and the lungs. One major type of disease that has effected thousands of people all around the world is Coronary Artery Disease. This disease is targeted towards the heart and
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Rheumatic Fever is a rare but can lead to a be a potentially life-threatening disease. Although it is far less common in the U.S., there have been a few outbreaks since the 1980s. Rheumatic fever affects primarily children between the ages of 6-15 and occurs approximately 20 days (usually within 1 to 5 weeks) Rheumatic fever is a complication of untreated strep throat caused by bacteria called group A streptococcus the main symptoms are fever, muscle aches, swollen and painful joints, chest pain
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Schistosomiasis, also known as bilharzia, is a disease caused by parasitic worms. Infection occurs when your skin comes in contact with contaminated fresh water in which certain types of snails that carry schistosomes are living. This infectious parasite can be found in 74 different tropical countries. As a healthcare practitioner my role is to help treat this dangerous disease after a patient has been infected. There are many different signs and symptoms that I will discuss as well as different
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the syndrome. What draw his attention of the family was that the males in the family affected them more than the females of the family. The males developed progressive renal failure and deafness. Why is it that the females are less affected of the disease? Well there is a pattern, and it is called “ X-LINKED “. The usual print of the gene onto the other chromosome is relatively protects female carriers who inherit an unusual alport gene on the X chromosome. Some females may develop renal insufficiency
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Abstract Peripheral Vascular Disease (PVD) is the most common disease of the blood vessels. Affecting about 8.5 million people in the United States of America, PVD is more prevalent in older adults, smokers, diabetics, and people with high blood pressure. Individuals who have a family history of Coronary Heart Disease (CHD), high blood pressure, high cholesterol, and stroke are also at increased risk. In diabetics and older adults, PVD is the leading cause of disability. Although PVD can be asymptomatic
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