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Essay / Research Paper Abstract
This 8 page paper provides an overview of the health condition called Amyotrophic Lateral Sclerosis. Amyotrophic Lateral Schlerosis (ALS), also known as Lou Gehrig's disease, is a neurological disease that is degenerative and no cure for this disease has been found. This paper outlines nursing protocols for dealing with this disease. Bibliography lists 10 sources.
Page Count:
4 pages (~225 words per page)
File: MH11_MHALSSym.rtf
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Unformatted sample text from the term paper:
as one of the motor neuron diseases, has led to further study of ALS and nerve cell research, in the hopes of developing a cure for the 5,000 new cases
of ALS that occur in the United States each year (LINDS, 2002). In understanding ALS and the impacts of ALS on individuals, families and the health care environment,
it is necessary to relate the general diagnostic characteristics of the disease, consider health care and nursing interventions and support, and also understand the magnitude of the problem in the
acute care setting. Because of the nature of this disease, specific characteristic responses have been noted in ALS patients, and the carative model must integrate a view of quality
of life for these patients as a nursing directive. DESCRIPTION OF THE DISEASE Amyotrophic lateral sclerosis is the most common form of motor neuron disease affecting adult
patients in the United States. ALS is a progressive disease that affects as many as 20,000 Americans, with over 5,000 new cases each year (LINDS, 2002). Classified as
one of the motor neuron diseases, ALS is the result of the degeneration of nerve cells in the brain and spinal cord that control movement (LINDS, 2002). The specific
etiology of the disease is not well understood, but substantive research suggests that individuals who suffer from ALS have mutations in the Cu/Zn superoxide dismutase (SODi) gene, and
that this is present in approximately 20 percent patients with familial ALS (Cluskey and Ramsden, 2001). Generally speaking, the process of degeneration of these specific nerve cells is gradual
and the initial symptoms of this disease include a weakening of motor function and a loss of motor control (LINDS, 2002). The nature of this disease, though, and the
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