The Voices Of L. L's Summary

ALS (Amyotrophic Lateral Sclerosis) or Lou Gehrig’s Disease is a classified as a degenerative neurological disorder that inhibits motor neurons in the spinal cord and brain to function properly. This disease eventually results in paralysis and imminent death over a period of time. ALS patients have anywhere from a few months, to a couple years to live after diagnosis since their nervous systems are slowly destroyed, rendering the body useless, and sustaining life impossible.

“ Amyotrophic lateral sclerosis (ALS), sometimes called Lou Gehrig's disease, is a rapidly progressive, invariably fatal neurological disease that attacks the nerve cells (neurons) responsible for controlling voluntary muscles (muscle action we are able to control, such as those in the arms, legs, and face).” By what A.L.S association.org says. A neurological disease is a disease that affects the brain and gives it many diseases like brain tumors, epilepsy, and, Parkinson's. “A.L.S is a neurological disease that weakens the muscles to where you can barely move or speak” said alsa.org. You can only live up to two to five years with als. A.L.S is a very rare disease every 100,000 people get it. By what alsa.org said. That means 73,571 people has it in the Whole world right now. Als is a very rare

Lou Gehrig’s Disease Thesis: Weakness in the hands, arms, legs or slurred speech. Imagine having these symptoms and not knowing what is wrong. Then the most dreaded words are uttered, “You have Lou Gehrig’s Disease”. Amyotrophic Lateral Sclerosis (ALS), or other wise known as Lou Gehrig’s Disease, is a disease that attacks muscles and brain cells. “ALS was first found in 1869 by French neurologist Jean-Martin Charcot,but it wasn’t until 1939 that Lou Gehrig brought national and international attention to the disease” (About).

Amyotrophic Lateral Sclerosis (ALS) is a terminal disease, also known as Motor Neurons Disease, Charchot Disease and Lou Gehrig disease. ALS destroys the Central Nervous System (CNS) and causes damage to the upper and lower motor neurons in the brain. Signs and symptoms are characterized as: muscles weakness, muscle atrophy, twitching and reduced muscle reflexes. Eventually the patient will become paralyzed and rely on a tracheostomy and ventilator for breathing (ALS Association [ALSA], 2010).

Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig’s disease, is a terminal disease that degenerates the nerves in the brain and spinal cord. Motor neurons run from the brain, through the spinal cord, and into the muscles of person; this is what allows a person to have control over voluntary movement. When an individual is diagnosed with ALS, their motor neurons begin to degenerate, thus eradicating their ability to walk, eat, and eventually breathe.

Amyotrophic Lateral Sclerosis was discovered in 1869 by a French neurologist named Jean-Martin Charcot. However, the disease did not become known worldwide until 1939 when famous baseball player, Lou Gehrig was diagnosed. The disease later took his life. Amyotrophic Lateral Sclerosis, also known as ALS, or more commonly known as Lou Gehrig's disease, is a progressive neurodegenerative disease that attacks nerve cells in the brain and the spinal cord. Motor neurons extend from the brain to the spinal cord and from the spinal cord to the muscles distributed throughout the human body. Degeneration of motor neurons eventually lead to death. Amyotrophic comes from the Greek language which translate into "No muscle nourishment. ALS can be summed

ALS, better known as Amyotrophic Lateral Sclerosis, is considered as a complex genetic disorder, in which multiple hereditary and environmental factors combine to cause this disease. This is seen as an illness of parts of the nervous system that control voluntary muscle movement. In ALS, the motor neurons (nerve cells that control muscle cells) are gradually lost. When these motor neurons turn out to be lost, the muscles they control become weak and ultimately nonfunctional. We see that “amyotrophic” is rooted in Greek origin meaning without nourishment to muscles and refers to the loss of signals nerve cells normally send to muscle cells. “Lateral” simply means to the side and refers to the location of the damage in the spinal cord. “Sclerosis” means hardened and refers to the toughened nature of the spinal cord in advanced ALS. This progressive neurodegenerative disease, that was first discovered 150 years ago, is associated with a life expectancy of approximately three years after symptom onset. In the United States, ALS is also known as Lou Gherig’s Disease, named after the Yankees Baseball player who passed away because of it in 1941. In the United Kingdom and other parts of the world, it’s often referred to as motor neuron disease in reference to the cells that are lost in the disorder (ALS Association, 2015).

Amyotrophic Lateral Sclerosis (ALS) is a progressive neurodegenerative disease affecting both the upper and lower motor neurons in the cerebral cortex, brainstem, and spinal cord. It is the most common motor neuron disease in the adult population with a prevalence of two to seven cases per 100,000 individuals. Survival rates in persons with ALS show considerable variation. Five-year survival rates vary from 7% to 40%, whereas 10-year survival rates range from 8% to 16% (cite).

Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig's disease, is a neurological disorder that involves the degeneration of motor neurons. ALS is commonly referred to as “Lou Grieg’s disease” after the New York Yankee Hall-of-Famer, who was diagnosed with the disease in 1939 (mayo Clinic,

Amyotrophic Lateral Sclerosis (ALS) or Lou Gehrig’s disease is a progressive nervous system disease. It constantly destroys the neurons responsible for muscle movements, especially the lower and upper motor neurons. ALS affects the nerves in your brain and spinal cord that controls your muscles. The nerves that are affected eventually break down and disappear. It got the name Lou Gehrig’s disease because of the famous baseball player, Lou Gehrig who died of ALS.

Amyotrophic lateral sclerosis, otherwise known as ALS or Lou Gehrig's disease, is a neurological motor neuron disease that slowly enables the body from doing everyday tasks. This disease blocks

Amyotrophic Lateral Sclerosis, otherwise known as ALS or Lou Gherig’s disease, is a neurological disease which attacks nerve cells causing them to die and leave the muscles paralyzed. People with ALS lose strength and control of muscles, weakening them and causing them to start to wear away. Eventually the muscles stop working all together and cause paralysis in places such as arms, legs and other parts of the body. When the nerve cells in the diaphragm and chest wall are attacked and the muscles are paralyzed, the person can lose the ability to breathe without assistance, or sometimes at all. Respiratory failure is the cause of death for most people with ALS. Currently there are approximately 2500-3000 Canadians that are living with ALS and according to www.als.ca “Every day two or three Canadians die of the

Amyotrophic Lateral Sclerosis (ALS), or Lou Gehrig’s disease, is a neurodegenerative autoimmune disease. This means that the neurons ( nerve cells of the brain and spinal cord), particularly the ones that control voluntary muscles (motor neurons), degenerate and die. Naturally, motor neurons in the brain send signals to the motor neurons in the spinal cord, which in turn, sends signals to the muscles. However, the degeneration and death of these neurons (upper and lower motor neurons) doesn’t allow the body to transmit signals to permit the movement of muscles. This eventually causes the weakening of the muscles, and the brain’s loss of controlling voluntary muscle movement. By this, people lose their ability to speak, walk, and breathe.

Amyotrophic does not affect the ability to see, smell, hear or recognize touch. A person with ALS have control of eye muscles and bladder control. Lou Gehrig's diseases mostly affects the nervous system (Amyotrophic Lateral Sclerosis Fact Sheet). When the muscles in the diaphragm and chest wall fail, thats when the patients start to lose the ability to breath without ventilatory support. Respiratory failure is a big cause of deaths with patients who have ALS; Patients die usually within 3 to 5 years from onset of symptoms (Amyotrophic Lateral Sclerosis Fact Sheet).

A distinctive characteristic of ALS is that although the motor neurons die, the brain, cognitive functions and sensory neurons stay intact (Porth & Matfin, 2009). This makes the disease especially devastating because patients become trapped inside their dying body, with a fully alert mind, but are unable to move. It is not known what causes the exact death of the motor neurons in the body, but “five percent to 10% of cases are familial; the others are believed to be sporadic” (Porth & Matfin, 2009, p.