Lou Gehrig's Disease

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), 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 also known as ALS or Lou Gehrig Disease, it's a disease that affect the neurons in the brain and its ability to communicate with other neurons leading to complications to the spinal cord. This disease affects the victim in various ways it's a progressive disease meaning it starts off slowly

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 is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. ALS causes muscle weakness and impacts physical functions this occurs in the nervous system. In the nervous system motor neurons of the body are being affected. Usually, ALS causes weakness and paralysis in the muscles. The muscles slowly waste away and a person’s legs and arms become much weaker. In some cases there may be muscle spasms, weight loss, and difficulty in breathing, eating, and swallowing. The mind does not get affected and there is no loss of sensation, or sense of touch during ALS. The average for a person with ALS is about two to five years from the time diagnosis. In some cases people can live with the disease for five years and more. ALS is mostly being develop between the ages of 40 and 70. Athletes usually get diagnosed between 30 and 34. It shows that athletes have had multiple head trauma and they also have abnormal

ALS or Amyotrophic Lateral Sclerosis is a neurodegenerative disease that causes muscle weakness, fatigue, and overall respiratory failure. It can also cause trouble breathing and swallowing.

ALS stands for Amyotrophic Lateral Sclerosis, and is also referred to as Lou Gehrig’s disease. After this disease is contracted, it weakens skeletal muscles and the body is eventually paralyzed. In some cases, ALS affects the limbs first, causing difficulty to move. Due to being a progressive condition, patients will suffer from many different symptoms as time goes by. After being diagnosed, only about fifty percent of patients live for at least two more years (Facts You Should Know 2010). Moreover, about twenty percent live five years after being diagnosed and only ten percent of people can expect to live for over ten years after the diagnosis (NINDS 2013). This being said, ALS is typically very rare. Approximately two out of one hundred

The brain is a complex organ that controls all of our bodies’ functions. In a normal functioning brain, there are thousands of neurons that lead to the muscles so they can control movement and feeling throughout the body. A rare disease called amyotrophic lateral sclerosis (ALS) affects these neurons in the brain, specifically in the medulla oblongata and the spinal cord. ALS is a neurodegenerative disease that leads to the inability of the brain to signal muscle movements, which cause the person to be unable to walk, speak, eat or breathe, and ultimately leads to paralysis and death.

Amyotrophic lateral sclerosis (ALS) is a fatal progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord (Plowman, 2015, p.1151). The motor neurons reach from the brain to the spinal cord and from the spinal cord to the muscles in the body. When ALS is in a degenerate stage, this causes paralyzation and loss of muscle control, which can lead to one’s death. The ALS Association is a national nonprofit organization that is dedicated to fighting Lou Gehrig’s disease by providing support and information to those that have this disease, as well as spreading awareness effective for change. The ALS Association aims to discover new treatment for those living with Lou Gehrig’s disease, while actively seeking a cure

There are many symptoms during the onset of ALS that are often overlooked that can include: Twitching, cramping, muscle stiffness or weakness, slurred and or nasal speech, or difficulty chewing or swallowing. Each patients symptoms vary depending on what muscles are damage first. Individuals can initially have the lower extremities affected or the upper extremities as well as noticeable speech problems. Damage to upper motor neurons can cause spastic muscles and contributes to an increase in reflexes, such as the gag reflex(7). Muscles may become weaker, however, patients are still able to perform voluntary muscle contractions with sensation still intact. Lower motor neuron damage is linked to muscles weakness, atrophy, cramps, twitching, and a decline of reflexes(BOOK). As the disease progresses throughout the patients body, they have increasing problems with muscle movement, maintaining weight, speaking, and swallowing. As muscles of the respiratory system weaken, patients also have difficulty breathing on their own and must depend on a ventilator

Amyotrophic lateral sclerosis is a progressive neurodegenerative disease (ALS Association, 2016). A neurodegenerative disease is a disease in which nerve cells are damaged or killed. In this particular case, the damaged motor neurons affect voluntary movements (Newton et al., 2000). Amyotrophic lateral sclerosis, commonly known as ALS for short, got its name from the Greek language. By breaking the name into a-myo-trophic; “a” means no, “myo” refers to the muscle cells, and “trophic” refers to nourishment (ALS Association, 2016; Gulli & Veillette, 2002; Hains, 2006). “Lateral” indicates the area of the spinal cord where the nerves are being affected (Gulli & Veillette, 2002). “Sclerosis” refers to the scarring and hardening of the spinal cord

Amyotrophic Lateral Sclerosis – also referred to as Motor Neurone Disease in most Commonwealth countries, and as Lou Gehrig's disease in the United States– is a debilitating disease with varied etiology characterized by rapidly progressive weakness, muscle atrophy and fasciculations which is a spontaneous contraction affecting small number of muscle fiber. This is often referred “Lou Gehrig’s disease”. Amyotrophic lateral sclerosis, or ALS, is a disease of the nerve cells in the brain and spinal cord that control voluntary muscle movement. Muscle cramps and muscle twitching all happens when people have ALS disease. First it damages the spinal cord pathway and through the motor neurons, bodies to move and is made up of the brain, nerve, and muscle. The things that we do every day like running all of that is controlled by the neuromuscular system. By the time that passes by the ALS disease causes these motor neurons in the brain and spinal cord to shrink and goes away, so muscle no longer receive signals to move. The result of this is that the muscle becomes smaller and weaker. About 2 out of 100,000 people will get Lou Gehrig’s disease. 5 out of 10% ALS cases in the United State are in Hereditary, means the disease runs through a certain families. At least 90% of cases are not inherited, this disease is called the Sporadic ALS disease.

Amyotrophic Later Sclerosis (ALS) is a progressive disease that occurs in the nerve cells which controls muscle movement. Over time it takes over the rest of the patient’s body until finally the heart gives up. Motor neurons make this disease progress. They reach from the brain to the spinal cord to the muscles throughout the rest of the body. Degeneration of the motor neurons is the cause of death in patients. The death of motor neurons leads to the brain not being able to control muscle movement. ALS is mainly a sporadic disease but 10% of cases are familial. Since the cause is still unknown it is hard to tell where people actually contract the disease from. Some theories about the cause of ALS is, some patients have had a head injury in

ALS is considered a neurodegenerative disease because it kills neurons, specifically, motor neurons. These neurons reach from the brain to the spinal cord, and from the spinal cord to muscles throughout the body. Motor neurons provide muscle control and voluntary movements such as reaching for something, or bending your knee. When a person has ALS, these neurons become damaged and can eventually die. The death of motor neurons causes the brain to lose control over movement of muscles. People with

Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig’s disease, is a progressive neurological disorder that destroy nerve cells causing death of motor neuron cells in the brain and spinal cord controlling voluntary muscle movements. It is considered a rare disease as only two out of 100,000 in a general population can develop it and there are approximately 20,000 to 30,000 cases in the United States (Miller et al 2004). It has also been shown that the disease affect men more than it does women with a ratio of three to two (Kiernan et al 2011).