Essay on What is Amyotrophic lateral sclerosis?

ALS is also known as Amyotrophic Lateral Sclerosis is a disease in which the brain, nerves, and spinal cord deteriorate. It attacks every part of the body except the brain. Causing major body malfunction along with muscle weakening. Which includes lack of strength, the ability to move arms, legs and body, eventually you lose the ability to breathe. The average time of life after being diagnosed is two - five years. It was believed to be inherited or maybe an infection. After years of research scientist have found a major

Amyotrophic meaning, “no muscle nourishment” in Greek, lateral meaning where the neurons are in the spinal cord, and sclerosis meaning “scarring.” ALS, often known as “Lou Gehrig’s Disease,” named after the New York Yankee who first brought awareness to the disease in the late 1930’s, is a neurodegenerative disease, which affects the neurons in the brain. The nerve cells in the brain and spinal cord that are responsible for sending and receiving motor signals progressively die off, causing the deterioration of simple motor skills in patients with ALS, such as walking, talking, and eventually speaking and breathing, however thinking is not affected by ALS. Early symptoms cause the person to slowly lose mobility of limbs, but in a matter of a few years, the person loses the mobility of most of their body and will eventually lose the ability to eat and breath, which will ultimately cause death. ALS deteriorates the patient's body, however does not affect the patient's state of mind or sanity while the rest of the body shuts down. People usually get ALS between the ages of 40 and 70. However, there is a growing trend where athletes are getting ALS in their thirties. ALS can be contributed to genetic predisposition, which means that the gene that is responsible for ALS is already in the person’s DNA. In recent studies, however, it was observed that individuals who have had suffered multiple concussions or any other head trauma are

Have you ever heard of ALS, better known as Lou Gehrig’s disease? For many people, ALS is a disorder that they may not know much about. I never heard of it either until my father was diagnosed with this disease in 2006. Because there is no known cure, it is important to detect this disease early, so that proper treatments and preparation can be done before it’s too late.

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.

It affects the motor neuron from the brain to the spinal cord then spreads to all the muscles in the body. You will not be able to simply reach for a smartphone or pick up trash off the floor because your muscles do not function the same and may not function at all. If you acquire ALS you could have full body paralysis. There are two types of ALS out there. There is familial and then there is sporadic. Familial is the type of ALS that can be inherited and passed down by parents or grandparents. But this only happens about 5-10% in the United States. It can almost happen to anyone out there. There is a 50% chance that it can be passed down but it does not always come into effect. Then there is sporadic ALS. You get this by seriously injuring your head or maybe even just a slight hit and it was just right to cause it. This is the more likely type you would get. In the United States you they are 90-95% chance of getting due to a brain traumatic injury. ALS can cause problems to your speech. It could make you have vocal cord spasms and impaired voice. It can cause difficulty of swallowing and can make you drool. You could have substantial weight loss, problems breathing, and it is hard to do everyday things depending on how severe your diagnoses is. It is normally in people ages between 40-70’s. It has a 100% fatality rate and the numbers in the US fluctuate year to year but usually makes it up to about 20,000 people could get it at any time but NFL players and military are more likely to get it because of the brain trauma they have been

In addition, people need to know the symptoms of ALS. In ALS, there is deterioration to a point that all movement, including breathing, stops. Muscle weakness first develops in the muscles, such as the hands, and spreads through other muscles closer to the brain. Such early symptoms as this can hardly be noticed. Early symptoms of ALS are very slight and often overlooked. They begin as simple things such as tripping or dropping things. Twitching or cramping of muscles and fatigue of the arms and legs may soon follow causing difficulty in daily activities such as walking or dressing (ALS Association). In more advanced stages shortness of breath or difficulty in breathing and swallowing show until the body is completely taken over by the disease. Intellect, eye motion, bladder function, and sensation are the only abilities left unharmed by the disease. There are many symptoms for ALS and if any of these symptoms are noticed, that person could have ALS.

The word “Amyotrophic” comes from the Greek language meaning “no nourishment”. ALS causes muscle weakness, problems with coordination, stiff muscles, loss of muscles, muscle spasms, over reactive reflexes, and fatigue. The symptoms of ALS increase rapidly, which makes an individual lose control of the muscles and begin having slurred speech. The arms and legs begin to feel weak and tired unexpectedly, while also experiencing cramps. When a medical professional diagnose someone with ALS they have about 2-5 years to live on average. Although about 10% of people with ALS live up to 10 years with the disease, while 25% live up to 5 years and 50% live up to 3 years. The average age that an individual is diagnosed with ALS is 55, but varies from the ages of

ALS got the name Lou Gehrig’s disease from a New York Yankee’s baseball player. Lou Gehrig had his first symptoms when his batting average had plummeted. He couldn’t hit long balls anymore. His strength was deteriorating. He also started to walk very slowly. After things started going downhill, he found out he had the disease which would later be named after him. He had ALS. On June 4, 1939 Lou said good-bye to his fans and Yankee Stadium. He was going to retire from baseball because of the condition he was in. He was dying of ALS. There have also been many other well-known people diagnosed with this disease. Stephan Hawking was diagnosed with ALS in 1963 when he was only 21 years old, and he is still alive.

ALS, otherwise known as Lou Gehrig’s disease, is a disease that attacks the muscles and impacts a person’s physical function. Overtime, the symptoms will

In 1939, the famous baseball player for the New York Yankees, Lou Gehrig was diagnosed with the incurable neurodegenerative disease called Amyotrophic Lateral Sclerosis. This time period is when ALS came to the forefront of the mind of sports fans. On June 2, 1941 , Lou Gehrig lost his heroic and inspiring fight against the paralyzing disease, ALS. Amyotrophic Lateral Sclerosis is now also known as Lou Gehrig’s Disease in the United States, mainly because of Lou Gehrig’s impact on American culture during his time. Amyotrophic Lateral Sclerosis is very fatal to its victims. There are many aspects of this disease that must be spoken about on occasion, but the biggest point to be made is that Amyotrophic Lateral Sclerosis can attack

Amyotrophic Lateral Sclerosis (ALS) 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 lateral sclerosis (ALS), also known as Lou Gehrig’s disease, is a progressive disease that affects motor control and muscle function. Although there are semi-predictable symptoms that will occur as the disease continues, what an individual patient will experience may be highly variable. There are also variants of the disease that affect symptoms and life expectancy.

Amyotrophic derives from Greek having ‘a’ mean ‘no’, ‘myo’ mean muscle and ‘trophic’ mean ‘nutrition’ translating to ‘no muscle nutrition.’ Lateral is the area in the spinal cord where signal cells are located and Sclerosis meaning scarring or hardening which is the result of no muscle nutrition. ALS is a progressive, degenerative disease meaning that as time passes, the conditions worsen and that it causes deterioration. The way ALS can be developed is through repetitive head trauma that causes toxic protein from the brain called “tau” to seep into the spinal cord and lead to the symptoms of the disease. The most heart wrenching aspect of the disease is that it attacks and destroys every part of the body, such as voluntary muscles, except the brain and the bladder. This essentially leads to the person with it able to know what is going on but has no control over it. Since ALS also impairs speech and mobility, one feels basically lifeless except for the fact that the brain can still process and think. The disease affects the voluntary muscles of one, throughout later stages, all mobility is lost and leads to paralyzation and eventual death. The ages where people are typically diagnosed with it are forty to seventy and the life expectancy is three to five years. However, athletes have been getting diagnosed with it at a younger age being 25 to 35 years of

Amyotrophic parallel sclerosis (ALS) is dangerous issue. It influences the piece of the sensory system that controls voluntary movements. ALS is some of the time called Lou Gehrig's sickness, after the well known baseball player who died because of the disease.In this disease the muscles gradually become weaker that leads to paralysis and even sometimes death.

ALS is a disease that damages the spinal cord and muscles in the body where toxic proteins get leaked into. There are several symptoms to ALS that will eventually lead to paralysis. When being diagnosed with ALS the muscles start to weaken and the brain loses control which causes no movement ot the body. The spine will soon be affected and it will become harder to speak and swallow, which will not allow a person to be able to communicate or eat. Age difference of ALS varies from an average person to an athlete. An average person can be diagnosed with ALS at the age of