Essay about 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.

Amyotrophic lateral sclerosis also known as ALS or Lou Gehrig’s disease, is a genetic disorder that has proven

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).

I had the opportunity to study the genetic mutation of Amyotrophic Lateral Sclerosis, or what is more commonly known as ALS or Lou Gehrig’s disease. Each year approximately 5,000 people are diagnosed with ALS, and statistics show that there are nearly 20,000 Americans who have it at any given time. French neurologist Jean-Martin Charcot is believed to be the scientist who discovered the disease in 1869.

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

The causes of getting ALS are getting multiple hits to the head, may not be all at once. It can cause serious problems that affects the daily life, for example hard to walk, speak, swallow, and breathe. People are being diagnosed with ALS at the ages of 40-70 with an average of 55 years. New studies state that athletes are being diagnosed at a younger age do to getting multiple hits to the head related to being in sports. After being diagnosed your life expectancy is 3-5 years, however it can increase with therapies and riluzole which is a drug and is very expensive. The disease isn't cured, it just slows down the disease. A well known person who had ALS is Lou Gehrig, he was a baseball player for the New York Yankees and was in the Hall of Fame in 1939. Started showing symptoms of ALS in 1938 and died on June 2nd

ALS is more commonly known as Lou Gehrigs disease. The progressive disease poisons the nervous system by a chemical that is released after a blow to the head; this chemical is known as Tou. Tou is released into the brain after a blow, poisoning the nervous system causing body muscles to shut down.

In early 1939, Lou Gehrig, one of the greatest New York Yankee baseball players ever, took himself out of a ballgame after playing in a record setting 2,130 consecutive games. He was noted by his teammates to drag his feet in the field, struggle with routine plays, and his batting average had plummeted. After baffling with many local physicians, he arrived at the Mayo Clinic where he was diagnosed with a “rare disease” – amyotrophic lateral sclerosis (Mitsumoto, 2001). Today ALS is no longer considered rare and is widely recognized as a relentless and devastating neurodegenerative disease. In recent years the media has covered ALS to promote awareness and support ongoing research to enhance diagnosis, treatment, and quality of life. Unfortunately, the disease is incurable and treatment options are currently limited.

ALS, CTE’s are the most common diseases in today, they usually cause by hitting the head. ALS is stand for amyotrophic lateral sclerosis(ALS). ALS is a disease which affects people’s brain and people’s muscles. CTE is stand for Chronic Traumatic Encephalopathy(CTE). CTE is a disease which is caused by hitting the head. CTE also include the disease which called ALS. Concussions and head trauma are part of Traumatic Brain Injuries(TBI), they are have differences. Those diseases are affecting the daily life of people, such as speaking, eating and walking. People need to take care about those disease, and understand what are those diseases.

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

Over the past decade, the medical community’s understanding of chronic illnesses has greatly increased. This increase is the result of improvements in technology and techniques that have clarified some of the unknown mechanisms associated with disease. For example, innovations in genetic sequencing have allowed researchers to analyze the genetic variables and abnormalities that could contribute to an individual’s development of Amyotrophic Lateral Sclerosis (ALS). In fact, over 20 different genes have been identified that increase one’s susceptibility of developing ALS. Therefore, an analysis of a recent research study, which elaborates on the genetics of ALS, is essential to understanding these types of investigations and how they are significant in modern medicine. With that being said, the purpose of this paper is to review a recently published investigation pertaining to ALS genetics by Cady et al. (2014) in JAMA Neurology.

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.