ALS Essay

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

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

People first need to know what ALS is. ALS is very difficult to diagnose. So far there is no

CTE occurs when there is a “build up of tau, a protein that spills out of cells due to blunt forced trauma.” (FORBES) This build up of tau can disable neural pathways in the brain that control things like memory, judgment, and fear. (FORBES) CTE has also been linked to Alzheimer’s disease, Parkinson’s disease, dementia and ALS (Lou Gehrig’s disease). CTE was discovered in 2002 by Bennet Omalu a forensic pathologist. The first player to be diagnosed with CTE was Mike Webster, a former center for the Pittsburgh Steelers. Webster died in 2002 from a heart attack. However, during his autopsy his brain showed severe damage which then became known as CTE. Ultimately, doctors believe that Webster’s death could have been a result of the CTE that they found. (coll.) According to Boston University and the U.S. Department of Veteran Affairs’ study, 87 out of 91 former NFL athletes have tested positive for the brain disease, CTE. It is important to note that this study was also performed on former high school and college athletes and the results were similar. Therefore, the danger of concussions is not just within the spectrum of the NFL.

However, those professional athletes competing in sports with a good deal of physical contact are in harm’s way of experiencing multiple concussions during their career as an athlete. According to recent research, scientists have discovered a neurodegenerative disease also known as chronic traumatic encephalopathy or CTE (Hard Knocks: The Science of Concussions). This disease was found in the brains of former athletes who have died mainly boxers and football players (What is CTE?). These athletes were those who have received continuous concussions or played in positions where they were vulnerable to experience a good amount of physical impact (Hard Knocks: The Science of Concussions). The repeated banging of the brain against the skull causes a gradual degeneration of the brain tissue, and also the forming of an unusual protein known as tau (What is CTE?). These activities in the brain can take place months or even years after the last concussion or retirement from the sport. Some of the symptoms associated with CTE include: memory loss, confusion, depression, aggression, hindered judgment, and dementia (What is CTE?).

Many scientists and doctors have researched to find the reasons why young athletes have gotten those diseases. Due to many concussions and hits to the head young athletes tend to have ALS and CTE at a younger age. Take Pete Frates, a baseball player, into consideration; he was diagnosed at the age of 27, which reveals the drastic age difference between an average person and an athlete. This occurred due to the head injuries he received playing baseball. Furthermore, the average age to being diagnosed for a regular person is 50. According to NCBI.gov, “ALS is rare before the age of 40 years and increases exponentially with age thereafter. This further proves that because of the number of concussions athletes receive they are below the age average of

Recent studies show that some athletes are now actually being diagnosed with either of these diseases as early as in their late 20’s. For example, Pete Frates, a former baseball player for the Boston College, was diagnosed with ALS at the age of 27. He first realized something was wrong when he was struck on the left wrist with a baseball and never fully recovered from the lingering weakness. He was diagnosed on March 13, 2012 and immediately started to raise awareness. In 2014 he launched the Ice Bucket Challenge along with the help of his friend Pat Quinn to raise money for ALS research. In addition, Chris Henry, who was a football wide receiver for the Cincinnati Bengals, was diagnosed with CTE at age 26. He is the only known player to have had CTE and was still active in sports. He was diagnosed after he had fallen from a pickup truck and died on December 16, 2009. Although his family had no knowledge of this, they did notice the mood swings, headaches, and anger management issues that he did not have before. Medical research show that athletes such as Pete Frates and Chris Henry are being diagnosed at an early age because they frequently suffer from head trauma and concussions. Athletes often do not realize the potential danger they are putting themselves in each time they play and get a brain

Diagnosed at such a young age, usually non-athletes get diagnosed with ALS at the age of 40-70 with average age at 55. Non-athletes don't suffer with injury to the head as much as Athletes do. Athletes however, tend to be diagnosed with ALS between 20’s and 30’s. CTE was discovered in 3 of 14 high school players and 48 of 53 college players. One Athlete named Junior Seau, who committed suicide in May, two years after retiring as one of the linebackers in the NFL. Seau suffered from the type of Chronic brain damage. The family of Seau stated “ a lot of head-to-head collisions over the course of 20 years of playing in the NFL, developed the detention of his brain and ability to think logically” (paragraph 4), resulted to the disease of CTE.

One of the diseases athletes are being diagnosed with is ALS, or Amyotrophic Lateral Sclerosis.

Tim Shaw is a former football player who was recently was diagnosed with ALS. He plays for the Tennessee Titans. Shaw, age 30 revealed his diagnosis in a video posted on the Titan's website. He is the latest NFL player to be diagnosed with ALS. Dave Mirra a BMX Star who had CTE died due to a gunshot on February 4. He is the very first action sport athlete to be diagnosed with CTE. An autopsy technician found out that he had CTE. Scientist believe repeated head trauma can cause CTE.

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

However, there are two types of ALS, which are Sporadic ALS and Familial ALS. Sporadic ALS can happen to anyone and makes up most of 90% to 95% of cases, while Familial ALS is inherited and that's about 5% to 10% of cases. Some ailments related to the disease are Primary Lateral Sclerosis (PLS), Progressive Bulbar Palsy (PBP), and Werdnig-Hoffman disease. PLS is a slightly less severe form of ALS, but it does affect the upper body. PBP is a muscle weakness of the body, however, the lower body is affected. Werdnig-Hoffman is a spinal cord disease that affects both children and infants. For all three types, there is no treatment or cure that will slow down the progression. In support of the patients with ALS, multiple support groups have been made, and in addition, patients will donate their brain to science to further the research in finding a cure. In result, ALS isn't the only disease that poses a big issue in sports, CTE also has a notable impact.

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.