The Ice-Bucket Challenge phenomenon that spread throughout the United States during the summer of 2014 was based on the disease ALS. Though the challenge raised money and awareness for the disease, many people still do not understand the risks and dangers of amyotrophic lateral sclerosis. ALS, or Lou Gehrig’s Disease, is a devastating disease that attacks the spinal cord and ultimately the body’s ability to move through the deterioration of nerve cells. Despite the serious danger, ALS has historically been overshadowed by other diseases that are perhaps more common. Nevertheless, ALS does not stop at anything to wreak havoc in the lives of ordinary people. To understand this menacing disease, one must first study the history and origin of it. In 1874, Jean-Marie Charcot observed a patient who had symptoms rarely ever seen in humans and documented the characteristics of the deterioration of the body. Though not much ALS activity is documented from 1874-1900, the disease erupted on the island of Guam between 1900 and 1940, proving devastating to the population. Around the year 1940, American awareness to the disease was heightened thanks in large part to a star baseball player for the New York Yankees named Lou Gehrig. Gehrig was forced to retire and give a speech about ALS in 1939 before dying in 1941 from complications of the disease. In the 1950’s, ALS studies received additional support from a company battling muscle diseases called MDA and their spokesperson Eleanor
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 (ALS), also known as Lou Gehrig’s disease, is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. ALS is also named Lou Gehrig’s disease because he was the first person to bring ALS to a national attention in the 1930’s. Lou Gehrig’s amazing professional baseball career was ended short by this horrific disease. There are multiple treatments for ALS, but no cure for this fatal disease. In 2014, ALS was brought to major attention by the ALS Ice Bucket Challenge. Although Lou has the disease named after him, there are several other notable individuals who have been diagnosed with ALS. These individuals include Stephen Hawking, Jim Hunter, Steve Gleason, George Yardley
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).
The article titled “The Voices of A.L.S. by Tara Parker-Pope has given me a better insight into A.L.S. In fact, it has made me more aware of it. Amyotrophic lateral sclerosis (ALS) also known as Lou Gehrig's disease, affects parts of the nervous system that control voluntary muscle movement. Motor neurons, among the largest of all nerve cells, reach from the brain to the spinal cord and from the spinal cord to muscles throughout the body. When these motor neurons die, the brain can no longer start and control muscle movement. At this time there is no cure for the disease; however, over the past few decades, we have made amazing strides in our understanding of the brain, the nervous system, and genetics. Discoveries in each of these areas bring
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 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).
This is why the Ice bucket challenge was invented. The ALS disease is an incurable cancer that many scientists don’t know what causes it. Some doctors think it is caused by a defective gene that prevents the body from producing a normal amount of an enzyme called superoxide dismutase.
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.
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.
Lou Gehrig was not the first person diagnosed with ALS, but he was diagnosed with ALS when the media started to begin and there was television . ALS is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. The disease affects all motor skills and muscle movement in the body which causes the muscles to become malnourished. When diagnosed with ALS, the face, arms, and legs slowly begin to paralyze and lose control of speech. The average time of life after diagnosis is two to five years and the average age to get ALS is fifty-five. However athletes are being diagnosed with ALS at ayounger age. Researchers think it’s probably due to the fact that they get hit in the head more often. ALS is without a doubt the most horrific disease because your brain is perfectly fine and you watch yourself slowly die without being to do anything about
Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig's disease, is a neurological disorder that involves the degeneration of motor neurons. Commonly, ALS is 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, 2010). According to the national institute of neurological disorders, ALS is a rapidly developing, consistently progressive, invariably fatal neurological disease that’s attacking the nerve cells needed for controlling voluntary muscles, or movement.” (NINDS, 2010). The muscles go through atrophy, which means the muscles gradually weaken and wasting away. Furthermore, ALS affects the neuromuscular system, which “enables our bodies to move
Thank you for your post. I do agree with you, ALS patients should not be charged to participate in a clinical trial.