Amyotrophic Lateral Sclerosis: Lou Gehrig's Disease

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

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

“ Amyotrophic lateral sclerosis (ALS), sometimes called Lou Gehrig's disease, is a rapidly progressive, invariably fatal neurological disease that attacks the nerve cells (neurons) responsible for controlling voluntary muscles (muscle action we are able to control, such as those in the arms, legs, and face).” By what A.L.S association.org says. A neurological disease is a disease that affects the brain and gives it many diseases like brain tumors, epilepsy, and, Parkinson's. “A.L.S is a neurological disease that weakens the muscles to where you can barely move or speak” said alsa.org. You can only live up to two to five years with als. A.L.S is a very rare disease every 100,000 people get it. By what alsa.org said. That means 73,571 people has it in the Whole world right now. Als is a very rare

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 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

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.

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

Those who suffer from Amyotrophic Lateral Sclerosis live the rest of their lives bedridden, or are embedded to a chair. The average patient diagnosed with ALS are males between the ages of 40-70. Athletes who are diagnosed in their late 20’s due to repetitive head injuries typically live 3-5 years after the diagnosis. Those who are fortunate enough may live 10 years post

There are 20,000 new cases of ALS diagnosed each year in the United States. This yields an incidence of 3 per 100,000 (Brown, 2006). There is no known cause for ALS in 95% of patients; however, 5% have an identifiable genetic mutation (Elman, 2016). The disease can present in individuals less than 30 years of age, but peaks between 40 and 60 years of age. Before the age of 65, more diagnoses are made in men; after the age of 65, gender incidence is equal. There is no clear-cut ethnic or racial predisposition in ALS (Ricks, 2016). The lifespan is approximately 3-4 years after diagnosis. However, in 10 % of

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 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

Have you ever wondered what Lou Gehrig disease is? If there is a cure for ALS or how many people have/had it. If so, then this article is for you. In this article I am going to be answering those questions and many more you might have. And in my opinion ALS is a negative mutation. Lou Gehrig disease (ALS) is a rare disease that takes place in the brain and spinal cord. A.L.S. affects the nerve cells. To be more specific in the motor neurons, which take place all through the body. When motor neurons die, which is what happens with this disease, the person that has it would lose brain functionality and muscle movement loss. With voluntary muscle affected the patient will be paralyzed only 2 people for every 100,000 are diagnosed with ALS. It is called Lou Gehrig disease because it is named after the famous Lou Gehrig, which was the first one to have ALS. The cause of this mutation is not yet discovered, but studies show that 90% of A.L.S is not inherited from other family members. This means it can’t only be passed down and there is an outside source. The symptoms of A.L.S. are hard time walking, weakness in legs, hand weakness, problems with speech, trouble swallowing, muscle cramps, twitching in the arms, bad posture.

Causes include gene mutation and will cause problems with your immune system. Your nerve cells are dying causing you to become weaker. At the chemical level gene mutation is the most common. ALS is a disease affecting the brain and nervous system, by sending signals to the spinal cord and nerves throughout the body. Weakness in your hands, arms, feet, legs or the muscles of speech are symptoms. You may experience tripping, dropping things, slurred speech, muscle cramps and twitching uncontrollably. Other symptoms include outbreaks of crying, laughing and difficulty with daily life activities. Diagnosing ALS is hard, because they symptoms are overlooked as a normal thing. 55 years old is the average age to have ALS.

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.