Symptoms And Symptoms Of Amyotrophic Lateral Sclerosis ( Als )

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.

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

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.

Amyotrophic lateral sclerosis or Lou Gehrig’s disease is a neurological disease that proves fatal for anyone diagnosed with it. Although this disease is not commonly heard of or most often diagnosed, numerous people a year (mainly those in their middle-age or older age generations) succumb to this terminal disease. This disease is progressive, meaning it continues to worsen with age, limiting one’s lifespan with only a certain number of years left to live. By definition, Lou Gehrig's disease is a rare neurological disease that attacks the motor neurons, thus affecting one’s ability to produce movements such as chewing, walking and talking (“Amyotrophic Lateral Sclerosis,” 2018). Although Lou Gehrig's disease is more prominent in the older-aged

ALS is one of the most common neuromuscular diseases worldwide (Amyotrophic Lateral Sclerosis Fact Sheet).There are three different types of ALS causes there is, familial, sporadic, and guamanian. Familial is 5-10% , sporadic is the most common which is 90-95% of all ALS causes and guamanian is rare variant. Guamanian is very similar to ALS almost the same and it happens because of something toxic that they are eating which messes with their nervous system (ALS[Lou Gehrig’s Disease]). It is also a disease varied with etiology characterized by rapidly progressive in weakness in the muscles.

Amyotrophic lateral sclerosis, also known as Lou Gehrig’s disease, is a neurodegenerative disease. Originally acknowledged by Jean-Marie Charcot in 1874, this disease kills over 140,000 people worldwide every year. The disease causes progressive paralysis and muscle weakness due to destruction of both upper and lower motor neurons. Due to its insidious nature and the irreversible negative effects on skeletal muscle innervation, ALS has a survival duration time of only 3 to 5 years (Rowland).

Amyotrophic lateral sclerosis (ALS) is a late onset neurological disorder characterized by motor neuron degeneration in brain stem, spinal cord and primary motor cortex. There is no single gene strictly associated with all ALS cases, the disease is thought to be caused by the interaction of many genetic factors as well as environmental influences. Most of ALS patients have no family history of this disease, familiar form accounts for only 5 to 10% and seems to be dominant in most cases. The dominance and high heritability of familiar ALS (FALS) led to identification of several high-risk alleles of few genes (among those, SOD1, FUS, TARDEP, C9ORF72 are the most frequent)

Amyotrophic Lateral Sclerosis (ALS), also known as Lou-Gehrig’s disease, was first described by Charcot in 1874. “Amyotrophic” pertains to the lower motor neuron signs of muscle weakness, atrophy, and fasciculations. “Lateral sclerosis” refers to the gliosis of the lateral column of the spinal cord found in autopsy specimens following degeneration of the corticospinal tracts. This is clinically manifested as upper motor signs like hyperreflexia, clonus, extensor toe signs, and Hoffmann

Amyotrophic lateral sclerosis, or ALS, is a disease where the nerve cells in the brain all together with brain stem and spinal cord that control voluntary muscle actions becomes weak progressively. The causes varies, can be from genetic defect or chemical imbalance, disorganized immune response, protein mishandling. Causes of ALS are unknown in most of the cases. In ALS, the neurons waste or die compromising the communications to the muscles. Causing a progressive inability to move getting worse by the time. Disease becomes a life threatening when reach the muscles in the chest area risking

Amyotrophic  lateral  sclerosis  (ALS)  is  a  devastating and fatal neurological disorder  that  causes  weakness,  atrophy,  paralysis,  and eventually respiratory failure due to the  selective  degeneration  of  neurons  responsible for voluntary movement. Since  its discovery in 1874, ALS has remained a  medical  mystery  ‐ researchers  remain  unable to identify any clear cause, cure, or  effective  treatment  for  the  disease.2   Throughout the history of research on the  disease, epidemiological and public health  research approaches have played a key role  in  informing  policy  and  advancing  knowledge on the disease. Epidemiological  studies  have  helped  change  early  perceptions  of  ALS  as  an  extremely  rare  disease,  and

Amyotrophic, no muscle nourishment, lateral, an area in the spinal cord in where the brain tells the muscles what to do, sclerosis, hardening, affects every part of the body except the brain. ALS is a specific disorder that involves the death of neurons . Symptoms usually start as a muscle stiffness or weakness, later leading to paralysis throughout the whole body including the speech, swallowing, and breathing. There are two types of ways you can encounter ALS,familial and sporadic. Familial is in the 5 to 10 percentage rate which is inherited. Sporadic, responsible for the other 90 to 95 percent, that can be associated with anyone.

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.