Sherkshire Walk Research Paper

“We are very community oriented. Each member must actively participate in the yearly fundraiser where all of our proceeds go towards DECA’s state-wide philanthropy, Muscular Dystrophy Associated (MDA). Our local chapter also requires members to work five community service hours per semester.”

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.

ALS, or amyotrophic lateral sclerosis, is a disease that damages motor neurons in the brain and spinal cord. It is a deadly disease that cripples its victims due to breakdown in the body’s motor neurons. Motor neurons are nerve cells that control muscle movement. They are important part of the body’s neuromuscular system. The neuromuscular system allows our bodies to move and is made up of the brain, many nerves, and muscles. People that are diagnose with ALS disease causes for the motor neurons in the brain and the spinal cord to shrink and disappear, so that the muscles no longer receive signals to move eventually causing the muscles to become smaller and weaker. Slowly the body becomes paralyzed, which means that the muscles no longer function. The average life expectancy for a person that has ALS after being

Amyotrophic lateral sclerosis, also called Lou Gehrig’s disease, is a neurodegenerative motor disease that results in the destruction of the neurons responsible for involuntary muscle movement (NINDS 2014). Patients are determined to have ALS if they have both upper motor neuron disease and lower motor neuron disease (Gordon 2011). Many people that have been diagnosed with ALS are seen in wheelchairs or if the person is in the early onset of ALS, using other walking devices. This is because in 65% of patients, ALS begins with weakness in the arms, legs, and body, therefore this results in the loss of capability to walk (Gordon 2011, A.D.A.M. 2012). Most patients live for approximately three to five years after symptom onset and usually die when the muscles in the chest stop working, which causes their heart and lungs to stop functioning as well (Gordon PH 2011, A.D.A.M. 2012). This is caused by muscles weakening until atrophy and fasciculations occur, leading to the brain being unable to control voluntary movement (NINDS). Amyotrophic lateral sclerosis is classified as a motor neuron disease (NINDS).

As a member of DECA, I have had the opportunity to network with the Muscular Dystrophy Association (MDA). While learning about the work the association does, I realized that I want to do similar work. In my effort, I worked on a promotional campaign for the Muscular Dystrophy Association. Neuromuscular diseases, like Muscular Dystrophy, take away physical strength and eventually life. The Muscular Dystrophy Association (MDA) fights to find a way to give back strength, independence, and life. The work they do truly changes lives; however, they need support from others.

Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig’s disease, is a progressive neurodegenerative disease that affects the brain and spinal cord nerve cells. The degeneration of these neurons result in their death, which prevents the brain from initiating voluntary muscle movement. Patients may not experience the same symptoms throughout the phases, early symptoms include difficulties swallowing, breathing, speaking, and increasing muscle weakness. Muscle atrophy occurs and paralysis may result in the later stages of the disease. The cause of ALS is unknown and although there is no cure, current treatment can halt the progression or possibly reverse it (ALS Association, 2010). Many people do not think twice about the early signs and symptoms of ALS, as the disorder progresses, the signs and symptoms can mimic other illnesses. Early signs usually begin in the upper and lower extremities. The patient appears to be clumsy. As ALS progresses, all voluntary muscle movements will be affected. The patient will have difficulty speaking, chewing, swallowing, breathing, and holding their head up. The average person lives 3 to 5 years after diagnosis, death of the motor neurons lead to death of the patient (Mayo Clinic, 2015). ALS is seen more in men than in women and more in Caucasian’s than any other race. Most patients are diagnosed between the ages of 40 and 75 (CDC, 2014).

What is ALS? ALS stands for Amyotrophic Lateral Sclerosis, it is also known to be Lou Gehrig’s and Charcot disease. ALS is a motor neuron disease, in this case ALS is a disorder that will involve the neurons cells to die. It is a result that in the death of the motor neurons control the voluntary muscles. Based upon what the patient’s symptoms and signs with testing will rule out any other potential causes. There is no cure for this disease, it is just a waiting process. Medicine that is call riluzole can however extent the life expand only by two to three months.

Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig’s disease is a neurodegenerative disease affects nerve cells in the brain and the spinal cord. Amyotrophic means no muscle nourishment, and this makes the body begin to atrophy, which means the tissues or organs start to waste away due to the degeneration of cells, this leads to the sclerosis. The degeneration of the cells eventually leads to death, this could be a very slow process lasting 5 years or more, or it could be faster lasting around a year or less. The motor neurons in the brain begin to die, and this affects their ability of the brain to initiate and control muscle movement. When the motor neurons die, people with ALS start to lose their ability to eat, speak, move, and

Amyotrophic Lateral Sclerosis (ALS) has been heard of at some point whether it was studied in school, talked about through word of mouth, or one decided to partake in the ALS Ice Bucket Challenge that swept the internet recently in support of the disease. This paper is going to delve into explaining the manifestations of this disease, its treatment and talk about the man this disease was named after.

Amyotrophic Lateral Sclerosis, more commonly know as ALS or “Lou Gehrig's Disease”, affects the nerves in the brain and the spinal cord. ALS is a disease of the nerve cells in the brain and in the spinal cord that control muscle movement. Over 5,600 people in the United States are diagnosed with ALS a year and about 30,000 Americans have ALS at a time. Some symptoms or signs of ALS are people’s arms and legs beginning to lose strength and muscles could become tight. Also, feet and ankles may develop weakness. General fatigue may develop and some muscles, like tongues, may twitch. Additionally, swallowing, speaking, and breathing may become harder to do. People with ALS may have slow eye movements and their

According the ALS website, the ice bucket challenge raised $115 million dollars and an additional $13 million dollars was donated to the association's regional branches. The website also states, as a result of the ice bucket donations, Scientist have discovered the NEK1 ALS gene. You can read about this discovery at http://www.alsa.org/fight-als/ice-bucket-challenge.html.

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

At the ALS meetings, group members introduced themselves to get to know each other. Each member narrated an experience that they thought was

I believe everyone at a time in life want to reach out and help give back to the community and really make a positive impact. Raising awareness for a new and unknown disease would help the diseases and keep people educated on it.

Ice Bucket Challenge encouraged donations through social media, such as Facebook and Twitter. Many people, including celebrities, participated in this campaign and ALS raised more than 100 million dollars. In the article “Does slacktivism work?”, “Campaigns for attention often assume that more attention would cause increased participant engagement”. However, most of the people primarily focused on fun or advertising themselves on social media rather than donating money to charity. Indeed, it seemed like people wanted to enjoy the last moments of summer by pouring a bucket of