This website uses cookies to ensure you have the best experience. Learn more

The Struggle Of Living With Amyotrophic Lateral Sclerosis

1339 words - 5 pages

ALS(Amyotrophic Lateral Sclerosis) is a progressive motor neurone degenerative disease. The disease has different subcathegories but will in the end develope equally and lead to death - usually within the shortness of 3-5 years. This disease has no cure, only a few possibilities of slowing down the progress to help the rapid developement of the life changing symptoms and effects.

History and general information
ALS, MND(motor neurone disease) or Lou Gehrig’s disease is first noted in a report by Charles Bell in 1824. Although the disease was made «famous» when the baseball player Lou Gehrig died from it in 1939, there is still little awareness of the disease, eventhough the incidence of ALS is five times more likely than Huntington’s disease and on the same level as Multiple Sclerosis. ALS usually develop within the ages of 40 and 70, but it can effect people earlier. There are no known boundaries when it comes to race or etniticity.(, 2013)

General characteristics
This progressive degeneration of motor neurones affects both the upper and lower motor neurons, which means both the brain and spinal cord are impaired. What happens is what we call demyelination of the axons. Demyelination is damage and dissapearance of the myelin sheath which is needed for the conduction of signals.
When the motor neurones can no longer send strong enough signals to the muscles, muscle weakness and atrophy starts taking it’s toll.
Although the disease impairs the patients ability to preform daily tasks, makes them lose the ability to move, ALS will not affect a person’s intellect, or senses.
There are two main types of ALS: Bulbar onset(25%) and limb onset (75%). Bulbar onset is the less contracted type, and the difference between the bulbar onset and the limb onset is where the symptoms start; Bulbar onset symptoms usually start with difficulties with the tongue, whereas limb onset is quite clearly when the limbs are the part to be affected first.

Early Symptoms
Most people(75%) diagnosed with ALS will say the earliest symptoms started with clumsiness. Being human, clumsiness is something that is not taken as a serious symptom if this is the only thing you are experiencing in an early stage. But the clumsiness starting when having ALS is often caused by drop foot. Drop foot is an abnormality in walking, which is characterized by the inability to flex the foot upwards. The next symptom which is mostly noted is cramping, tremors and fasciculations. These cramps may also be regarded as normal by the person and the tremors often start out so small one would not give it another thought or even notice.
These symptoms will after a while start becoming more severe, and what is repeatedly seen in patients medical records is what led them to seek medical attention is often severe falls without any reason for them. The earliest symptoms of the bulbar onset ALS are slurred or hoarse speech, difficulty swallowing and problems related to the tongue.

Find Another Essay On The struggle of Living with Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis Essay

2105 words - 9 pages Amyotrophic lateral sclerosis, also known as ALS or Lou Gehrig's disease, is a disease of the nerve cells in the brain and spinal cord that control voluntary muscle movement. Jean-Marie Charcot was the first to recognize ALS as a distinct neurological disease with its own unique pathology. In ALS, nerve cells degenerate and deteriorate, and are unable to transmit messages to muscles. In around 90% of the cases of ALS, the cause remains unknown

Amyotrophic Lateral Sclerosis Essay

2204 words - 9 pages Amyotrophic Lateral Sclerosis ABSTRACT At this time, Amyotrophic Lateral Sclerosis(ALS) is a very confusing and elusive disorder. While the clinical presentation and diagnosis of ALS dates back to the early 1900’s, with Charcot being the first to scientifically report and document his findings, there simply has not been definitive evidence since that time for the etiology for ALS. This fundamental problem has befuddled the most

Amyotrophic Lateral Sclerosis

1278 words - 5 pages , they included, loss of strength, slipping and falling, and loss of coordination (Lou, 2011). After Lou was diagnosed with this disease he decided to retire from baseball (Lou, 2011). Lou will always be remembered as “The Iron Horse” due to his ability to keep playing despite suffering many injures due to his loss of coordination (Lou, 2011). Amyotrophic Lateral Sclerosis is a disease that affects the motor neurons from contracting muscles

Amyotrophic Lateral Sclerosis

927 words - 4 pages ; A French doctor named Charcot first identified ALS in 1874. It is one of the most devastating diagnoses a person can receive. ALS is said to start between the years of 40 and 70, with the exact average being 45.6 years old. The most classic case of Amyotrophic Lateral Sclerosis is Lou Gehrig. Lou Gehrig was a New York Yankees first baseman, who from 1923 to 1939, had never missed a game and had a life time batting average of .340. However

Amyotrophic Lateral Sclerosis

1175 words - 5 pages 11727 Amyotrophic Lateral Sclerosis Amyotrophic Lateral Sclerosis (ALS) is a disease that affects the nerve cells in the brain and spinal cord, specifically the motor neurons. Motor neurons carry signals from the brain and spinal cord to all of the muscles in your body. When a person has ALS, they are not able to generate enough motor neurons, and the brain cannot then initiate and control muscle movement. After some time, when the disease gets

Amyotrophic Lateral Sclerosis

1078 words - 5 pages Amyotrophic lateral sclerosis (ALS) It is not surprised that one of the common progressive motor neuronal disease, ALS, is also genetically connected to the mutations of degradation machineries with varied etiology. Even the majority of ALS is sporadic, two of familial ALS is mainly associated with simple monogenic factors, the mutation of SOD (D90A) and a large hexanucleotide (GGGGCC) repeat expansion in chromosome 9 open reading frame 72

The Fatal Disease: Amyotrophic Lateral Sclerosis

3700 words - 15 pages The Fatal Disease: Amyotrophic Lateral SclerosisAmyotrophic Lateral Sclerosis (ALS) is a progressive incurable neuromuscular disease that attacks nerve cells and pathways in the brain and spinal cord. Motor neurons, among the largest of all nerve cells, reach from the brain to the spinal cord to muscles throughout the body with connections to the brain. When they die, as with ALS, the ability of the brain to start and control muscle movement

What is Amyotrophic lateral sclerosis?

1373 words - 5 pages activity in muscles. Certain EMG findings can support the diagnosis of ALS. The muscles in the body are the big factors of ALS which makes electromyography an accurate test to support the diagnosis of amyotrophic lateral sclerosis. When there is a possibility that a patient has ALS the doctors prepare the patients with new ways communication and ways of living so when they go through a later stage in ALS they can be prepared. Gentle aerobic

Amyotrophic Lateral Sclerosis (ALS): Lou Gehrig's Disease

1696 words - 7 pages Amyotrophic lateral sclerosis (ALS), commonly known as Lou Gehrig’s disease, affects approximately 20,000 - 30,000 U.S. citizens, with an estimated 5,000 new diagnoses made each year. ALS is a rapidly progressive neurological disease which attacks neurons responsible for the control of voluntary muscles, and is habitually fatal. ALS is part of the class of disorders called motor neuron diseases (MNDs). Motor neuron diseases are characterized by

The disease, Amyotrophic Lateral Sclerosis, better known as Lou Gehrig's Disease

579 words - 2 pages Amyotrophic Lateral Sclerosis (ALS) is a disease that causes muscles to stop working. ALS is a rare disease found mostly in very active people. Another name for ALS is Motor Neuron Disease (MND) and the most common name is Lou Gehrig's disease. Lou Gehrig was a hall of fame baseball player who played with Babe Ruth on the Yankees. He once hit four homeruns in one game. He fell victim to ALS in the late 1930's.ALS was discovered in Paris, France

Amyotrophic Lateral Sclerosis: Pathophysiology and Implications for Physical Therapy

3308 words - 13 pages Amyotrophic Lateral Sclerosis: Pathophysiology and Implications for Physical Therapy This work will provide a basic overview of the pathophysiology for amyotrophic lateral sclerosis (ALS) as well as the medical interventions used in treatment of the disease. Physical therapy interventions for ALS and therapeutic exercise recommendations are the major focus of this study, and will be discussed in greater detail in the later portion

Similar Essays

Mutations Of The Superoxide Dismutase Gene Are Associated With Amyotrophic Lateral Sclerosis

1771 words - 7 pages Recent studies have provided some insight for the possible causes of the familial type of amyotrophic lateral sclerosis (FALS). This disease occurs only in 10% of the known cases of ALS with the sporadic, non-hereditary form being predominant [7, 9]. ALS in general has an occurrence of 0.4 to 1.8 per 100,000 live births [1]. ALS has been called Lou Gehrig’s disease, Charcot’s disease and motor neuron disease in other literature [4]. ALS is

Amyotrophic Lateral Sclerosis (Als) Essay

1087 words - 5 pages Imagine if you loss control of your body but your mind stayed unaffected. You would be a prisoner in your own body, all leading up to your death sentence. That is the sad fate for the people diagnosed with Amyotrophic lateral sclerosis (ALS). “Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder was first described by Ran in 1850. This description was then expanded in 1873 by Charcot, who emphasized the involvement of the

Amyotrophic Lateral Sclerosis Essay 2937 Words

2937 words - 12 pages Part I: Amyotrophic Lateral Sclerosis (ALS) is an age-related disorder which results in rapid, selective deterioration of motor neurons of the central nervous system. ALS was first described by Jean-Martin Charcot in the 1870s and is the most common motor neuron disease, with an incidence of 2 per 100,000 people. It predominantly includes primary lateral sclerosis, a disease restricted to upper motor neurons and progressive muscular

Amyotrophic Lateral Sclerosis Essay 2486 Words

2486 words - 10 pages , which allows them to synapse with muscles throughout the body. Thus, in a normal situation, messages from UMNs are transferred to LMNs, and from there are transferred to specific muscles. UMNs and LMNs are responsible for movements such as walking and chewing, and movement of the arms, legs, chest, and face, respectively. This permits healthy individuals the ability to voluntarily move their muscles with ease. Amyotrophic Lateral