Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease, is a neurological disease that affects voluntary muscle movement. ALS is named after the famous baseball player Lou Gehrig, whose career was cut short when he started quickly lose control of their muscles. Twelve years after the diagnosis of ALS, Gehrig died of the disease. According to the ALS Association, approximately two out of every 100,000 people suffer from ALS, and have much to learn about the disease. To get an idea of what the doctors today know here is a guide to the basics of ALS:
General Information
ALS is also known as motor neuron (MND) disease affects the cells of the spinal cord and spinal nerves that are responsible for controlling voluntary muscles. While specialized neurons in the brains that are responsible for different functions such as thinking and memory, ALS affects only associated with muscle strength and coordination. These muscles begin to degenerate and, after a certain point, stop working. ALS is a progressive disease. Over time, the disease affects more areas of the body. In the end, the victims find it impossible to complete. Basic tasks such as chewing, swallowing or standing
symptoms
Early symptoms of ALS are often small enough to ignore. These early symptoms include difficulty breathing, speaking and swallowing. Other symptoms include muscle weakness and spasms and cramps in the arms and legs. Many patients feel uncomfortable at first, stumbling on sidewalks, curbs repeatedly removing objects. Symptoms vary from person to person, and affect different parts of the body, but most often show signs of muscle weakness. Prolonged symptoms of ALS often fatal. As the disease progresses, the affected people have trouble breathing. Choking is a frequent complication, and patients who lose control of their swallowing muscles will only be fed. By means of a probe
causes
According to the National Library of Medicine of the United States, only 10 percent of the ALS cases been associated with a family history. The vast majority of cases of unexplained, and researchers have yet to find. Definitive set of causes of the disease A current hypothesis mutation of a gene that is inherited cause developmental genetic diseases. Other possible causes include the unbalance of glutamate, a chemical messenger in the brains and cerebrospinal fluid or disorganized immune response in which the immune system of a person's body mourning. Although the cause is not clear, there are several known risk factors for ALS, hereditary predisposition. ALS is also more common in people between the ages of 40 and 60, and it is slightly more common in women than in men.
prevention
There is no known way to prevent premature ALS but the key to slowing the progression of the disease. Can Healthcare providers can be a series of tests intended primarily to carry determine muscle weakness. Into different parts of the body Physical examination may reveal signs, as is apparent from spasms, tremor, muscle twitching, or loss of muscle tissue. Of decay Other means for measuring the motor control involves the testing of the breathing, swallowing studies and studies of the nerve conduction. Blood tests, MRI scans, or scans can also be administered to any underlying disease or ALS. With these tests, an expert of a patient to a drug can help to start the control of the symptoms. Program
treatment
Although there is no cure for drugs that are too slow. The progression of the disease ALS, Riluzole is a drug specific for ALS, and has been used to reduce the spread of muscle atrophy and prolong life. There are also a number of recipes that are used to symptoms that daily life, including influencing antiseizure medications and drugs are usually used to alleviate. Parkinson's disease In the end, the person with ALS who needed a wheelchair or braces, stomach help. Feeding tube and mechanical ventilation
General Information
ALS is also known as motor neuron (MND) disease affects the cells of the spinal cord and spinal nerves that are responsible for controlling voluntary muscles. While specialized neurons in the brains that are responsible for different functions such as thinking and memory, ALS affects only associated with muscle strength and coordination. These muscles begin to degenerate and, after a certain point, stop working. ALS is a progressive disease. Over time, the disease affects more areas of the body. In the end, the victims find it impossible to complete. Basic tasks such as chewing, swallowing or standing
symptoms
Early symptoms of ALS are often small enough to ignore. These early symptoms include difficulty breathing, speaking and swallowing. Other symptoms include muscle weakness and spasms and cramps in the arms and legs. Many patients feel uncomfortable at first, stumbling on sidewalks, curbs repeatedly removing objects. Symptoms vary from person to person, and affect different parts of the body, but most often show signs of muscle weakness. Prolonged symptoms of ALS often fatal. As the disease progresses, the affected people have trouble breathing. Choking is a frequent complication, and patients who lose control of their swallowing muscles will only be fed. By means of a probe
causes
According to the National Library of Medicine of the United States, only 10 percent of the ALS cases been associated with a family history. The vast majority of cases of unexplained, and researchers have yet to find. Definitive set of causes of the disease A current hypothesis mutation of a gene that is inherited cause developmental genetic diseases. Other possible causes include the unbalance of glutamate, a chemical messenger in the brains and cerebrospinal fluid or disorganized immune response in which the immune system of a person's body mourning. Although the cause is not clear, there are several known risk factors for ALS, hereditary predisposition. ALS is also more common in people between the ages of 40 and 60, and it is slightly more common in women than in men.
prevention
There is no known way to prevent premature ALS but the key to slowing the progression of the disease. Can Healthcare providers can be a series of tests intended primarily to carry determine muscle weakness. Into different parts of the body Physical examination may reveal signs, as is apparent from spasms, tremor, muscle twitching, or loss of muscle tissue. Of decay Other means for measuring the motor control involves the testing of the breathing, swallowing studies and studies of the nerve conduction. Blood tests, MRI scans, or scans can also be administered to any underlying disease or ALS. With these tests, an expert of a patient to a drug can help to start the control of the symptoms. Program
treatment
Although there is no cure for drugs that are too slow. The progression of the disease ALS, Riluzole is a drug specific for ALS, and has been used to reduce the spread of muscle atrophy and prolong life. There are also a number of recipes that are used to symptoms that daily life, including influencing antiseizure medications and drugs are usually used to alleviate. Parkinson's disease In the end, the person with ALS who needed a wheelchair or braces, stomach help. Feeding tube and mechanical ventilation
As a sign of gratitude for how my husband was saved from the dreaded ALS, i decided to reach out to those still suffering from this.
ReplyDeleteMy husband was diagnosed of ALS in 2013 and it was really tough and heartbreaking for me because he was my all and the symptoms were terrible, he had difficulty swallowing, all his joints were dead and that made him immobile to mention but a few. we tried various therapies prescribed by our neurologist but none could cure him. I searched for a cure and i saw a testimony by someone who was cured and he left the contact of the doctor who had the cure in 2015. I never imagined ALS has a cure not until i contacted him and he assured me my husband will be fine. I got the herbal medication he recommended and my husband used it and in three months he was fully okay even up till this moment he is so full of life. ALS has a cure and it is a herbal cure contact the doctor for more info on josephalberteo@gmail.com on how to get the medication. Thanks for reading my story.