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Recommended: Als disease
In the summer of 2014 a social media phenomenon swept the world and newsfeed of every Facebook, Instagram and Twitter account. It was called the “ALS Ice Bucket Challenge”. How it worked was someone who had previously been challenged, challenged someone else and they had to accept it, dump freezing water on their head in the most creative way possible and pass it on or donate to the Amyotrophic Laterals Sclerosis Association (ALSA) to help research the disease. Then I knew nothing about Amyotrophic Laterals Sclerosis (ALS) though I participated in the challenge myself, nor did I realize that this challenge that I took part in to join the crowd was going to become a challenge that would change my life in a few short years. Jean Martin Charcot …show more content…
There is not one specific test created to determine whether or not someone has ALS. It is all done through a series of test and examinations to detect if the symptoms mimic those of ALS. When diagnosing physicians look for signs of muscle deterioration in the lower motor neurons, which are located in the spinal cord and brain stem, signs of deterioration in the upper motor neurons, located in the brain. Both are done by clinical examination and specialized testing. From there they begin to rule-out other neurological diseases and begin an in-depth medical and family history and physical examination to start a neurologic work-up, testing specific nerve points and nerve functions. The next step if ALS is suspected is an electromyogram (EMG). This test measures the signals that run between nerves and muscles and the electrical activity inside muscles to see if there is a pattern consistent with ALS. If there is additional test may involve imaging the spinal cord and brain by magnetic resonance imaging (MRI) and they will test the fluid surrounding the spinal cord (spinal tap or lumbar puncture), this is done by inserting a needle into the back between the two lower vertebrae. Even then diagnosing ALS is often a “rule-out” procedure. Meaning that ALS is only diagnosed after all possibilities of any other kind of neurological disease has been ruled out by specific tests, and still the physician will usually
It is truly remarkable how Randy Pausch and Morrie Schwartz stories are so similar but yet so different. They both seem to have an outlook on life in a positive way, not sad or demeaning. The only crippling difference is the fact that Morrie was at the age that wasn’t abnormal to be sick and Randy was just dealt the cards for a short life. One of Professor Randy Pausch’s many quotes during The Last Lecture makes a similar point between his experience and Morrie’s when he says, “…it’s hard to raise awareness of pancreatic cancer – people who get it don’t live long enough.” ALS is such a rehabilitating disease that scientist have issues pinpointing the causes to even get close to a cure, which didn’t hinder either of their strive to keep going as far as they could.
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 corticospinal tracts. In the United States, ALS is often referred to as Lou Gehrig's disease, after the famous ball player who was stricken by the disease in the midst of his career. (Yale School of Medicine, 2014)” In this paper will go through the definition, the process, the signs, the risk factors, etiology, and discus the known people that have suffered with this terminal disease.
There is no cure for ALS at this time and treatment is focused on management of the symptoms, involving a combination of physical therapy, occupational therapy, and speech, respiratory, and nutritional therapies. Moderate exercise may help maintain muscle strength and function. Drugs can also treat excessive saliva and drooling, and speech therapy can help compensate for loss of muscular control of the mouth. As the disease progresses and muscular degeneration spreads throughout the body, various devices may provide support, such as ankle braces, neck collars, reclining chairs, wheelchairs, and hospital beds. Respiratory support and feeding tubes are required when the person loses cont...
INTRODUCTION The winter season can be a major hassle for some people while others just have to deal with a slight cool down in temperatures. Over the northern portions of the country, people are faced to deal with the harsh conditions that Mother Nature has in store. Some winter seasons are less brutal than others. Besides the typical storm systems that come through the area and drop different types of precipitation whether it is snow, sleet, or freezing rain, there’s another weather event that affects not everyone in the country, but primarily around the Great Lakes.
As motor neurons degenerate, this obviously means they can no longer send impulses to the muscle fibers that otherwise normally result in muscle movement. Early symptoms of ALS often include increasing muscle weakness, especially involving the arms and legs, speech, swallowing or breathing. When muscles no longer receive the messages from the motor neurons that they require to function, the muscles begin to atrophy (become smaller). Limbs begin to look thinner as muscle tissue atrophies (Choi, 1988).
ALS is a degeneration of motor neurons that move from the brain and down the
Survival and Love in Charles Frazier’s "Cold Mountain" I lie In vacant or in pensive mood, They flash upon that inward eye Which is the bliss of solitude; And then my heart with pleasure fills, And dances with the daffodils.
Doctors need a sure way to diagnose the disease before treatment or studies can be done. The diagnosis is an autopsy of brain tissue examined under a microscope. In addition, medical history, a physical exam, and mental status tests are used for diagnosis (Posen, 1995). Often, tests are done to rule out other potential causes of the dementia. This allows the identification of other causes of thinking and behavioral changes to be made before concluding that the patient has Alzheimer’s or another form of dementia. The tests that are requested to be done include CT and MRI scans to rule out strokes or brain tumors which could account for change in memory and behavior; thyroid and psychological tests which can also detect thinking and behavior problems (Posen, 1995).
Amyotrophic lateral sclerosis, or ALS, is a degenerative disease affecting the human nervous system. It is a deadly disease that cripples and kills its victims due to a breakdown in the body’s motor neurons. Motor neurons are nerve cells in the brainstem and spinal cord that control muscle contractions. In ALS, these neurons deteriorate to a point that all movement, including breathing, halts. Muscle weakness first develops in the muscles of body parts distant from the brain, such as the hands, and subsequently spreads through other muscle groups closer to the brain. Such early symptoms as this, however, can hardly be noticed.
Terry Fox is an individual who has had an enormous impact on society as we know it today. Although losing his right leg to cancer at a young age, he wouldn’t let that stop him from running across the nation of Canada in hopes of raising money and awareness for cancer research. The run, officially named, “The Marathon of Hope” would be recognized by many as an incredible journey which from its start to end would overall distance around 5373 kilometers in 143 days. Still to this day, Terry Fox is widely regarded as a Canadian hero for his sacrifice in order to help others who are also suffering from such a deadly disease reach care and awareness. The “Terry Fox Run”, organized by many groups and schools across the continent, also runs to raise
The ice bucket challenge of 2014, on the other hand, managed to progress empathy one step further. As a fundraiser for amyotrophic lateral sclerosis (ALS), and the act of ‘passing it on’ by tagging someone after completing the challenge led the challenge to extend across an entire summer (The ALS Association). Several months of donations, in contrast with the Syrian cause’s much briefer donation spike, led to millions of dollars in donations to ALS (The ALS Association). However, in this case, many participants dropped “ALS” from their video titles and neglected to donate. The ice bucket challenge thus succeeded in extending the duration of its donations, but failed to propagate the empathetic element of its
Shortly after her second birthday, doctors had discovered that her tumors had grown and she needed a stem cell transplant. People from all over the world held their own lemonade stands and donated the money they made to Alex and her family. This helped the foundation reach a goal of $1 million dollars raised to help children battling cancer. In August of 2004, Alex passed away at the age of eight, knowing that, with the help of others, she had raised more than $1 million to help find a cure for the disease that took her life. Throughout all of this, she helped create the foundation today known as Alex’s Lemonade Stand Foundation (ALSF).
This is a neurodegenerative disease, meaning it results in progressive loss or death of neurons. It often starts off with effecting simple motor skills like writing and holding things, after a few months usually patients start losing the ability to walk, talk, or move any of their limbs. Although the brain trauma is what causes it, ALS has little-no-effect on the brain. This fatal disease is typically diagnosed around age 60 and most patients are given about 3-5 years to live after being diagnosed. It has been found that 10% of cases are shown as genetic. It was brought to attention that athletes were beginning to get diagnosed with ALS at a younger age than most. After extensive research in the early 2000’s, Brain Analyst, Dr. Mckee ran tests and finally came to the conclusion that the toxic proteins in the brains of ALS patients were coming from repeated blows to the head. It was then made evident why so many athletes in contact sports such as football, soccer, boxing, etc… were being diagnosed at such a young age and more frequently than
My involvement as Founding Member and UCLA President of the Youth Movement Against Alzheimer’s non-profit has sparked within me a desire to guide a team of individuals towards a greater cause. I have dedicated much of my time to generating inventive ways to involve the youth population across the U.S. in the fight against this disease.
During eleventh grade, I hoped to aid the victims of Alzheimer’s Disease by raising money for the Alzheimer’s Research Foundation. I organized a fashion show, Catwalk For A Cause, and with the help of local businesses, I raised over $2,000.