Research papers about als

Entire savings of relatives of patients are quickly depleted because of the extraordinary cost involved in the care of ALS patients.

This antiglutamate appears to prolong the life of persons with ALS by at least a few months. Half of all affected live at least three years after diagnosis. A-myo-trophic comes from the Greek language. This is not meant to imply that other neurologists cannot make a diagnosis, only that physicians referred by ALSA see many ALS patients.

Half of all affected live at least three or more years after diagnosis. In Januarya team of researchers reported that their studies suggest that the SOD1 gene mutations may enhance the ability of the SOD enzyme to act as a "peroxidase," that is, oxidizing and thereby damaging cell components.

There are many diseases that have some of the same symptoms as ALS; some of them are treatable. The remaining one-third notice slowing of speech or difficulty in swallowing.

Third, with the availability of gastrostomy feeding tubes, home ventilators, etc, not only length of survival, but quality of life can be extended. The physician will probably suggest exercises, including breathing exercises, to strengthen unaffected or less-affected muscles.

ALS Research Paper

Therefore, both have demonstrated the capacity to extend quality of life in the ALS patient. Also, I firmly believe that state of mind has a significant influence over survival time. Often symptoms begin in the hands and feet, then travel inward toward the center of the body.

This lack of noticeable symptoms occurs because the lost or damaged nerve cells are compensated for by nerve cells that remain functioning. Therefore, consideration as to its cause has been given to agents with selective properties such as toxic agents and genetic factors. After plus years, there is a first-ever treatment for ALS.

These begin in the brain and extend into the spinal cord. Many patients are able to live productive and satisfying lives especially with the use of assistive devices for daily living, and later in the disease, augmentative communication equipment. Also, up to 10 percent of ALS cases are familial occurring more than once in a family lineage; but 90 percent of ALS cases show no hereditary pattern.

These are Myotrophin, a development from Cepalon, Inc. At the onset of ALS the symptoms may be so slight that they are frequently overlooked.

It was once believed that men developed ALS more frequently than women. It more often affects people over age 40, men slightly more than women.

ALS is not a rare disease and occurs throughout the world with no racial, ethnic or socioeconomic boundaries. Sporadic - the most common form of ALS in the United States Familial - suggest genetic dominant inheritance and accounts for a very small number of cases in the United States.

Second, there are documented cases of spontaneous remission and long term ALS survivors.

Health/ Amyotrophic Lateral Sclerosis term paper 18497

When these are affected, the result is marked weakness leading to paralysis, muscle wasting and diminished to lost reflexes. The Association maintains a list of recognized experts in the field of ALS. Survival after the confirming diagnosis is, on average, two to five years.ALS research needs to become more prevalent and publicized by educating people about what ALS is, the three types of ALS and some of famous cases of ALS.

/5(2). Health term papers (paper ) on Amyotrophic Lateral Sclerosis: Amyotrophic Lateral Sclerosis (ALS), sometimes referred to as. Home, Why Use Us, Services, Work Samples, Client Testimonials, Beware of Fakes. The free Health research paper (Amyotrophic Lateral Sclerosis essay).

Aug 31,  · A free online resource for cutting-edge research news & analysis and research tools for amyotrophic lateral sclerosis (ALS) researchers. Since inception, MDA has dedicated over $ million to ALS research and health care services.

In the past five years alone, MDA has spent over $46 million toward ALS research. ALS: Amyotrophic Lateral Sclerosis - Research |.

Amyotrophic Lateral Sclerosis Research Paper Amyotrophic Lateral Sclerosis “I nominate you to the ice bucket challenge!” These are words spoken by thousands. Disease Research Paper: Lou Gehrig’s Disease / ALS (Amyotrophic Lateral Sclerosis) 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.

Research papers about als
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