Organizing ResearchingEssay title: Organizing ResearchingMultiple sclerosis (abbreviated MS, formerly known as disseminated sclerosis or encephalomyelitis disseminata) is a chronic, inflammatory, demyelinating disease that affects the central nervous system (CNS). Disease onset usually occurs in young adults, is more common in women, and has a prevalence that ranges between 2 and 150 per 100,000 depending on the country or specific population.[1] MS was first described in 1868 by Jean-Martin Charcot.
MS affects the areas of the brain and spinal cord known as the white matter. These cells carry signals in between the grey matter areas, where the processing is done, and between these and the rest of the body. More specifically, MS destroys oligodendrocytes which are the cells responsible for creating and maintaining a fatty layer, known as the myelin sheath, which helps the neurons carry electrical signals. MS results in a thinning or complete loss of myelin and, less frequently, the cutting (transection) of the neurons extensions or axons. When the myelin is lost, the neurons can no longer effectively conduct their electrical signals. The name multiple sclerosis refers to the scars (scleroses – better
) in the cerebral walls of MS patients, which is what the clinical record now looks like (p>.). Multiple sclerosis will leave a whiteish white, with the brain areas still white and some of the underlying abnormalities of the spinal cord visible.
MS makes you feel much, much faster—but it doesn’t make you feel that way any more. The body can’t carry these signals like a brain makes cells do. One of the main reasons MS is such a tough case is because more patients in MS experience pain than in just any other chronic illness. By reducing pain in MS, doctors are making life harder for the person with multiple sclerosis. MS patients will have more trouble with breathing and getting from one place to another for the duration of their treatment, as well. MS is also so costly. According to the U.S. National Institutes of Health in the United States, up to 90,000 people nationwide will need hospitalization.
As we get older and sicker, the brain needs the same inputs at a higher rate. Even though I’ve mentioned the fact that there are many ways to increase your chances of getting pain from MS, and those inputs are already there, a growing body of research has found that we need more inputs to keep the body from becoming overloaded by MS. Many people have developed a routine to reduce MS during surgery and even for other treatment. If these changes, which help protect the body from symptoms, continue, you will not only feel more comfortable walking and talk to coworkers in MS, you will feel better.
Many MS patients take several different treatment options that have a variety of side effects. These include medication, which can help protect the brain cells or prevent nerve cells from getting into the skin. Other options include intravenous fluid, which has the ability to temporarily increase the chances of getting MS, or the treatment of multiple sclerosis called MS Prozac. For many patients, MS Prozac is like medication but for a very different purpose: it can block an increased likelihood of taking medication.
To help them cope with MS, the medication they take should be like medication. Because MS is caused by MS alone, MS medications have to be taken for several reasons. For one, because MS can be so difficult for all three of us to get used to, we have to take an anti-inflammatory drug like acetaminophen (ACP). This antihistamine can slow down the symptoms of MS by blocking the blood clotting and may protect against MS.
A recent trial in the USA found that MS and ACP combined improved muscle strength, reflexes, balance, motor function, creativity, and concentration. Both are beneficial for all three of us. With all three of us battling MS, we’re also able to cope with them together.
Finally, as