Chronic Fatigue
Imagine feeling exhausted after walking two blocks, having chronic sore throats, muscle and joint pain. Imagine your head feels like it is stuffed with wet sand and when you try to read, words swim on the page. Imagine feeling heavy and sluggish after a nights sleep. And imagine that these ailments last for years. These are just a few of the symptoms associated with Chronic Fatigue and Immune Dysfunction Syndrome, betters known as CFS, a serious and disabling illness that affects and estimated 800,000 persons a year. I can imagine these symptoms because I was diagnosed with CFS in 2001. I first began to notice a change in my health in 1998. I had always been healthy, outgoing and full of energy. My favorite phrase was "I will sleep when I die", but in 1998 I began to notice that I was abnormally tired. For a few years I was aware of this feeling but always blamed it on other factors such as my mom's passing, working 12-16 shifts at my job, just not getting enough rest, not eating properly, etc. All part of a busy lifestyle. But late in 2000 I began to take a turn for the worse, the tiredness I was feeling turned to exhaustion. I began to have migrane headaches, earaches, swollen lymph nodes, sore throats, upset stomach and fr
equent diarreha. I remember in Feburary 2001 I took a trip to Florida and literally slept all the way there and back. I went to see my doctor and we did some blood work checking my thyroid, looking for viral infections and even multiple sclerosis. We found nothing from the blood work and I was rescheduled for September. The symptoms continued and got worse. I began to have problems with my sleeping from insomnia to sleeping on nearly all of my off time. I would even fight sleep at work and on the drive back and forth to it. I found it hard to concentrate and had short-term memory loss. I remember a time I went to answer the phone and when I picked it up I "forgot" what I was supposed to say when I answered it. I could read a page in a book and not know what I had just read. Simple everyday tasks grew more confusing and difficult. I got chills and night sweats, dissiness and balance problems, problems with my stomach got worse. I carried a low grade fever most days and would experience tingling in my feet and lower legs. It was becoming harder and harder to function on a daily basis. I would sleep so hard at times it would take 3 alarm clocks to awaken me and I would still feel exhausted, no matter how much sleep I had. My social life became nil. In June, I came down with bronchitis and it took 3 months, two visits to minor-emergency centers and a visit to the emergency room to get past it. In September, I returned to my doctor and was diagnosed with CFS. A study done in 1999, conducted by Depaul University, estimated that as many as 800,000 people nationwide suffer from the illness. 90% of these have not been diagnosed and struggle through life without medical care. Research has shown that CFS is 3 times more common in women, a rat
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Dysfunction Syndrome,
Depaul University,
CFS CFS,
Disease Control,
People CFS,
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Approximate Word count = 1176
Approximate Pages = 5 (250 words per page double spaced)
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