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Since any website that is trying to increase awareness of multiple sclerosis must attempt
to at least give some information about this disease, I will try. I will not get into a great deal of details and
will also use wording that I have found to be understandable by those of us without medical degrees.
If you want to know the medical terminology and details, please go to the
National Multiple Sclerosis Society
website or to a medical site with definitions (in Friends & Resources).
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You can not catch multiple sclerosis from someone who has it. However, you could have it for many
years before it is diagnosed. It is a chronic, often disabling disease that randomly attacks the central nervous system.
You may have many attacks, and recover from them with no physical changes. Many of the changes are invisible simply
because the nerves control the muscles. If the nerve becomes damaged, the muscle quits. If it is a leg or arm muscle,
you lose the use of it. If it is not an often used and seen muscle, no one except you knows it.
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A friend calls multiple sclerosis his designer disease, because the symptoms are many and varied.
Seldom will two people with ms have the same symptoms. They range from severe fatigue, blurred vision, numbness
in the arms and legs, muscle weakness. These symptoms may come and go, or they could become permanent
anytime. There is no cure for multiple sclerosis, but there are medications that can slow the devastating symptoms,
thanks to the many dollars given to research by the
National Multiple Sclerosis Society
and others.
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Many people seem to confuse this disease with muscular dystrophy. That is the disease that the
Jerry Lewis telethon raises funds for. I support that effort as much as I can, but you are born with
muscular dystrophy. At this time, multiple sclerosis seems to be different. Any person can get it,
at any time in their lives. It has been diagnosed in children as young as 10 and in adults older
than 50. The cause of multiple sclerosis has not been determined yet. Each year, the cause and
cure get a little closer, thanks to the research funded by the
National Multiple Sclerosis Society
and others.
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As a victim of this disease, I have found that finding current information about ms can be difficult
at times. In July of 2000 when I was diagnosed with multiple sclerosis, there were less that
350,000 ms patients in the United States. Since there is a relatively small number of people
diagnosed with ms, there is not a great deal of exposure for the need for research into the
cause and cure. As someone told me, the more widespread the cause becomes, the easier it will
become to get donations. Most people will tell you they know of someone with multiple sclerosis,
and it either disabled them completely, or they have no visible symptoms. Of course, sometimes they
simply tell you that the person seems to fake problems often. They act like they have problems
at different times of the day, but since they don't have them all day, there probably is nothing
wrong with the person. This very issue is what makes multiple sclerosis so difficult to diagnose
and deal with. Perhaps an individual needs a wheelchair in the mornings, but can carry the wheelchair
home within an hour or two! These symptoms are very difficult for both the multiple sclerosis victim
and all the individuals around them. |
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For more information about multiple sclerosis, please contact the
National Multiple Sclerosis Society.
You may also want to check out one of the websites in the
Friends & Resources. Please insure the information
has been reviewed or updated recently. Information about this disease changes rapidly, sometimes monthly.
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Here are a few books that are excellent at explaining symptoms and issues involved for the
multiple sclerosis patient:
- Climbing Higher by Montel Williams; published by New American Library, January 2005
- Curing MS; How Science Is Solving the Mysteries of Multiple Sclerosis by Howard L. Weiner, MD;
published by Crown Publishers, 2004
- Managing the Symptoms of Multiple Sclerosis, Fourth Edition by Randall T. Schapiro, MD;
published by Demos Medical Publishing, Inc, 2003
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