Saturday January 11, 2025
SNc Channels:

Search
About Salem-News.com

 

Feb-28-2007 11:43printcomments

The Sometimes Invisible Disease – Multiple Sclerosis

MS affects the central nervous system, restricting nerve fibers from conducting electrical impulses to and from the brain.


medicalprogress.org

(SALEM) - Four-hundred thousand Americans suffer from Multiple Sclerosis which has the subtleness of invisibility to others, but is devastating to those afflicted with this debilitating disease.

In researching Multiple Sclerosis, I came to realize how little I knew about it, and was soon to learn that those not specifically educated on MS have very little insight.

Several years ago there was an instructor at the business school I attended who told his students about the disease he had. He informed us if we were to see him stagger or act a little “out of it”, that he was not on drugs but was suffering from MS. What an eye opener for some of us because we had heard rumors that Mr. “?” was acting strange and of course some thought he was abusing drugs. It is nasty how “little” minds work when the unknown prevails - it is so easy to think the worse. His disease progressively worsened and the last I heard he was in a wheelchair. MS had taken its toll!

I have a cousin with MS and she said many times people have looked at her strangely when she parked in the handicapped zone. Their look was very clear, “You certainly don’t look handicapped.” There were times people told her, “But you look so normal!” The devastating effects of MS are just not understood. That's the invisible disease. People don’t know that suddenly an MS sufferer could lose their balance and fall, or a devastating headache could occur, or just as suddenly, one with MS can become so dizzy they cannot stand by themselves. These assaults of symptoms could occur at any time.

MS affects the central nervous system (CNS) and is thought to be an autoimmune disease. The CNS is made up of the brain, spinal cord, and the optic nerves. There is a fatty tissue called myelin that surrounds the nerve fibers of the CNS and this tissue helps nerve fibers conduct electrical impulses. Once myelin is lost in multiple areas, it leaves scar tissue called sclerosis, hence multiple sclerosis. The destroyed or damaged nerve fibers inhibit the ability of the nerves to conduct electrical impulses to and from the brain causing a myriad of symptoms.

The symptoms include changes in cognitive abilities which deal with memory, lack of attention and problem solving; and fatigue, difficulty in walking, balance, vision problems, vertigo, dizziness, numbness, sexual dysfunction, depression, spasms, and bladder and bowel dysfunctions and pain.

As with most misunderstood illnesses, individuals who suffer from the symptoms of MS often refrain from telling the people around them about the disease they are suffering from. The fear of rejection, being different, and losing social status is prevalent and many tend to keep it a secret for as long as possible.

If you have a loved one, a co-worker, or a friend who suffers from this disease, you will be doing yourself a favor by becoming as informed as possible about Multiple Sclerosis.

There are 400,000 Americans who suffer from MS. The average range is 20 to 50-years of age, and it is more prevalent in women than men. The disease does, although rarely, afflict children.

www.nationalmssociety.org/Who%20gets%20MS.asp

There are many websites that give information and there are chat sites where people interact and help each other through difficult times. Following are some of the sites that give excellent information to help understand this complicated and elusive disease.

www.nationalmssociety.org

www.nationalmssociety.com

www.mswatch.com/community/

www.msinbalance.com/




Comments Leave a comment on this story.
Name:

All comments and messages are approved by people and self promotional links or unacceptable comments are denied.



Staci Indiana March 6, 2007 10:59 am (Pacific time)

I am trying to understand what article people read. The comments made no sense, the article said nothing about dying? It was very imformative and it reminded me of when I got on an elevator, too go up one floor and people said I was lazy. I was diagnosed 6 years ago.


Flora March 3, 2007 10:43 am (Pacific time)

I'm afraid I also found your well-intentioned article misleading, regressive and misguided. And as for your "resources", get ready for a shocking news flash: a LOT of us MS patients are TOTALLY fed up with the NMSS and their obvious bias in favor of their advertisers. So how about some equal time from less biased sources? Like these: http://www.thisisms.com/index.php http://www.lowdosenaltrexone.org/ http://www.remedyfind.com/HealthConditions/21/ http://ldners.org/


Hank Ruark March 3, 2007 9:08 am (Pacific time)

Good job in overview-depth article, Lela. Wish more writers included links to sources --believe we owe it to readers, as well as proving up sources-used for the overwhelming flow of information these days.


Meranda Vieyra-Blass March 2, 2007 12:21 pm (Pacific time)

I live in Colorado and came across this article today. Hopefully everyone knows, March 5th begins National MS Awareness Week and I am hoping more articles on this subject will surface. As a person living with MS, I appreciate all press on this disease. Thank you for exploring MS in a truthful, positive and non-judgmental manner.


Michael Conti March 2, 2007 4:56 am (Pacific time)

Linda, good article. I was Dx'ed 15 years ago. Have gone through the humiliation of traffic sobriety tests, and the funny stares for handicapped parking. Still living a fairly normal life thanks to the latest in biotech. It is important to start taking the disease modifying drugs as soon as possible. I have been on Avonex since 1996. There is hope. My neurologist told me shortly after diagnosis that "MS rarely affects the quantity of life - only the quality".


Lela March 1, 2007 6:19 pm (Pacific time)

Thank you Gina. One of the aspects of Salem-News.com is that we supply additional website links for more information on whatever subject being written about. I try to do this with my articles so people can look up and make their own conclusions or gain more knowledge on a subject.


Gina March 1, 2007 2:46 pm (Pacific time)

I was diagnosed with MS 3 years ago and I appreciate you shedding some light on the disease. Pointing people to solid websites for more information as well as bringing awareness to the forefront. Thank you!


Lela March 1, 2007 11:29 am (Pacific time)

Linda, I really appreciate your comments and want you to know I had read a lot of information on this and have talked to individuals. This article was not meant to be an indepth medical discussion on MS, just an article to bring awareness to the disease. I do appologize if I upset you and in no way meant to imply anyone with MS does not live a rich life. My cousin is very active and lives life to the fullest.


Linda Dunn March 1, 2007 6:26 am (Pacific time)

I have had MS of 13 years and find your article frock with misconceptions. Instead of disspelling the myths surrounding MS, you have added to them. People with MS dont suddenly die at the age of 50. Most live rich lives into their 70's and 80's. And, being wheelchair-bound does not negate one's ability to live a rich, enjoyable and productive life. You need to get past your stereotypical view of people with handicaps and do your homework!

[Return to Top]
©2025 Salem-News.com. All opinions expressed in this article are those of the author and do not necessarily reflect those of Salem-News.com.


Articles for February 27, 2007 | Articles for February 28, 2007 | Articles for March 1, 2007
Sean Flynn was a photojournalist in Vietnam, taken captive in 1970 in Cambodia and never seen again.

Special Section: Truth telling news about marijuana related issues and events.

googlec507860f6901db00.html
Support
Salem-News.com:

Annual Hemp Festival & Event Calendar