Aug
31

Q&A: Why won’t my computer recognize this website?

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Question by mysticduder: Why won’t my computer recognize this website?
I’m trying to go to the multiple sclerosis society, at www.nationalmsscoiety.org
I can do it from work no prob, but on my laptop at home it says either “server not found” or redirects me to “estparking.com” where it offers to sell me the domain name…..any answers?
Thanks
I mean “nationalmssociety.org”

Best answer:

Answer by mrgone2a
http://www.nationalmssociety.org

Try this. It just worked for me.

What do you think? Answer below!

Aug
31

Can Sunshine Prevent an effect on MS?

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Article by Vanesa Estrada

Over the last few years we have all been bombarded with messages about how important it is to keep out of the sun. We’ve realized exactly how real a risk skin cancer can be and are doing everything we can think of to prevent it from happening. We slather on layers and layers of the largest SPF sunscreens that we can purchase. We wear huge hats. We wear long sleeves in addition to pant legs even in the warmest of heat. We do our best to stay only in the shady areas–some have even started carrying parasols and umbrellas around so that their skin never comes into contact with direct sunlight. Now we’re beginning to find out that sunlight can sometimes be really helpful. Can sunshine truly help you?

A new study has been performed and it indicates that people who allow some time in direct sunshine aren’t as likely to get MS as the people who do everything they can to keep out of the sun. At the starting point, the study was much more about Vitamin D and it’s effects on Multiple Sclerosis. It didn’t take much time for them to realize that it is the Vitamin D our bodies make after exposure to the sun’s rays that is at the center of the issue.

It’s been recognized for a very long time that Vitamin D and the sun’s rays can effect the way the immune system works and how it can contribute to Multiple Sclerosis. This study, however, focuses on the affects of the sun’s rays on people who are experiencing the very earliest symptoms of the disease. This study is trying to figure out the results of Vitamin D in addition to the sun’s rays on the precursory signs and symptoms of the disease.

Unfortunately, there are not all that many approaches to truly quantify the study’s theory. This study is seeking to demonstrate whether or not sunlight can truly help a person prevent Multiple Sclerosis. Sadly, the only real way to know whether or not this is true is to monitor a person over his or her entire life. This is just about the only solution to actually assess the levels of Vitamin D that are already present in a person’s blood before the precursors to MS start to become apparent. The way it stands these days, and has stood (widely recognized) for a long time is that people who live in warm and sunny climates and who get more exposure to direct sunshine are less likely to develop MS than those who live in dark or cold climates and get very little exposure to the sun.

The fact that the chance of developing skin cancer goes up proportionally to the amount of time you spend in direct sunlight (without protection) is also a problem. So, in an attempt to stave off one condition, you could be causing yourself to create a different one. Of course, skin cancer—if caught early on—has an improved chance of being cured. MS still isn’t curable.

So should you acquire more sunlight to prevent MS from setting in? Your doctor may help you figure out whether or not this is a plan for you. Your physician can evaluate your current health status, your medical history and even your genetics to determine if you are even at risk for the disease in the first place. From there your physician may help you discover the best ways to keep the disease at bay.

About the Author

Vanesa’s websites: Plastic Jar, Pottery Painting, Sugar Maple Cabins and Bottle Labels.

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Aug
31

New Insight into Tissue Damage in Multiple Sclerosis – Mayo Clinic

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A new Mayo Clinic study has found that the type of tissue damage changes throughout the course of multiple sclerosis (MS). This work provides important information at the microscopic level regarding the dynamic changes occurring in MS white matter plaques over the course of the disease which can help inform subsequent studies that characterize the disease based on advanced imaging techniques or clinical outcomes. A better understanding of the pathology of MS may eventually lead to new therapeutic targets.

Aug
30

Latest Symptoms Of Multiple Sclerosis auctions

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symptoms of multiple sclerosis eBay auctions you should keep an eye on:

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Aug
30

Drug and alternative treatments for multiple sclerosis

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Article by Groshan Fabiola

Multiple sclerosis is a disease that affects the central nervous system and makes it attack the sensitive membrane that protects the many nerve endings that can be found throughout the body. When one of these attacks occurs the sense that corresponds to the affected nerve endings is damaged and in some cases it’s temporary lost. For example, the patient can temporary lose his/her vision or suffer severe balance problems.

The cause of multiple sclerosis has not been discovered yet, it is not known why when the nervous system is affected by multiple sclerosis sends the white blood cells and antibodies against the myelin steath membrane which protects the nerve endings. The cells mentioned above are sent to attack viruses and bacteria that enter the body and can cause an infection, so the reason for the attacks is mysterious.

So because the cause is unknown there is no treatment that can cure multiple sclerosis, but many things can be done against it.Currently the goal of the multiple sclerosis treatment is to decrease the frequency of the attacks and their severity, and to make the disease advance slower.

One of the most popular treatments for multiple sclerosis is immunotherapy. Immunotherapy drugs are usually injections with substances that can reduce the frequence and severity of the multiple sclerosis attacks by slightly modifying the way the immune system works. Immunotherapy is done with the help of drugs called beta interferons, that aid the immune system in its fight against infections and make the multiple sclerosis attacks less severe.Unfortunately immunotherapy drugs have side-effects that include fever and coughing, indigestion, skin irritation, and drowsiness, any many patients avoid using them for this reason.

Some doctors say that Mitoxantrone,a chemotherapy drug used to treat cancer, has great effects against multiple sclerosis, but it’s side effects are really bad and it can even damage the body if it’s administered for a long time.

Other medication must be administered in the multiple sclerosis treatment, depending on the symptoms that it presents. If it causes loss of balance and muscle coordination then the patient should receive physiotherapy and take muscle pain reliving drugs.

If the visual sense is affected and the patient experiences blurry vision, or even loss of vision then doctors recommend steroids. Steroids can fight and relieve these symptoms.

Other drugs depend on the nerves that multiple sclerosis affects. Consult your doctor for more information about the secondary multiple sclerosis treatment.

Drug therapy can be combined with alternative therapy for best results. Alternative treatment for multiple sclerosis is acupuncture, yoga or massage.

If you suffer from multiple sclerosis you should also consult a support group. There are many organizations that have the purpose of aiding those that suffer from multiple sclerosis and to give them the best treatment options.

About the Author

We recommend you clicking this site http://www.multiple-sclerosis-center.com for more multiple sclerosis subjects like multiple sclerosis treatment or symptoms of multiple sclerosis

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Aug
30

Q&A: Can somebody check my essay?

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Question by BF1222: Can somebody check my essay?
Brittany Falussy

If you would have told me two years ago that the most influential person in my life would be a man who couldn’t speak, walk, or go to the bathroom by himself, I probably would have laughed out loud. Two years ago I was a different person. Two years ago I met a man named Henry. I never learned his last name, and I probably never will. Henry was the man who couldn’t speak, walk or go to the bathroom by himself. Despite these maladies, Henry was in fact the most influential person in my life.

I began volunteering at the Gurwin Geriatric center during my summer between sophomore and junior year of high school. The Gurwin center was a great opportunity to gather community service hours that were mandatory in my participation in the National Honor Society. Volunteering there was a blast. I spent Tuesday mornings in Arts and Crafts, Wednesdays at bingo, and Thursdays working in the nail salon.

Now it shouldn’t be surprising my favorite part of the week was Arts and Crafts, nor should it be that I became very close with its instructor, Ms Julianne Cutolo. Noticing my interest in the arts, she told me that she had a degree in art therapy, and that she held an art therapy program at Gurwin each Friday. I agreed to help, not realizing what I was getting myself in to.

The Art Therapy program was located in the section of the home dedicated to the people with extremely bad conditions. The room was filled with about twenty elders, each with worsening conditions. I began helping everyone get situated before we began the program when I noticed a man in a wheel chair huddled in fetal position in his wheel chair. His clothes were about three sizes too large, and had a Yankee cap sitting on his head. I walked over to him noticing he had a red colored pencil in one hand, a ruler in the other, and a white piece of paper on his lap.

At first he was reluctant to my help. He was a very humble man, and you could tell it pained him to have to have someone constantly helping him. He took the ruler and extended it towards me, and pointed on the paper. So, I took the ruler from him and placed it on the paper where he pointed. He drew a red like across the paper. We repeated this step about thirty times when I noticed the lines he was drawing were beginning to form a red convertible.

Each day was the same routine. He pointed, I placed, and he drew. He couldn’t speak very well, but as time went on I learned to decipher his mumbles. We laughed, told jokes, and shared stories every time he came to the program. We never introduced ourselves, but we always acted as if we had known each other forever. It wasn’t until my last day at Gurwin that I learned his name was Henry.

On the outside, Henry and I seemed very different. He was an eighty-five year old man with Multiple Sclerosis, and I was a young and light-hearted fifteen year old with the rest of her life ahead of her. On the inside, Henry and I were very much alike. We came to Gurwin for the same reason: we were alone and needed some company in the world.

If I could never speak, walk, or go to the bathroom by myself ever again, I would have one thing going for me. Henry taught me that if you can look for the good in life instead of accepting the bad, you would forever be happy. He told me he was very content in his life because even though he had it really bad at that very moment, he lived his dream of pursuing his art, and never regretted anything.

Best answer:

Answer by Someone
I placed notes at the bottom and asterisks to denote where a possible problem is. Overall, it seems pretty good, but you may want to elaborate more about WHY Henry is influential to you(to address the prompt well) and HOW he was optimistic despite his situation. Anyway, here’s the edited version:

If you told me two years ago that the most influential person in my life would be a man who couldn’t speak, walk, or go to the bathroom by himself, I probably would have laughed out loud. Two years ago I was a different person. Two years ago I met a man named Henry. I never learned his last name, and I probably never will. Henry was the man who couldn’t speak, walk or go to the bathroom by himself. Despite these maladies, Henry was in fact the most influential person in my life.

I began volunteering at the Gurwin Geriatric Center during the summer between my sophomore and junior year of high school. The Gurwin Center was a great opportunity to gather community service hours that were mandatory in my participation in the National Honor Society. Volunteering there was a blast. I spent Tuesday mornings in arts and crafts, Wednesdays at bingo, and Thursdays working in the nail salon.

Now, it shouldn’t be surprising that my favorite part of the week was arts and crafts, nor should it be that I became very close with its instructor, Ms. Julianne Cutolo. Noticing my interest in the arts, she told me that she had a degree in art therapy and that she held an art therapy program at Gurwin each Friday. I agreed to help, not realizing what I was getting myself into.

The art therapy program was located in the section of the home dedicated to the people with extremely bad conditions. The room was filled with about twenty elders, each with worsening conditions.* I began helping everyone get situated before we began** the program when I noticed a man in a wheelchair huddled in a fetal position. His clothes were about three sizes too large, and had a Yankee cap sitting on his head. I walked over to him noticing he had a red colored pencil in one hand, a ruler in the other, and a white piece of paper on his lap.

At first, he was reluctant to my help. He was a very humble man, and you could tell it pained him to have to have someone constantly helping him. He took the ruler, extended it towards me, and pointed to on the paper. So, I took the ruler from him and placed it on the paper where he pointed. He drew a red line across the paper. We repeated this step about thirty times when I noticed the lines he was drawing were beginning to form a red convertible.

Each day was the same routine. He pointed, I placed, and he drew. He couldn’t speak very well, but as time went on I learned to decipher his mumbles. We laughed, told jokes, and shared stories every time he came to the program. We never introduced ourselves, but we always acted as if we had known each other forever. It wasn’t until my last day at Gurwin that I learned his name was Henry.

On the outside, Henry and I seemed very different. He was an eighty-five year old man with Multiple Sclerosis, and I was a young and light-hearted fifteen year old with the rest of her life ahead of her. On the inside, Henry and I were very much alike. We came to Gurwin for the same reason: we were alone and needed some company in the world.

If I could never speak, walk, or go to the bathroom by myself ever again, I would have one thing going for me. Henry taught me that if you can look for the good in life instead of accepting the bad, you would forever be happy. He told me he was very content in his life because even though he had it really bad at that very moment, he lived his dream of pursuing his art, and never regretted anything.

* You used ‘conditions’ in two sentences in a row. Consider finding a different word.
** Redundancy. You used ‘began’ twice in the same sentence here.

Add your own answer in the comments!

Aug
29

Not To Worry: 92 Affirmations That Apply How To Stop Worrying Techniques For Curing The Symptoms Of Anxiety Reviews

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Not To Worry: 92 Affirmations That Apply How To Stop Worrying Techniques For Curing The Symptoms Of Anxiety

Not To Worry: 92 Affirmations That Apply How To Stop Worrying Techniques For Curing The Symptoms Of Anxiety is a simple and easy-to-apply book in which you will discover ninety-two affirmations you can immediately use to apply how to stop worrying techniques for curing the symptoms of anxiety in the shortest time possible.

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- Full access to the “3 Powerful Tips To Help Manage Everyday Stress” video
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Aug
29

Walk MS 1 of 5 – National MS Society

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Aug
29

Latest Multiple Sclerosis Symptoms auctions

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Multiple Sclerosis Symptoms on eBay:

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Aug
29

Living with Multiple Sclerosis

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Article by Rob Parker

Although it is a disease that has seen a major expansion as far as awareness over the past couple of years, most people don’t know a lot about multiple sclerosis. The impact of the disease, what causes it, the different types, its treatments, and what a person living with MS can expect are all areas shrouded in mystery.

When it comes to living with multiple sclerosis, then, the first step is to become as educated about the disease as possible. There is always a certain amount of fear after diagnosis is made, and this fear is both natural and abiding. Don’t let it keep you from doing in-depth research on the disease, as many times the facts you find may actually serve to alleviate some of the fears involved.

Different people will react to their diagnosis in different ways. There will be a certain amount of anger that arises from time to time when confronting the fact that you have the disease. It can be very hard to channel this anger, but refusing to acknowledge the feeling is not a good tool. Other people in your life – family, friends, and spouses above all – will also feel the effects of multiple sclerosis in their lives even though they will not display the symptoms. If you don’t feel like talking about it, that is understandable, but sometimes it can help if you can point the people who care about you to other sources of information that can help them understand the disease.

During the research process, you will undoubtedly come across several drugs and treatments which can help alleviate, delay, or prevent some of the symptoms of the disease. It’s really important to explore the options here with your doctor, and once you have settled on a plan to follow it every day. Many of the treatments have proven to be very effective in preventing symptoms or lessening the effects and duration once they occur.

One thing that can be very hard when living with MS is facing a future in which the specter of the disease looms large. Many people diagnosed with MS will avoid support groups and the like as they often include patients in later stages of the disease. While this type of gathering may indeed be intimidating, it can also be extremely uplifting to take note of how these people deal with their day to day realities and recoveries. Let them motivate you, and don’t be afraid to feel a connection with them.

Living with multiple sclerosis on a day to day basis will bring sundry reactions in different people. It’s always important to have a support network about which you feel confident and secure, and a plan for the future.

About the Author

Approximately 50,000 Canadians have MS and dealing with it can be hard, but contacting the Multiple Sclerosis Society of Canada is a good way to get support.

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