Oct
12

Multiple Sclerosis Symptom Improvements Part 1: Melissa Morgan discusses Colostrum 1 year on

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helpingeachother.com.au Greatly reduced fatigue, improved vision and walking ability has increased from 600meteres, is now able to walk 2.2Klms. Melissa is getting great results with her MS Symptoms using a combination of natural Colostrum supplements. In this video she discusses her symptoms prior to starting on these products on 1 November 2009, compared to now.

Oct
1

Healthy Living with MS Featuring Clay Walker Part 3 – National MS Society

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MS Learn Online is the National MS Society’s online educational webcast series. This video features part three of a three-part series of discussion with country music star Clay Walker, who talks about living with multiple sclerosis.
Video Rating: 5 / 5

Sep
25

Gait and MS Part 1 – National MS Society

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MS Learn Online is the National MS Society’s online educational webcast series. This video features part one of a discussion with Francois Bethoux, MD, who talks about the common issues associated with gait and multiple sclerosis.

MS Learn Online is the National MS Society’s online educational webcast series. This video features part two of a two-part series on cognition and multiple sclerosis. www.nationalmssociety.org

Sep
15

Fatigue: Take Control Part 4 — National MS Society

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MS Learn Online is the National MS Society’s online educational webcast series. This video features part four of a six-part series about fatigue and multiple sclerosis. www.nationalmssociety.org

MS Learn Online is the National MS Society’s online educational webcast series. This video features a discussion with Sarah Minden, MD, who discusses pseudobulbar affect, or uncontrollable laughing and crying, in people with multiple sclerosis.
Video Rating: 5 / 5

Sep
11

Questions and Answers about Multiple Sclerosis and Family Part 2

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Article by Akrista L’Bert

Multiple Sclerosis is a chronic disease that can eventually cause mobility problems in some and severe disability in others. It is very difficult to tell how the disease will take it’s course. And because of this, it’s difficult to plan your life when it can be so unpredictable. We’ve always been told to expect the best but plan for the worst. The financial, social, emotional, physical, employment, and housing issues bring special challenges when living with multiple sclerosis.

Living with Multiple Sclerosis involves a myriad of issues that will affect your family. These include:

financial

social

emotional

physical

employment

housing

How you deal with them is unique to your situation, just as your MS is different from everyone else’s. You need to think about each issue and make decisions along with your loved ones as to what is best for you and your family.

Keywords: multiple sclerosis, ms, financial issues, social issues, emotional, physical issues, family,

Financial Issues

Raising a family as we all know, is hard enough nowadays as a healthy person. When you or a family member has MS, everyday can be a challenge. Family finances can be strained to the limit when health care costs come into the picture. And if you have always been the sole income earner or even the second income:

What do you do if you can no longer work?

Have you looked into working at home as an option?

Have you thought about another retraining for another career that is less stressful or physical?

Again, preparation is the key. Expect the best, but prepare for the worst. Make sure your finances are in order. Begin now to make plans for the future. Even if you never become disabled, being prepared is still a good thing. It definitely can’t hurt.

Emotional and Physical Issues

Managing the stress of daily living as well as your symptoms can sometimes be difficult on your own. The emotional and physical issues associated with MS may eventually require the help of professionals. It’s not a sign of weakness to know when you may need a little help. Making the ultimate decision to turn to a professional is best made with the help of your family and your doctor.

To deal with physical issues, your doctor may suggest a physical or occupational therapist, or both depending on your needs. Emotional issues may range from cognitive problems to severe depression. Cognitive impairment may be helped by daily planning, learning memory tricks and organizing. The treatment for severe depression may be medication and or professional help. There is help available, so you don’t need to suffer needlessly.

Employment Issues

If you have gotten to the point where you feel you can no longer work, then what happens next?

Does your job know that you have been diagnosed with multiple sclerosis?

If so, have they made every reasonable accommodation to help you keep working if you want to? The Americans with Disabilities Act has put several laws in place to deal with these issues. Learn about your rights and what is available to you.

If you have health insurance, is there a disability clause?

Will it be enough to cover your health needs and expenses if and when you decide to stop working?

These types of questions should ideally be asked before you let your employer know and if possible even before you receive your MS diagnosis. That way if you need to make changes to your insurance you can do so before you become disabled and are no longer able to work.

If you have made the decision to stop working, and know that you won’t have insurance, the question of Social Security Disability Insurance is an inevitability. Applying for it and getting approved can be a daunting task. It doesn’t have to be. Doing your homework before you leave work, will make working through this task a whole lot easier.

Find out everything, and I mean everything, that will be required and follow it to the letter. Answer every question on the application truthfully and thoroughly. Follow-up with your doctor to make sure they have submitted everything they need to submit. If you are not approved the first time, try again. And above all, don’t give up. You will succeed.

Social Issues

Depression and loneliness can become a big problem if you have limited mobility and no longer feel like going out. Many people with MS, have led active lives and while some can continue to do so, others just can’t. There are several ways to get around this issue.

First of all, are there support groups in your area?Have you joined your local National MS Society? For those of you who have stopped working, what do you do with your time?

They are a great source of information and support for events happening in your area. If you have a computer and internet service, get on-line. There are many support groups and several chat rooms where people with MS get together regularly.

If you are still mobile, (and about 75% of people with MS will never need a wheelchair), consider doing yoga or some other exercise to stay healthy. The MS clinic in our area offers a water exercise class, yoga, and a Tai Chi class as well. All of these are geared toward multiple sclerosis patients and people with limited mobility. So whether you can walk or even if you can’t, there are ways to be involved in these types of classes. You can learn something new and meet new people in the process.

Housing Issues

Accessible housing may be something that you may never need to worry about. But our little mantra comes into play in this area, too. Expect the best, but prepare for the worst. It won’t do for you to have a dream house planned for your retirement that has multi-level living. If you become disabled to the point where you can no longer navigate the stairs, what will happen then?

Plan your dream home for this eventuality and include things like wheelchair ramps, accessible bathrooms with grab bars and kitchens with easy to reach counters and cabinets. Wide open spaces, hardwood floors, tiles, or Berber carpeting, are just a few of the other things you may want to consider when planning your home. Condominiums may also be a good choice so that yard work won’t be an issue.

As you can see, living with MS brings up a myriad of challenges that you as a person with multiple sclerosis will inevitably deal with from day to day. But living with MS is not impossible to do. Watching my husband live with this disease has taught me a lot of things. One thing stands out. It may not always be easy, but people with MS have the strength and determination to live fulfilling lives in spite of having multiple sclerosis.

About the Author

Akrista L’Bert has been married to her husband, who is also her best friend, for 28 years. He has been diagnosed with multiple sclerosis since 1992. She is his caregiver. They both have a heart for helping others who live with MS. To read more about the challenges above and how to deal with them, visit their site Life in Spite of MS for a unique perspective on living with multiple sclerosis. To read more about Living with MS, click here.

Sep
7

Multiple Sclerosis – Prevention And Treatment part 2

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Article by John Daniel Rivera

PreventionThere is no known way to prevent the onset of MS according to conventional medicine.

The TreatmentOral corticosteriods, such as prednisone, or intravenous corticosteriods, such methylprednisolone, may be prescribed to shorten the duration and reduce the severity of attacks. Your doctor may prescribe interferon beta 1b or interferon beta 1a injections, a form of biological therapy, to treat MS. These medications are synthetically engineered to be identical to a naturally occurring protein and reduce the frequency and severity of attacks by altering many of the body’s immune responses. Alternatively, your doctor may prescribe glatiramer acetate injections to modulate the immune dysfunction in MS. The choices among these therapies are complex and usually require the assessment of an MS specialist your doctor may prescribe antispasmodics or tranquilizers, including diazepam or baclofen, to relax spastic muscles and provide pain relief, or anti depressants to treat associated depression. A variety of medications may be administered to treat incontinence, frequency, hesitancy and other bladder control problems. Try not to become overheated. Avoid excessive sunbathing, heavy exertion, and hot baths and obtain prompt treatment for fevers; a raised body temperature may trigger or worsen symptoms. Taking a cool shower, swimming, or sitting in air-conditioned room may relieve the severity of symptoms during an attack. Pursue a program of moderate exercise to help keep muscles as flexible and strong as possible. Physical and occupational therapy may help patients adjust to muscular and sensory changes. Psychological counseling may help patients and their families cope with depression and the lifestyle changes imposed by MS. Be wary of unproven remedies, such as bee venom. Obtain more information by contracting your doctor. A powerful and revolutionary alternative therapy in treating Multiple Sclerosis and is highly recommended by almost 15,000 European doctors. Take the time to discover and study this one, we highly recommend this therapy for Multiple Sclerosis – Prevention And Treatment.

Just follow the link and watch the 5minute video presentation:http://www.curewithinoneminute.com

About the Author

This article is written by john daniel rivera who is an advocate for natural health and healing, and has been in the field of health for quite a few years. He is interested in illuminating individuals and helping others return to a better quality of health. If you would like to learn more about his approach, please feel free to visit http://www.curewithinoneminute.com

At Hadassah, stem cell therapy comes another step closer to a cure for Multiple Sclerosis
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Aug
22

Multiple Sclerosis – My Story Part 1 – 18/5/11

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How MS bit me on the arse – Part 1 2010 was a really crappy year, it all started for me back in May…
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Aug
19

Primary-Progressive Multiple Sclerosis: Perspectives on Moving Forward Part 2 – National MS Society

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MS Learn Online is the National MS Society’s online educational webcast series. This video features part two of a six-part series that profiles four people with primary-progressive MS and tips for managing the disease.

Join the movement at www.jointhemovement.org. Multiple sclerosis interrupts the flow of information from the brain to the body and stops people from moving. Every hour in the United States, someone is newly diagnosed with MS, an unpredictable, often disabling disease of the central nervous system. Symptoms range from numbness and tingling to blindness and paralysis. The progress, severity and specific symptoms of MS in any one person cannot yet be predicted, but advances in research and treatment are moving us closer to a world free of MS. Most people with MS are diagnosed between the ages of 20 and 50, with more than twice as many women as men being diagnosed with the disease. MS affects more than 400000 people in the US, and 2.5 million worldwide. MS stops people from moving. The National MS Society exists to make sure it doesn’t. We help each person address the challenges of living with MS through our 50 state network of chapters. We fund more MS research, provide more services to people with MS, offer more professional education and further more advocacy efforts than any other MS organization in the world. The Society is dedicated to achieving a world free of MS. We are people who want to do something about MS now. Join the movement at www.jointhemovement.org.

Aug
9

Multiple Sclerosis: BUILDING the North American CCSVI Society Part 2

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www.kvmr.org THE link for Wed. 2 at 1200 Pacific TIME This is a community radio show. The programme is called Rabble Rousing. John Fletcher will be hosting the show. Special thanks to Susan ThePennygirl (youtube user) Great news this week in CCSVI research. Canada and Italy have allocated several million dollars toward CCSVI research. A group of cardiovascular specialists from over 47 countries have UNAMIMOUSLY come to the consensus view that CCSVI comes before MS CCSVI is congenital (we are born with it). I have a radio interview scheduled on Feb 10th at 1200 noon PACIFIC TIME the radio show is Rabble Rousing with John Fletcher This is huge on getting CCSVI some public exposure. Please check out Joan Beal’s radio interview it has been posted on several CCSVI facebook spots. Also, I had alluded in this video about a link between FIBRIN and stress. FIBRIN is present in the blood and it causes blood to thicken or have higher viscosity. During times of stress it is proven that FIBRIN production increases. With chronic cerebrospinal insufficiency the veins that drain deoxygenated blood from the brain become narrowed. I have often wondered why my MS attacks have been during very stressful times in my life. Well….If under stress my blood thickens and it makes it that much harder to drain because of CCSVI. This makes a lot of sense. Thank you everyone for your continued support and for getting the word out and standing up for what is right. Together WE WILL. Mark
Video Rating: 5 / 5

Aug
4

Multiple Sclerosis: Journey to Diagnosis – Part 7 – 22/6/11

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This video talks about the dreaded brain MRI and the lonely wait for results. Sorry the last video cut off at a bad time, and the break between videos – I have been struggling emotionally for the last little while. Infusions and weight gain are not fun :(
Video Rating: 5 / 5