Columns

Multiple Sclerosis Fatigue: Puzzling over the Jigsaw

Feeling tired?Ā  No surprise there.Ā  Fatigue is as much a part of living with Multiple Sclerosis as sand is a part of the beach where I live. It’s interesting, then, that neurologists seem to have no good system for measuring levels of MS fatigue or any treatments that are…

Bloom, Wherever You Fall! An MS Detour

Editor’s Note: MS Patient Specialist and Columnist Judy Lynn writes from her unique and engaging perspective as an MS patient reflecting on the challenges that the disease presents and how to cope with them in her daily life. In her debut article for her new Column “You’ve Got Some Nerves,”…

Is Your Neurologist Listening to What Your MS Is Saying?

Editor’s Note: Debi Wilson’s column “Faith of the Mustard Seed” explores a range of important topics that relate directly to the patient experience. In her debut article, she discusses her own experiences with neurologists, and encourages MS to not settle on a specialist until they feel as though their…

REAL MS Research Needs You

  You want to help find answers about multiple sclerosis but donā€™t know how, and I hear your frustration about being unable to contribute in meaningful ways. Let me share with you the news that REAL MS (Research Engagement About Life with MS) was launched this summer, and I…

Wondering How MS Will Affect Me Today

Waking up in the morning and facing the world brings a sense of wonder. Not in the sense of awe, just in wondering how MS will affect me today. Is it a good day or a bad day? What will it bring? Like most people,…

Stem Cell Clinics Under Critical Scrutiny in US

Stem cell clinics are proliferating in the U.S., where there are now 570 in operation, according to a paper quoted by the New York Times. And concerns are being raised that these clinics are often operating and making claims beyond those allowed by the countryā€™s public health regulatory…

MS Patients in US and UK Face Very Different Treatment

  We may have international cooperation and worldwide this and that, but the fact remains that countries vary drastically from one another in all sorts of ways.Ā Take healthcare as an example, and the costs of treatment. Yes, we have the World Health Organization and there are various health-related initiatives…

Action Is Needed: Costs Limit MS Patients’ Access to DMTs

A recent survey of more than 6,000Ā multiple sclerosis patients in the United States found that health insurance coverage can decide their access toĀ disease-modifying therapies (DMTs), and that that coverage is worsening, leaving a good numberĀ struggling to be able to pay for their treatment. As an MS patient myself, I find…

‘My Super Diet Cured My MS! Buy My Book!’

There seems to be general agreement that achieving and keeping an overallĀ level of good health is very important for people living with multiple sclerosis, or with any chronic illness for that matter. And one way to reach that goal, many will say, is to eatĀ a healthy, well-balanced diet. Itā€™s at…

Patients Need To Know What Drugs Do Inside Our Bodies

Oral therapy Tecfidera (dimethyl fumarate) seems to be emerging as a first-line treatment for relapsing multiple sclerosis ā€“ according to Biogen, the company that developed it. Thatā€™s good news, and something we need to know. The company agrees that for some time, the long-term effectiveness and safety of this oral…

Have Your Say About Disease Modifying Therapies for RRMS

You have just one week from today to have your say about the effectiveness of various disease modifying therapies (DMT) used to treat relapsing remitting multiple sclerosis (RRMS). Public comments are welcome in response to an early draft paper that is planned to be the basis for…