multiple sclerosis research future

//multiple-sclerosis-research.blogspot.com/ ). It's run by some UK neuros/researchers for people with MS. What's nice about this blog is that not only do you get the research abstracts, but they also give some sort of context or commentary as to why you might be interested or how promising they think whatever it is will be. As a bonus, if you have a question about the research, they will often answer it in the comments.

I found this site the other day and it also has good articles on MS research. file:///Users/Charley/Desktop/Multiple%20Sclerosis%20Resource%20Centre.

//www.medhelp.org/posts/Multiple-Sclerosis/Trend-for-decreasing-Multiple-Sclerosis-Severity-Scores-MSSS-with-increasing-calendar-year-of-enrollment-into-the-New-York-State-Multiple-Sclerosis-Consortium-/show/1451038?

my sister (24) was diagnosed Multiple Sclerosis in 2010, responded to steroid. now she suffered sudden & complete loss of vision in her left eye. she has been put on SOLUMEDROL. please suggest any available treatment modalities world over ? chances of return of vision ??

Stem-cell transplants may control and even reverse multiple sclerosis symptoms if done early enough, a small study has suggested. "Not one of 21 adults with relapsing-remitting MS who had stem cells transplanted from their own bone marrow deteriorated over three years." link to article: http://news.bbc.co.uk/2/hi/health/7858559.

30 AM – Forum Starts Hyatt Regency Century Plaza 2025 Avenue of the Stars Olympic Ballroom (Plaza Level) Please join us for this unique opportunity to speak with our MS doctors about the advances that have been made in multiple sclerosis research and patient care. Thanks to your generous support, we are even closer to finding a cure for this debilitating disease.

Despite this pivotal link, not all people with vitamin D deficiency develop multiple sclerosis. More research is needed to fully understand why only some people develop multiple sclerosis from vitamin D deficiency and why others don't. However, a distortion of the CYP27B1 gene is increasingly apparent in MS cases and it's possible that the gene generates other, yet undetected, complications that lead to the disease—such as genetically caused rickets.

1. NARCOMS registry (North American Research Committee on Multiple Sclerosis, a project of the Consortium of Multiple Sclerosis Centers, http://www.cmscnarcoms.org/). They run a Global Patient Registry in order to "facilitate multi-center research in the field of multiple sclerosis." They currently have "an active database of over 34,000 individuals who have MS." If you sign up, all you have to do to participate is fill out a survey every six months.

//www.msimmunology.com/multiple-sclerosis-subclinical-clinical-disease-activity?cid=ocr_DI_MNOCMSH0062_1&c=MNOCMSH0062 We already knew there was approximately 25% more lesions detected on a 3T in comparison to a 1.5T and whilst I realise that 7T's are not available outside research purposes but missing 34%, is a lot....

The Partners MS Center is equipped to provide the best level of care for MS patients and is committed to continuous clinical and laboratory research, in an effort to discover a cure for multiple sclerosis. This web site is designed for both patients and health care professionals. It provides information for lay individuals and practice guidelines for professionals treating multiple sclerosis.

Hypoxia-like tissue injury as a component of multiple sclerosis lesions. Lassmann H. http://www.ncbi.nlm.nih.gov/pubmed/12559509 Ischemic Demylination: http://www.ingentaconnect.com/content/maney/nres/2006/00000028/00000003/art00018 Multiple Sclerosis: The Role of MR Imaging Y. Ge From Department of Radiology/Center for Biomedical Imaging, New York University Medical Center, New York, NY http://www.ajnr.

Are you a participant in the NARCOMS registry Sarah? That's the North American Research Committee On Multiple Sclerosis. It was started almost 20 years ago by the Consortium of Multiple Sclerosis Centers (cMSc). It's a global registry for Multiple Sclerosis research, treatment, and patient education. You complete a comprehensive (confidential) survey when you register (free) and then are notified of update surveys each fall and spring.

Recent studies In 2005, researchers at the Serono Genetics Institute (SGI) achieved a major milestone in identifying and creating a register of genes involved in Multiple Sclerosis (MS). For the first time in this disease area, researchers identified 80 genes involved in the inflammatory and neuro-degenerative pathways of MS, based on a 40% genome scan comparing the genetic profile of a total of 1,800 people with MS and healthy individuals in different populations.

OTTAWA - Health Minister Leona Aglukkaq is bucking some of the latest research and giving the go-ahead for clinical trials of a controversial treatment for multiple sclerosis patients. Aglukkaq says the federal government will fund trials of the so-called liberation therapy in spite of recent studies that have cast doubt on narrowed neck veins as the primary cause of multiple sclerosis.

I did a little research and see that it is associated with many things including some drugs and autimmune disorders and multiple sclerosis. See our discussion on the MS Forum: http://www.medhelp.

Another worthwhile project (that is easier to participate in because all you have to do is fill out questionnaires) is the North American Research Committee On Multiple Sclerosis (NARCOMS) Project (patient registry) at www.mscare.org/cmsc/CMSC-NARCOMS-Information.html Also on the Consortium of Multiple Sclerosis Centers website is their MRI for MS protocol which people ask about periodically: www.mscare.org/cmsc/images/pdf/MRIprotocol2003.

"EHE International and the Nancy Davis Foundation for Multiple Sclerosis Celebrate the 'Orange You Happy to Erase MS' Campaign at Rockefeller Plaza LOS ANGELES, April 1 /PRNewswire/ -- For the month of April 2010, the Nancy Davis Foundation for Multiple Sclerosis and Race to Erase MS will take over the window at 10 Rockefeller Plaza as they promote their "Orange You Happy to Erase MS" campaign which raises funds and awareness for multiple sclerosis.

UNFORTUNATELY, I COULD NOT BECAUSE I HAVE MULTIPLE SCLEROSIS. I DID END UP TRYING TMS. IT WORKED BUT FOR ABOUT 6 MONTHS. I HAD THE LOWEST DOSE AND TIME FRAME DUE TO MY MULTIPLE SCLEROSIS. IF YOUR INTERESTED TO TO YOIUR MD AND SEE WHAT THEY SDAY. CAN'T HURT TO ASK... GOOD LUCK IN YOUR SEARCH FOR ANSWERS.

//www.medhelp.org/health_pages/Multiple-Sclerosis/MS-Mimics---Part-I/show/375?cid=36 Be sure and come back and ask any more questions you may have.

Multiple sclerosis research future

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