multiple sclerosis research relief fund

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.

//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.

s help with getting the new administraton to fund more and better research and education regarding Multiple Sclerosis. As my brain is a little fuzzy, I'm asking for some bright person to help develop a petition. I can at least provide the link to where we can get the petition started; http://www.thepetitionsite.com/create-online-petition I think it's worth a try, don't you?

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

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.

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.

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 ??

Cree reported the conclusions as follows in a poster presentation to the World Congress on Treatment and Research in Multiple Sclerosis, held in September 2008 in Montreal, Canada.

” Wynick then turned to Professor Neil Scolding who studies the use of stem cells in the treatment of multiple sclerosis. Scolding provided human brain tissue affected by multiple sclerosis and, as the team predicted, galanin was also shown to be upregulated in this brain tissue. Professor Scolding said: “The results of this research are very significant and provide new insights into how the disease might be treated”.

so ive been to a neurologist an have been diagnosed with multiple sclerosis, i am 21 years old and hae been tryng o figue this out since i was 18 years old ive done lost of research and t makes since, every symptom experienced all this years and feel relieve that i have an answer and its hard to know that there is no cure but for some reason feel relieve and some weird way happy and thankful to be alive.......if any one has multiple sclerosis plzzzz i cold might use some advise..... thank u....

//www.medhelp.org/posts/Multiple-Sclerosis/Low-Dose-Naltrexone-for-MS/show/453613 http://www.medhelp.

Reuters 8/31/10 The clinic, based at the University of Edinburgh in Scotland, will be named after Rowling's mother Anne and the author said she hoped it would become a world center for excellence into neurological conditions. "I have just turned 45, the age at which my mother, Anne, died of complications related to her MS," Rowling said in a statement on Tuesday.

s going to be very interesting to see if they give you an explanation. seems like a no brainer to fund research that seems to very promising....

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.

//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?

//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....

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.

http:// www. cbc .ca/ health/story/2010/08/02/pei-ms-treatment-584.html Premiers to debate MS treatment Leaders differ on approach to 'liberation therapy' An experimental treatment for multiple sclerosis will be discussed at a meeting of Canada's premiers this week, P.E.I. Premier Robert Ghiz said. P.E.I. Premier Robert Ghiz said he has heard Islanders' calls to investigate an experimental treatment for MS.

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.

"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.

Multiple sclerosis research relief fund

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