multiple sclerosis research funding

//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.

Quantitative high field imaging of sub-cortical gray matter in multiple sclerosis. Multiple Sclerosis. 2011 Oct 27. Epub ahead of print] DETAILS Drs. Alan Wilman and Gregg Blevins at the University of Alberta measured iron levels in the brains of 22 people who were newly diagnosed with MS and 22 people who did not have MS. They discovered that people with MS have higher levels of iron in areas of the brain responsible for relaying messages to the rest of the body.

” 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”.

On December 1, the US National Multiple Sclerosis Society has issued a statement regarding CCSVI. You can read it in its entirety at http://www.nationalmssociety.org/news/news-detail/index.aspx?

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?

She has friends and a close relative with multiple sclerosis and the possibility that this research could help those with the disease adds significance. "MS is a difficult disease because it's so life altering. To watch people lose their mobility is always difficult." The research was funded by about $200,000 in annual grants from Canadian Institutes of Health Research, Alberta Innovates and the MS Society.

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

"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.

//www.businessweek.

Ten years ago one patient, his caregiver, a doctor and a nurse opened Oak Clinic for Multiple Sclerosis to treat individuals living with MS regardless of their ability to pay. They offer a variety of treatment services to their patients in an encouraging and relaxed, yet very professional environment. 'Oak Clinic for MS' has entered the 'Pepsi Refresh Challenge' for 25K in grant funding to help mobility impaired MS patients stay connected to the world.

As heartening as the news from Tisch is it is disheartening that NMSS has chosen not to provide essential funding for Phase 2 of Dr. Sadiq’s research. The Tisch study is FDA approved and Phase 1 has shown real results in real people. I would like to learn more about the NMSS’s decision not to financially support this important work. Thanks in advance for your reply.

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 ??

au/news/queensland-researchers-make-major-breakthrough-ms-treatment 5 February 2014 NEW Queensland research suggests that controlling infection with Epstein-Barr virus (EBV) – the most common cause of glandular fever – may be beneficial in treating multiple sclerosis (MS), a chronic inflammatory demyelinating disease of the brain and spinal cord affecting more than 23,000 Australians.

I agree that there is need for better research in this area and a way to make conducting such research more appealing, whether through orphan drug legislation and funding, direct MS Society funding, or funding for academic research at universities. But stories of positive experiences are just that. Stories. As they say, the plural of anecdote is not data. As someone with MS myself, "show me the data.

Please sign both of these if you are interested in seeking increased funding for hsv research. They both target the decision makers that determine funding that is granted to researchers. http://www.petition2congress.com/373...earch-funding/ http://health.change.org/petitions/v...search_funding Thanks!

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....

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.

Multiple sclerosis research funding

Common Questions and Answers about Multiple sclerosis research funding

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