Multiple sclerosis foundation com

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multiple-sclerosis

572651 tn?1530999357 One of the rare but not unheard of symptoms of multiple sclerosis (MS) is pruritis (itching), which can be included in the category of sensory abnormalities known as "dysesthesias." Because this type of itching is neurologically based, it does not respond to topical treatments like those used in allergic reactions. Anti-epileptic medications (gabapentin, carbamazepine, and phenytoin) are sometimes helpful in treating this problem." this is from sharecare .
382218 tn?1341181487 "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.
382218 tn?1341181487 Member organizations of the MSC include Accelerated Cure Project, the Consortium of MS Center, Can Do Multiple Sclerosis, the International Organization of MS Nurses, Multiple Sclerosis Association of America, Multiple Sclerosis Foundation, National Multiple Sclerosis Society, and United Spinal Association. Find the Multiple Sclerosis Coalition online at http://ms-coalition.org or visit MSC on Facebook at www.************/MSCoalition and on Twitter at @MS_Coalition.
6507866 tn?1381935797 Hi, there, and Welcome! I can't believe this got by without anybody answering. My apologies! Seizures! Wow! Scary!! They're not completely unheard of in MS, though, as we're twice as likely to get them as the general population. But that's 5-6% as compared to 3% of the general population. I snagged this from the MS Foundation site: One of the less common problems associated with MS is seizures.
20866773 tn?1551913127 See your primary care physician, or go to urgent care, describe your issue (webmd[DOT]com/multiple-sclerosis/multiple-sclerosis-symptoms -is a decent resource for potential symptoms) and ask about getting an MRI. As far as I know, that's the only way to diagnose (or rule out) MS. I hope that this helps, and I very much hope that you don't have MS, I wouldn't wish it on my worst enemy... If you do, stay strong and try your best to stay positive.
382218 tn?1341181487 16 Apr 2009 - 3:00 PDT www. medicalnewstoday .com/articles/146211.php Decision Resources, one of the world's leading research and advisory firms focusing on pharmaceutical and healthcare issues, finds that surveyed neurologists anticipate that less than 30 percent of their use of emerging oral agents --- Merck Serono's oral cladribine, Novartis/Mitsubishi Pharma's fingolimod (FTY-720) --- for the treatment of multiple sclerosis will be in the first line.
Avatar m tn In adults, vitamin D deficiency contributes to bone loss, causing conditions of osteopenia and osteoporosis. Vitamin D deficiency is also widely seen in patients with multiple sclerosis. Vitamin D deficiency is considered an environmental risk factor for autoimmune disease. Problems with Supplements Trevor Marshall, Ph.D. a professor at Australia?s Murdoch School of Biological Medicine and Biotechnology explains that increased ingestion of vitamin D affects more than bone health.
4478309 tn?1356061667 board membership, Editorial Board of Multiple Sclerosis; grants/grants pending, National Research Foundation Switzerland, Rubatto Foundation, Swiss MS society, European Union, Roche Foundation, Novartis Foundation; speaking fees, various companies involved in development of MS therapeutics; paid educational presentations, Neurostatus System for Standardized Neurological Assessment. F.D.L.
Avatar n tn Does psilocybin (an active component in magic mushrooms) cause multifocal demyelination, which leads to multiple sclerosis? A few my friends do mushrooms couple times a year, and I myself done them 2 or 3 times, neither I or them have symptoms, but I'm worried. Found only few clues about connection between psilocybin and demyelination on the Internet. Thank you.
1710955 tn?1309446473 How Science Is Solving the Mysteries of Multiple Sclerosis by Howard L. Weiner (Oct 25, 2005) it explains where MS research and treatment has developed.
382218 tn?1341181487 15 Dec 2008 - 0:00 PST www. medicalnewstoday .com/articles/132947. php "FTY720 (fingolimod), an experimental oral drug for relapsing MS is more effective than current treatments according to new research reported today. The trial, called TRANSFORMS, is the first of three studies of FTY720 to report. TRANSFORMS was a one year study involving 1,292 participants receiving either 0.5 mg or 1.25 mg FTY720 or interferon beta-1a (Avonex).
382218 tn?1341181487 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.
382218 tn?1341181487 6% had relapsing remitting multiple sclerosis, 9.4% primary progressive multiple sclerosis and 6% clinically isolated syndrome. Nearly 40% of our multiple sclerosis patients with disease duration >10 years (mean = 16.2 ± 5.3 years) remained with no or mild disability (Expanded Disability Status Scale [EDSS] 3). Also, about 30% of patients with relapsing remitting multiple sclerosis showed benign disease evolution (EDSS 3) more than 20 years (mean = 24.0 ± 3.3) after onset.
Avatar m tn Hi, everyone: The Multiple Sclerosis Foundation celebrates every year in the month of March "The MS Education and Awareness Month". If you ask, they will send you "Awareness Kits" that you can distribute in your home state. These kits have valuable information that may help the public and even our families understand what MS is, how it strikes differently in each individual and even motivational information. You can contact the MS Foundation at www.msfocus.org.
Avatar m tn 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 ??