multiple sclerosis news and views

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.

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 ??

The study was partly funded by the National Multiple Sclerosis Society, The Wellcome Trust and the support of science investor, Jeffrey Epstein and The Jeffrey Epstein VI Foundation. Multiple sclerosis is a neurological disease caused by the decay of myelin, the fatty sheath that protects the axons around the brain and spinal cord. Myelin is an essential part of neural communication because it not only protects the nerve circuits but promotes efficient conductivity.

//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.

Canadian researchers say they have found new links between low levels of vitamin D in children and an increased risk that they may develop multiple sclerosis. Dr. Brenda Banwell told an international meeting of MS specialists in Montreal on Friday that low levels of vitamin D in some children may explain why doctors are seeing more kids developing MS in Canada and other parts of the world.

Primary Progressive, Relapse-Free Secondary Progressive Multiple Sclerosis Drug Masitinib Still In Phase 2b/3 Testing http://bionews-tx.

[Robert] Zivadinov, director of the Buffalo Neuroimaging Analysis Center, is careful not to hype the new theory as groundbreaking medicine. Multiple sclerosis is a complex disorder, and skeptics raise questions that have not yet been answered. "But Zivadinov and others also view the early evidence as compelling and are excited about the potential prospects for patients and for the MS medical programs in Buffalo that might get a head start in pioneering a new treatment.

//www.theherald.co.uk/news/news/display.var.2504159.0.Lifechanging_benefits_for_patients_using_addiction_drug.

D., Professor of Neurology, Director, Multiple Sclerosis Center, Wayne State University and lead investigator of the study. "These data further substantiate our previous research into the potential neuroprotective effect of COPAXONE®, as well as the use of NAA measures as a reliable marker for assessing a patient's disease progression and response to treatment.

Sorry his is old news. No one else has had any success with replicating his findings. He only had like 19 in the study. Most neurologists dismiss it. I wish I had better news.

Many of us are in limbo and have symptoms like yours. Many have been trying to get an accurate dx for years. It's awful! You are in good company here. I doubt if any of us can say what the chances are that you have MS. There are so many things that mimic the disease. If you think your doctor has stopped looking, find a good neurologist. Read the health pages here and elsewhere, and don't give up on finding out what is wrong, whether it is MS or something else!

One of them said it is all due to ur anxiety ( Cause i do not have any bladder problems and dizziness, numbness tingling all is due to anxiety) but one said its Multiple Sclerosis+ anxiety. My MRI and EEG were clear. Currently i have high frequency of muscle tingling through out my body only when i am lying on bed plus i see double vision of any statement especially ( white in colour) on TV and laptop. Is it MS? Should I start taking Med for MS or just let it be and hope it will go away?

My dad was also sprayed with Agent Orange and has numerous medical problems and so do my brother and I; both conceived after Vietnam. I would go to www.publichealth.va.gov/exposures/agentorange/ Then under "Related Diseases" click on "Veteran's Disease's" or under the heading "Benefits" click on "Disability Compensation" and then read and click on other links within those categories.

My feet are cold all the time, with electric sensations in my legs on and off. I also have pins and needles in my arms and legs intermitently. Starting this past August, my toes on my right leg were having Charlie Horses in them every night. I have times where I trip over my right foot when walking. I am out of breath at times, and cannot sleep through the night. I have pain in my lower legs. My family practice doctor currently has me on meloxicam and soma and oxycodone.

I have been diagnosed with HHV6, EBV, coxsackie B4, Post Osterial Tachycardia, Chlamydia Pnemonia, and CFS. My symptoms go on and on. I have dizziness, muscle weakness and pain, strange sensations through out body especially arms and legs, ringing in my ears, tremors/shakiness, strange vision disturbances, headaches and facial pain, and extreme fatigue. I had an MRI that showed one lesion in my brain, a hemangioma in the thoratic region and some mild degeneration in my cervical spine.

Now, I have injuries from a car accident, there are some things wrong with the c6 and c7 in my neck and i have carpel tunnel. Also the L5 and 6 or L3 and 4. I have a panic disorder but I do not take medication at all. It really affects me when the weather changes. I do know that my dad died from als and my grandfather had ms but it was that bad. He just drug his leg and walked with a can. I have vertigo and have had it for years and did not realize what it was.

org/brochures and you can get many publications from The Basic Facts, The History of Multiple Sclerosis, to publications on Newly Diagnosed, Employment issues, Staying Well, Managing Specific Issues, Managing Major changes, And the list goes on and on.

Ya I just got back my MRI the third one in 1 year and the results are the same, the MRI shows an area 9mm in length on the left side of my brain, it represents an area of demylenation, I have now been too 3 neurologists and none of them know what it is, I was hoping I could list some of my symptoms and someone here could help me out, here goes Right side of my body only numbness face, Vertigo, insomnia, anxiousness, stress, trembling, spasms in my face, ear and leg, my stomach also will jerk fro

Hi, kak- I'm sorry to hear of your bf diagnosis. That in itself is scary enough for both of you and your family and friends. I don't know how much you know about MS so I encourage you to check out our Health Pages, as wobbly said. I assume that your bf is now on some meds for his MS, namely Disease Modifying Drugs (DMD)? If not, I urge him to get started on one of those asap. They do not cure MS but they have good results of slowing down the progression.

He had an MRI of the brain that showed multiple foci of T2 and FLAIR hyperintensity in the white matter of both cerebral hemispheres including approximately 5 small lesions in the periventricular white matter, lovated at the callosal sptal margin and oriented perpendicular long axis of the lateral ventricles. THere are 2 Flair hyperintense lesions along the undersurface of the copus callosum. Focus of T2 hyperintensity is seen in the deep white matter of the right frontal lobe.

The headache has not returned but stranger yet was a interesting sensitivity to my scalp at the rear center top of my head. It lasted 6 days and was moderate in pain and hurt when touching my hair or trying to sleep on that side. It has since left and then a few days later I noticed a swelling, or puffy area in that little crevice on my left collar bone at base of my neck. The collar bone feels weird. My regular doctor has requested a CT scan of neck and chest.

I was dignosed with Raynaud's disease about four years ago. My feet were like ice cubes both winter and summer. My right leg was as cold. I wore leg warmers winter and summer. Errrrrr...and now, four years later, gone. Isn't it something how those vascular disorders disappear? I have no idea why. Just gone.

So I haven't gotten any better although my vitamin D levels have improved. My walking gait is horrible and I am having tingling, muscle spasms really bad at nights especially. My doctor says he thinks the viruses have attacked my nervous system and has prescribed physical therapy. He's done a brain mri and it shows normal, but I've been suffering for a long time with multiple problems. Does anyone think this EBV stuff could be ms???

Multiple sclerosis news and views

Common Questions and Answers about Multiple sclerosis news and views

multiple-sclerosis