Multiple sclerosis foundation of america

Common Questions and Answers about Multiple sclerosis foundation of america

multiple-sclerosis

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.

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 .

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.

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.

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.

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.

2 million worldwide. According to the Multiple Sclerosis Association of America, about 80 to 85 percent of MS patients are initially diagnosed with relapsing-remitting MS.

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.

t really know the underlying mechanism of MS. There are a lot of drugs developed on the basis of the autoimmune theory and certainly the immune system is involved in MS, but it's still not been shown that that is the underlying cause of MS.

Lulu has shared with us before that the MSAA - Multiple Sclerosis Association of America - helps with some MRI costs. Although I believe there's is limited to diagnostic level imaging, they may well be able to point you toward so good resources for follow-up imaging. I believe you can find them at msassociation.org. Good luck to you! Any chance you can see a more reasonable neuro who will begin treatment based on history and then see you quickly for follow-up?

I have had increased symptoms of fatigue and in recent weeks a tingling along both of my legs, my feet hurt and I am having alot of back pain that sort of circles around. Should I start with my PCP to see if it is my back or go straight to my neurologist? I am on Copaxone, but I was off of the shots for 6 mos prior to this last MRI for insurance reasons.

You would benefit from seeing a neurologist. You need a complete work-up to determine the cause of your neurological symptoms. The neurologist should do lots of blood tests to help them figure out what it is and run other tests to determine the cause of your neurological symptoms. Because you have had so many viruses, my guess is that you have an autoimmune disease.

The cause of meralgia paresthetica is compression of the nerve that supplies sensation to the skin surface of your thigh." https://www.mayoclinic.org/diseases-conditions/meralgia-paresthetica/symptoms-causes/syc-20355635 If it's possible i'd get it seen by your family dr, the odds of this type of situation being the first presentation of a neurological condition like MS is very unlikely. Hope that helps.....

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.

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 may also be on some other drugs for his symptoms. Is he? I ask because some drugs have side affects that affect you sexually. This could be one of his problems or it could be something else. I am no doctor and as wobbly did, I urge you to have your bf address this with his doctor.

Also after my delivery I had problem of DVT. What is the cause of DVT? Is it related to MS? I was admitted in the hospital for 15 days.

Recommended