ABCs of the MS Diagnostic Process

ABCs of the MS diagnostic process

A – Ask a Neurologist

Is it MS, or is it something else? If you are experiencing numbness and tingling in your body, these symptoms could be caused by MS. On the other hand, there are many illnesses that easily mimic MS symptoms. To help figure out what is going on, the next step is to make an appointment with your primary care physician. If your doctor suspects MS, you’ll probably be referred to a neurologist for a definitive MS diagnosis.

B – Brain MRI

The MRI scans the brain using a computer, radiofrequency stimulator, and a huge magnet. Good news, MRIs do not expose patients to radiation, and helps doctors get a clear picture of what’s happening in the Brain. The MRI is used to assess the size and location of lesions in persons with multiple sclerosis. Contrast enhancement is often used to help to better assess inflammation and determine if MS is present in the Brain.

C – Consider Your Treatment Options

MS can be treated with a variety of effective FDA-Approved drugs. These medications can be recommended for all three types of MS. There are three main goals of MS treatment. Firstly, is to limit MS activity and development. Secondly, is to lessen the severity and duration of a relapse. And lastly, is to treat MS symptoms. All of these medications are typically administered by a doctor who specializes in MS or a neurologist. To download a list of FDA-Approved MS medications, please click here.

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About MSAA

The Multiple Sclerosis Association of America (MSAA) is a national nonprofit organization and leading resource for the entire MS community, improving lives today through vital services and support. MSAA provides free programs and services, such as: a Helpline with trained specialists; award-winning publications, including, The Motivator; MSAA’s nationally recognized website, featuring educational videos, webinars, and research updates; a mobile phone app, My MS Manager™; safety and mobility equipment products; cooling accessories for heat-sensitive individuals; MRI funding; My MSAA Community, a peer-to-peer online support forum; MS Conversations blog; a clinical trial search tool; podcasts; and more. For additional information, please visit www.mymsaa.org or call (800) 532-7667.

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