Patient Resources

Clinical Care

Managing MS requires a comprehensive care approach that maximizes and enhances the brain's ability to protect and repair itself and to promote quality of life for patients and their families. It is also an ongoing process, beginning with the very first symptoms and continuing throughout the disease course. It’s never too soon or too late to think about how to access and best utilize quality care. Knowing what to look for, where to find it, and how to work effectively with your doctor and other health professionals is a vital part of managing MS.

Medications

For many years, certain diagnoses—such as childhood leukemia and HIV/AIDS—meant quick disease progression and a life cut short. That reality, however, has changed dramatically as new, successful treatment regimens have taken hold, specifically combination therapies. As we look to the future of MS treatment—all the while making small steps toward the discovery of a cure—combining on and off-label treatments holds great potential. As with other diseases, combination therapies could revolutionize MS treatment as a whole.
You should let your doctor what types of medicines, herbs, and supplements you are taking before beginning a new medication.
 

 

Symptoms

The symptoms of MS depend on which areas of the brain and spinal cord develop MS lesions. For example, if the nerve that is involved in vision (the optic nerve) develops a lesion, blurring of vision occurs. This is referred to as optic neuritis. If a lesion develops in the part of the brain that produces movement on the left side of the body, left-sided weakness develops. In addition to visual blurring and weakness, other common MS symptoms include fatigue, depression, urinary difficulties, walking unsteadiness, stiffness in the arms or legs, tingling, and numbness.

 

Living with MS

After a multiple sclerosis diagnosis, it is common to experience many unique emotions.  People often report feeling irritable, tearful, anxious, or distracted.  They may describe themselves as depressed as a result of the diagnosis and unable to tolerate the idea of an uncertain future.  These experiences are very normal. After any surprising, traumatic event, we are expected to take some time to adjust and come to grips with our feelings.  Well-meaning friends and family members will sometimes  encourage newly diagnosed people to "put mind over matter”, to “be strong”, to "not think about the MS", or to “get over” their fears.