Multiple sclerosis - discharge

Symptoms vary from person to person. With time, each person may have different symptoms. For some people, symptoms last days to months, then lessen or go away. For others, symptoms don't improve or only very little.

Over time, symptoms may get worse (progression), and it becomes harder to take care of yourself. Some people have very little progression. Others have more severe and rapid progression.

Make sure you understand which medicines you should be taking and how you should be taking them. Some medicines require periodic blood tests or MRI scans. A pill box or app on your phone can prevent you from forgetting any doses.

Try to stay as active as you can. Ask your provider what kind of activity and exercise are right for you. Try walking or jogging. Stationary bicycle riding is also good exercise.

Benefits of exercise include:

• Helps your muscles stay loose
• Helps you keep your balance
• Good for your heart
• Helps you sleep better
• Helps you have regular bowel movements

If you have problems with spasticity, learn about what makes it worse. You or your caregiver can learn exercises to keep muscles loose.

Increased body temperature can make your symptoms worse. Here are some tips to prevent overheating:

• Exercise in the morning and the evening. Be careful not to wear too many layers of clothes.
• When taking baths and showers, avoid water that is too hot.
• Be careful in hot tubs or saunas. Make sure somebody is around to help you if you become overheated.
• Keep your house cool in the summer with air conditioning.
• Avoid hot drinks if you notice problems with swallowing, or other symptoms get worse.

Make sure your home is safe. Find out what you can do to prevent falls and keep your bathroom safe to use.

If you are having trouble moving around in your house easily, talk with your provider about getting help.

Your provider can refer you to a physical therapist to help with:

• Exercises for strength and moving around
• How to use your walker, cane, wheelchair, or other devices
• How to set up your home to safely move around

You may have problems starting to urinate or emptying your bladder all the way. Your bladder may empty too often or at the wrong time. Your bladder may become too full and you may leak urine.

To help with bladder problems, your provider may prescribe medicine. Some people with MS need to use a urinary catheter. This is a thin tube that is inserted into your bladder to drain urine.

Your provider may also teach you some exercises to help you strengthen your pelvic floor muscles.

Urinary infections are common in people with MS. Learn to recognize the symptoms, such as burning when you urinate, fever, low back pain on one side, and a more frequent need to urinate.

Do not hold your urine. When you feel the urge to urinate, go to the bathroom. When you are not at home, take note of where the nearest bathroom is.

If you have MS, you may have trouble controlling your bowels. Have a routine. Once you find a bowel routine that works, stick with it:

• Pick a regular time, such as after a meal or a warm bath, to try to have a bowel movement.
• Be patient. It may take 15 to 45 minutes to have bowel movements.
• Try gently rubbing your belly to help stool move through your colon.

Avoid constipation:

• Drink more fluids.
• Stay active or become more active.
• Eat foods with lots of fiber.

Ask your provider about medicines you're taking that may cause constipation. These include some medicines for depression, pain, bladder control, and muscle spasms.

If you are in a wheelchair or bed most of the day, you need to check your skin every day for signs of pressure sores. Look closely at:

• Heels
• Ankles
• Knees
• Hips
• Tailbone
• Elbows
• Shoulders and shoulder blades
• Back of your head

Learn how to prevent pressure sores.

Keep up to date with your vaccinations. Get a flu shot every year. Ask your provider if you need a vaccination to prevent pneumococcal infections (sometimes called a pneumonia shot) and a COVID-19 vaccine.

Ask your provider about other checkups you may need, such as to test your cholesterol level, blood sugar level, and a bone scan for osteoporosis.

Eat healthy foods and keep from becoming overweight.

Learn to manage stress. Many people with MS feel sad or depressed at times. Talk to friends or family about this. Ask your provider about seeing a professional to help you with these feelings.

You may find yourself getting tired more easily than before. Pace yourself when you do activities that may be tiring or need a lot of concentration.

Your provider may have you on different medicines to treat your MS and many of the problems that may come with it:

• Make sure you follow instructions. Do not stop taking medicines without first talking to your provider.
• Know what to do if you miss a dose.
• Store your medicines in a cool, dry place, and away from children.

Contact your provider if you have:

• Problems taking medicines for muscle spasms
• Problems moving your joints (joint contracture)
• Problems moving around or getting out of your bed or chair
• Skin sores or redness
• Pain that is becoming worse
• Recent falls
• Choking or coughing when eating
• Signs of a bladder infection (fever, burning when you urinate, foul urine, cloudy urine, or frequent urination)

MS - discharge

Calabresi PA. Multiple sclerosis and demyelinating conditions. In: Goldman L, Cooney KA, eds. Goldman-Cecil Medicine. 27th ed. Philadelphia, PA: Elsevier; 2024:chap 380.

Fabian MT, Krieger SC, Lublin FD. Multiple sclerosis and other inflammatory demyelinating diseases of the central nervous system. In: Jankovic J, Mazziotta JC, Pomeroy SL, Newman NJ, eds. Bradley and Daroff's Neurology in Clinical Practice. 8th ed. Philadelphia, PA: Elsevier; 2022:chap 80.

National Multiple Sclerosis Society website. Living with MS. www.nationalmssociety.org/managing-ms/living-with-ms. Accessed August 23, 2024.

Updated by: Joseph V. Campellone, MD, Department of Neurology, Cooper Medical School at Rowan University, Camden, NJ. Review provided by VeriMed Healthcare Network. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.