If you have MS, some lifestyle strategies, including regular physical activity, a nutritious diet, and connection with others, can help support your overall physical and emotional well-being.

With the help of new treatments, modern technology, and the dedication of scientists, researchers, and activists, it’s possible to live your best life with multiple sclerosis (MS).

These 15 tips can get you started on your journey to living well.

Learning everything you can about your diagnosis is the first step you can take to effectively manage your condition. A doctor can provide informational pamphlets about MS, or you can read about it from reputable organizations like the National MS Society.

Finding out the facts and clarifying any misconceptions about MS may give you a greater sense of your options as you manage your diagnosis.

Scientists are also learning more and more about MS each day. So, it’s essential to stay up to date as new treatments make their way through the pipeline.

The National MS Society is a good resource for finding new clinical trials in your area. Trials help researchers determine whether new treatments are safe and effective.

Participation in a clinical trial is a very personal decision. In addition to helping scientists uncover new treatments or combinations of treatments, there are other benefits to participating in clinical trials.

Participation in some sponsored clinical trials may be free of cost. People who haven’t received satisfactory results from traditional treatments can explore new drug combinations or drugs that have been previously approved by the Food and Drug Administration (FDA) to treat other conditions.

You can find a comprehensive listing of all past, present, and future clinical trials on ClinicalTrials.gov. If you find a clinical trial in your area that interests you, you can speak with a doctor to find out whether you could be a candidate.

Exercise can improve muscle strength and fitness, improve posture, and reduce symptoms, such as pain and fatigue, in people with MS. Low to moderate aerobic exercise can improve heart health and reduce fatigue.

According to a 2021 review of research, regular exercise in people with MS may support:

  • physical fitness, strength, flexibility
  • walking mobility
  • cognition and sleep quality
  • depression
  • sleep quality
  • slowed disability progression
  • a reduced relapse rate
  • a reduced risk of cardiovascular and metabolic diseases, such as diabetes

You can stay active in many ways. Doing what works for you may be the best place to start. Some ideas include:

  • general physical activity, like gardening, cooking, walking a dog
  • adaptive sports or recreational opportunities at a local community center
  • swimming, which allows for a range of movement that may not be possible on land
  • yoga for balance, flexibility, and stress reduction
  • resistance bands or light weights for muscle strength

No matter what activity you choose, prioritize your safety first. You may want to talk with a doctor about which options to try.

Good sleep hygiene can help relieve MS fatigue.

Some ways to help get more restful sleep include:

  • establishing a bedtime routine, such as taking a warm bath and listening to soothing music right before bed
  • trying to go to bed and wake up at the same time each day
  • avoiding bright screens before bedtime and dimming the lights as you get closer to bedtime, if possible and safe for you to do so
  • avoiding caffeine in the late afternoon and evening

You don’t have to go through this diagnosis alone. If you’d like to connect with others living with MS, consider joining a group like Bezzy MS.

Bezzy MS is a place for you to safely share your concerns through online forums. You can connect with others who may be going through some of the same experiences as you. Bezzy MS also has stories, information, and a forum.

MS support groups can connect you with other people living with MS and help you establish a network for exchanging ideas, new research, and good vibes.

You can also join a volunteer program or activist group. You may find participation in these types of organizations empowering.

The National MS Society’s activist website is another good place to get started. You can also look for upcoming volunteer events near you.

MS is a lifelong condition, so it’s important to be under the care of an MS specialist who is a good match for you. A primary care doctor can refer you to a team of other healthcare professionals to help you manage all of your symptoms.

Or, you can use this Find Doctors & Resources tool from the National MS Society.

The healthcare professionals you may choose to work with as part of a multidisciplinary team can include:

  • a neurologist who specializes in MS
  • a neuropsychologist to help manage thinking ability, like memory, focus, information processing, and problem-solving
  • a physical therapist to work on overall strength, joint range of motion, coordination, and gross motor skills
  • a psychologist or mental health counselor to help you cope with the diagnosis and living with MS
  • an occupational therapist, who can give you the tools to perform day-to-day tasks more efficiently
  • a social worker to assist with finding financial resources, entitlements, and community-provided services
  • a dietitian or nutritionist to help you maintain a balanced diet
  • a speech-language pathologist if you’re having problems with speech, swallowing, or breathing

Current research is looking at the potential benefits of the Mediterranean or MIND (Mediterranean-DASH Diet Intervention for Neurodegenerative Delay) diet to support the health of people with MS. These diets typically avoid ultra-processed foods and red meat. They prioritize:

  • fruits
  • vegetables
  • whole grains
  • healthy fats
  • lean protein
  • nuts and seeds

A small 2020 study found an association between obesity and higher clinical disability and inflammation in people with relapsing-remitting MS (RRMS).

Here are some other diet tips to consider:

  • Eat a low fat or plant-based diet: Another 2020 study found that people with MS who largely ate a Mediterranean-like diet had improvements in their fatigue levels after 12 months. However, it didn’t show improvements in relapse rates or disability levels, so more research is needed.
  • Get enough fiber: According to the USDA Dietary Guidelines for Americans, the recommended intake is at least 25 grams of fiber each day for women ages 31–50 and 31 grams of fiber each day for men in the same age range. This helps promote good bowel function.
  • Reduce alcohol consumption: Alcohol can impair balance and coordination and increase the need to urinate. Alcohol can also interfere with some MS medications.
  • Drink enough water: Many people with MS limit water intake to manage bladder issues. Dehydration from lack of water can lead to higher rates of fatigue.
  • Eat foods high in omega-3 fatty acids: Examples include fatty fish (like salmon, tuna, and mackerel), soybeans, canola oil, walnuts, flaxseeds, and sunflower oil. A 2021 review of studies found that omega-3 and fish oil supplements may help reduce relapse rate and inflammation and improve the quality of life for people with MS.

Household tasks can seem overwhelming, but you don’t have to do them all at once.

You can divide things to make them more manageable. For example, make a reasonable schedule for home repairs and errands like cleaning the yard and replacing HVAC filters, so they’re done over several weeks instead of a weekend.

You can try to clean one room a day or divide it into smaller time segments throughout the day, with rest periods in between. Depending on your symptoms, you can get cleaning done on your own. But you’ll want to take steps to avoid injury.

Some people plan out weekly meals and freeze portions for use on later days. You can use small tools for the kitchen that can make ordinary tasks easier and safer. For example, a jar opener can help you open up vacuum-sealed jars.

Try to think strategically about how your home and workplace are set up.

You might need to make some adjustments to suit your needs. For example, consider storing the kitchen tools that you use every day on the counter and in the most easy-to-reach cabinets. You may want to place heavy electric appliances, like blenders, on the countertop so you don’t have to move them around often.

Consider rearranging or getting rid of furniture, rugs, and decor that take up too much floor space or could trip you. You can also declutter to reduce cleaning time.

You can also talk with your employer to see whether they can provide ergonomic equipment. Examples can include glare protection on computer screens. It may also help to move your workstation to an accessible location, such as closer to the entrance, restrooms, and other essential areas.

MS can cause symptoms like memory loss and issues concentrating. This can make it difficult to remember day-to-day tasks, like appointments, and when to take your medication.

Use the technology you already have to make things easier. Most smartphones have apps and tools to help you work around memory challenges. You can also use your calendar, take notes, make lists, and set alerts and reminders.

Many people with MS are sensitive to heat exposure. When your body temperature rises, your symptoms may worsen. Even just a slight temperature increase can impair nerve impulses enough to cause symptoms. This experience actually has its own name: the Uhthoff phenomenon.

Try to keep yourself cool by avoiding hot showers and baths. Use air conditioning in your home and stay out of the sun when possible. You can also try wearing a cooling vest or neck wrap on hot days.

It’s important to take your medications on time. Forgetting to take a medication or refill a prescription can have major consequences on your day-to-day life.

To avoid this issue, consider setting up auto-refills for prescriptions with your local pharmacy. You can have the pharmacy text or call you to let you know that your prescription is ready for pickup. Many pharmacies can even mail your prescriptions in advance.

Managing life in the workplace can pose a challenge for people with MS. If you’re living with a new diagnosis, take some time to do a bit of research, such as about potential workplace accommodations.

This can involve a discussion between you and your employer and may include everything from physical accommodations like grab bars in restrooms to telecommuting arrangements.

Travel can be a wonderful way to enjoy life’s pleasures. This is entirely possible if you live with MS. The National MS Society has these tips for making your next getaway the best it can be:

  • pre-arrange assistance at the airport
  • pack extra medication and back it up with documentation, like doctors’ notes
  • confirm the accessibility status of hotels and attractions at your destination
  • schedule breaks and rest days during your trip

Having water and nutritious snacks on hand can also help make your visits more comfortable, along with traveling during cooler months.

Although there’s no cure for MS right now, newer treatments can help slow the disease. Research is being done to improve treatments and reduce disease progression.

If you’re having a hard time managing life with MS, consider meeting with a psychologist or a mental health counselor to discuss your needs.

Can you live a typical life with MS?

Depending on your symptoms and level of disability, you may need to make some modifications. However, many people with MS have long and active lives.

How long does MS take to disable you?

Each person with MS can have different symptoms and disease progression. Different types of MS can also progress differently. In many cases, treatment can help prevent or slow disability.

How does MS affect a person’s daily life?

Different people with MS may experience different symptoms and disease progression. At least half of participants with MS in a 2020 survey reported fatigue, weakness, issues with balance or coordination, sensitivity to hot and cold temperatures, issues with memory and concentration, and numbness or tingling.

How do you cope with living with MS?

Some people find that connecting with others who have MS or talking with a mental health professional helps them cope with MS. Other lifestyle strategies, such as getting regular exercise or eating a nutritious diet, can help reduce MS symptoms like fatigue.

Life after a diagnosis of MS can be overwhelming. Some days, your symptoms might prevent you from doing what you love or leave you feeling emotionally drained.

While some days may be difficult, it’s still possible to live well with MS by implementing some of the above changes into your life.