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Energy Conservation for Multiple Sclerosis

A senior woman resting on a bench.
Key Points
  • Energy conservation helps people with MS manage fatigue by changing how they complete daily tasks to use less energy throughout the day.
  • The 4 Ps framework provides a simple approach to conserving energy: Plan your activities, Pace yourself with breaks, Prioritize what matters most, and Position your body to work efficiently.
  • Small modifications make a big difference. Sitting instead of standing, organizing your space, and breaking tasks into smaller steps can significantly reduce how much energy you spend.
  • Tracking your fatigue patterns reveals important insights about when you have the most energy, which activities drain you most, and how to structure your day for success.
  • A Solace MS advocate helps you get the support you need by connecting you with occupational therapists, coordinating between your specialists, and ensuring your care team understands how fatigue affects your daily life.

You wake up, and the day stretches ahead. Getting dressed feels like climbing a mountain. By the time you've showered and made breakfast, you're already exhausted. The rest of your to-do list seems impossible.

This isn't regular tiredness. If you have multiple sclerosis, you know that MS fatigue is different. It affects up to 90% of people with MS, and for at least half, fatigue is the symptom that causes the most problems in daily life. It's not about needing more sleep. It's about your body working harder to do everything because the messages between your brain and body aren't traveling efficiently.

The good news is that you don't have to just accept it. Energy conservation techniques can help you manage fatigue so you can keep doing the things that matter to you. These aren't complicated medical treatments or expensive programs. They're practical strategies for getting through your day with the energy you have.

Man assisting an older man using a wheelchair. Banner text: MS is tough, but so are you. Get the steady care you need. Includes a button: Find an advocate.

What Is Energy Conservation?

Energy conservation means completing your daily tasks in the most energy-efficient way possible. Think of it like managing a budget, except instead of dollars, you're managing your energy. You only have so much to spend each day, so you want to be smart about how you use it.

Research shows that energy conservation programs can reduce the physical and social impact of fatigue and improve quality of life for people with MS. The idea isn't to stop doing things you care about. It's about finding ways to do them that don't leave you completely drained.

Unlike just resting more, energy conservation is about working smarter, not harder. It involves planning ahead, modifying how you do things, and using your body more efficiently. When you conserve energy well, you'll have more consistent energy throughout the day instead of running out by noon.

Understanding the Fatigue Cycle

To understand why energy conservation matters, it helps to know what's happening in your body. MS damages the myelin that surrounds nerve fibers in your brain and spinal cord. This myelin works like insulation on an electrical wire, helping signals travel quickly and efficiently. When it's damaged, those signals slow down or get blocked entirely. Your body has to work much harder to do everything, which causes fatigue.

But there's more to it than just the disease itself. Many people with MS get caught in what doctors call the fatigue cycle. You feel exhausted, so you do less. Doing less leads to muscle weakness and deconditioning. That makes you more tired. The exhaustion and limitations can lead to depression. Depression saps even more energy. You might develop muscle stiffness or have trouble sleeping. All of this feeds back into more fatigue.

Breaking this cycle requires active management. It's about finding the right balance between rest and activity. You need to conserve energy so you can stay active enough to avoid deconditioning, but not so active that you crash and burn.

The 4 Ps: Your Framework for Energy Conservation

Healthcare providers who work with chronic conditions often teach something called the 4 Ps. This framework gives you four simple principles to guide your energy conservation efforts: Plan, Pace, Prioritize, and Position. Let's break down each one.

Plan

Planning ahead is one of the most powerful energy savers you have. When you plan your activities, you can reduce unnecessary steps, gather everything you need before you start, and avoid that draining feeling of running around looking for things.

Start by thinking about your week. What needs to happen? When do you typically have the most energy? Put your more demanding tasks during those high-energy times. Spread out the heavy lifting so you're not trying to do everything in one day.

Even planning within a single task helps. Before you start cooking dinner, for example, take a minute to get out all your ingredients and tools. This saves you from making repeated trips to the pantry or searching through drawers while you're already tired.

Pace

Pacing means maintaining a steady, manageable speed throughout your activities. The key is taking breaks before you get tired, not after you're already exhausted. This is harder than it sounds because it requires fighting the urge to just power through and finish.

Think of pacing like running a marathon instead of a sprint. You don't want to use all your energy in the first mile. Break large tasks into smaller chunks. If you're folding laundry, do one load and then rest. If you're cleaning, tackle one room and take a break before moving to the next.

The "10-minute rule" works well for many people. After working on something for 10 minutes, pause and check in with yourself. Are you starting to feel tired? Take a quick break, even if it's just sitting down for a few minutes.

Prioritize

You can't do everything, and that's okay. Prioritizing means deciding what actually needs to happen today and what can wait. It means focusing your energy on the things that matter most to you.

Make a list of what you need and want to accomplish. Be honest about what's truly essential. Does your house need to be spotless, or is "good enough" actually good enough? Can someone else handle some of these tasks? Are there things on your list that don't really need to be there at all?

Pay attention to when you have the most energy. Most people with MS have more energy in the morning, but everyone is different. Schedule your high-priority tasks for your peak energy times. Save the less important stuff for when you're running lower.

Position

How you position your body during tasks makes a bigger difference than you might think. Sitting uses about 25% less energy than standing, which adds up over the course of a day.

Look for opportunities to sit instead of stand. Get a stool for your kitchen so you can sit while cooking or washing dishes. Sit at your bathroom counter while you brush your teeth or do your hair. If you garden, use a low stool or bench so you're not bending and standing the whole time.

Your posture matters too. Sit and stand as upright as you can. Slouching makes your muscles work harder. When you're doing a task, bring things to your level instead of reaching or bending. Use proper breathing techniques to stay relaxed and maintain a steady breathing rate.

Man assisting an older man using a wheelchair. Banner text: MS is tough, but so are you. Get the steady care you need. Includes a button: Find an advocate.

Tracking Your Energy Patterns

Before you can manage your energy well, you need to understand your patterns. This is where keeping a fatigue diary becomes incredibly valuable.

For at least four days, track what you do and how tired you feel. Write down your activities and rate your fatigue level on a scale of 1 to 10 at different times throughout the day. Include what you ate, when you rested, and any other factors that might affect your energy.

After a few days, you'll start to see patterns. You might notice that you always crash after lunch. Maybe certain activities drain you more than others. Perhaps you have more energy on days when you do a specific activity or eat certain foods. This information is gold because it helps you make informed decisions about how to structure your day.

Pay attention to which tasks are most meaningful to you. Which activities bring you joy or fulfillment? Which ones feel like they're just checking boxes? Your energy is precious. Spend it on what matters.

Practical Strategies for Daily Activities

Energy conservation isn't abstract. It shows up in the real, everyday things you do. Here are specific ways to conserve energy in common activities of daily living.

Morning Routine

Your morning routine sets the tone for the whole day. Small changes here can save significant energy:

  • Lay out your clothes the night before so you're not making decisions or digging through drawers when you're already tired
  • Sit on your bed or a chair while getting dressed
  • Put on your underwear and pants before standing up
  • Use adaptive equipment like a long-handled shoehorn, sock aid, or button hook if fine motor tasks drain you
  • Consider a shower chair or bench so you can sit while bathing
  • Dry off with a terry cloth robe instead of toweling off with your arms raised
  • Organize your bathroom so everything you need is within easy reach

Meal Preparation

Cooking requires a lot of energy, but you have to eat. Here's how to make it easier:

  • Use a high stool or chair in the kitchen so you can sit while prepping food or washing dishes
  • Plan your meals ahead and do any prep work during your high-energy times
  • Try batch cooking on days when you feel better, then freeze portions for days when you don't
  • Use time-saving appliances like slow cookers, instant pots, or air fryers that do the work for you
  • Keep frequently used items at counter level so you're not reaching or bending
  • Consider meal delivery services or prepared meal kits on particularly difficult days

Household Tasks

The house doesn't clean itself, but you can make these tasks less draining. Spread chores throughout the week instead of trying to do everything in one day. Do laundry on Monday, vacuum on Wednesday, clean bathrooms on Friday. On each day, you're only tackling one thing.

When you do tackle these tasks:

  • Sit whenever possible (fold laundry on the couch, sit while wiping down surfaces)
  • Use a rolling cart to move supplies or items from room to room instead of carrying them
  • Push, don't pull (pushing requires less energy)
  • Use lightweight tools and long-handled tools that reduce bending
  • Take breaks between tasks, even if you don't feel tired yet

Don't be afraid to ask for help or consider hiring services for the most demanding tasks. Using grocery delivery or having someone else clean your bathroom isn't giving up. It's making smart choices about where to spend your limited energy.

Personal Care and Grooming

Getting ready shouldn't exhaust you. Install a bench or chair in your bathroom. Organize your grooming supplies so everything is at counter level. If applying makeup or shaving requires a lot of fine motor work that tires you out, consider simplifying your routine.

Use adaptive aids like electric toothbrushes, which require less effort than manual ones. Long-handled brushes can help you reach your back without straining. Weighted utensils can sometimes be easier to control if you have tremors.

Man assisting an older man using a wheelchair. Banner text: MS is tough, but so are you. Get the steady care you need. Includes a button: Find an advocate.

Temperature and Energy

People with MS often experience heat sensitivity. When your body temperature rises, damaged nerves conduct signals even less efficiently than usual. This means heat can trigger or worsen fatigue and other symptoms.

Staying cool helps conserve energy. Use fans, air conditioning, and cooling vests if needed. Keep cold drinks handy. Take cool showers instead of hot ones. In warm weather, plan outdoor activities for early morning or evening when it's cooler.

But be careful not to cool down too quickly, as rapid temperature changes can also trigger symptoms. The key is maintaining a comfortable, consistent temperature throughout your day.

The Role of Exercise

This might seem contradictory. If you're trying to conserve energy, why would you exercise? But research consistently shows that appropriate exercise can actually help reduce MS fatigue over time.

The key word is "appropriate." You're not training for a marathon. You're staying active enough to prevent deconditioning, which makes fatigue worse. When your muscles are strong and your cardiovascular system is functioning well, everything takes less energy.

Types of exercise that often work well for people with MS include:

  • Aquatic exercise (the water supports your body and keeps you cool)
  • Chair yoga or gentle stretching
  • Walking at your own pace
  • Resistance training with light weights or resistance bands

Talk to your doctor or a physical therapist before starting an exercise program. They can help you find the right balance and intensity. Always warm up with stretches, use proper body mechanics, and stop if you feel your symptoms worsening.

Working with an Occupational Therapist

Occupational therapy is incredibly valuable for people dealing with MS fatigue. Occupational therapists (OTs) specialize in helping people do the daily activities that matter to them. They don't just give generic advice. They assess your specific situation and create individualized strategies.

An OT will typically start with a fatigue assessment. This helps measure the severity of your fatigue during different activities, including physical, sensory, cognitive, and emotional components. They'll ask about your daily routine, what's most challenging, and what's most important to you.

From there, they'll work with you to develop practical solutions. This might include teaching you energy conservation techniques, recommending adaptive equipment, suggesting home modifications, or helping you develop better routines. They can also help with work accommodations if you're employed.

OTs understand the balance between staying active and conserving energy. They can show you how to modify activities so you can keep doing them without exhausting yourself. If you haven't worked with an OT, ask your doctor for a referral.

Assistive Devices and Adaptive Equipment

Sometimes the right tool makes all the difference. Assistive devices and adaptive equipment are designed to help you complete tasks with less effort. You're not being weak by using them. You're being smart about your energy.

Common helpful devices include:

Reachers and grabbers let you pick things up without bending over or stretching. They're especially useful for getting items from high shelves or off the floor.

Dressing aids like sock aids, long-handled shoehorns, and button hooks make getting dressed easier when bending or fine motor control is difficult.

Shower chairs and benches let you sit while bathing, which saves significant energy and reduces fall risk.

Rolling carts can transport items around your house so you're not making multiple trips carrying things.

Ergonomic tools with specially designed handles require less grip strength and reduce strain on your hands and wrists.

Many insurance plans, including Medicare, may cover some adaptive equipment if it's medically necessary. Your occupational therapist can help identify what you need and write documentation for insurance approval.

Man assisting an older man using a wheelchair. Banner text: MS is tough, but so are you. Get the steady care you need. Includes a button: Find an advocate.

Environmental Modifications

Sometimes changing your environment is easier than changing how you do things. Look at your living space with fresh eyes. What could you rearrange to reduce energy expenditure?

Organize frequently used items so they're easy to reach without bending, stretching, or climbing. If you have a two-story house and going up and down stairs exhausts you, consider whether you can move some essentials downstairs. Maybe set up a bedroom or bathroom on the main floor.

Improve your lighting so you're not straining to see. Make sure rooms are well-ventilated so you stay cool. Remove tripping hazards and clutter that force you to navigate obstacles. If possible, create dedicated workspaces where you can sit comfortably with everything you need within reach.

Think about the flow of your day. If you're constantly moving between the kitchen and dining room, could a rolling cart help? If getting mail requires walking to the end of a long driveway, could you move the mailbox closer or ask someone else to handle it?

Managing Energy at Work

If you're working, balancing your job demands with MS fatigue presents unique challenges. Many people worry about disclosing their diagnosis, but under the Americans with Disabilities Act (ADA), you may be entitled to reasonable accommodations.

Accommodations might include:

  • A modified work schedule that lets you work during your peak energy times
  • The option to work from home some or all of the time
  • More frequent breaks
  • An ergonomic workspace setup
  • The ability to sit instead of stand, or vice versa
  • Reduced physical demands

You don't have to disclose your diagnosis to everyone, but you'll likely need to talk to HR and provide medical documentation to get accommodations approved. Your doctor or occupational therapist can help with this documentation.

Be strategic about when you schedule meetings and tackle demanding projects. Use your energy conservation techniques at work just like you do at home. Take your breaks even when you're busy. Eat lunch sitting down, not at your desk. Your job is important, but so is managing your health.

Man assisting an older man using a wheelchair. Banner text: MS is tough, but so are you. Get the steady care you need. Includes a button: Find an advocate.

When Energy Conservation Works Best

Energy conservation doesn't work the same for everyone. Research suggests that certain factors affect how well these techniques work. People who have a less negative perception of fatigue and stronger social support tend to see better results. Your outlook and support system matter.

That doesn't mean if you're struggling, it's your fault. It means that addressing the emotional and social aspects of living with MS is part of managing fatigue. Consider joining a support group. Talk to a therapist who understands chronic illness. Build a team of people who get what you're going through.

Energy conservation works best as part of a comprehensive approach to managing MS fatigue. It's not a magic cure, but it's a proven tool. Combine it with medical treatment, exercise, stress management, good sleep habits, and support from others. Be patient with yourself. It takes time to learn what works for you and to build new habits.

Set realistic expectations. Energy conservation will help you do more of what matters, but it won't eliminate fatigue entirely. Some days will be harder than others. That's part of living with MS.

How a Solace Advocate Can Help

Managing MS fatigue isn't just about learning techniques. It's about coordinating care, getting the right referrals, ensuring your insurance covers what you need, and making sure all your doctors understand what you're dealing with. That's where a Solace advocate becomes invaluable.

Connecting you with occupational therapists and specialists. Finding an OT who has experience with MS and understands energy conservation takes time and research. Your advocate can identify specialists in your area, check whether they're in your insurance network, handle the referral process, and get you scheduled.

Coordinating between your healthcare providers. You might be seeing a neurologist, primary care doctor, physical therapist, and other specialists. Your advocate ensures everyone is on the same page about your fatigue and how it's affecting you. They make sure test results and treatment plans are shared across your care coordination team.

Following up on referrals and recommendations. When your doctor suggests occupational therapy or adaptive equipment, your advocate tracks it from recommendation to completion. They ensure referrals get processed, appointments get scheduled, and nothing falls through the cracks.

Helping you communicate patterns to your care team. Tracking your fatigue patterns is important, but translating that information into something useful for your doctors can be challenging. Your advocate helps organize your observations and presents them in ways that lead to better treatment decisions.

Researching coverage for adaptive equipment and therapy services. Insurance coverage for occupational therapy and adaptive equipment varies widely. Your advocate investigates what your plan covers, handles prior authorization if needed, and finds financial assistance programs if you have coverage gaps.

Supporting workplace accommodation requests. If you need accommodations at work, your advocate can help gather the medical documentation you need, communicate with HR, and ensure you get the support you're entitled to under the ADA.

Keeping everything organized. When you're managing fatigue, the last thing you need is to spend energy tracking appointments, following up on referrals, and calling insurance companies. Your advocate handles the administrative burden so you can focus on taking care of yourself.

One Solace advocate stays with you through the whole process. You're not repeating your story to different people or getting bounced around. Just one person who learns your situation and keeps working on your behalf.

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Frequently Asked Questions about MS Energy Conservation

Will energy conservation make me weaker because I'm doing less?

Energy conservation isn't about doing less. It's about doing things more efficiently. The goal is to conserve enough energy that you can stay active and avoid deconditioning. You'll still exercise, move throughout your day, and do activities that matter to you. You're just being strategic about how you use your energy. Think of it like packing a suitcase more efficiently so everything fits, not leaving half your clothes at home. Studies show that people who use energy conservation techniques while staying appropriately active often maintain better function long-term than those who just rest all the time.

How long does it take to see results from energy conservation techniques?

Most people start noticing small improvements within a few weeks of consistently using energy conservation strategies. You might find you can make it through the day without completely crashing, or that you have energy left for an evening activity. More significant changes often take a couple of months as you refine what works for you and develop new habits. Remember, energy conservation is a skill that improves with practice. Your first attempts might feel awkward or like you're slowing yourself down, but over time these approaches become natural.

Can I still exercise if I'm using energy conservation strategies?

Absolutely. Exercise and energy conservation work together, not against each other. The key is choosing appropriate types and intensities of exercise and timing them strategically. Many people find they can exercise more consistently when they're using energy conservation in other areas of their life because they have more energy available. Talk with your doctor or physical therapist about an exercise plan that fits your current abilities and energy levels. They can help you find the balance between staying active enough to prevent deconditioning and overdoing it.

What if my family doesn't understand why I need to change how I do things?

This is a common challenge. MS fatigue is invisible, which makes it hard for others to understand. Start by educating your family about how MS affects your body and why fatigue is different from regular tiredness. Share resources from reputable organizations or bring family members to a doctor's appointment where your fatigue can be discussed. Be specific about how fatigue affects you. Instead of "I'm tired," explain "when I shower standing up, I don't have enough energy left to make breakfast." Ask for specific help rather than general support. And remember, it's okay to set boundaries. You don't need anyone's permission to use energy conservation techniques that help you function better.

Are energy conservation techniques covered by insurance?

Occupational therapy, which is where most people learn energy conservation techniques, is typically covered by Medicare and most private insurance plans. You'll usually need a doctor's referral. Coverage limits vary, so check your specific plan. As for adaptive equipment, coverage depends on the item and your insurance. Medicare covers some durable medical equipment if it's medically necessary and prescribed by your doctor. A Solace advocate can help navigate your specific coverage and find financial assistance if needed for items that aren't covered.

This article is for informational purposes only and should not be substituted for professional advice. Information is subject to change. Consult your healthcare provider or a qualified professional for guidance on medical issues, financial concerns, or healthcare benefits.

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