August 25, 2026

MS Relapse Triggers: 7 Things to Watch When Living With MS

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Picture of Patti Bevilacqua

Patti Bevilacqua

Dr. Patti Bevilacqua is a workplace culture speaker, TEDx speaker, bestselling author, and hidden challenges advocate. Diagnosed with multiple sclerosis in 1990, she holds a PhD in Teacher Development from the University of Toronto. Through her writing, speaking, and advocacy, she helps people see beyond a diagnosis and recognize the hidden challenges that shape how we live, lead, and connect with one another. She is the author of MS doesn't define ME, a memoir that explores identity, resilience, and rebuilding life after an MS diagnosis. Her work encourages readers and audiences alike to see the whole person, not just the condition. Patti lives in Grand Forks, British Columbia, Canada.

I was diagnosed with multiple sclerosis in 1990, during my first year of teaching high school physical education. In the years that followed, I learned, sometimes the hard way, that MS rarely announces itself loudly.

Changes tend to begin quietly.

A symptom that feels slightly off.

Fatigue that does not lift.

A shift you almost explain away because hard days are part of life with this disease.

Over time, I learned to recognize the MS relapse triggers behind those changes, long before they turned into something bigger.

Learning to distinguish between a difficult day and a genuine warning sign took time. It also took better conversations with my care team, more honest self-observation, and a willingness to stop minimizing what my body was telling me.

This post reflects my lived experience alongside guidance from organizations including the National MS Society, MS Trust, MS Society UK, Cleveland Clinic, and NHS. It is not medical advice. It is meant to help you recognize changes, understand what may be happening, and know when it is time to contact your MS care team.

MS Relapse vs. Pseudo-Relapse: Know the Difference

Before looking at what to watch for, this distinction matters.

A true relapse involves new or significantly worsening neurological symptoms that last at least 24 hours and occur in the absence of fever or infection. The National MS Society defines a relapse as neurological symptoms lasting at least 24 hours, separated from the previous episode by at least 30 days.

A pseudo-relapse is different. Existing symptoms temporarily become worse because of factors such as heat, fatigue, or infection, without new inflammatory activity. Symptoms typically improve once the triggering factor is removed.

The MS Trust notes that pseudo-relapses are temporary and do not represent new disease activity.

Understanding the difference can help you recognize what is happening and give your care team better information when you contact them.

1. Infection: A Common MS Relapse Trigger

Infection is one of the most consistently documented factors associated with an increased risk of MS relapse, particularly urinary tract infections.

When your immune system responds to an infection, that broader immune activity may also be associated with increased inflammatory disease activity in MS. Research has found that common infections, including respiratory and urinary infections, are associated with an increased short-term risk of relapse.

From my own experience, even a mild infection that might not slow most people down could noticeably change how my body felt.

Learning to take infections seriously, rather than simply pushing through them, was an important adjustment for me.

What to watch: Increased MS symptoms alongside signs of infection, including fever, unusual fatigue, or burning during urination. Contact your healthcare provider and let your MS care team know what is happening.

2. Heat

Heat typically causes a temporary worsening of existing MS symptoms rather than a true relapse.

That distinction is important.

An increase in body temperature can temporarily slow nerve conduction in pathways already affected by MS. This is known as Uhthoff’s phenomenon. Cleveland Clinic notes that heat sensitivity is common in MS and that symptoms generally improve once the body cools.

What to watch: A sudden worsening of weakness, vision, balance, or other existing symptoms in the heat or after exercise.

If your symptoms improve after cooling down and resting, it may be a pseudo-relapse. If they continue for more than 24 hours, contact your MS care team.

3. Severe or Prolonged Stress: A Hidden MS Relapse Trigger

Managing stress when you live with MS is not simply about feeling better emotionally. Research suggests that severe or prolonged stress may be associated with an increased risk of relapse.

The relationship is not simple, and stress does not automatically cause an MS relapse. But research has found an association between stressful life events and subsequent relapse risk.

I noticed early in my diagnosis that sustained stress, not the ordinary pressures of everyday life but prolonged, unmanaged stress, seemed to leave me more vulnerable.

That was one of the reasons I eventually began treating stress management as an important part of taking care of myself rather than an optional extra.

What to watch: New or returning neurological symptoms during or following a period of intense or prolonged stress. Keep track of patterns and discuss them with your neurologist or MS care team.

4. Disrupted Sleep

Sleep disruption does not necessarily cause an MS relapse, but poor sleep can have a significant effect on fatigue, cognitive function, and existing MS symptoms.

Sleep problems are common among people living with MS. And when you are already managing limited energy, poor sleep can make an already difficult day considerably harder.

What to watch: A noticeable worsening of existing symptoms following a period of disrupted sleep, particularly increased fatigue or cognitive difficulties.

If sleep problems continue or significantly affect your daily life, talk with your healthcare provider rather than assuming they are simply another part of living with MS.

5. Hormonal Changes

Hormonal changes can influence MS disease activity, particularly during pregnancy and after giving birth.

The National MS Society notes that relapse rates often decrease during pregnancy, particularly during the third trimester, and may increase during the postpartum period.

If you are planning a pregnancy, conversations about MS management should happen with your neurologist and obstetric care team before, during, and after pregnancy.

What to watch: New or noticeably worsening neurological symptoms during periods of significant hormonal change, particularly after giving birth.

If you notice changes, contact your MS care team.

6. Physical Overexertion

Pushing yourself physically can worsen fatigue, weakness, and other existing MS symptoms, but overexertion usually causes temporary symptom worsening rather than a true relapse.

This is why learning to pace yourself matters.

For me, that has not always been easy. There is a big difference between knowing you should slow down and actually allowing yourself to do it, especially when you remember everything you used to be able to accomplish in a day.

But pushing harder is not always the answer.

The MS Society UK recommends energy-management strategies such as planned rest, pacing activities, and setting realistic goals as part of managing MS.

What to watch: A significant increase in fatigue or other existing symptoms after doing more physically than your body can comfortably manage.

If symptoms do not improve after resting and cooling down, or continue for more than 24 hours, contact your MS care team.

7. New or Returning Neurological Symptoms: The Most Important MS Relapse Trigger to Watch

This is the one that deserves particular attention.

New neurological symptoms, or a significant worsening or return of previous symptoms, may signal a true relapse.

These changes can include:

● Vision changes
● New numbness or tingling
● Weakness
● Balance problems
● Changes in bladder or bowel function
● Other neurological symptoms that are new or significantly different for you

The NHS advises that new or worsening neurological changes should be assessed by a healthcare professional.

From my own experience, I learned that minimizing new symptoms rarely helped me.

Getting them assessed, even when I was not sure whether they were significant, gave me clearer answers and helped me make better decisions than simply waiting and hoping they would disappear.

What to watch: Any new or significantly worsening neurological symptom that lasts more than 24 hours and is not explained by factors such as heat, infection, or extreme fatigue.

Contact your MS care team so they can determine what may be causing the change and what you should do next.

What to Do When You Notice Warning Signs

Recognizing that something has changed is only the first step. Knowing what to do next matters too.

Keep a symptom diary. Write down when symptoms appear, how long they last, what they feel like, and what else was happening at the time. This gives your healthcare team useful information and may help you recognize patterns.

Contact your care team early. Do not wait until symptoms become severe. Your care team can help determine whether you may be experiencing a true relapse, a pseudo-relapse, an infection, or something else that needs attention.

Do not self-diagnose. You may become very good at recognizing your own patterns, but a healthcare professional should assess new or significantly worsening symptoms and determine whether treatment is needed.

Rest without guilt. This one took me time to learn. When your body is telling you something has changed, pushing harder does not prove anything. Give yourself permission to slow down while you figure out what is happening.

For a closer look at how MS affects relationships, routines, and the people around you, my post about how MS affects daily life explores that side of living with the disease in more depth.

And if you are looking for an honest account of what living with MS actually looks like beyond symptom lists and medical appointments, MS doesn’t define ME tells that story.

It is not a medical guide.

It is my story of diagnosis, identity, loss, resilience, self-advocacy, and learning that MS could change my life without defining who I am.

Frequently Asked Questions

Q1. What are the most common MS relapse triggers?

Factors associated with an increased risk of MS relapse can include infections and severe or prolonged stress. Hormonal changes, particularly during the postpartum period, can also affect relapse risk.

Other factors, such as heat, fatigue, poor sleep, and physical overexertion, may temporarily worsen existing MS symptoms without causing a true relapse.

If you notice a pattern in your own symptoms, keep track of it and discuss it with your MS care team.

Q2. How long does an MS relapse last?

A true MS relapse involves new or significantly worsening neurological symptoms lasting at least 24 hours. Symptoms may continue for days or weeks, and recovery varies from person to person.

Some people return to their previous baseline, while others may experience lasting changes. Your MS care team can determine whether treatment is appropriate.

Q3. Can heat cause an MS relapse?

Heat does not typically cause a true relapse. It more commonly causes a temporary worsening of existing symptoms, sometimes called a pseudo-relapse.

Symptoms generally improve once your body cools down. If symptoms continue for more than 24 hours after cooling and resting, contact your MS care team.

Q4. How can I tell a relapse from a pseudo-relapse?

A true relapse generally involves new symptoms or a significant worsening of existing neurological symptoms that lasts more than 24 hours and occurs without fever or infection.

A pseudo-relapse involves a temporary worsening of existing symptoms, often related to factors such as heat, fatigue, or infection.

It is not always easy to tell the difference yourself. If you are unsure, contact your MS care team.

Q5. Can stress cause an MS relapse?

Research suggests that severe or prolonged stress may be associated with an increased risk of relapse, although the relationship is complex and stress does not automatically cause a relapse.

Finding ways to manage prolonged stress can still be an important part of taking care of yourself when you live with MS.

Q6. When should I contact my MS care team about symptoms?

Contact your MS care team when you experience new neurological symptoms, when existing symptoms become significantly worse and continue for more than 24 hours, or when you suspect an infection.

If you are uncertain about what you are experiencing, you do not have to figure it out alone. Contact your care team and let them help you determine the appropriate next step.

Q7. What is the difference between relapsing-remitting MS and progressive MS?

Relapsing-remitting MS involves distinct relapses followed by periods of partial or full recovery.

Progressive forms of MS generally involve a more gradual accumulation of disability over time, although individual experiences vary.

Knowing what type of MS you have can help you and your healthcare team understand changes in your symptoms and make appropriate treatment decisions.

Author Profile

Picture of Patti Bevilacqua

Patti Bevilacqua

Dr. Patti Bevilacqua is a workplace culture speaker, TEDx speaker, bestselling author, and hidden challenges advocate. Diagnosed with multiple sclerosis in 1990, she holds a PhD in Teacher Development from the University of Toronto. Through her writing, speaking, and advocacy, she helps people see beyond a diagnosis and recognize the hidden challenges that shape how we live, lead, and connect with one another. She is the author of MS doesn't define ME, a memoir that explores identity, resilience, and rebuilding life after an MS diagnosis. Her work encourages readers and audiences alike to see the whole person, not just the condition. Patti lives in Grand Forks, British Columbia, Canada.
Dr. Patti Bevilacqua is a workplace culture speaker, TEDx speaker, bestselling author, and hidden challenges advocate. Diagnosed with multiple sclerosis in 1990, she holds a PhD in Teacher Development from the University of Toronto. Through her writing, speaking, and advocacy, she helps people see beyond a diagnosis and recognize the hidden challenges that shape how we live, lead, and connect with one another. She is the author of MS doesn't define ME, a memoir that explores identity, resilience, and rebuilding life after an MS diagnosis. Her work encourages readers and audiences alike to see the whole person, not just the condition. Patti lives in Grand Forks, British Columbia, Canada.

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MS doesn't define ME

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is a powerful and transformative book by Dr. Patti Bevilacqua, sharing her journey with multiple sclerosis (MS). More than a memoir, it’s a beacon of hope for anyone facing chronic illness. Patti’s story is one of resilience, courage, and the strength she found in redefining herself beyond her diagnosis.

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