MS careLiving with MS

Heat sensitivity and MS: why symptoms flare in warm weather

A hot afternoon, a warm bath or a temperature can bring back MS symptoms that were settled at breakfast. It is called heat sensitivity, or Uhthoff's phenomenon. It is not a relapse, and the symptoms ease once the body cools down. This guide explains how to tell the two apart, when to ring the MS nurse, and how to plan a hot day at home.

By James Bowdler, founder of PrimeCarers  ·  Updated September 2026  ·  10 min read · See the hot day plan

A woman in her forties resting in a chair under a tree with a cold drink, her partner nearby, in a shaded garden

Part of our guide to ms care.

Why heat does it

Heat makes existing MS symptoms worse for a few hours

When the body warms up, even a little, symptoms a person already has can come back or get worse. The effect is named after Wilhelm Uhthoff, an eye specialist who noticed it in 1890. It passes as the body cools.

6 in 10

people with MS report heat sensitivity, according to the MS Trust.

MS Trust, Heat sensitivity and MS (Uhthoff's phenomenon).

The MS Trust's page on heat sensitivity describes it as a temporary worsening of symptoms in response to a rise in temperature. It says the extra symptoms are not usually caused by new MS damage, and that once body temperature returns to normal they should settle within a few hours. The symptoms it lists are the ones a person already knows: fatigue, blurred vision, numbness and tingling, weakness, poor balance, and trouble concentrating.

The same page lists what can set it off:

  • warm weather, and humid weather most of all
  • a room that is overheated or crowded, including a house with the heating turned up in winter
  • warm baths and showers, saunas and steam rooms
  • exercise, because it raises the body's core temperature
  • stress or anxiety
  • a fever or an infection
  • hormonal changes around periods and the menopause

This matters for the family because the change can look alarming. Your relative may be fine at breakfast, and by three o'clock their legs are weak, their vision is blurred and they are too tired to talk. Knowing it is heat, and that it usually passes, makes a hot afternoon less frightening. MS care at home sets out how the rest of the illness shapes a week.

Flare or relapse

How to tell a heat flare from a relapse, and when to ring the MS nurse

A heat flare and a relapse can look alike on the day. Three questions separate them: what came before it, whether the symptoms are new, and whether they ease when your relative cools down.

What came before

Heat flare
A hot day, a warm bath, exercise, a stuffy room or a temperature.
Possible relapse
Nothing that usually brings their symptoms on.

Which symptoms

Heat flare
Ones your relative has had before.
Possible relapse
New symptoms, or old ones that are clearly worse than usual.

After cooling down

Heat flare
Better within a few hours.
Possible relapse
No better, and lasting at least 24 hours.

What to do

Heat flare
Cool down, drink something cold, rest, and keep a note of it.
Possible relapse
Ring the MS nurse or the MS team, and ask the GP to check for an infection.

From the MS Trust pages on temperature sensitivity and on MS relapses. If you are unsure which it is, the MS Trust's advice is to contact the GP or the MS team.

The MS Trust's page on temperature sensitivity says to contact the GP or MS team if heat symptoms are new or much worse, last longer than they usually do, do not improve after cooling, or come with signs of infection or a fever. Its page on relapses explains that a relapse means symptoms lasting at least 24 hours with no other explanation, such as an infection or heat. It also says the GP practice can test for a urine infection, which can make MS symptoms worse for a while, and UTIs and sudden confusion covers what to look for. If it does turn out to be a relapse, MS relapse cover at short notice explains how to get extra help at home quickly.

Keeping cool

Keeping the house and the person cool

The MS Trust and the NHS give much the same advice. Keep the heat out of the rooms during the day and keep the body cool from the outside, while drinking enough.

The rooms

Close the windows, curtains and blinds during the day, and open them at night when it is cooler outside. Blackout curtains help on the sunny side. The NHS says an electric fan helps while the temperature is below 35 degrees.

Keep the sun out during the day

The body

A cool shower rather than a warm bath. A plant mister of iced tap water for the face and wrists, or cold water run over the hands and feet. Cooling scarves, vests, hats and wristbands can be worn through the day.

Cool from the outside

Food and drink

Iced water, ice lollies, and foods with plenty of water in them such as cucumber, watermelon and berries. The NHS advises avoiding alcohol, caffeine and hot drinks in a heatwave.

Cold, and little and often

Clothes and the bed

Loose, light clothes in cotton or linen. At night, breathable bedding, a cooling pillow or a gel pad on top of the usual one, and nothing made of memory foam.

Light and breathable

Drinking enough in the heat can worry someone whose bladder is already a problem, and the temptation is to drink less to avoid getting caught out. The MS Trust's page on bladder problems advises against cutting down. It gives at least 1.5 litres in 24 hours as the general guide, and explains that too little fluid makes urine more concentrated, which irritates the bladder and makes infection more likely. Caffeine, alcohol and fizzy drinks can irritate the bladder too. Bladder and bowel care with MS covers what a continence service can do. The NHS advice on the rooms, fans and drinks is on its page about coping in hot weather, and hot weather and heatwaves covers the wider advice for older people.

The hot day plan

Planning a hot day around the cooler hours

The simplest change is to move the effort to the cool of the morning, spend the hottest hours still and cool, and bring the house back down in the evening. Here is one hot day in three parts.

  1. Morning

    Until about 11am

    The coolest part of the day, so the effort goes here.

    What to plan for

    Washing and dressing, appointments, the shopping and any exercise. Anything that needs the most energy is best done before the heat builds.

    Keeping cool

    Open the windows early while the air outside is cooler. Close them, with the curtains and blinds, before the sun comes round to that side of the house. A cool shower rather than a warm bath.

    Where a carer helps: Helps with the shower and dressing so they are finished early, closes the curtains, and puts a jug of water in the fridge.

  2. Afternoon

    11am to 3pm, and after

    The hottest hours. The NHS advises staying out of the heat between 11am and 3pm.

    What to plan for

    Indoors in the coolest room, with rest planned in rather than waited for. Light jobs done sitting down, and a cold lunch rather than a hot one.

    Keeping cool

    A fan while the room is below 35 degrees. Cold drinks through the afternoon, a plant mister of iced water for the face and wrists, and a cooling scarf or vest. Loose, light clothes.

    Where a carer helps: Keeps the cold drinks coming, walks alongside on the way to the toilet if balance is worse, and notices when symptoms are building.

  3. Evening

    From about 6pm

    Cooling the house down for the night.

    What to plan for

    A short walk or time in the garden once the sun is lower, a light meal, and the bed made ready before tiredness sets in.

    Keeping cool

    Windows open once it is cooler outside than in. Cotton or linen bedding, a cooling pillow or gel pad, and a lukewarm shower before bed.

    Where a carer helps: Opens up the house, changes the bedding for something lighter, and writes down any symptom that has not settled since the afternoon.

Cooling steps are from the MS Trust and the NHS heatwave advice. The times are a guide: on the hottest days the morning is shorter, and a house that holds the heat may need the curtains closed earlier.

Fatigue is the first symptom on the MS Trust's list of those that heat makes worse, so a hot day needs more pacing than a cool one. MS fatigue and managed days explains how pacing works and why a rest planned before an effort helps more than one taken after it. On a hot day the same rule applies, with the rests moved into the hottest hours.

Poor balance is on the same list. If your relative's balance gets worse in the heat, keep walking in the hot hours to short, familiar routes inside the house. A perching stool in the kitchen, a shower seat, and a walking aid kept where it is needed all make the hot hours safer. Mobility aids and the home with MS covers what to ask for and who pays.

Travel and holidaysSection titled Travel%20and%20holidays

The MS Trust's guide to holidays and MS suggests choosing a time and a place with a climate that suits your relative. It also suggests keeping medication in hand luggage in its original packaging, with a copy of the prescription. If the room temperature is likely to be above 25 degrees, it suggests asking the travel company about a fridge for any medication that needs one. It also warns that standard travel insurance is unlikely to cover mobility aids. If a carer's help would make the trip possible, can you take a carer on holiday with you explains how that is arranged.

How a carer helps

What a carer can do on hot days

A carer cannot stop the heat from affecting MS. What they can do is take on the jobs that cost the most in warm weather, keep the cooling going through the day, and notice when something has changed.

  1. 1

    Plan the week around the forecast

    Before the hot spell
    When hot weather is coming, agree with your carer to move the shower, the shopping and any appointments into the mornings, and keep the afternoons free for rest.
  2. 2

    Keep the cooling going

    Through the day
    Curtains closed before the sun comes round, the fan on, cold drinks refilled, a cooling scarf or vest on, and the windows opened again in the evening.
  3. 3

    Notice what changes, and write it down

    Every visit
    What time the symptoms came on, what came before, and whether they eased once your relative cooled down. That note is what the MS nurse will ask for.
  4. 4

    Know when to ring someone

    Agreed in advance
    Agree with the family who the carer calls, and when. New symptoms, symptoms that do not settle, a fever or signs of heat exhaustion all mean a phone call rather than waiting.

Hourly visits from carers on PrimeCarers cost £18 to £25 an hour with our fee included, against £28 to £35 an hour through an agency. An hour each morning through a week of hot weather is seven hours, which comes to £126 to £175 on PrimeCarers. If your relative with MS would like help on hot and tiring days, you can search for carers near you and compare their rates.

Carers on PrimeCarers are self-employed people you find, interview and book directly. We are an introductory service, not an agency or a care provider, so we do not provide or manage care. Before a carer appears, we check their identity and right to work, run an enhanced DBS check (or PVG in Scotland, Access NI in Northern Ireland) issued within the last 18 months, and interview them online. Every visit booked through PrimeCarers is insured, either by the carer's own policy or by cover we arrange where they do not hold one. We do not check qualifications, training or references. What a carer says about their MS experience is their own account on their profile, so ask them about it when you speak to them.

Questions

Questions about heat and MS

Usually it does not. The MS Trust says the extra symptoms brought on by heat are not usually caused by new MS damage, and should settle within a few hours of cooling down. If symptoms are new, clearly worse, or do not ease after cooling, ring the MS nurse or the GP.

The MS Trust says they should improve within a few hours once body temperature is back to normal. A relapse lasts at least 24 hours and does not ease with cooling. If you are not sure which it is, contact the MS team.

For someone with heat sensitivity, a warm bath is one of the common triggers, along with warm showers, saunas and steam rooms. A cool or lukewarm shower does the same job without raising body temperature, and a shower seat makes it less tiring.

No. The MS Trust advises against cutting down on fluids, because concentrated urine irritates the bladder and makes infection more likely. It gives at least 1.5 litres a day as a general guide. The MS nurse or the continence service can help if the bladder is making this hard.

For some people it is. The MS Trust says around 15 in 100 people with MS report cold sensitivity, which is much less common than sensitivity to heat. Its page on cold sensitivity and MS explains what helps.

If you need help at home

Start with our guide to ms care

Support that flexes with relapses. What it costs, what a carer does day to day, and how to hire one directly.

Carers near you

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