The short answer
- Heat brings back old symptoms for a whileA rise in body temperature can make existing symptoms worse for a few hours. The MS Trust says this is not usually caused by new MS damage.
- If cooling down does not help, ring the MS nurseSymptoms that are new, clearly worse, or still there after cooling down need the MS team, and so does a fever.
- Do the hard things in the cool of the morningKeep the hottest hours for rest in the coolest room, and cool the house down again in the evening.
- A carer can take on the cooling and the heavy jobsThey can help with the morning wash, keep drinks coming and watch for a change that needs a phone call.
Carers on PrimeCarers charge £18 to £25 an hour with our fee included, typically £20. Agencies charge £28 to £35 for the same hour.
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.
| Heat flare | Possible relapse | |
|---|---|---|
| What came before | A hot day, a warm bath, exercise, a stuffy room or a temperature. | Nothing that usually brings their symptoms on. |
| Which symptoms | Ones your relative has had before. | New symptoms, or old ones that are clearly worse than usual. |
| After cooling down | Better within a few hours. | No better, and lasting at least 24 hours. |
| What to do | Cool down, drink something cold, rest, and keep a note of it. | Ring the MS nurse or the MS team, and ask the GP to check for an infection. |
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
Keep the sun out during the day
The body
Cool from the outside
Food and drink
Cold, and little and often
Clothes and the bed
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.
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.
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.
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.
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
Plan the week around the forecast
Before the hot spellWhen 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
Keep the cooling going
Through the dayCurtains 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
Notice what changes, and write it down
Every visitWhat 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
Know when to ring someone
Agreed in advanceAgree 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.

