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Ask Nurse Amy: Staying cool and confident this summer

Heat sensitivity is common in MS, but you can still enjoy the warmer months. Planning ahead, using cooling strategies and pacing yourself can make warmer weather much more manageable, so you can continue enjoying activities, barbecues, beach trips and summer events.

ArticlePublished 14 October 2026

Feeling anxious about summer is understandable, especially if you’ve experienced symptoms worsening due to heat in the past. Planning ahead and being prepared can help restore your confidence so you can continue enjoying the warmer months.

Why does hot weather make my MS symptoms and fatigue worse?

Heat sensitivity is common in MS. MS damages the myelin, which is the protective coating around nerves. Even a small rise in body temperature can temporarily make signalling through affected nerves less efficient, and everyday activities may require extra effort.

On top of this, hot nights can disturb sleep, and social activities or changes in routine can also add to fatigue.

This can lead to a temporary worsening of symptoms, including increased fatigue, weakness, balance difficulties, or cognitive symptoms such as ‘brain fog’.

These temporary symptoms are sometimes referred to as a ‘pseudo-relapse’ and do not mean there is new damage or progression of your MS. Symptoms usually improve after you rest and cool down, although this may take longer for some people.

How can I stay active during summer?

What should I consider when socialising?

What are the best ways to keep cool?

It’s often easier to stay cool than to cool down once you’ve become overheated.

Sun safety should be a consideration

Using a broad-spectrum SPF 50+ sunscreen, along with UV-protective clothing, a hat and sunglasses, and seeking shade where possible, can help protect you from harmful UV rays.

Some medications also increase sensitivity to the sun, so check with your pharmacist if you are unsure.

What should I do if my symptoms worsen?

After resting and cooling down, if you have any new or persistent symptoms lasting more than 24-48 hours, you should let your medical team know.

If you experience severe symptoms, such as vision loss, fainting, collapse, significant weakness, or you are unable to safely manage at home, you should seek urgent medical review.

Have questions about managing MS in the heat?

Our MS nurses can discuss your individual circumstances, symptoms and concerns, and help you find practical strategies that work for you. Call the free MS Nurse service on 1800 042 138.

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If you or someone close to you has been diagnosed with a neurological condition, we’re here to support you – both now and throughout your journey.

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