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Beginner 4 min read

Wigs, scarves, or nothing at all: choosing during hair loss

NCI lists wigs, scarves, turbans and hats among the ways people cope with treatment-related hair loss, and notes some choose to cut or shave their hair first.

NCI source:NCI last reviewed 2020-01-15

Review status: AI-assisted, source checked. Not reviewed by a clinician. How we check pages

The short answer

There is no right answer here — only what feels bearable to you. NCI lists wigs, scarves, turbans and hats as options, notes that some people cut their hair short or shave before treatment, and advises protecting the scalp from the sun with sunscreen and headwear.

  • NCI names wigs, scarves, turbans and hats among ways to cover the head during hair loss.

  • Some people choose to cut their hair short or shave before treatment starts.

  • NCI advises using sunscreen and protective headwear outdoors, because the scalp is exposed.

  • After chemotherapy, NCI says hair often grows back in 2 to 3 months once treatment has ended.

Choose how you want to read this

The whole article, with every detail and caution.

Three legitimate answers

Some people wear a wig every day and would not answer the door without it. Some rotate a drawer full of scarves. Some walk out bald on day one and never cover their head again.

All three are correct. NCI lists head coverings such as wigs, scarves, turbans and hats as options, not requirements. What follows is meant to help you work out which of these fits you, rather than to point you at one.

Getting ahead of it

Hair loss can be hard to face. NCI notes that some people cut their hair short to make it easier to deal with when it starts to fall out. Others shave their heads. The appeal for many is control over when it happens.

Others cannot face pre-empting it and would rather it happen in its own time. That is equally reasonable.

There is no version of this that is braver than the others.

If you want a wig

Practical points worth knowing:

  • NCI suggests buying a wig while you still have hair, so you can match its color to your own
  • Some people choose something close to their own hair, others treat it as a chance to try something different entirely
  • Comfort matters as much as appearance, since a wig that is hot or itchy will not get worn
  • Ask your center whether they have a wig service, a lending scheme or a local charity contact

NCI's page does not address insurance coverage for wigs, so ask your own plan directly. It is worth asking rather than assuming either way.

If you prefer scarves and hats

Scarves, turbans and hats appear on NCI's list alongside wigs. Many people find them lighter and quicker to put on than a wig. NCI suggests choosing a comfortable scarf or hat that you enjoy and that keeps your head warm.

Soft fabrics are kinder to a scalp that may be sensitive. Having several means not thinking about it. And there is no rule against wearing a hat indoors.

If you go without

Plenty of people find covering up more uncomfortable than being bald — physically or emotionally. Going without is a real option.

One genuine piece of care goes with it. NCI advises applying sunscreen and wearing protective headwear outdoors, because an uncovered scalp is exposed to the sun. This applies whichever choice you make, whenever your head is uncovered.

NCI also recommends gentle handling of whatever hair remains: a soft-bristled brush, mild shampoo, and avoiding heat styling tools.

Mixing it up

Most people do not settle on one answer. A wig for work and a bare head at home. A scarf for the school run and nothing on the sofa. A hat when the weather is cold and no covering at all in summer.

You are allowed to change your mind daily, and you are allowed to change it because of who is going to be in the room.

The feelings that come with it

NCI is straightforward that many people experience anger, depression or embarrassment about losing their hair. It suggests connecting with others going through similar experiences, and talking openly with family, as sources of support. It also points to the Look Good…Feel Better program.

Hair loss is often the point at which an illness that was private becomes visible to everyone. That is a real change, not a superficial one, and it is a legitimate thing to raise with your team or a counselor.

What comes back

NCI says that after chemotherapy, hair often grows back in 2 to 3 months once treatment has ended. After radiation therapy, it says hair often grows back in 3 to 6 months, though higher doses can mean permanent thinning or no regrowth in the treated area.

Expect the return to be its own adjustment. NCI notes that new hair may be very fine at first, and can come in curlier, straighter or a different color — which catches many people by surprise, and is a reason not to give the wig away too quickly.

A woman with a shaved head looks in a mirror while buttoning her collar.

Common questions

Should I get a wig before treatment starts?

Many people prefer to sort head coverings in advance. NCI suggests buying a wig while you still have hair so you can match its color, and notes that some people cut their hair short or shave their head.

Is it fine to go without anything?

Yes. NCI lists coverings as options, not requirements. If you do go without, NCI advises sunscreen and protective headwear outdoors.

Will my hair grow back?

After chemotherapy, NCI says hair often grows back in 2 to 3 months after treatment has ended. After radiation therapy it says hair often grows back in 3 to 6 months, and higher doses may cause permanent thinning or no regrowth in the treated area.

Why does the new hair look different?

NCI notes that new growth may be fine at first and can differ in texture or shade before returning to normal.

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Sources last checked: 2026-10-02 what this meansLast updated: 2026-08-11Next planned review: 2027-08-11

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Cancer Explained does not originate medical claims. Every page restates guidance already published by the National Cancer Institute, the CDC, the USPSTF and the FDA, in plain language, with the source cited so you can check the original yourself. AI does the translating and organizing; automated checks test claims, citations, clarity and safety before anything publishes, and this is translation and navigation, not clinical judgment. Nothing here is personal medical advice, and no page can account for your particular situation.

Editorial status: Source checked — This page was written with AI assistance and then compared with the sources listed on it, looking for statements those sources do not back up. That check is not a sentence-by-sentence record and can miss errors. It is not a medical review, and it does not confirm the page is complete or right for your situation.

Human medical review: not completed. Pages here are not signed off by a clinician before they publish. That is not an oversight we are quietly working around: we restate published guidance and cite it, so the authority belongs to the source rather than to us, and every page names where its claims come from — you can verify us instead of trusting us. Where a volunteer clinician has reviewed a page, their name and credentials appear on it; where no name appears, no clinician has checked it. We are glad to have reviewers and are recruiting them, and we do not hold pages back waiting for one. Use this site to understand your situation and to ask better questions of the people treating you.

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