Sharing scalp cooling experiences

6 minute read time.
Sharing scalp cooling experiences

There’s no one size fits all when it comes to cancer treatment and dealing with side effects. Although there can be common side effects such as hair loss, sickness and fatigue, not everyone will experience them.

Hair loss seems to be a side effect that many people worry about when having chemotherapy treatment and the use of a scalp cooling system (also referred to as the cold cap) may have been mentioned to you.

If you’re wanting to hear from those who have used the scalp cooling system (cold cap), or are curious about what scalp cooling is, then this blog has what you are looking for.

Here on the Online Community we often see questions like the following posted on the site. If you have a similar question, why not start a discussion in our Community groups or post a question in the Ask an expert section

“Did anyone opt for cooling caps and is there evidence that they work? I would be interested in hearing anyone’s experiences. Hair loss is the most upsetting bit at the moment for me. I am interested in trying cool caps but don't want to feel that it is for no point and it will come out anyway. If you have used them- what’s the actual procedure? I will obviously ask at my appt but just trying to prepare the best I can.”
Community member, Womb (uterus) cancer forum

“Hi has anyone else tried the scalp cooling before Chemo and does it work?”
Community member, New to the community forum

“Hi, just wondering how you go about getting a cold cap to help with hair loss?  I've had my 2nd round and it's coming out extremely fast now.”
Community member, Ask an Expert section

Green cold cap on a person's head with them looking away from the cameraWhat is scalp cooling (cold cap)?

Scalp cooling tends to be a preventative method of stopping hair loss during cancer treatment. There’s more information about what the Cold cap is on the information pages on the Macmillan website. You may want to read the ‘Reducing hair loss during chemotherapy’ blog written by one of our content developers here at Macmillan.

Don’t forget you can also contact the Nurses and support teams on the Macmillan Support Line if you have questions about scalp cooling or coping with hair loss. They’re there to help every day from 8am to 8pm when you call 0808 808 00 00, send an email or start a live webchat during the opening hours.

Why not look at some of the questions already posted in our Ask a Nurse section like this one here. You’re welcome to ask a question of your own if you would like more information or guidance on your situation.

There’s also some tips for hair loss towards the bottom of the page if you’re looking for some additional guidance.

Community member’s experiences and thoughts

Below are some of the experiences that have been shared with others in our Community groups about using scalp cooling. Please remember that everyone is different and members are speaking from their own personal experience.

“I've just finished my chemo and managed to keep a lot of my hair using the cold cap. I found I got a bit paranoid about my hair falling out as I went along. I cut it short before starting treatment. The advice to get through the first 15 mins of cold capping worked for me - I stopped noticing it after that. It is a bit uncomfortable, but I would say try it and see how you get on.”
Community member, Breast cancer forum

“On my cycle a different nurse put on a smaller cap and I remember I kept touching the top of the cap and pushing it down to make contact. I lost a lot of hair and maybe it's because the cap didn't fit snugly enough. I also know of a younger lady has used the Cold cap, she also lost some hair around hairline due to cap not making good contact, she had long hair and was advised to get it cut to a long bob otherwise too much hair needs to be squeezed under the cap and again contact won't be as good.

It's very very cold, painfully cold for the first 20 minutes but bear with it as it doesn't last long and you will get used to it.”
Community member, Womb (uterus) cancer forum

“I didn’t find it too bad at all, as others have said after the first 10 mins or so you stop feeling it.  It did make me very cold, the nurses would give me a heat pad to help keep me warm! So do take a warm cardi or blanket with you even though we’re getting into summer now.

it worked very well for me.  I shed throughout from about 2 weeks after the first dose.  But I kept around 70% of my hair I’d say, just a bit thin on top and a wide parting by the end.  By about 6 weeks post chemo you couldn’t tell as the regrowth covers the scalp, and now my eyebrows and eyelashes have come back I’m feeling I look much more like myself again.  So I’d recommend giving it a go and see how you get on.”
Community member, Breast cancer forum

Deciding to have scalp cooling is a personal choice and something to be discussed with your health care team. Hopefully the experiences above can offer some guidance and reassurance if that’s what you were looking for.

If you’ve decided to not have scalp cooling during your chemotherapy treatment like the following members have, then you may be looking for some hair care guidance. Towards the bottom of the page, there’s some resources you may find helpful.

“I choose not to cold cap due to the next weekly chemo I couldn't face bring at the hospital for an extra 3 hours.”
Community member, Breast cancer forum

“Hi my sister is due to start chemo soon (just had mastectomy and lymph nodes out), she's not going to use the cold cap as she already gets migraines, so we expect her to lose her hair. I said I'd look into options for her as she's got enough to get her head around with chemo treatment plans etc.”
Community member, Breast cancer forum

If you are experiencing hair loss at the moment, you may find the Macmillan Information pages about this helpful. It covers different topics that may be concerning you such as how to get a wig, emotional effects of losing your hair and practical advice.

·       Let’s talk about cancer and hair loss- Community news blog

·       Coping with hair loss- information booklet

·       Post-surgical menopause, chemotherapy, and hair loss- Sunita’s blog

·       Hair loss: information and guidance - Community news blog

Have you used the cold cap and want to share your experience with others? Use the comment box below to share how you're coping with this. Also if you have any hair loss tips, please share them for an upcoming blog we are planning to feature. 

Anonymous
  • I started chemo in June 2023 and opted to use a cool cap. Unlike the comments I have read hear I did not find the cold uncomfortable at anytime. My first session though the nurse used a medium cap on me and not all areas of my scalp was coming in contact with the cap. I kept trying to push the top down to make contact. After about 10 days a small handful of hair came out in my hand after washing it. This hair came from the crown, temples and side and front hairline, the parts the cap hadn’t been in contact. From the second session onwards I had a small size cap which was the rightsize for me and made contact all over my scalp. My hair did thin and go from grey to white. I completed chemo in November 2023. My hair didn’t start to grow back until my chemo finished. Now my hair is growing back where it fell out and these areas seem to be slightly thicker! Also on one side and at the back on the same side the ends have gone a bit curly and the other side is a bit wavy! My hairdresser has been very good throughout, fitting me in to have bits trimmed when I have felt I needed it. He is now telling me my hair is in very good condition, and that it was all through my chemo, and that he loves the colour - white. I am 75 so white is the expected colour! I have, and still am, using Simple shampoo and conditioner. My hair is definitely drier than it was pre cancer.  During the time I was using the cool cap the time I had to wear it for at the end of treatment increased from 30 minutes at the start to 1 hour at the finish. Each chemo session I had 2 different infusions, and by the last treatments I was spending  6 - 7 hours in hospital. It was a very long day! It gave me a lot of back ache. Would I use a cool cap again if I had to - yes, definitely but the cool cap is not for everybody. If you are not sure if it is for you, give it a try and if you can’t cope with it just remove it and tell the nurses you no longer want to use it. Nobody will judge you, it’s your prerogative.

  • Hi ,

    Thank you so much for sharing your experience here. You're absolutely right about it being a personal choice, and it's a great reminder that if you do try it, you can always discontinue using the cap should you find it too uncomfortable.

    It sounds like you tolerated the cap very well, though. It's always good to hear about the positive outcomes alongside the many challenges, so thanks again for sharing. Slight smile

    Matthew
    Macmillan Online Community Team

  • I have been having weekly chemotherapy for breast cancer and decided to try the cold cap. I have found it do-able and recommend people try it . So far so good. 5 sessions in. 
    I have also tried some pre-loved wigs at the Force Charity. This also gave me confidence and a measure of control over the process! 

  • Hi Flower lover,

    Thank you for sharing your personal experiences with using the cold cap, I am sure those who read this blog will find it helpful to hear how you found using it.

    It’s good to hear you have found support with finding a wig and have posted in the Triple negative breast cancer forum to connect with others who share similar experiences. 

    Please remember that alongside accessing peer to peer support from our Community groups, the Macmillan Support Line has specialist teams who are also there to support you. Sometimes it can help to talk things through with someone who’s there to listen. They’re available 7 days a week, 8am-8pm on freephone 0808 808 00 00email or live webchat.

    If you have any questions or need any help using the site, you can contact the Online Community team every day by sending a private message to the Moderator account, or by emailing community@macmillan.org.uk.

    Best wishes, 

    Megan
    Macmillan's Online Community team