The dreaded mask

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When I went to the Radiotherapy planning appointment, I was introduced to my own personal mask. I was far from comfortable in fact I started having nightmares about this mask clamping me down to the machine . I can tell you while that mask will never be my friend I have learned to tolerate the treatment. My initial worry that having COPD I would really struggle laying on my back and having my face covered. The Radiology team at the Christie in Manchester could not have been more helpful. I was given appointments that did not happen to early in the day, which is when my cough was more persistent. Now I am in my second week of Radiotherapy, so far I have had 8 sessions. To be honest it gets easier each session. I hope this post is helpful to anyone awaiting the same treatment. As an afterthought if your hospital has a Maggies I would recommend a visit to see if you like, if only to get a free brew. 

  • The mask was the easy part IMHO by some considerable margin. 
    How long were you kept waiting for your “appointment”?

  • Hi Ricky

    It's heartening to read that things do get easier. It will encourage others so thank you for the update

    Dani 

    Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019

    I BLOGGED MY TREATMENT 

    Macmillan Support Line -  0808 808 00 00 7 days a week between 8am-8pm

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  • Glad they rescheduled for you.  Almost every single one of the RT radiographers we deal with are absolutely brilliant Heart️

    Peter
    See my profile for more details of my convoluted journey
  • I had the Radiotherapy planning meeting one week after meeting the Oncologist that was a Friday, then started Radiotherapy the Monday after.

  • Hiya

    I have just joined the community after having two surgeries for SCC - left lump neck removal and then last Thursday Pandescoscopy and back tongue layer removal.

    Histology report from neck removal showed cancer had gone to a couple of lymph nodes and the tongue layer removal to try and locate primary cancer site.

    Currently in lots of pain still and struggling to eat and drink Cry

    My major worry is having the mask fitted as chlostraphobic and struggled with PET Scan and MRIs I am literary having palpitations as I think about it!!!

    Being feeling a bit low today I was told diagnosis 7th January 2026 as initial thoughts by MDT was a cyst but my consultant wasn't convinced so even the MDT were shocked by results!!!

    I am usually so positive but just dreading the radiotherapy Sob

    Any advice would be really appreciated.

    Nanzo

  • My major worry is having the mask fitted as chlostraphobic and struggled with PET Scan and MRIs I am literary having palpitations as I think about it!!!

    Hi  Honestly if you can get through a head and neck MRI the mask will be a doddle. practice at home lying on the bed with a towel draped over your face. It sounds funny but it works both for the mask fitting and the treatment. It's a tip from Hazel, a mate and a stalwart of the group. I'm sure she will be on soon to say hello.

    For the fitting, but not the planning scan, you can have somebody in with you but truthfully it's not that bad. Just feels like a warn wet flannel on your face. 

    You can ask for sedation which might be useful for your first few RT sessions too

    Ask for eyeholes to be cut....actually don't just ask...insist. Some masks come with pre-cut holes so you might be lucky

    Dani 

    Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019

    I BLOGGED MY TREATMENT 

    Macmillan Support Line -  0808 808 00 00 7 days a week between 8am-8pm

    Community Champion badge
  • Hi Nanzo. I really dreaded this too, as I am claustrophobic, and for what it’s worth this is what helped me the weeks leading up to the treatment.

    I was told I’d be on the table for around 7 minutes in all (only 2 minutes of which was actual treatment). I figured that if I take slow breaths (which is calming in itself) I take about 20 breaths per minute, so that’s about 140 breaths in all whilst on the table. 

    In the weeks leading up to the treatment I trained myself by lying in a nice hot bath with a clock near my feet end, put a wet flannel over my face and slowly start counting my breaths.  When I got to 30 breaths I knew I was nearly a quarter of the way through. When I reached 70 I knew I was half way and was basically counting down. When I reached 140 I knew the team would be in back in the room unclipping me. (And they always were.)

    It might sound weird but it worked for me and after a few sessions I didn’t need to count my breaths any more. I just lay there thinking this is saving my life.

    Wishing you all the very best. M

    ps I also asked for eye holes to be cut out of my mask so I could see what was going on. 

  • Hi  the mask fitting isn’t too bad it’s like a warm towel being put over you honestly the staff are quick and efficient. I had eyehole nose hole snd mouth hole cut out on mine. Picture below 

    you can practise fir the radiotherapy sessions as well I used to lie on my bed close my eyes plus a playlist on and take my head off on a walk or favourite cycle ride I tones them around 12 -15 mins. Once you’ve done the first few you get into a routine. 
    Hazel x

    Hazel aka RadioactiveRaz 

    My blog is www.radioactiveraz.wordpress.com  HPV 16+ tonsil cancer Now  6 years  post treatment. 35 radiotherapy 2 chemo T2N2NM.Happily getting on with living always happy to help

    2 videos I’ve been involved with raising awareness of HNC and HPV cancers 

    https://www.instagram.com/merckhealthcare/reel/DBs8Y0niJ8N/

  • Thank you for sharing this put my mind at rest a little knowing I can request holes!! Glad to hear you are on the other side x

  • Thank you so much for sharing really am appreciating all the advice it's really helping Grin