Hi, new to the group

FormerMember
FormerMember
  • 8 replies
  • 153 subscribers
  • 621 views

Hi,

My husband was diagnosed with throat cancer, right Vallecula SCC with right neck metastatic disease p16 positive squamous cell carcinoma, in November 2021.  He has finished his chemo and radiotherapy and all things point to it having been successful at treating the cancer, which is fabulous news. We just have his final scan to do and then the results will be in!

At the moment, one of the main problems he is dealing with is a thick catarrh like phlegm at the bottom of his throat, which makes him cough and spit stuff up, or he chokes on it. I will be talking to his oncologist when we see her but I wondered if anyone, who has been through a similar type of cancer, has any insight into how he can deal with this better. As he has virtually no saliva at night, he doesn’t get much sleep and coughing/choking/spitting happens a lot…sleeping, not as much!

He is using artificial saliva, which has helped, but has this improved over time for people, or is he going to be stuck with this forever?

Many thanks,

xx

  • Hi Scooby. I’ve posted similar on another thread 

    Well done on getting through the treatment.

    Yes thick mucous is par for the course. I managed just by steaming over hot water but lots of others got help from a nebuliser. Keeping a vaporiser by the bedside can be useful. Drinking lots of water does thin it down too. If none of these help you could ask your team if they might consider a drug called carbocysteine which can do the trick with some people. The sticky stuff does go. Mine went practically overnight by six weeks but we are all different. 
    i spat into kitchen roll by the bedside a lot and always had a glass of water handy. I got quite adept at sipping it almost in my sleep. 
    The lack of saliva is another problem. Mine has come back slowly and by six months was acceptable. 
    Have a look at my blog. There’s a couple of posts on acupuncture which helped me loads. 
    Chewing xylitol gum stimulates saliva too

    At night I still use xylimelts which keep my mouth moist. They are worth trying. 
    It all takes time I’m afraid. 
    i hope this helps. 

    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
  • has this improved over time for people, or is he going to be stuck with this forever?

    Dani has covered the short term very well Scooby, but from a longer perspective, I'm eight years post treatment now and I'd say my saliva is now as good as it was pre-treatment. That's obviously a way down the road for your husband, and progress is slow at times, but there is light at the end of the tunnel!

    Community Champion Badge

    Metastatic SCC diagnosed 8th October 2013. Modified radical neck dissection November, thirty-five radiotherapy fractions with 2xCisplatin chemo Jan/Feb 2014. Recurrence on larynx diagnosed July 2020 so salvage laryngectomy in September 2020.

    http://mike-o.blogspot.co.uk/

  • FormerMember
    FormerMember in reply to Beesuit

    Thank you Beesuit, I will suggest a nebuliser to my husband, all suggestions are gratefully received. Two hearts

  • FormerMember
    FormerMember in reply to MikeO

    Thank you MikeO, it’s really good to know that it isn’t necessarily going to be permanent, light at the end of the tunnel is all I need! Two hearts

  • Hi scooby 

    This is normal and should improve over time

    Good luck

    Chas

  • FormerMember
    FormerMember in reply to Chicotime

    Hi Chas, thank you, good to hear! Two hearts

  • Hi. I’m Hazel over 3.5 years post radiotherapy for tonsil cancer with several affected lymph nodes.what yiurour husband is going through is normal fir our types of cancer. It doesn’t last forever I found the nebuliser and and humidifier invaluable. It does go as quickly as it came.  The dry mouth ..I found chewing sugar free gum helped and I also had a course of acupuncture. In tge daytime I can cope with the dry mouth niw but at night time I too use xyimelts.

    for niw get him ti drink water I used bottled   water as tap water I found horrible. Water does help with the phlegm.

    Hazel 

    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/

  • FormerMember
    FormerMember in reply to RadioactiveRaz

    Hi Hazel, thank you for your advice, I shall definitely be looking into the nebuliser and humidifier for Paul, anything to help him. I will also show him everyone’s responses as they have been so incredibly encouraging to read! So thank you to everyone who has replied.

    xx