The information on this site is not intended or implied to be a substitute for professional medical advice, diagnosis or treatment. Content within the patient forum is user-generated and has not been reviewed by medical professionals. Other sections of the Melanoma Research Foundation website include information that has been reviewed by medical professionals as appropriate. All medical decisions should be made in consultation with your doctor or other qualified medical professional.

Is “dry mouth” permanent?

Forums General Melanoma Community Is “dry mouth” permanent?

  • Post
    gmschmidt
    Participant
      Hi Everyone,

      My husband is off treatment (for now), after two years of nivolumab. It’s been three months and most the side effects have subsided, which is great. However, the extreme dry mouth and slimmy film in his mouth continues, and hasn’t changed one bit. I’m just wondering if there is anyone else on this forum who dealt with dry mouth and is not longer getting treatment, that could tell me if the dry mouth ever went away.

      Thank you
      Gail

    Viewing 3 reply threads
    • Replies
        Hukill
        Participant
          While on the combo I went 11 weeks with no saliva, even got a prescription for artificial saliva. Nothing I tried worked. I had to carry water everywhere I went and a bottle of salt/baking soda mix water to rinse my mouth due to my breath being horrible. I had to eat very wet food also. After 11 weeks and done with the combo it went away and it has been almost 3 years now. At least once a week my mouth goes dry for several hours and it happens very suddenly.
          lkb
          Participant
            I’m still on immunotherapy (switched from nivo to pembro) and still have dry mouth. The only things that help (temporarily) are wet fruits–baked pears, baked apples, juicy melons.
            tedtell1
            Participant
              Over a year since my last treatment (Opdivo) and my dentist has told me that I still don’t produce saliva the way I should. I don’t notice it much, except when I get up in the morning. It isn’t anywhere near as bad as when I was on the treatment though.
              Ted
              Bubbles
              Participant
                I took nivo for 2 1/2 years and had a great deal of difficulty with “dry mouth”, altered taste, and severe mouth ulcers. Those problems did not resolve immediately upon ending my treatment by any means, but over time they would wax and wane….never becoming as bad as they had been when I was on treatment. It was strange because after a good spell, I would suddenly, for no apparent reason, have “road rash” (small cuts and laceration like lesions) all over my tongue and inner cheeks!! But, all of these issues have gotten better gradually and incidents much less frequent. Hopefully, your husband will start feeling a lot better soon. The best news is that I remain NED for melanoma with my last nivo infusion in June of 2013! celeste
            Viewing 3 reply threads
            • You must be logged in to reply to this topic.
            About the MRF Patient Forum

            The MRF Patient Forum is the oldest and largest online community of people affected by melanoma. It is designed to provide peer support and information to caregivers, patients, family and friends. There is no better place to discuss different parts of your journey with this cancer and find the friends and support resources to make that journey more bearable.

            The information on the forum is open and accessible to everyone. To add a new topic or to post a reply, you must be a registered user. Please note that you will be able to post both topics and replies anonymously even though you are logged in. All posts must abide by MRF posting policies.