Saliva and dry mouth: Head and neck cancer and treatments
Many of us have this problem. Three years after RT and lots of talks by oncologists at our meetings and I'm still learning new details about this side effect. Some people have no saliva for life because their glands have been wrecked by the treatment, some recover some function as late as 2 years after (is that right?). Most people though have to manage a more or less dry mouth with constant to frequent sips of water or gels and sprays.< r />Even worse is what lack of saliva does to your teeth. I've learnt that normal saliva is continually building up the teeth and that without it we are in danger of rampant dental decay without extra fluoride treatment or heroic effects to keep out mouth acid neutral.< r />How do other manage this problem? What tips do you have?
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My husband had his first round ot RT in the fall of 2015 at Mayo jville. Before treatment began he was sent to a dentist to be fitted for fluoride trays, with directions to use them every day. He has since had two more rounds of RT. He is not compliant with the daily floruide, but probably 2 x week. I make an appt with our family dentist every six months. (Give him 24 hrs notice, so he can't back out)
He tried a new product called SalivaMax rinse which showed promise, but after a couple of weeks it gave a metallic taste and he stopped using it. Maybe it would help someone else. It is prescription: http://www.forwardscience.com/salivamax
@jeffk @lisa_sj99 @jtw96 @mrsjhagen18 @sylviapf @lzzie @loli @karly @trudivo @angelag @ssimons @deborahe @gaybinator @emmur16 @merryinman0811 @udderplace @carebear Hi folks. I still have my training wheels and forgot to tag people who might be interested in this topic.