Hi. Has anyone got any advice on how to deal with excessive saliva? This is a new symptom for my husband. We are still waiting for a date for the chemo and immunotherapy to start. Hopefully will be in the new year. Many thanks folks
This is a really horrible ! I never found a way to deal with it i had to make sure I always had a bag with me and it didn’t always give you much notice ! But after my second cycle of chemo the tumour had shrunk and I could eat and the collection of saliva stopped it was such a relief !! Tricia
Thank you for taking the time to answer my query.
He’s having a bad day today and is struggling with the saliva. Cannot even get him to drink the Fortisips, just sips of water.
Yes all I could have was sips of water so I had a jej feeding tube it’s not fun for the both of you is he on a curative pathway ?
He will be on pallative treatment, as unfortunately it has spread to other parts. Hoping to hear today for a start date. Feel in limbo and helpless. They said the treatment (if he can tolerate it) will help and should strink the tumour. So trying to stay positive x
Yes the waiting is dreadful once you have a plan and the treatment starts hopefully the wallpaper paste regurgitation as we call it will stop and he will be able to eat more !
Sorry to be a pain. When you had the tube fitted for feeding is it done as a day patient? My husband is scared to go into hospital, as he was admitted before Christmas and it really upset him x
Well I was in for a month being fed by a picc line while they did all my scans and tests ! I had my jej tube fitted when I had my laparoscopy then I was in a couple of days after that to teach me to use the pump so I guess he might have to stay in to learn how to use it but I’m not sure ! Someone on here is sure to know where in the country are you as some hospitals prefer to fit NG tubes through the nose !!
Hi
I had the feeding tube fitted when I had the laparoscopy. This was due to be as a day patient but due to a complication I had to stay in longer. As it was only fitted as a precaution at that stage I was not shown how to use it until after my operation a few months later but that only took a few minutes.
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