Salivary duct carcinoma

FormerMember
FormerMember
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Has any one opted not to have surgery ?

  • Hi and a very warm welcome to the online community

    Having to make treatment decisions can be very hard and I hope that some of them other members of this group will be along soon to tell you about their experiences.

    In the meantime I'm tagging this groups Community Champions and as they may be able to help you further.

    When you have a minute, it would be really useful if you could pop something about your journey so far into your profile as it really helps others when answering or looking for someone with a similar diagnosis. It also means that you don't have to keep repeating yourself. To do this click on your username and then select 'Profile'. You can amend it at any time and if you're not sure what to write you can take a look at mine by clicking on my username.

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  • Thanks Latchbrook

    Im sorry I should have been here earlier. I did see the post and went away to think about it. 
    As far as I know this is a fairly aggressive tumour and surgery plus radiotherapy are the standard options. 
    so  what aspects of surgery are you worried about? I know there is a danger of facial nerve damage. Have you discussed this with your surgeon? I can’t really suggest much else and a search on this forum reveals few posts about it reflecting the cancer’s rarity. 
    Come back  and give us a little more detail and maybe we can help. 

    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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