Oral cancer

  • 9 replies
  • 73 subscribers
  • 466 views

In late march i was at the dentist because i had found white dots within 5 kins she was doing an email to head and neck dr, i saw dr on the following tues and within the next 4wks i had ct and mri scans, plus biopsy, i was then told yes i had oral cancer over the next month i had meeting with oncology teamsand told i had staging  T4a N1 M0, squamous cell carcinoma of Oral Cavity, Alveolar Ridge.

However i was told because of other issues with my health i.e kidney transplant, and diabetic they would not operate however we went down the route of chemotherapy started it 8wks ago 2 have had 2 treatments, i saw my oncology dr on weds and he is very pleased with the way my cancer is shrinking so he has authorised 2 more treatments befire doing a head and chest ct scan if that shows no issues then he is looking at radiotherapy

Just wonder if anyone else has had this and has any advice 

  • Hi  

    Welcome here but really sorry to see you here. I've been here five years and I can't recall anybody else reporting this type of oral cancer so I did a search for gum cancer and that came up blank too. However, lots of forum members just lurk here without posting so your post might prompt a reply.

    There are folk here who have had induction chemotherapy before radiotherapy for throat cancer, then progressing onto the curative radiation.

    There are similarities in reaction to treatment. Radiotherapy will give you a pretty sore mouth and you might find eating very difficult or impossible. You may be offered a feeding tube.Your oncologist will go through all the side effects and there are a few but nobody gets them all. 

    You have to be in the same position at every treatment so you'll have a mask made which clips to the treatment table. Sounds awful but it's not.

    I have a few details in my blog linked at the bottom of this post.

    Stay with us and we can help you through. You'll have more questions on the way.

    Good luck

    Dani 

    Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019

    I wrote a blog about my cancer. just click on the link below 

    https://todaymycoffeetasteslikechristmasincostarica.com 

    Macmillan Support Line - 0808 808 00 00, 7 days a week between 8am-8pm

    Community Champion badge
  • Good evening Sussexguy, i have not had cancer in specific area and did not have any health issues at the time i cannot comment on that side of things but it is very encouraging to hear that the cancer tumour is shrinking  as it shows the treatment is doing its job, i expect your consultant is making sure that the treatment is continuing to work before comminting to a course of radiotherapy so dont be to alarmed about the radiotherapy . Wishing you all the best with your recovery, take care.

                                                       Chris 

    Its sometimes not easy but its worth it ! 

    Community Champion Badge

  • Hi Sussecguy

    Not sure if my cancer is quite the same as yours but I had a mandibulectomy in 2013 after having an ulcer that would not heal on my gum near one of my teeth. I then had a course of radiotherapy but no chemo. My cancer was caused by lichen planus an inflammatory condition that I had since I was 40. I was 59 when it developed into cancer.

    It is great that the chemo is shrinking your cancer. If you do need radiotherapy this forum is a great place to get advice from those who have walked the walk.

    Sending best wishes for your ongoing treatment.

    Lyn

    Sophie66

  • Thank you very much think mine will be a long road 

  • Yes the road is long but the treatment is worth the outcome. You have to take it a day at a time. The radiotherapy can make you feel like '******' for a while but the end does come. It took me about 3 months to feel that I was back to normal but now am back to enjoying my life. The radiotherapy I had was aimed at my jaw so I did not have the swallowing difficulties that those that have tongue and tonsil cancer have but my mouth got very sore with ulcers. Regular pain relief is vital and your medical team will make sure you have plenty of it. Not everyone gets all the side effects.

    The forum will be a great source of help along the way.

    Lyn

    Sophie66

  • Hi Sussexguy

    Welcome to the group.

    What great news that the Oncologist has shared with you that the tumour is shrinking from.Chemo.

    Sorry to hear about your other health  issues but I’m sure the team you are under will take care of you throughout your treatment plan.

    Your CNS can lease with other medical professionals and they can offer great support . Dont be afraid to ask them any questions or discuss any worries you have .

    The lovely people on here are also a great source of comfort and support .

    All the best for your scans and radiotherapy ( if needed).

    Debbie

  • Thank you for your lovely comment

  • Thank you for you comment

  • Thank you for your reply