Tongue Cancer - Diagnosed two days ago

Hi, I am a 32 year old single mum to my two year old daughter and I found out two days ago that I have tongue cancer.  I'm waiting for an appointment for an MRI scan and a CT scan which should hopefully be within the next few days and this can find out if the cancer has spread.  I then have to have an appointment to discuss a treatment plan but I have already been told that this will involve cutting out the lump in my tongue and a neck dissection to remove Lymph nodes.

It's all such a lot to take in and I'm trying to come to terms with the fact that in a few weeks time my life will never be the same again.  I have read some horrific stories about what I have to come and I am willing to face any of it so long as I stay alive for the sake of my daughter.  I have only told my parents and one friend so far, no piont telling everyone until I have more facts after the scans but I'm concerned at how far the cancer could have spread.  I have had this painful lump on my tongue for six months but the doctors kept giving me prescripotions for other things which has delayed diagnisis.  I have also had pain in my throat and more recently I've noticed ear ache and jaw ache and neck pain.  I'm trying to stay positive until I know more information from the scans but I know I will crumble if it has spread beyond repair.

From reading stories from others on here and other websites, I'm a little confused that I haven't yet been told what stage the cancer is at.  Isn't that something that could be identified from my biopsy?  How could the doctor be so sure that I will need a neck dissection before knowing what stage it's at?

None of this has come of much of a surprise.  I googled my symptoms of a persistent ulcer back in April, before I first went to the doctor and was alarmed to see the word "cancer" everywhere I looked.  I had all the symptoms but was just hoping I was wrong.  The first two doctors I saw about this reassured me that it was nothing more sinister than an ulcer, which put my mind at rest a little, how wrong were they?!  I am just glad that I stayed persistent and kept going back to the doctor about it.  I don't think they treated it as an urgency as I don't fit in with the usual risk factors, I've never smoked, I hardly drink and I'm not in the right age bracket.  I'm now feeling annoyed at the waiting game.  I want to know when the scan will be.

It helps to come on here and read other threads but I still don't think it has fully sunk in yet but when it does, positivity for the sake of my little girl will just have to get me through.  I would love to keep hearing stories from others or any advice would be greatly received.

Nicola xx

Parents
  • Hi Nicola.

    It seems I am in a similar boat to you, I delayed going to the gp for a month as I have had tonsiliis a lot so tried all the thing I normally do, then the gp tried strong anti biotics but as soon as I knew they were not working I went back.

    As I said to her a sore throat should not last for 6 weeks so within 2 weeks I had an ENT appointment.

    Things moved fairly fast then, they booked me into a onestop clinic for neck lumps(idea was to be seeen by everyone in one visit and be told what was wrong on the day) but also a ct and surgery to put a camera down and take samples. by the time i went to the clinic i had already had the ct scan (the day before) and a date for surgery(biopsy) I was only in the clinic a few min as they told me about the mass on the ct and needed the samples and MRI to know more. at no time has anyone told me in the way your gp has, it seems bad untill the have formulated a plan as it seems to me not all are the same. I am ecpecting a combination of chemo r/t and surgery.

    I have only told one other person apart from my wife as timings are not good and untill I have answers it will just be harder. 

    Seems like a heavy burdon at the moment.

    Ken.

  • Hi all how are we all doing?

    sorry not been around but it's been crazy at work

    welcome aboard all you new peeps I know you prefer not to be here but this is a great place to be if you are in our club

    mutant of which you are not I had throat cancer I got away with not having surgery and am now 7 months post treatment and very much on the mend although I have still got a way to go to get back to what I was

    i diarised my experience on my blog page so it might give you some idea about what you are about to go through gammaraygary.wordpress.com/about/

    so what's doing all looking forward to meeting you all in AprilApril

  • Hi Ken

    Sounds like your treatment has started and so you have a bit of a rocky road ahead of you.  Good to see that your sense of humour hasn't deserted you despite what life has thrown at you - try and hang onto that!

    As you will see from Simon's post above, this site is great for helping you through the treatment.  It will be tough, but you will get through it.  So come on here to ask questions, have a good moan and know that you will be listened to by others who have 'been there'.  

    Good luck, and keep in touch.

    Irene

  • Sorry to interrupt the thread, but as I'm not able to PM I wanted to ask if Guzzle posts in here, could you take a look at the fundraising section? We are doing the 'Thunder Run' in July to raise awareness for Head & Neck cancer, and as I know you are a keen runner it'd be great to get you involved.

    If anyone else is interested please feel free to check it out too!

    All the best to everyone in their battles

    Leo

  • Hi Leo

    Just to let you know that I've spoken to Gary (Guzzle) and he has already committed to doing the Thunder Run, which is great news!  

    Best of luck

    Irene

  • Hi Everyone 

    I have spoken before but I was just reading your comments about chocolate and I was pleased to read I'm not the only one who struggles with it. My cancer and treatment was nearly the same throughout as Nic but I kept my teeth. I was diagnosed in Dec 2013 and now on three monthly checkups ( hi Nic, I've followed all your story) Chocolate sticks all around my mouth and becomes a mass of gloopy mess which I cannot get rid of without a drink! It tastes like pepper and burns my mouth after a few seconds so I avoid( still love the smell though) The other things I've never been able to eat is fruit which I loved. I tend to make smoothies now but mainly Banana . Im down in Canterbury in Kent if anybody comes this way? This site is such a comfort to me as it has helped me to accept that I'm just going through the normal process of post RT/ Chemo treatment for head and neck cancer. I have worriies  that you have all been chatting about which had mostly answered and put my mind at rest many times so thank you guys for posting.

    All my best wishes and admiration to everyone who has been on this journey 

    God bless everybody with heathy futures 

    Carol xxx

  • Carol

    good to hear from you and glad it's going well for you

    ok so we miss chocolate, I can accept that one and to be honest I have lost the enjoyment of it .... and it hurts so a good reason to stay off the stuff

    i hope you have had a good Christmas and that 2017 holds even greater things for you

    keep us all updated

     

    vat h

  • Your so right Vatch keep well. 

    Happy New Year to you too and every one else on this site! 

    My very best wishes

    Carol 

     

  • Just wanted to post a pic of some of us from this thread. We had a meet up in Liverpool at the weekend which was our second meeting since we all met on this chat forum a few years ago.

    We all came from different parts of the country and it was great to see everyone again and find out how we are doing with life after cancer. Hopefully this will give some inspiration to those of you who are fighting the fight right now. 

  • Dear all

    we all came together with a common goal, we are all achieving that goal and try to help others through it

    great to see you all again

    xx

  • I'd have loved to have met you all but I'm in Canterbury which is a long way from Liverpool. Glad you had fun x

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