Coming to the end of my chemo

It's been a bit of a rollercoaster to say the least. But I can see the light at the end of the tunnel now and wowsers I am so lucky. 

At the beginning of this year been so ill not knowing why

- then having a MRI scan to be told I have terminal advanced cervical cancer stage 4

having to tell my two young sons that I was going to heaven. 

To be then been told 6 weeks later after a biopsies that I was misdiagnosed at I actually have NH lymphoma. 

Treatable!  I am having my last chemo next Wednesday - I was told after my PET scan my third round of chemo that my cancer mass had totally gone but had to completely finish my treatment. 

I am so grateful the outcome so far and fingers crossed the next few months continue with good results too. 

I feel like a totally different person but still got 101 questions to ask about radiotherapy... which is next ... 

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    Hi Channy,

    Welcome to Cancer Chat.

    What a rollercoaster you’ve been on. Fortunately, it sounds as if the final diagnosis has come out well and I sincerely hope that the outcome remains good for you.

    Make a list of those radiotherapy questions and bring it to your next appointment. That way you shouldn't forget any of them.

    Please keep in touch and let us know how you get on. There is always someone here whenever you feel like talking.

    Kind regards,

    Jolamine xx

  • lucky escape ?  let's hope luck continues.  I have just had radiotherapy, no complaints - only that  DIDN'T get the skin burning and the fatigue...

  • Thank you for your reply, hope all is well with you now x 

  • Thank you for your advice, I will be sure to write my questions down before next week x 

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    I think that you will find it helpful to have everything written down.

    Regards,

    Jolamine xx

  • Hi Im new to all of this hope i get it right. I got out of hospital yesterday after chemo.TACE is the type of chemo I had for liver tunours they insert a catherter through the groin directley to the tumour's it's high dose chemo all though I dont know what would be low dose they got 3 last time hopefully they got the last one yesterday. The first time I had it I didnt know what was worse the thought of having cancer or the after efects of chemo Im very positive I've always stayed fit I laugh about the strangest things now! As I said Im new to all of this any advice would be much appreciated.

                                                                                                              Garry xx

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    Hi Gazza,

    I notice that this is your first visit to Cancer Chat, so welcome.

    I am sorry to hear about your diagnosis. When were you first diagnosed and what stage is your cancer? How many chemo have you had altogether and have you had any side-effects? I'm glad to hear that you can laugh, even if about the strangest things - most of us complain of crying for no particular reason.
    Have you got a date yet for further tests to see if the chemo has worked?

    I cared for my Mum before she died of secondaries to liver, lungs brain, bone and breast. I have now had breast cancer myself for 7 years, so I am afraid that I don't have that much advice to give. However, I am sure that someone else who has liver cancer will soon come along to chat to you.

    I have had 2 bouts of breast cancer and I am just relieved when I wake up in my bed each morning. I try not to dwell on what might be the eventual outcome, instead, I try to make the most of each and every day.  If you can keep up the positivity and continue to laugh, you are three quarters of the way there.

    Please keep us informed about how you are getting on. There is always someone here whenever you feel like talking.

    Kind regards,

    Jolamine

  • Hi Jolamine, Sorry its taken so long to get back to you.My cancer is stage one I am lucky in a way because of previous liver problems I have been in the liver program at my local hospital for 7 years so I have regular MRI's and scans so they picked it up earlier than most people they are very small and localized to the liver I was diagnosed 10 months ago I have to have my next scans after I have settled down from the chemo the only side effects have been severe nausea and headaches this is only my second bout of chemo as I said TACE chemo is targeted directly at the tumour through the blood vessel that supplies them depriving them of oxygen and nutrients (embolisation) in that way I'm also lucky because it hasn't spread so because of all the treatment my chances of recovery are higher than most. I am sorry to here that you have had to face 2 bouts of breast cancer my Nan died of breast cancer when I was 15. how do you deal with it? I have wonderful Doctors and especially liver specialist nurses who's instructions I follow to the letter I feel very positive that I will beat this. My biggest worry at the moment is that my family and friends don't know, apart from my wife and son, they are the only people that know I only told my wife and son 7 months after being diagnosed we have a long history of cancer in my family I just don't want my brother or sister to have to go through this again I,m not sure what to do.
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    Hi Gazza,

    I am glad to hear that you have caught it early - there had to be some benefit from being in the liver programme for all these years! I too have a marvellous liver specialist nurse, who takes all my bloods as well as monitoring my liver. I have Lymphoedema in both arms and hands, so all my bloods need to be taken from my feet - not a pleasant thing to have done. It makes such a difference when you have faith in your doctors and nurses.

    I am sorry to hear that you lost your Nan to cancer. This must have been difficult for you when you were only 15? You must be a very strong person if you were able to keep your diagnosis from your wife and son for 7 months. Cancer runs rife in my family too. I told my family immediately and I  have been very open with friends and colleagues.

    I understand that you don't want your siblings to go through another cancer journey. Nobody can tell you what to do. It has to be your decision. Put yourself in their position. If the boot were on the other shoe, and it was one of them who had cancer, how would you feel if they never confided in you?

    Do let us know what you decide to do and, I hope that you come up with the right decision.

    Kind regards,

    Jolamine