First Chemotherapy Session

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Today I had my first chemotherapy session - intravenous 0xaliplatin. I had been feeling anxious about it, but on the day felt much calmer. The nurses were lovely and explained everything. The whole procedure took about 3.5 hours. Not too many side effects as yet, sore & tender arm, tingly fingers and slight nausea. I felt very shaky and emotional when I saw my husband in the waiting area, then my voice went very squeaky and I felt I couldn't breath - fortunately someone, can't remember who, posted about having a squeaky voice the other day so I knew what it was and took some deep breaths which helped. I took the advice to get a hot drink for the journey home, which takes almost one hour. Oh, I've had the 'first bite' pain and also sharp jaw pain when I sneezed!  I start the capecitabine tablets this evening.

The whole experience wasn't anything as stressful as I had imagined - the unknown is always harder to cope with - so I'm feeling a lot better mentally. I am so grateful for all the supportive advice I've read here.

  • Well done . That’s a great start you got off to .

    Its not easy for people starting treatment but I could see mum developing a routine as it went on .

    Now it’s an evening of getting wrapped up and spoilt for you .

    Have a good sleep and glad you have found support here .

    Court 

    Helpline Number 0808 808 0000

  • Thank you, Court. Yes, I am looking after myself. I have a "wheatie" which has helped with my sore arm. 

    My chemotherapy nurse told me to be careful of cold things for 7 days - is that normal? Also, I find that when I wash my hands in hot water, my finger get tingly afterwards - I didn't touch the taps, got hubby to run the water for me! I suppose it is a learning curve.

  • Hi 

    I think she was careful but it certainly was not the same issue as the first few days .

    Hope you had reasonable sleep . L x 

    Helpline Number 0808 808 0000

  • Hi Court, thank you for that. I hope your mum is doing well. If it's not too cheeky, may I ask how old your mum is? I'm 70.

    I didn't sleep too well, but that's not unusual for me at the moment. Perhaps I'll have a nanna nap later!

    Alyson xxx

  • She was 67 -69 when she went through the bulk of her treatment 73 when she had her lung  resection . Managed to get to 80 before it raised its ugly wee head again .

    Not sure what will be potential possible just now . She is currently in hospital but hoping to get home soon and we will build her back up and see her oncologist in the future . However given she was a stage 4 patient back in 2009 we think she has done amazingly well .

    However late 60 early 70 she was full steam ahead with active treatment and I can’t tell you how much quality living , fun , family gatherings and family holidays we packed it . I am so grateful she subjected herself to it all . As she gave us a wonderful happy decade together . 
    She did do a lot of wee naps during the day when on treatment. Her favourite saying was she was listening to her body and doing what it needed .

    Enjoy your nap and here’s to a bright future .

    Court 

    Helpline Number 0808 808 0000

  • What a very difficult time you must all have been through. Your mum sounds amazing, what a remarkable, brave and resilient lady! I'm so glad she just got on with life and those happy memories will stay with you forever.

    I wish your mum all the very best for the future - and will definitely take her advice of listening to your body.

    Take care. 

    A xxx

  • Hi Sopra

    Oxy really is filthy stuff and the nasty effects I found were cumulative. Your Oncologist could reduce the dosage as its based on body volume by say 20 per cent.Thats what I did.

    It worked pro tem for me. From a complete S4 basket case I am scheduled for surgery now because of Capox  x6 snd 5 weeks of chemoradiation.

    If things get impossible then switch to Folfox and a pump. I whined a lot about pain and have been offered a central line and pump but there are no cost free options. 

    Try and suck it up for as long as possible. Your job is to eat well, exercise gently and stay positive.  No point worrying about things you cannot effect. It's treatable not curable. 

    My disease was very extensive at the start with a Tumour marker CEA of 96 at the start but these ghastly therapies can work. So hope for the Ok hand and continue doing the things you enjoy albeit at a reduced level.

  • Hi Anthony

    Thank you for sharing your experience. I am struggling a bit at the moment, but I know I have to keep going with it.

    I hope your surgery goes well. Take care. xxx