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serenity11's avatar
13 years ago

Final chemo DONE!

I have my final chemo swishing around my body as I type this blog. Final chemo - done. Happy dance for me.

I expect the dex zing, the lack of sleep, foggy eyes, aching muscles, and I should forget the purging poohs, will all happen yet again in the next week and I will tick them off one by one as they pass. As the symptoms ease I write in my journal in my “chemo handwriting” and record their disappearance as a celebration.  If ever I publish my journal I think I will call it “ The day my life became about shit”.  Because it does in so many ways and on so many levels :P

Woke up with a headache, my second headache ever on chemo, “this bodes well I think (not)”. The first one was a knockout due to hormones and chemo I was told, this one due to muscle tightness I think. Off to chemo. Climb into "The Chair" for the last time. Make myself comfy with the pillow and blanket. Uncover the PICC line for the last time, uncover the good arm for blood and obs. And would you believe it, the PICC line behaves and gives the blood samples! Hasn't done this for the last 5 weeks but today it works beautifully. Celebration, no needles today. And off we go with the chemo routine.

My Oncologist bounces in singing “ So long, far well, aufiderzein, goodbye....” (in tune to my amateur ears).  Taps me on the feet.  Tells me I should drop in for a visit during the first or second day of radiation but otherwise unless there is more chaos, go home and get well.  And then out he cruises humming away.  OK then, so it shall be.

As I am sitting, I listen to the chatter around me. The lady next to me is having bone marrow transplant chemo. She has been in that chair for hours already and will be for hours more as she now needs a top up of blood and some more stuff. Then there is my other chemosaubie who is having a combination of drugs to help her through the combination of chemo. It is part of a trial as they seek to navigate her through to successful treatment of her cancer.

And I think, "How lucky am I?" I'm not putting it out there that I am free of cancer, but my treatment regime has been nothing compared to these strong women. I haven’t been "hurling like a pro" as one husband gleefully told the doctor when he came to speak with them. Nor have I had to deal with a raft of symptoms that requires a medical arsenal to provide some comfort. I have plodded through the chemo relatively unscathed. There have been some scary physical side effects but they have eased and will continue to do so. Psychologically I have had the most amazing support from family and friends and medical team and I feel although there have been moments of blue I am well.

And then I think, “I will miss these people”.  The humour and strength that surrounds the patients and nursing staff is infectious.  It has had such a positive effect on me during my treatments, no matter how awful the day became.  I can see why people feel the withdrawal when they no longer get this top up every week or month.  But then I think “I don’t ever want to see them again”.  And I mean this in the nicest way.

So chemo on board, flush done, PICC line out, wait ten minutes and then off I go.  I’d like to say goodbye to everyone but they are busy supporting others so I just wave and say “see you”.  I have sent a chocolate bouquet with a message which I hope will express my gratitude to them all.

To celebrate the strong one and I head to the coffee shop and I have the second coffee in six months.  An iced latte frappe.  I savour the flavour, dairy and all.  Tomorrow I return to the no dairy diet. 

My final chemo is done.  I now prepare for the daily zapping, or as one pink chick has put it the “toasting of tits”. 

Onwards I go, but this time there will be a couple of wines and a surprise 50th for the strong one before my next clinic visit.  Oh, and the planning of the WA Christmas adventure.  What could go wrong J

 

10 Replies

  • Thoroughly enjoyed your post as always!  Congratulations on reaching and blitzing another milestone!  Hope the 50th will be a huge joint  celebration, and that you have fun planning your WA getaway - on to the t-of-t - big hug, Michelle x

  • Thoroughly enjoyed your post as always!  Congratulations on reaching and blitzing another milestone!  Hope the 50th will be a huge joint  celebration, and that you have fun planning your WA getaway - on to the t-of-t - big hug, Michelle x

  • Hey Serenity

    Congratuations to you, woo hooo.  Party party party.  Keep looking forward  sweety and keep well.

    Radiotherapy will be a walk in the park after chemo kiddo.

    LOL

    Mich xoxo

  • It would be lovely to meet up for morning tea.  At the moment we are meeting on Friday at Garden City ( Upper Mt Gravatt) but I am happy to pop into town for a visit.  Perhaps you can work adjusted hours to suit your "good days" once you know how you are going to react to the chemo.  At this time I think it is important to be gentle on yourself, your body is going through hell right now (so is your mind).  Are you on fortnightly treatments?  Perhaps one day next week will suit you as you might be feeling better?  Or I can meet up before your treatment if it suits you. Let me know.  Take care.

  • Hi Toni My doctor is Maree. I'm still working full time (allegedly), supposed to be going tomorrow but not sure I can do it. I work at QUT so not affected by Premier but husband has been. Hasn't lost his job but has a very big new one at same level, of course, that doesn't sound much fun. Not sure he needs the extra stress right now but can't change that. If I hadn't changed jobs in May I'd have taken leave through chemo, may still, will just see how it goes. Anyway, my appointments are Thursday morning, but I could walk over from work at Gardens Point (on a good day :)) another day for morning tea, too.
  • Yes I am at HOCA Mater.  There are a few of us that I know of now. Let me know if you need a chemo buddy or just someone to go out with or someone to pick up the shopping.  Also available for home visits as I wont be returning to work (thanks to our Premier) if you need someone to help you or just the company.  I am happy to help in any way I can.  There is a group of us who  have finished the chemo and are heading into radiation we meet for morning tea one day a week.  We all had FEC.  Our doctors are Maree and Paul. When you are up to it, you are welcome to join us.  Take care.  

  • For both getting through the last chemo, and for sharing it with us. I've just started first FEC100 last Thursday and travelling OK so far, although not looking forward to the chemo journey, I have to say. So it is very good to hear you coped so well. I think you were at HOCA Mater too? Or perhaps I've got that mixed up. Anyway, yay for no more chemo and good luck for the radiation. Not far to go now.
  • For both getting through the last chemo, and for sharing it with us. I've just started first FEC100 last Thursday and travelling OK so far, although not looking forward to the chemo journey, I have to say. So it is very good to hear you coped so well. I think you were at HOCA Mater too? Or perhaps I've got that mixed up. Anyway, yay for no more chemo and good luck for the radiation. Not far to go now.
  • and thank you......

    for sharing your story here, there were times when I felt very alone, and your blog, amongst others helped me feel part of a very lovely collective.

     

    I wish for  you, great health, the discovery of beautiful things, journeys to travel and enjoy.

    All the very best,

    Ruth

  • Anonymous's avatar
    Anonymous
    Not applicable

    That was written so well serenity11! Thank you for sharing your final Chemo experience. I hope those that are just about to start Chemo take comfort in the fact that you made it through and with a smile. ~ Daina