Reactions after a few days of treatment

2 minute read time.

First of all, a huge thanks for all the wonderfully supportive messages I got in reaction to the round-robin e-mail informing friends and family of my illness. A real shot in the arm (pardon the pun...)

I guess the impact of treatment is never predictable, never quite what you expect, no matter how much you read beforehand.

I came home on the Monday evening, after my first (hefty) dose of Chemo (Cisplatin) and first radio session. I felt fine, I really did. I ate heartily and went to bed. Things went pear-shaped at about 2.30 am though, when violent hiccuping set in. Whoah, not just hiccups, but real spasms. 3 of these bouts ensued, lasting about an hour each, unfortunately accompanied by reflux and major heartburn, really quite painful and exhausting.

The hospital recommended I get a prescription for a medication called Haloperidol, which I duly did. HIghlight of the morning was when the GP prescribing it said "Oh, I bought your book by the way, the kids really liked it." (Quick plug: "The Cat, the Mountain and the Hot Air Balloon", for kids about 8 years old. Drop me a line if interested.. :-)) Somewhat lower point was when I realised that Haloperidol is normally prescribed for schizophrenia ... so now my chemist thinks I'm schizophrenic too! Never mind.

Anyway, hiccups have now subsided though not disappeared entirely. A little bit of research shows that these violent hiccups are not due to the Chemo, but to the anti-emetic (anti-nausea) drug Dexamethasone which is given as standard. And it turns out this reaction is quite common. Hmmm. I had asked not to have anti-emetics at all but was advised against this line .... Of course, what I don't know is how sick I would feel had I not had the Dexamethasone. Interesting study on this here http://www.ncbi.nlm.nih.gov/pubmed/24107973 

The other effect, which is hard to described in terms of its extent, is sheer lethargy. One feels robbed of all energy and simply wants to lie on the couch. This feels slightly better this better morning, hence the ability to write a blog, and hopefully the effects will continue to wear off before the next dose of chemo in 2.5 weeks time.

Also slightly surprising is the speed at which the side-effects of radiotherapy have kicked in. I have 6 weeks in total, but already my toast tastes like cardboard. Keeping up my weight is going to be a challenge.

OK, that's it for now, thanks if you read this far! Best wishes to all.

Anonymous
  • FormerMember
    FormerMember

    Hi Dave,

    Cardboard toast and hiccups, you should try my dads cooking is very much the same effect.

    I can't help thinking what can I do, I don't what to send messages without substance and look to find news and energy for you, its sunny today and I know you must see it too just like me which make us see the same and I hope feel the same....

  • Ha! My cooking ain't much better! Thanks Jeff. No need to seek substance (not sure I am doing that on my side!) Your friendship is more than enough

  • FormerMember
    FormerMember

    What about work, do you feel able or is it time to give yourself time later for that. Cooking mmm I don't mind it but perhaps like many its not on the top of my "to do list" still a nice curry is easy. I had a chat with Tom and ask if Dylan would like to chat via Skype... I guess you have a tablet PC?

  • FormerMember
    FormerMember

    Hi David, it was a great shock hearing your news. It brought home to me the point of doing those MAC 4X4s with Malachy! Food tasting like cardboard - well you chose to go and live back in the UK ;-) I was really glad to read your GP had bought your book. It is really nice and has pride of place for encouraging Ariane's nieces and nephews to learn English! Best wishes to you. Ian

  • FormerMember
    FormerMember

    Hi dear David rough rough  ride .. and this is how we find out that you wrote a children's book. How wonderful.. is there no end to your talents? thinking of you, Caroline et al

    ps. your experience with the drugs just  shows how  doctors do not communicate  adequately with patients.. believe it or not, patient empowerment our health policy agenda..