There is light at the end of the Chemo Tunnel

FormerMember
FormerMember
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Hi,

This is my first post ,so hope I've got it in the right place. 

I just wanted to offer a word of encouragement to those of you

who are struggling with the after effects of Chemo, in particular

the dreaded Chemo brain,  IT DOES GET BETTER,

I had chemo following an op for bowel cancer 3 years ago.

At first I was preoccupied with the obvious side effects;

Vomiting, diarrhea, first bite syndrome etc, but as these subsided,

I began to notice more the tiredness, fatigue - and - Chemobrain;

unable to concentrate on anything for more than a few minutes.

I had a few chats with the wonderful guys at the local Macmillan Centre,

and they assured me it would get better, I just needed to be patient.

Well I guess I gradually got used to it, and tried to live with it.

Then one day, just over a year after the Chemo, I realised I wasn't feeling

quite as tired as I had been, and the concentration had improved a bit.

Again I gradually got used to this better but still not good way of life.

Recently, three years after the chemo, I noticed another step in improvement.

Still not as much as I'd like, but still better than it has been; 

(probably not helped by the fact I'm now the wrong side of 70) ;).

So for those of you still struggling through the chemo tunnel,

yes it is a long one, but look out for those corners it turns which

gradually let in a bit more of the light of normality

  • Hi  and welcome to the board. Thankyou for sharing your experience with chemo brain? It’s a funny one isn’t it? I often use it as a reason for not remembering something but then wonder if it’s an age thing or I’m just not concentrating? 
    It’s good to hear that you’re 3 years down the line though and I hope you’re enjoining retirement in your new bungalow?

    Take care

    Karen x

    Macmillan Support Line - 0808 808 00 00, 7 days a week between 8am-8pm
  • FormerMember
    FormerMember

    How many chemo cycles did you have? My husband gets the brain fog and hates it most out of all the side effects. Glad to hear it’s easing up for you! 

  • FormerMember
    FormerMember in reply to FormerMember

    Hi,  Yes the chemobrain is so frustrating.

    I was supposed to have 4 lots of chemo,

    but was so ill (omitting and diaorea) after

    the second lot  that the chemo was stopped.

    When did your husband have his last chemo.