Scan delayed!

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Haven't posted for a while, just working on keeping things as normal as we can during the pandemic and all the restrictions. Dave's had 6 rounds of chemo, Folfoxiri and Avastin to hopefully impact his stage 4 cancer with mets to liver and peritoneum. He was due a halfway scan after the 6th cycle but due to Covid the CT scans are cut back hence the delays. The radiology unit say it will be a few more weeks so he'll plod onto round 7 this week.

It's a real conundrum as we'd like the scan to know what's happening and perhaps some shrinkage (we dare to hope), but there's also a small comfort in not knowing just in case it's bad news.

On the bright side his bloods which were incredibly troublesome at the outset at 7.9, which almost stopped the chemo, have continued to increase each time before chemo and at the last session were 12.1, hoping this is a good sign. We've made loads of dietary changes and we walk at least 5km a day (except for the 3 days post chemo when he has the pump and steroids) and think this is contributing. He's been an absolute trooper throughout this gruelling treatment, fingers crossed we see some positive results soon. 

Love Frances xx 

  • Oh dear . A delay to a scan is a tough one but I know exactly what you mean . You start to feel safe with the chemo routine.

    Your husband has actually done really well reversing his bloods . That’s quite incredible given he has been on chemo .

    You have both faced this with a fantastic approach . Great effort with the exercising. 
    I hope everything goes well with his scan . I am holding out for some good news . It’s so nerve racking! Sounds as though he has actually improved on treatment !

    Take care ,

    Court 

    Helpline Number 0808 808 0000

  • Hi Court, you are so right he has improved through treatment which is surprising as its such a heavy weight chemo. His back pain disappeared after a couple of cycles and the fatigue has gone since the bloods have risen and he's a better complexion colour too. After chemo he feels weird, and the next 2 days with the pump and steroids he has less appetite, but once the pump is off he recovers quickly. He's not had too many side effects as his team seem to preempt the possibility and send meds through his chemo line.

    Just making the most of his new found energy as we never know what's around the corner.

    Never daring to hope out loud, but certainly allowing it in my mind. 

    Hope your Mum is doing well,

    Love Frances xx