Cannula problems

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Hello all

My husband has has 2 rounds of chemo for his lymphoma but today after 6 failed attempts to get a cannula in he’s been told he has to have a PICC line fitted so he couldn’t have his 3rd round. 

Can anyone who’s had this issue advise me how this works please as he’s a bit down about it. 

I’ve reassured him that it won’t affect the outcome of his treatment (he was worried he’d have to start again from the beginning!). 

I wasn’t with him today (I went to the first 2). If I’d been there I would have asked more questions.

Thanks

Frankie

  • Hi Frankie  good that all was ok…… unfortunately there are significant differences between treatment centres and heath boards with regards to the availability of Cancer Nurse Specialists…… I never had a CNS for the first 14 years  

    Mike (Thehighlander)

    It always seems impossible until its done - Nelson Mandela

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  • I was given a specialist number to call while on chemo - could call it for anything. Like any side effects or picc line. 

    Does he have a ‘cancer treatment book’? The number was supplied in that for me. 

    I even called the number on Monday and I haven’t had any treatment since November - just for advice. 

    Between like 9-5 it was directed to the chemo unit and then out of hours it went through to on call oncologist specialist nurses. 

    Are you in the UK? I am north west England xx

  • Yes we are in Stockport - he’s being treated at Stepping Hill Hospital in the Laurel suite. 

    He did get a phone call yesterday from someone asking how he was doing but that’s the first contact of that kind since his diagnosis.  

    it’s all been a bit shambolic. Maybe I’m expecting too much but he’s got cancer! 

  • Hi - I live in the South and was treated in what I believe is a relatively big hospital (650 beds, for reference). I had a booklet with numbers and details... 9 to 5 Mo-Fri I just had to ring hospital reception and say extension number and that called the pager of the two CNS. Out of hours and weekends I had to call the ward (there was a section of the hospital for hematology patients staying at the hospital overnight etc) and a nurse would advice, they'd have my details to hand easily as well. 

    I contacted the line the first day of chemo as I was having palpitations in the evening, then another time cause I had bone pain and breathlessness, due to the filgrastin injections... and I think that's it. But it gave me so much reassurance to have those numbers. I contacted them via email for what I thought was non-urgent stuff too, and I still do (for example now to ask if I should get covid spring booster).

    Then I hope you are seeing the consultant before the start of each cycle (??). 

    I guess it's a bit of a postcode lottery