AnthonyMoore

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Viewing 6 posts - 1 through 6 (of 6 total)
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  • #121134

    blueant107
    Participant

    Thanks Carol can see how that helps lol. Just back from Jamaica and currently obsessed with booking my next trip…
    Probably to Aus to see my extended family and the barrier reef hopefully.

    #121125

    blueant107
    Participant

    Wow. This is so me right now. Struggling with concentration, bored all the time and feeling depressed a lot.
    im planning a new hobby brewing and trying to get into that, need to drop a few kilos which hopefully will help my mood and going to start swimming.
    I got told in clinic that Im mildly depressed so going to take their advice I think and seek help .
    so glad I read this, thank you

    #114328

    blueant107
    Participant

    Hi just at the end of my 6 month chemo so meeting the stem cell team next. Just not sure who you ask these questions too without looking like an idiot lol. When first found out asked if i could delay treatment till after christmas as had a big job on my consultant basically went mad at me. Can see his point now but at the time was unsure and my first thought was making sure my family had bread on the table.
    Glad your doing well and playing Tennis it gives me a lot of hope for me reading all these things and enjoying going to what my wife calls cancer club having my zumatra and bloods taken.everyone is so cheerful its great.
    Obviously I want to get to the point where i can do normal stuff and not be wrapped in cotton wool by everyone. So have followed the doctors rules too the letter not drunk alcohol fizzy drinks, i swear i can now tell the diference between bottled water brands, the lot. I havent driven either since i found out.
    Keep up the tennis and thank you for answering my dilema so quickly.
    regards
    anthony

    #114326

    blueant107
    Participant

    Hi
    off to meet my consultant at Christies next week and wondered how long between then and being treated I had to look forward too. Currently finding as many small things to do to keep my mi d active as I can. July would be good for me as can cram some small jobs and little break in to give my wife q treat as guessing its been no bed of roses these last few months for her.
    would like to get thru my birthday fit and well too which is at the end of june. Or am I just being stupid and should do as I am told by the consultants?

    #114227

    blueant107
    Participant

    Hi
    Sometimes its the fault, as with me, of the person who has the mm. I thought I had a hernia and was eating painkillers when I found out. We had run out so went to AE at my local hospital hoping for something stronger than paracetemol which werent working.
    I had an xray and at 8pm. It was reviewed at 9am next morning by a specialist and they found a lesion on my left leg. By 10am I had been contacted and was returning to hospital where further tests and x rays were taken. They talked to me about the possibility of cancer and by 1pm I had had a bmb and went back to work.
    Luckily (I think) my wife was visiting family in Austrailia so I had a few days to get my head round the whole thing.read up on the subject and got ready to tell my wife. Sometimes its harder for the spouse who watches from the outside I think and trys to look brave 7nfront of the person going thru it.
    my hospitalnis Stepping Hill within a week I had been assessed made to feel part of it, had so much information and help from macmillan, the NHS and the local community nurses as well as my GP it was overwhelming in a good way.
    I am about to xtart stem cell surgery and hoping to be well by wimbledon which is what I set myself when this journey began, I work as a chef at the championships, whether I go to work it or not this year is a different matter but want to be well by then.
    I found if I needed a question answered there has always been someone to answer it who has more knowledge of the subject than me or google. My Consultant has always made sure I understand as much as I have wanted to know, the nurses have tried to keep the room light hearted and still business like. Now Im about to go to Christies to see s8meone who is a myeloma specialist.
    my opinion is if your not getting what you need then ask everyone you have contact with. Its a t3am thing and as the patient you are involved. For me I have foccussed on whats in hand in the 3 weeks coming up. Currently I have found out about sct and all the stuff that goes with it. Recovery seems to be down to the individual, I find work sometimes is easier than being at home. I suffer with being unable to sit still for too long. I can now make a mean cupcake tho
    first thing I said to the consultant was can I start treatment in jan as I had a lot of work on. He told me no, I must stop work immediately. So I did. Looking back the initial month of adjusting to the drugs and the whole thing sinking in I was in no state to do anything at all. I know ive gone off topic at times I apoligise for that.
    hope you get the treatment you want and have great clinicians looking after you as I have. My hospital all over the news currently but you need to have faith in your team, if not ask for another team!

    #114224

    blueant107
    Participant

    Hi all,
    seems I’ve been lucky on the dex front. My reactions have been sleepless ness going dizzy in supermarkets and bad flatulence. Initially the co phosphates sent me dool alley and the tramadol make me confused a little. My main reaction has been sweating badly.
    I just got my date to go and see the consultant and move onto the sct part of this.
    Its a hard slog as people dont realise the energy drain that just happens anywhere and anytime with this daren’t go to the pictures as when the lights go down my eyelids seem tooas well.
    Hope everyone hassuccess this forum has given me so much information thanks.
    regards
    Anthony

Viewing 6 posts - 1 through 6 (of 6 total)