Chris Cluff

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Viewing 5 posts - 91 through 95 (of 95 total)
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  • #85361

    bikerchris
    Participant

    HI David,
    Quite happy to meet up in Taunton some time. Give me a ring, 01823 270304.
    Regards, Chris

    #85356

    bikerchris
    Participant

    HI Bridget,
    Sorry it has taken me ages to reply, I hope you are feeling ok. I am pleased to say that my radiotherapy seems to have helped me and my back is much less painful now, I am still taking the Oxycontin at night and morning but none during the day. I saw the specialist today, and she was very pleased with my last set of blood results. I am starting on my third cycle of Chemo now, and if it carries on working I may be looking at Stem Cell treatment at Easter.
    You mentioned about sedation during the Bone Marrow sample, no they did not offer it, and when we enquired they said there wasn't time, so I was rather bulldozed into it – I did have gas and air though. I would be pretty apprehensive before going into it again, but all part of the 'pain to get some gain' I guess.
    Regards, Chris

    #85375

    bikerchris
    Participant

    Hi Heather, it is good to hear from you, and I hope you are finding the comments useful. I am only 6 weeks into my treatment, and I am feeling a lot better than I did a month ago. It is interesting to hear your comments about work. I have my own firm, and have been struggling on, keeping things going for now, but I accept that if I have a transplant I may not be able to work at all. I have decided that I will sell the firm if I can, and retire – I have no desire to see out my last years sitting behind a desk at work when I could be doing other things. Did you give up your job completely when you started treatment? Why do you want to go back? The problem is that I guess we all need some money to survive, and so far I have received no real financial advice. Travelling sounds like a great idea, and it doesn't have to be tiring unless you intend to climb Mount Snowdon!
    I would be interested to hear from you, Regards, Chris

    #85360

    bikerchris
    Participant

    Hi Tom, yes I have seen your replies, but I havn't been at the laptop to reply until now, but many thanks to you, and to everyone who has commented and replied to my post – it is great to see that a few members of the site have read my ramblings!
    I agree, it seems to be a brilliant site, and your comments have already been of help to me as some of the medical mumbo jumbo can be pretty confusing.
    Since last time I have had my first monthly meeting with the Consultant, to renew my drug supplies. The only alarming thing was that my neutrophils are only 0.7, so they have taken me off the chemo for now, and I am just on the thalidomide and steroids. He was worried that the chemo would lower the immune system even more, but the fall may be down to the radiotherapy. My PP level is down from 55 to 34.5. On the positive side, the radiotherapy seems to have reduced my back pain slightly, and without the chemo I am feeling much livlier and less queasy. It is very tempting to rush around doing too much, but my family are good at nagging me to take it easy – and that is the message from other sufferers too.
    No-one has spoken to me about SCT yet, but I guess it is early days for me yet.
    Happy New Year to everyone on the site, and I will raise my glass of shandy to 'positive thinking'! Cheers! Chris

    #98594

    bikerchris
    Participant

    Hi David,
    I am new to the site, and live in Taunton. My partner Lena has been following your story on the site since I was diagnosed last month, and then we realised that you are local to us. I have posted my story on the newcomers page, and hope to get some replies.
    I keep waking up at night too, maybe the steroids, but I was so fed up lying in bed thinking about things that I was up at 6.00 today and clicking away on the keyboard! >:-(
    Am up at Beacon tomorrow 10.45, so we will keep an eye out for you!
    Regards, Chris

Viewing 5 posts - 91 through 95 (of 95 total)