NickiFord

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Viewing 15 posts - 16 through 30 (of 39 total)
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  • #91079

    nickinoo
    Participant

    Thinking of you Bridget xx

    #90960

    nickinoo
    Participant

    Hi Sarah,

    Sorry for the late message I do not visit the site very often at the moment.

    So so sorry to read the news about Gordon.

    My thoughts are with you and your family.

    Nicki xxx

    #90838

    nickinoo
    Participant

    Hi guys,

    I really wanted to watch this, but couldn't bring myself to as programmes like that upset me much more since Sam's diagnosis, he sounds like an inspirational young man though.

    xx

    #90530

    nickinoo
    Participant

    Hi Jet,

    Thanks for your kind reply, and I am glad to hear that you found my post uplifting.

    I didn't actually speak to you on the day but I did see you at the Myeloma UK Infoday (I recognised you from your pic on here and also your name badge), I hope you found it as interesting as I did xx

    #90558

    nickinoo
    Participant

    Thinking of you and Peter, Min, and I really hope they come up with something suitable soon.

    Nicki xx

    #90528

    nickinoo
    Participant

    Hi guys,

    Thanks so much for all of the good wishes.

    It was so lovely to see yourself and Janet and it was really nice for Sam to meet you both as I have told him all about you. David I am so glad to hear that you too are feeling mostly well after your transplant, long may it continue.

    Liz, glad to hear that my post has given you a boost, and I hope that your hubby continues to make a speedy recovery.

    Take care all.

    Nicki xx

    #89926

    nickinoo
    Participant

    Thank you guys for your good wishes!

    We leave for Edinburgh airport at about 1am, I am used to going to bed about 10pm most nights (boy do I love my bed!) so feeling tired already!

    Sam on the other hand is downstairs fit as a fiddle watching Match Of The Day!

    Very excited for our little trip as it is the first one that sam has been cancer treatment free from since diagnosed.

    Take care all.

    Nicki xx

    #89923

    nickinoo
    Participant

    Hi guys,

    Thanks for all of your kind words, it really does mean a lot.

    Although I haven't posted on here much in the past I follow everyones journeys regularly and this site was truly a god send in the early dark days.

    Its Only Me I wish you and your mum and family all the best and please keep us updated on how she is doing.

    Eve I also wish you all the best on this awful journey and will be thinking about you and your family.

    It is now my turn to try and offer some reassurance to newbies, as other members of this forum did for me. And I am so happy that it may do so.

    Night all.

    Nicki xx

    #89902

    nickinoo
    Participant

    Hi David,

    So pleased to hear that your results so far are very good, and disappointed for you that you are only on cloud 8 amd cloud 9 🙂

    Sam will be 16 weeks post transplant on wednesday and time has flown, his Myeloma wasnt the paraprotein type (if you know what I mean!) but he was told by his consultant last time that he was in a virtual complete remission pending his bone marrow results so we were over the moon with that.

    How are you feeling generally?

    Nicki xx

    #108688

    nickinoo
    Participant

    I love this poem, I found it online shortly after Sam was diagnosed xx

    #89387

    nickinoo
    Participant

    Thats so lovely Roz, I too had a little cry when I read it.

    Thinking of you xx

    #96859

    nickinoo
    Participant

    Pleased to hear the good news Shirley, I hope you continue to make a good recovery!

    Nicki xx

    #108679

    nickinoo
    Participant

    Right back at you 🙂

    Have a good one!

    Nicki xx

    #89326

    nickinoo
    Participant

    Hi Roz,

    Words fail me I am afraid, I just wanted to say how sorry I am that you are going through this, if it is any consolation I think you are so so strong and brave, an inspiration, and you certainly won't be upsetting anyone with your post, we all just feel so very upset for you, Micheal and your family.

    Micheal will be so proud xx

    Take care xxx

    Nicki

    #105822

    nickinoo
    Participant

    Hi there,

    Wanted to reply to this post as saw as I read it as it struck a chord with me but have only just gotten round to it!

    When Sam was first diagnosed we were treading on eggshells and it just wasn't normal for us and it really didn't feel right, in fact I think it made things worse. Until his mum, who nursed her husband through Myeloma said to me "treat him the same, be as normal as possible" so I did and things were much better.

    I think secretly he likes being nagged! Ha ha!

    Nicki xx

Viewing 15 posts - 16 through 30 (of 39 total)