Relapse official

This topic contains 33 replies, has 22 voices, and was last updated by  KWilson 13 years, 9 months ago.

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  • 7th January 2011 at 6:29 pm #89446

    KeithH17
    Participant

    Well it's official the relapse is a reality.
    Was due to see consultant on 13th but had a call today saying he wanted to see me Mon at 4pm.
    He said the Bone Marrow showed the Myeloma was active and he want's to discuss treatments open to me with a view to starting all over again Tues.

    Happy days are here again:-(

    Keith.H.

    7th January 2011 at 6:47 pm #89447

    susannah
    Participant

    H Keith So sorry to hear of your relapse, just wanted to wish you all the very best for Monday. Ive always appreciated your kind words over the months,and now its my turn from Michael and myself good luck

    Regards
    Sue

    7th January 2011 at 7:13 pm #89448

    michelleakitt29
    Participant

    Hi Keith

    Sorry to hear that you have had your worst fears confirmed, I am wishing you look for monday. Keep touch and let us know how you get on.

    with much love michelle x

    7th January 2011 at 7:38 pm #89449

    gina45
    Participant

    Hi Keith i am so sorry that the myeloma is back. i hope the hospital can get you back on the right track.
    Take care x

    8th January 2011 at 12:51 am #89450

    brocho
    Participant

    Hi Keith I am sorry that you are now relapsed , its a real pig when you hear those wordsBut having heard them myself a few times now take strenghth from the fact that active treatment can get cracking and knock it back again love Bridget x

    8th January 2011 at 1:30 am #89451

    KeithH17
    Participant

    Thank's girls your thoughts are much appreciated.
    I'm getting ready for round 2 as I like to call it.
    Treatment is due to start on Tues after Monday's consultation.
    The Doctor said he wanted to discuss at least 2 treatment options with me before deciding which way to go.
    I can't really complain as I've had over 2 years of mainly good health and
    knew it was only a matter of time before the ticking timebomb went off.
    When I've been to Hospital on Mon I'll post the latest news for you all.

    I thank all you lovely people once again and hope you all stay well.

    Keith.

    8th January 2011 at 7:39 am #89452

    tom
    Participant

    Hi Keith

    Well thats a Bugger aint it.

    Am sure you will cope with round two Better than you did with round one as they say it gets easier:-/

    All the best for Monday and hope the treatment you decide on will have little or no side effects 😀

    Tom "Onwards and Upwards"

    8th January 2011 at 7:43 am #89453

    Roz
    Participant

    Hi Keith

    So sorry your going through this. :'-( I wish you all the best in your next round.

    Be thinking about you, so come on lad lets fight it:-)

    All the best
    Roz

    8th January 2011 at 8:06 am #89456

    Perkymite
    Participant

    Tough Keith, I wish you the very best of luck on Monday.

    You have beaten it once and I am sure you are the sort of guy that can do it again. Seconds Out, clang, clang of the bell – Give it h**l buddy.

    kindest regards

    David

    8th January 2011 at 10:51 am #89457

    zasrs
    Participant

    hi keith

    sorry to hear about round two. gordon is on round two and responding slowly but he is getting there. there seems to new treatments coming on line all time for mm.

    good luck

    sarah

    8th January 2011 at 11:51 am #89458

    SharonG
    Participant

    Hi Kieth
    Sorry to hear about your relapse, I am in the same boat myself having just had the tumour at the bottom of my spine confirmed as a plasmacytoma and evidence of speckles of small plasmacytomas up my spine :'-( like you I am gutted. I am in hospital having radiotherapy at the moment and am waiting to see whether my consultant thinks I should go for valcade to try to knock all the other smaller tumours on the head now.
    I haven't given up yet, I know there are still plenty more treatments available and I intend to try them all if necessary!
    Wishing you luck
    Sharon x

    9th January 2011 at 1:23 pm #89465

    Amelie
    Participant

    I am really sorry to read that Keith. I send you all my best wishes and thoughts.

    9th January 2011 at 2:12 pm #89466

    DaiCro
    Participant

    Hi Keith,

    I'm sorry my take was proven wrong but I wish you all the best in catching it quickly and maintaining a repression of your MM.

    Regards

    Dai.

    9th January 2011 at 2:40 pm #89467

    Eva
    Participant

    Dear Keith,
    I seem to be in a simliar position to you. I haven't had a bone marrow test yet for absolute confirmation. Remember that for many of us this will be a journey( and sometimes a long one) rather than an event.
    Thinking of you,
    Eva

    9th January 2011 at 9:41 pm #89459

    brocho
    Participant

    H Sharon I hope you are back home now and all went well .I have my appointment with radiologist this week and cant wait for my radiotherapy . Although I know a lot about it I am still a bit nervous about having radiotherapy so I would love to hear how you found the experience When will you find out about having velcade? Keep smiling your beautiful smile love Bridget x

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