Relapsed and starting VCD – keen to hear from others on same journey!

This topic contains 2 replies, has 3 voices, and was last updated by  andyg 12 years ago.

Viewing 3 posts - 1 through 3 (of 3 total)
  • Author
    Posts
  • 29th April 2012 at 4:50 pm #99243

    PhilipVanessa
    Participant

    Hi all – new to Myeloma UK so this is our first 'post'.
    Husband, Philip, diagnosed June 2008 – had CTD and then sct in Sept 2010. Unfortunately has just relapsed. Started VCD last week – back to the dreaded Dex! Would love to hear from anyone else on VCD – how you are coping etc.
    Vanessa

    29th April 2012 at 6:24 pm #99244

    tom
    Participant

    Hi Vanessa and Philip

    A warm welcome to the group.

    Cant give advice on VCD as all I have had is CDT then SCT all done in 2009 and now am drug free.

    Just wanted to say Hi 🙂

    Love Tom "Onwards and Upwards" xx

    29th April 2012 at 11:30 pm #99245

    andyg
    Participant

    Hello Vanessa and Philip.

    Welcome to the forum. We are all friends here.

    Sorry I can't help you with your question. I was only diagnosed October last year and haven't reached a stage for a sct yet. I'm sure you'll receive an answer from someone who has had a similar experience as Philip soon. If not you could give Ellen a call on the helpline and she will be able to guide you.
    Good luck with the new treatment.
    Take care.
    Andy

  • Author
    Posts
Viewing 3 posts - 1 through 3 (of 3 total)

The topic ‘Relapsed and starting VCD – keen to hear from others on same journey!’ is closed to new replies.