lncooje

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  • #121330

    lncooje
    Participant

    Hi carol, I live in Yorkshire and not far away from the countryside so I don’t think its living in Lindon but I do think its related to mm x linda

    #121316

    lncooje
    Participant

    I was told I couldn’t absorb vitamin d I’m beginning to wonder if it related to mm also

    #121306

    lncooje
    Participant

    Fingers crossed its good news and he still smouldering.  I am also on a fantastic face book page for myeloma called UK meyloma support and have made friends with some fantastic people who all support each other.  I have found myeloma .org fantastic too.  I would phone your husbands consultant secretary and find out where you can get your support from, there should be someone locallyxx

    #121302

    lncooje
    Participant

    Hi there, I was diagnosed on 1st Oct 14 with smouldering meyloma and was still smoulder when I had my last bloods at the end of Dec.  I’ve just had my bloods taken and I’ve got everything crossed i m still smouldering when I see my consultant on the 23rd march.  Re the tingling I have the tingling in my arms and back. This was the reason I went to see my gp in the first place but never expected the outcome would be meyloma. Do you have a support group in your area or can you contact his nurse to ask if you are worried. I was told I could contact them anytime especially when I was worried. It may be worth having a chat with them. Please keep us informed on his progress Jan, we are all fighting together lots of love linda x

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