TeaRose

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  • #147346

    tearose
    Participant

    Kho305

    Thank you for your reply and for your good wishes for my husband and my grandson. I am sorry that your dad relapsed but, sadly, we know that that is inevitable at some point with MM.

    I think Covid affected a lot of things in the medical world and it will take time to get things back to where they were before it struck. I am pleased that your dad is now getting more regular consultations and I hope that continues from now on.

    I wish you dad all the best. xx

    #147339

    tearose
    Participant

    Hello Mulberry

    Thank you so much for your good wishes for my grandson and for your positive and encouraging post about your treatment. The words ‘world class therapy’ are reassuring. and your confidence in Myeloma Support UK tells me that I have found the perfect forum.

    Being reasonably close to a big hospital is one of our criteria when it comes to looking for a house in the UK and so is being able to take part in drug trials which are so important, especially in the rare cancers. My husband will be more than happy to take part in them.

    All in all, I have had some great responses to my first post on here and I am feeling so much more positive about our move back now. Thank you.

    #147337

    tearose
    Participant

    Thank you so much, Tony, for your kind words about my grandson, and for your reassurance about the care that you have received. I wish you all the best.

    with kind regards

    TeaRose

    #147333

    tearose
    Participant

    Hi Znab

    Thank you so much for your good wishes for my grandson.

    I am sorry that you have been diagnosed with MM and I wish you all the best with your treatment. It’s very reassuring to hear what you say about the NHS. Where in the UK are you based?

    My husband has had excellent treatment in France. His consultant is in regular contact with MM consultants in the UK, the US and in other parts of the world and they share knowledge and information which means that there is always research going on somewhere in the world which I find reassuring.

    I wish you all the best with your treatment. My husband has had ups and downs since he was diagnosed but he has done very well since his transplant so the ups and downs are worth it.

    Take care

Viewing 4 posts - 1 through 4 (of 4 total)