Hello

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Hi pleased to be accepted . I was diagnosed with multi myeloma  2020 been on chemo pushed it back a bit had pneumonia  but still trying to be positive my children are taking it badly but I keep strong so far  

  • Hi  and a warm welcome to this corner of the Community although I am sorry to see you joining us and hear about the journey you are on.

    I am Mike and I help out around our various Blood Cancer groups. I don’t have Myeloma but I was diagnosed way back in 1999 with a rare, incurable but treatable type of Non Hodgkin’s Lymphoma (Stage 4 in late 2013) so although my Blood Cancer ‘type’ is different I do appreciate the challenges of this journey rather well but not the specifics of you condition.

    In the early days it’s all about understanding and once you get more information and talk with others the journey will get more understandable.

    So let’s look for the group members to pick up on your post. There are a number of active group members at the moment so why not click on the main ‘Myeloma Group’ title and this will bring up all the group posts. Have a look at the posts and as always you can hit reply to any post and connect in with the wider group conversations.

    Our Support Line teams are available 7 days a week, 8am-8pm on freephone 0808 808 00 00email or live webchat where you will find one of team there to help you out.

    We also have our Ask an Expert section but do allow a few working days for a reply.

    For good information do check out Myeloma UK who produce very good information and run various support platforms including their Buddy Scheme, they also have a Support Line on 0800 980 3332

    You may also want to check to see if you have a Maggie's Centre in your area as these folks are amazing and most centres do run monthly Heamatology Support Groups most are online at the moment….. the one I attend does have a few folks with Myeloma in it so worth checking.

    Always around to help more or just to chat.

    Mike (Thehighlander)

    It always seems impossible until its done - Nelson Mandela

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  • Hello Suki

    i had a stem cell transplant for Myeloma on 21/09/21. I was diagnosed in May 2019. Mine was delayed because of Covid. Stay strong and if you have any questions or just want a “ rant “ just let me know. xx