Hello

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Hi

I was diagnosed with Myeloma in Feb 20. Had chemo then SCT in Dec 20. Relapsed in June 22 back on chemo now

Feel like I have a gun to my head !  not the life I imagined.  Married Easter 2019 . my husband is amazing I don't know what I would do without him

Work retired me in April 21 thank goodness & give me a pension even though I am only 52

I live in South Yorkshire 

Happy to chat  xx

withI was diagnosed Myelona 

  • Hi Janey,

    thanks for your email and really sorry to hear you’re back on chemo. I think that is my biggest fear that I’ll go through transplant and be back on chemo. 

    The first year on chemo was dreadful and I wasn’t sure I could cope and I totally understand you feel like you have a gun to your head. 

    id be interested to know your experience of SCT and how you coped and what things I need to be aware of, and also how your husband coped.

    thanks

    Adrian

  • Hi

    I had my SCT at Sheffield Hallamshire Hospital. I wasnt allowed visitors due to covid. I was quite ill afterwards with the dreaded S&D and didnt want to eat much. Had lots of ice lollies which were nice

    I refused a 2nd SCT as I only got 18mths remission & was told the 2nd transplant would give me less

    Good luck on your journey 

    Janey x

  • Hi,

    I think that’s my biggest fear is going through everything and the remission isn’t as long as expected. If I’m honest I’m still in two minds……

    Hope things work out for you 

    Adrian

  • Adrian, it’s all about the bigger picture and what the overall outlooking is. As I have said before I have a different blood cancer but I was given a few years on the clock with SCT the only hope, my first Allo failed within 6 months but I seven and half years out from my second Allo and doing great…… and over the past 7 years two new treatments for my rare condition have come on line so I now have a few fall backs.

    Mike (Thehighlander)

    It always seems impossible until its done - Nelson Mandela

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