It is just coming up to one year since the love of my life died after she had been diagnosed with lung cancer 11 months previously. We did all the things we could, and if you could die a good death, she certainly did. And we lived it all together. However, I have now been told that there is a chance I may have myeloma. On the 14 day pathway. And though it is not yet confirmed and the prognosis is not as bad (probably get 5 years at my age if confirmed), I still feel that pain that the one person that lived this all with me in her last year is now not here. I feel a little lonely. Gosh life doesn't make things easy sometimes. Still, not even had confirmed diagnosis. Just wanted to say this to people who would know what I was feeling.
Hello padjo59
Firstly I am very sorry to hear of your wife's passing after her lung cancer. I hope that you can take some comfort from being able to do all the things you could with her and were able to support her when she did die. I can only imagine how difficult it must have been. Please remember Macmillan is here when you need us.
I am sorry to hear of your possible myeloma and I hope that you soon have some answers about what is going on and what may happen next. It must bring it home as well after your experiences over the last couple of years. Feeling lonely at these times is to be expected. Do you have other family/friends around you?
I hope that it has helped to say how you are feeling on here and people will indeed understand how you are feeling. if talking things through would help then please do give the Support Line a call.
Please do let us know how you are getting on and if there is anything you need, then please do ask.
Jane
Macmillan Support Line - 0808 808 00 00, 7 days a week between 8am-8pm
Well they have confirmed it's definitely myeloma and it's incurable and kills you in about 5 or 6 years on average. Chemo underway and stem cell transplant coming in December.
Main feelings are:
Hello Padjo59
I am very sorry to hear of the loss of your wife and I know that you are taking comfort from the fact that you had such a love and such an important anchor in your life that still, and will always, bring meaning and richness to you in your life.
I know that you will really feel the loss of this anchor now when you face your own tough roller coaster of a journey. Not every human being gets to experience this priceless love we have had with our deceased partners - we were the really lucky ones.
I wish you the very best of success with your stem cell transplant. Hopefully you will also draw on the strength of your wife's love, and your mutual strength as a romantic, loving couple that you had through her illness. That spirit and her strength will still be with you now.
As Jane said I hope you can keep in touch with us through this journey and please ask us for help. I pop on here less now but it is such a source of help.
Florence
Well, it is now four months on and tomorrow I go into hospital to have the stem-cell-transplant which the consultants are confident is the best way forward for the myeloma.
I have been blogging and writing for my own benefit the whole time this last two and a half years since Caro got her first diagnosis. And I still feel very lucky in all of this, even though from one point of view it has been one hit after another. Not all of us find the love of our lives and share a third of our lives with such happiness. Not all of us fulfil that promise of "I want to spend the rest of my life with you" by holding her hand as she breathed her last. And even now, feeling confident in Cro's love, I know that she doesn't have to know about my illness and all the pain that would cause her. I know she would have been brilliant with it but she doesn't have to be.
And I am not alone. I have loads of friends and family on my side. I have the knowledge that Caro would have been right by my side, so I do not feel abandoned, just 'unwillingly left'. And I feel loved. And I have even met a nice woman that I am cautiously building a relationship with. But I do not feel that she has any need to take any responsibility for how I feel in the treatment (as she was bold enough to take me on, knowing my diagnosis).
So, all in all, the last two and a half years has left me more aware, better-armed, and feeling hugely loved. If anyone wants the link to my blog, please message and I will send it.
And to all of you bereaved carers, whether you are on the same road as me or not, remember you stuck it out, and showed your love in what you did. And that is exactly what being human is about.
Whatever cancer throws your way, we’re right there with you.
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