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@baeph
You wrote:
Bc his cancer is so unpredictable it’s hard to believe that this is what the rest of our lives will look like.

I was the sole caregiver for my wife from the time of her pancan diagnosis in July 2019 to the time of her passing September 14, 2022. My wife had no family and my family all live in other states. As we left the hospital after her distal pancreatectomy in March of 2020, the country went into COVID lockdown. Due to her immune compromised status and all the unknowns of COVID, my wife would only leave the house for medical appointments. She wouldn't allow friends to visit; she wouldn't even do zoom calls because she was afraid that well-meaning people would say upsetting things. My wife was normally the happiest, outgoing and giving person you'd ever meet. We were both convinced that she would get well and we'd resume the wonderful lives we had for 42 years together. Together, we decided to maintain hope by never believing that failure to be cured was inevitable. Ultimately, everything that I did to make my wife's path comport with her desires made my path harder after her passing. It's very difficult to suddenly change from being ever hopeful to be faced with losing the love of my life. But she knew that she was cherished and loved to the very last. Every patient and every caregiver is different. I tried my best. Maybe there were better ways, maybe there would have been better outcomes but our hopes gave us strength.

@baep you'll never know everything that's going through his head even if he starts communicating. The only advice I can give, is if you learn his desire, do what you can so he can work towards it. You don't have to like it, you don't have to agree with it, you just have to accept it.

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Replies to "@baeph You wrote: Bc his cancer is so unpredictable it’s hard to believe that this is..."

First, I am so sorry for your loss. I’m sure you miss your wife terribly and it’s kind of you to share your experiences with me. It helps so much to hear how you managed care and especially support for her needs and expectations. I have found that depression is a huge part of this journey and I’m trying daily to spend time outdoors, in the garden, and at the beach for sunrises when he isn’t too exhausted. We are choosing to take an optimistic attitude about recovery and, even though it’s difficult, I think it is necessary to keep hope alive.
The last paragraph gave me much to think about and I will keep it in mind. I think you must’ve been a good caregiver and I hope your mind is at peace.