Ashamed: I think about (and plan for) dying. Do you?
Hi, did anyone, after there cancer and COPD diagnosis start to think about dying? After almost four years, I still do, all the time. Planning my funeral, how to leave my children, how it will be to be in a coffin. Bizarre, I know.
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You go girl!!!! 🏍️
I've had stage IV breast cancer for 2.5 years, other medical issues and scary side effects from meds, but I still have decent quality of life. I tend to think about what all I need to take care of before I go so my son won't have to do it. I've taken care of and organized all the paperwork, cleaned out closets of excess stuff. I even have a stack of letters I've written and dated to those closest to me to go out after I've passed or maybe if I'm in hospice, but I wanted to have something written prepared in case something happened suddenly. I don't delay in writing kind letters and notes now, but some things are better said at the end or might worry people if I sent the letters now. My last "need to do" is to do something with the thousands of photos and get them organized and down to a more reasonable amount. Due to fatigue, getting through my list has taken longer than I had hoped. I do make sure I'm enjoying my days and having some fun in between tasks. I don't dwell on it all, but try to use the advanced notice to my advantage. I feel lucky in that respect.
You have no reason to feel ashamed. Just allow yourself to enjoy life to the fullest while you're taking care of business. Let people remember the best version of you laughing and smiling. Prayers for you.
@soupycampbell I love your screen name. It made me smile. I love that you bought a scooter and plan to make the most out of the time you have left. It seems you made a good decision. Prayers for you. Enjoy!
I love your post and agree about life being so much better when you retire from shoulds . Enjoy your time and blessings. Haven’t read you NETs story anywhere but hope you are seeing NETs specialists. Prayers for you.
@ellengrubb It sounds like you have a good plan and are taking care of business. We OCDers get things done. Prayers for you. Enjoy your time.
Thank you so much. Yes, last thing I was told s Few days ago when I pushed for answers was depending whether they go other organs I should have months to a year and because I am in such good shape possibly longer. My daughter had to go to Hawaii (with regards to her business) and I’m going with her tomorrow! Haven’t been there for several years now so that will be nice. I live in White Rock , BC which is close to the ocean and usually pretty warm by now but it’s been unseasonably cooler. I will enjoy the heat.
All the best to you and prayers being sent! Keep us informed.
Joan
I'm glad you are feeling well. Enjoy Hawaii! I'm excited for you. I've never been, but it's on my list. Take care, Lisa
Joan, I love that you are going to Hawaii! One of my favorite places, but it has been a long time. So beautiful! It will bring you peace and, yes, warmth. Even California has been unusually cool this winter. Enjoy!!! Prayers for you, Lori
As for your lung NETS, I still want to be sure you've seen a NETs specialty team. There is a support organization in Los Angeles LACNETS.org with tons of info, links, videos of NETs specialists around the US giving talks about various treatments. NETs is treated very differently than other cancers and the patients tend to survive much longer. There is also a different treatment plan for each patient -- not standard like common lung cancer. It's more operable even in organs. It's a rare cancer with programs only at top cancer facilities. If your decision to stop treatment is just a quality of life issue and not wanting more surgeries or meds then I understand. I expect to make that same decision at some point. But my local oncologists were not familiar with NETs so I to go UCLA (Los Angeles) for NETs treatment and my local oncologist for unrelated breast cancer treatment. They coordinate. Not sure about Canada, but there is a NETs specialty team in Seattle, WA -- a couple hours from you. I hope the LACNETS site will be helpful.
Joan, I think I mixed up your cancer history with someone you replied to so I guess the NETs info doesn't apply to you. Have fun in Hawaii! Lori
LACNETS.org has a lot of info and contacts, videos from NETs experts regarding treatments for neuroendocrine cancer. Treated very differently than other cancers. It has a better survival rate than most cancers if treated properly. I hope that site has some useful information for you. It's rare so most doctors are not familiar with neuroendocrine cancers. A NETs specialty team like Mayo or other top cancer centers might be worth while for a second opinion. Prayers for you.