Adenocarcinoma NSC Lung Cancer Stage 3. Advice? Success stories?

Posted by detroitmom23 @detroitmom23, Feb 7, 2023

I recently found out that I have stage 3 adenocarcinoma NSCLC with mass in lung and spread to lymph nodes in neck, they want to do four rounds of chemo and if shrunk enough possibly radiation afterwards. I have asked them not to give me a prognosis because my fragile mind can’t handle it.
My first chemo treatment is tomorrow and I’m a nervous wreck. Any advice on getting through it?
Any success stories would be SO welcome right now.

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@lls8000

Hugs to you! You have a lot to manage, and these conversations aren’t easy to get started. He’s likely always felt that he needs to be strong.
He may need the upcoming trip as something to look forward to also. Don’t be afraid to ask for help, especially with logistics of traveling.

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My husband realized last night, after making all the special arrangements to travel, that he is not strong enough to move forward. I had “known” for the last few weeks and needed for him to come to that realization. My mantra, since his diagnosis has been, it is his body, his cancer and I am not his mother.
As long as he is capable of making his own decisions and choices I am willing to set aside. Even if I disagree.

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If it has metastisized that would be stage IV. I recommend you ask your oncology to send pathology samples of your tumor(s) for genetic testing to see if you might qualfy for a targeted therapy. Keytruday, Xalkori (I am on this...) or one of the many others. Also be willing to participate in possible trials being run by the hospitals and drug companies. Wishing you the vety best.

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@millie5737

My husband realized last night, after making all the special arrangements to travel, that he is not strong enough to move forward. I had “known” for the last few weeks and needed for him to come to that realization. My mantra, since his diagnosis has been, it is his body, his cancer and I am not his mother.
As long as he is capable of making his own decisions and choices I am willing to set aside. Even if I disagree.

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@millie5737, Thanks for letting us know, I had been thinking of you. I'm glad he came to this realization, it's hard to admit that you aren't able to do the things that you could when you were younger and healthy. You've been married for a long time!, so you know best how to approach each other with delicate situations. If your mantra works in for you then use it, everyday if need be. This is still a relationship where there's give and take, make sure you take care of your own needs too.
Is the inflammation getting any better, or worse?

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@angel42

You just made me so happy for the first time in weeks! My husband has been wanting to give up, but you, you had a similar diagnosis and survived! I am going to share your story with him. I know it will inspire him as it did me, the wife and caregiver who battles beside him. I pray Mayo can do for him what they did for you as our one-horse, one hospital/clinic, and outsourced oncology and radiation facilities failed him miserably. Blessings to you!

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Hi @angel42, There are many success stories here on Mayo Connect. I am a three-year survivor. I am hopeful that your husband receives the care that is best for him. Unfortunately, access to good healthcare isn't always easy, and there are disparities between health care systems.
Do you know what type of lung cancer he has? Do you have an upcoming appointment with Mayo Clinic?

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@lls8000

@millie5737, Thanks for letting us know, I had been thinking of you. I'm glad he came to this realization, it's hard to admit that you aren't able to do the things that you could when you were younger and healthy. You've been married for a long time!, so you know best how to approach each other with delicate situations. If your mantra works in for you then use it, everyday if need be. This is still a relationship where there's give and take, make sure you take care of your own needs too.
Is the inflammation getting any better, or worse?

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You are ever so full of compassion, thank you. The inflammation has been the most difficult to respond d to treatment. We are always told the next cat scan will determine the effectiveness of the cancer treatments and then it is murky due to the inflammation. More steroids. Well the next scan scan might tell us if it has improved. He seems much weaker, more difficulty breathing, catching his breath, more effort speaking, needing more rest, pulse high…..

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@fef

I had fourth stage Rectal Cancer, I know not the same, but I thought important to let you know that cancers can be cured today. I had months of chemo and now have been ckean forn10+ years.
So, bottom line NEVER GIVE UP HOPE.

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Hi @fef, your story and experiences with stage 4 rectal cancer are also welcome in the Colorectal Cancer Support Group here: https://connect.mayoclinic.org/group/colorectal-cancer/

Ten years in remission gives hope to many. Thank you.

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This is tough. All I can advise is to make sure you do what is necessary for you to keep a high nutrition diet, stay hydrated and do stretches (even in bed) to keep up your strength. They are one of those things no one feels like doing when they are not well. Enriching activities, like movies, audio books might help. Best wishes.

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@katiesue

After awhile I learned to embrace the treatment effects. They didn’t last that long. Keep a diary or a checklist and you may start seeing a pattern. The steroids made me feel energized at first and then I knew I’d be spending a few days on the couch barely eating. So I had my cream of wheat and bananas; soup and crackers at the ready. Easy reading ( books I’d already read and loved so it would be easy to focus), and my favorite movies so if I fell asleep I wouldn’t miss anything. I got rid of any guilt I might feel for just staying low for a few days. Then gradually work myself out of it again until I was back to normal. ( Knowing I was going to have to do it all over again I three weeks)

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Hello Katiesue,
I go through the same challenging days after the treatment. It’s hard, isn’t it? I dislike being so sick and weak. My heart pounds just walking outside to sit in a chair. Fortunately it’s only about three days and then it lifts. I’ve gone through four rounds of a standard therapy along with keytruda following three rounds in a clinical trial. Next week I have the scans at Mayo to determine what next for treatments. I am hopeful no more carboplatin.

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@soupycampbell, I am truly motivated by what you said..it apparent that you know yourself well and what is best for you..I on the other hand tend to freeze up when I hear what some doctor says… I always had a strong voice but I’ve become more withdrawn and I don’t like it, thank you for the strength you show, it’s very inspiring for me and I truly wish only the best for you.

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@millie5737

Thank you for you continued positive kind words. His spirits remain good. He avoids any “real life talk” with me. No need for me to be specific, it’s just that sometimes I feel that he is in denial. I have a need to get a few things out in the open and I suppose that is my issue and not his. I am frightened when his oxygen levels go way down with a minimal amount of exertion. He refuses to cancel a long plane trip to see one of our sons and his family. We are seasoned travelers but never with oxygen, wheelchairs, and with cancer, blood clots and lung inflammation. Am trying to be strong and support his wishes. It’s his life, his cancer, and I am not his mother.

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OMG! He is one brave soul, just the kind that can get cured, hopefully.
I wish him oceans of love and peace!
This is a picture of me last summer at Jone Beach. I was 88 the now 89 and not in the best of health but enjoying every day like it’s my last.
As a point of info I have been dead once and alsmost twice more during the Korean War, so always stay strong and when I was gone no pain, no worries etc., lola

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