3-month survival for stage IV lung cancer? Is it true? Need hope

Posted by rlf66 @rlf66, 2 days ago

I was on internet checking for stats on survival time for stage IV lung cancer. One site mentioned that most people have a 3 month survival time!! Obviously, I was shocked and very discouraged re: my diagnosis over month ago. I have still to consult doctor and find out what type of cancer I have. I know it is NSCC non small cell cancer which metastiziced to my right temple which makes it stage IV. I will need to go for further test to see where it may be surfaced. A PET scan over month ago found it left lung.
rlf66

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Please give me any information to what you may have experienced and what type of therapy worked and what did NOT work.

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@rlf66 Hello. I was diagnosed with nsc lung cancer, stage 4 in September 2022. I am still here, using supplemental oxygen and my nebulizer daily.
I am a Mayo MN patient and they have treated me well. I’ve been in two trials and have had standard therapies. I had a run of 22 good months on an oral trial medication. Now I’m waiting to see if they have a new recommendation next week. I have a brain mri and ct scan on Monday. I have empathy for you, it’s hard not to be scared and anxious. I try to take things one day at a time. I hope I’ve given you encouragement.

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@rlf66 , There are many different types of lung cancer.
The general statistics are lagging behind the advancements that have been made in the past 5-10 years. They are a picture in time, but the treatments have improved, so they aren't always accurate today.
We are not statistics. We're individuals, and we react individually to treatments. No one can predict how well we'll do on any treatment.
I hope you are able to get some of your questions answered. The waiting and the unknown is one of the hardest things in this process of being diagnosed. Is your appointment still scheduled for this week?

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@frouke Thanks so much and God bless you.
rlf66

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@rlf66 God bless you too 🙏

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Profile picture for frouke @frouke

I’m sure you will get some good feedback here regarding stage IV lung cancer and it’s not as hopeless as you might think, I also look up everything and it can get scary. I do know that many people are living long and happy lives with cancer due to better treatments and drugs to make it possible, ask lots of questions from the doctors and get as much information as you need to help you get through this difficult time, eventually you’ll start to adjust to changes that come along, also please stay connected with this site so that you can ask questions about what is happening and you will definitely not feel overwhelmed and alone because you’re not alone, best wishes for a good recovery.

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@frouke Thanks so much and God bless you.
rlf66

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Profile picture for mally007 @mally007

I was diagnosed with stage 4 lung cancer with the ALK+ gene mutation. That was over 5 years ago. I take oral pills daily. I just had progression with mets to the brain in late July. I had 12 small spots, I got them zapped and started a different oral pill. It didn't slow me down and it is just the waiting game to see if it worked with a brain MRI in December. It is hard not to think the worst and when you see what the internet says you do think the worst. Look for the sites like this one that are informative and supportive. There are constant changes going on and new treatments, clinical trials etc. Once you know you biomarker that will help as well. Always ask questions, stick with the positiveness and best to you on your new journey.

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@mally007
Thanks so much for taking time to inform me. God bless you and best to you during your difficult journey.
rlf66

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I was diagnosed with stage 4 lung cancer with the ALK+ gene mutation. That was over 5 years ago. I take oral pills daily. I just had progression with mets to the brain in late July. I had 12 small spots, I got them zapped and started a different oral pill. It didn't slow me down and it is just the waiting game to see if it worked with a brain MRI in December. It is hard not to think the worst and when you see what the internet says you do think the worst. Look for the sites like this one that are informative and supportive. There are constant changes going on and new treatments, clinical trials etc. Once you know you biomarker that will help as well. Always ask questions, stick with the positiveness and best to you on your new journey.

REPLY
Profile picture for rlf66 @rlf66

Please give me any information to what you may have experienced and what type of therapy worked and what did NOT work.

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Hiya@rlf66 I was diagnosed with stage IV nSCLC that had spread from lung to liver, pelvis, hips, spine and clavicles. Immediately started radiation then chemo. My oct scan showed 8 of 10 tumors had reduced or eliminated. Now on keytruda to attack the others. I too read the horror stories on the internet but with today’s drugs it’s beatable.

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hi @rlf66 - that information is frightening. I'm including a blurb from the American Cancer Society about caution in looking at overall survival numbers. when do you see your doctor to get your biomarker diagnosis and discuss your treatment options? is it possible for you to get a second opinion as well? when I was diagnosed, I was able to see a new thoracic oncologist at our cancer center in Seattle very quickly (I think it took about a week.) they understand time is of the essence!

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