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Starting immunotherapy Keytruda

Lung Cancer | Last Active: 18 hours ago | Replies (28)

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@sglaza

Hello Burdyblue,
Sorry to hear about your chemo journey to date......what you have described in detail sums up what one should expect although everyone does respond differently (I'm guessing that journaling your ups and downs is actually therapeutic for you). Good that your oncologist listened to you and lowered your dosage accordingly. As you are probably learning, managing your supportive medications during your chemo treatments is an exercise in trying to figure out what works best for you without some of the unwarranted side effects (mental fog for one). Whether to undergo chemotherapy for Stage 2 lung cancer is a personal choice that should be made in consultation with your oncologist's feedback. Personally, I would have second guessed myself to this day if I hadn't taken that "insurance" step.

I apologize for assuming Tagrisso targeted therapy would be in your future after completion of your chemo treatments. Tagrisso is indicated for a certain type of cellular genetic mutation (ie. EGFR mutation) that leads to a common form of lung cancer predominately in non-smokers. You may want to confer with your oncologist to determine if the genetic marker testing they performed on your tumor indicated any specific genetic mutation as that would perhaps dictate which subsequent drug therapy might be beneficial in your case.

I had the pleasure of working in South Texas for a period of time and my lasting memory is how strong, resilient and supportive the people are there.......we can tell you have those same traits. Continued good luck and keep expanding your husband's domestic skills!

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Replies to "Hello Burdyblue, Sorry to hear about your chemo journey to date......what you have described in detail..."

Thanks, sglaza. You put some sunshine in my day. Today is day 6 from my second treatment and no longer needed the anti emetics at last. My legs feel like rubber, but they get sturdier after several day with walking and stretching. I do notice the mental fog. It hadn't occurred to me that it might be all the anti emetics, steroids and so on aside from the cisplatin and pemetrexed. I don't know, will see if it becomes clearer before treatment #3. Have warned my husband to make sure I don't leave the dogs outside like I did the other day, for instance, or the stove top on.

It was nice to hear your perspective on the stage 2 to do chemotherapy option. I erred on the side of caution, too, and look at like added insurance, although I do know that it can still crop up again for no rhyme or reason at any time. And that we are not statistics. But I'll take what I can get as there is a lot of life I'd like to live yet. That's what this whole stuff does to me, makes me think about what I put off and could have done. I know I am not alone there on that happening.

I was told initially my biomarkers were not positive for immunotherapy as I may have mentioned already. I will start researching what means what that means in my reports my oncologist gave me. Very complex compared to what I was tested for 20 years ago in the breast cancer department.

Thank you for the compliment and well wishes, sglaza.

Happy Thanksgiving. 🌾🍇