Stage IV lung cancer: Just had my 2... - Lung Cancer Support

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Stage IV lung cancer

Jackiefilebacin profile image
9 Replies

Just had my 23 chemo treatment. Cancer has not spread bit tumor grew. Now on to cyberknief. I am afraid but staying strong. God is good. As always Jackie

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Jackiefilebacin profile image
Jackiefilebacin
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9 Replies
pbjb profile image
pbjb

Jackiefilebacin.

I will have treatment 20 next week. So far no change. Stage 4 also with mets to bones. Will keep you in my prayers. It's ok to be nervous and afraid. An unknown we have never faced.

pbjb

Denzie profile image
DenzieModeratorVolunteer

Best hopes for good results on the radiation.

stutheit profile image
stutheit

I had CyberKnifeon on my left lung very non aggressive the only thing is you have to lay still for an hour at each treatment but it definitely worked wish you the best

GMC1 profile image
GMC1 in reply to stutheit

Would you tell me about the Cyberknife? My husband's tumor has grown to 5 inches. Is that too big for cyberknife? How many treatments do you need? Thanks for any information you can give me.

FtB_Peggy profile image
FtB_Peggy

Jackie, Thanks for letting us know how things are going for you. I am sorry about the growth, but excited that they are addressing that with Cyberknife. Good luck to you, please keep us posted. And, yes, I can only imagine how you feel right now - but whatever those feelings are, they are normal and yours! We can't help feeling what we feel, this is scary stuff, but please know you have a lot of people cheering for you here.

MartyFaccenda profile image
MartyFaccenda

Prayers and wishing you good luck! I hope you will post results of the cyber knife results. I've been contemplating that treatment as well for my nsclc.

4 different chemo drugs have failed me over the past 2 years. Currently receiving immunotherapy(Opdivo) with good results but interested in the cyber knife treatment. God bless!

Jackiefilebacin profile image
Jackiefilebacin in reply to MartyFaccenda

Won't know about cyberknief until December. Dr said it takes st least 6 months for results. I am currently having opdivo infusions every 2 weeks. Makes me really sick. Have #7 on Thursday. Trying to stay strong. They just diagnosed my husband with a 5 centimeter mass on his right side of brain. They give him 3 months. Going to Jefferson for s second opinion on the 7. Penn wants to operate but dr said he can not get it all. Praying for strength.

FtB_Peggy profile image
FtB_Peggy in reply to Jackiefilebacin

Oh Jackie, how hard to wait, and then to get the news of your husband's diagnosis. I am more sorry than I can say. Will pray for strength for both of you. I am glad you are getting a second opinion (takes so much energy, doesn't it) but is truly worth it, as you know. Prayers, hugs and caring thoughts coming to you.

rdflynnjr profile image
rdflynnjr

Jackie, I never prayed much before, but be assured that you and your husband are in my prayers now. Please include all of us in yours also.

Rick

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