Hey Cabo You WIN
I stopped taking the CABO on Tuesday the side effects have made my daily life so miserable that I don't want to get out of bed. The pain in my esophagus has been the worst and it just keeps getting worse by the day. I spoke to my doctor and I told him I can't do this anymore even though it is working I am no longer happy, he agreed that it is time to stop. I also asked him to give me a five week vacation from any drugs while I decide what I am going to do, and give my body a chance to detox from the CABO. I may go back to CABO if we lower the dose to 20 mg's and I don't have the same issues otherwise I am done. Sorry everone about quitting but I really want to be happy and limit pain. Good luck to those of you who are still continuing CABO I hope it continues to work for you.
Mark
Comments
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Sorry to hear
I was just taken off of Votrient because it wasn't working for me.
I'm sorry to hear that you were unable to tolerate the Cabo that was working for you, but I thank you for your post.
I've been given a choice of my next course of action. One includes Cabo and one includes Opdivo. I've pretty much made up my mind for Opdivo, and I think your post solidifies the choice for me.
Don't appologize for taking a break.
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Just curious
I'm curious as to how much flexibility a patient has with these cancer meds. Fox, you seem to have adjusted your medical regiment in a way that works for you. Mark, will your doctor give you that option? If he/she does, can you experiment with a dosage regiment/break cycle that will give you a good quality of life and still battle the cancer? I'm praying for you, Mark!
Stub
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The final wordstub1969 said:Just curious
I'm curious as to how much flexibility a patient has with these cancer meds. Fox, you seem to have adjusted your medical regiment in a way that works for you. Mark, will your doctor give you that option? If he/she does, can you experiment with a dosage regiment/break cycle that will give you a good quality of life and still battle the cancer? I'm praying for you, Mark!
Stub
Over the last three years I've had two oncologists and both have graciously given ME the final say on dosages and breaks.
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Hey Foxy, I see you changedfoxhd said:Mark,
I'm taking 40 every other day. By about 3 weeks I need to skip another 2 or 3 doses. It makes a big difference. I'm taking a break now because of the buildup of side effects.
Hey Foxy, I see you changed your picture! Good one!
Always appreciate your input on here.
Hugs, Jan
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I am still on Sutent. Since it is working my oncologist at Moffit does not want me to change to Opdivo or Cabo. I researched a lot about Cabo and company Excelsis and it seems to be working well.
My Oncologist id say that some people have been having bad side effects and dosage adjustment maay be necesary.
One reason I woul opt for Cabo is not to have a port put in eventhough that would make scans and blood work easier
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Flexibilitystub1969 said:Just curious
I'm curious as to how much flexibility a patient has with these cancer meds. Fox, you seem to have adjusted your medical regiment in a way that works for you. Mark, will your doctor give you that option? If he/she does, can you experiment with a dosage regiment/break cycle that will give you a good quality of life and still battle the cancer? I'm praying for you, Mark!
Stub
Stub my medical team gives a great say in what goes on with the meds and such. I met with my ONC today and he said that if I want to be done with CABO that is fine with him, and that he things 20 mg's would probably do the same so he is reluctant to even go down to a reduced dosage. We are going to take a break from chemo and decide what the next course of action will be after I detox. As for doctors letting their patients do things like this they should it is your life and you should not be subject to unhappiness, and that is what my ONC said today, he said does not want to see my unhappy. If you don't find your doctor in your corner like that I would get a new doctor.
Mark
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Hey, Mark, glad you are going
Hey, Mark, glad you are going to get a break, well deserved! Glad too you can advocate for yourself and that your doctor listens, so important.
Just know, I care...still
Sending you love, from my heart to yours,
Jan
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QT,Qt34167 said:I am still on Sutent. Since it is working my oncologist at Moffit does not want me to change to Opdivo or Cabo. I researched a lot about Cabo and company Excelsis and it seems to be working well.
My Oncologist id say that some people have been having bad side effects and dosage adjustment maay be necesary.
One reason I woul opt for Cabo is not to have a port put in eventhough that would make scans and blood work easier
never change a med until it does not work or the side effects become intolerable. If a med works, you can try to decrease dosage to deal with side effects.
Opdivo and cabo are not chosen based on what is easier. That would be wrong. Opdivo is a immunologic. That means the drug works with your immune system to eliminate the tumor cells. It could cure you. Cabo is a drug hat blocks the developement of blood capillaries to stunt tumor growth. It kills nothing. Except the patient if toxicity occurs. Opdivo does not need a port. An iv is placed when you have blood work. It is removed after infusion.
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Jan,Jan4you said:Hey Foxy, I see you changed
Hey Foxy, I see you changed your picture! Good one!
Always appreciate your input on here.
Hugs, Jan
it took me 5 years to figure that out. I'll bet I tried to change it 50 times. Tex never believed me when I told him I don't know how to use a computer. I've only recently stopped changing my texts because I finally found the "Q". Maybe I need a new selfie but I have no idea how to get it out of my poloroid. I have no other pictures.
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True JanJan4you said:Hey Foxy, I see you changed
Hey Foxy, I see you changed your picture! Good one!
Always appreciate your input on here.
Hugs, Jan
Still wearing the same jacket and T-shirt tho' (and he hasnt aged a day!)
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Big difference
Mark between taking a break & quitting. Nevertheless, even if you decide down the road that you're done with it all, in my eyes you're still a warrior. Funny, having dealt with cancer patients in a professional setting, including family members, I have never once viewed any as quitters, not in my vocabulary I guess. It's just a personal choice that each person is entitled to make. Certainly the side effects can be so limiting it makes it difficult to feel the joy of life. You deserve the best. I have you in prayers.
Donna~
Donna~
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HDfoxhd said:QT,
never change a med until it does not work or the side effects become intolerable. If a med works, you can try to decrease dosage to deal with side effects.
Opdivo and cabo are not chosen based on what is easier. That would be wrong. Opdivo is a immunologic. That means the drug works with your immune system to eliminate the tumor cells. It could cure you. Cabo is a drug hat blocks the developement of blood capillaries to stunt tumor growth. It kills nothing. Except the patient if toxicity occurs. Opdivo does not need a port. An iv is placed when you have blood work. It is removed after infusion.
Thanks for the great advice!
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Agree with Apny and Donna -
Agree with Apny and Donna - this is not quitting. And pleasecdo not apologise to us - you owe us nothing. The only person you should care about is you ( and you family), not us!
the break will help you to make the right decision. It is hard to do a good choice when you feel awful and overwhelmed.
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My prayers are with you
I pray for peace and wisdom as you have this break. Thanks for your strength and courage!
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