Cabo?
Comments
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Foxfoxhd said:Donna
I am currently on steroids for inflammation and it has relieved all pain. As to adding a diet componet of anti inflams, it would be a drop in the bucket. Besides it is far to late to use supplements to affect my prognosis. Living pure from day one is too difficult because of the chemicals we have absorbed in our life time. Our body is an enviornmental filter damaging our dna and random cell mutation happens. I exist at the stage of managing symptoms for as long as I can. And hopefully with as few side effects as possible. 3-4 years ago I said,"Bring it on!" Now I say, "Lets hang on as comfortably as I can."
But NEVER count me out. I have remarkable healing powers. There is a loss from the battles but I tolerate a lot.
During the last few daysFox
During the last few days I was in the hospital in Feb after my nephrectomy I read ALL the posts on this entire site. You have been through hell and back my friend. But you always come back. You are a inspiration to me to keep dredging through the mouth sores diarrhea insomnia nausea etc. I have no great words of wisdom for you. Just continue posting with your updates. You're important to more of us than you may realize.
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Thanks Airiehardo718 said:Ditto to Airie's comments
Fox....you're a keeper!
Donna~
You guys too. Donna keep the faith. Jojo, You know where my head is at. Keep defying the odds. Airie, that's a lot of reading. Even if you just read mine. You must know stuff I've forgotten. I have an ability to let things go so that I don't dwell on them. So I forget things like esophogeal sores, skin peeling and sensitive hands and feet, etc. I couldn't imagine how many tumors I've had. Or the amount of radiation. And here I am. Out in the garage working on an old motorcycle. This ones for you Ron. I'm cleaning, painting, and rebuilding a vintage Honda. Doing it the way a kid builds a model car. Nothing fancy. Just bigger pieces. I'm having a ball.
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So sorry to hear this foxy!foxhd said:Thank you
sweetheart.
So sorry to hear this foxy! How about the link I sent you? I really think you should look into it. I have bought some for mysefl and for my son with ASD. He has shown some great results. There are all kinds. One you can inhale in a nebulizer for the lungs mets. Drops you can take orally, creams you can rub on and even injections. I cannot name the product here or i will be banned. You know what i am talking about. Please, give it some thought, others have great results with it.
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Fox... that is great that thefoxhd said:Thanks Airie
You guys too. Donna keep the faith. Jojo, You know where my head is at. Keep defying the odds. Airie, that's a lot of reading. Even if you just read mine. You must know stuff I've forgotten. I have an ability to let things go so that I don't dwell on them. So I forget things like esophogeal sores, skin peeling and sensitive hands and feet, etc. I couldn't imagine how many tumors I've had. Or the amount of radiation. And here I am. Out in the garage working on an old motorcycle. This ones for you Ron. I'm cleaning, painting, and rebuilding a vintage Honda. Doing it the way a kid builds a model car. Nothing fancy. Just bigger pieces. I'm having a ball.
Fox... that is great that the growth is inflammation. That just might be the case. So, was there also new growth or they think those nodes are just reactory? I am not going to count you out by any means. There are still too many other things to do.
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Ange,angec said:Fox... that is great that the
Fox... that is great that the growth is inflammation. That just might be the case. So, was there also new growth or they think those nodes are just reactory? I am not going to count you out by any means. There are still too many other things to do.
my scans lit up everywhere. Everywhere. Bones, lung, nodes. Like a field of dandelions.
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Foxy, I love you to the moon and back...foxhd said:Ange,
my scans lit up everywhere. Everywhere. Bones, lung, nodes. Like a field of dandelions.
just don't tell your wife and I wont tell my husband!
Summer will be here in no time so its a good thing you are working on that vintage Honda and probably shining that Harley of yours, and oh, remember to tune up the guitar for some good ol' blue grass playing! As for the rest, not that I want to put a lot of pressure on you but you know how so many of us look up to you and care for you. We are hoping, wishing, praying and sending good vibes that your treatment will have positive results this time around. Im wishing with all my heart you have a good Summer like you did last year.
Im having a difficult time lately with both my parents health so I come around not so often as usual. I'll be checking on news from you. Please be well.
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Hmm.. makes me wonder what isfoxhd said:Ange,
my scans lit up everywhere. Everywhere. Bones, lung, nodes. Like a field of dandelions.
Hmm.. makes me wonder what is going on. That seems like too much for it to be cancer. Must be inflammatory. Any side affects with the cabo?
It looks like mom has to be removed from Votrient after almost 4 years. She was ned then a node will show, now show, show not show. Seems like the two that show on and off coincide with infections. So, votrient worked good in that matter. But, she has started to get brain symptoms, seeing people, talking to them etc. I a not sure if that could be the medicine. But, each time to refill it the pharmacy always asks if she is having mental issues. Where is TW when you need him? He would know about that. Does anyone else have a clue? Mom is also 83 but it came on so suddenly it seems weird.
I am praying for you, Fox. Glad the pain is gone. Keep us posted! ELF! xxoo
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cabo plan on holdEliezer2 said:cabo is new , from sutent family
not sure how much track recod there is
Wow. This has been something. Sarah, I am betting my life on everything being inflammed. Many pow wow's with my care givers. Believe me when I tell newbies that I am so sorry that you are here. I know how scared you are. How do you make decisions? I'll also tell you that after a while you get less frieghtened and much smarter. That may be it's own problem. It's a good thing that I feel ready to fight. I'm getting the sbrt/gamma knife to my spine. And 2 more nivo infusions then scan. The radiation is mandatory. Neurosurgeon will do myelgram for mapping. Then it will be a one shot procedure. This is the second course thru my neck and the last. Risks we won't bring up here. I don't look forward to reliving last years struggle or worse. No options here. But I'm ready. Well, maybe more ready next week, or november, or never but I don't get to choose. I am playing my hand for extending quality of life. Cards are on the table.
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You're always in myfoxhd said:cabo plan on hold
Wow. This has been something. Sarah, I am betting my life on everything being inflammed. Many pow wow's with my care givers. Believe me when I tell newbies that I am so sorry that you are here. I know how scared you are. How do you make decisions? I'll also tell you that after a while you get less frieghtened and much smarter. That may be it's own problem. It's a good thing that I feel ready to fight. I'm getting the sbrt/gamma knife to my spine. And 2 more nivo infusions then scan. The radiation is mandatory. Neurosurgeon will do myelgram for mapping. Then it will be a one shot procedure. This is the second course thru my neck and the last. Risks we won't bring up here. I don't look forward to reliving last years struggle or worse. No options here. But I'm ready. Well, maybe more ready next week, or november, or never but I don't get to choose. I am playing my hand for extending quality of life. Cards are on the table.
You're always in my thoughts. I have the feeling those cards on the table will be a good hand!
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Data showing it superior to AffinitorEliezer2 said:cabo is new , from sutent family
not sure how much track recod there is
With regard to Cabozaitinib: I'm looking over my notes from Kidney Cancer Association conference in Los Angeles
States "may eventually be a front line drug" and "superior to Affinitor" written down
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An interesting discussion todayfoxhd said:cabo plan on hold
Wow. This has been something. Sarah, I am betting my life on everything being inflammed. Many pow wow's with my care givers. Believe me when I tell newbies that I am so sorry that you are here. I know how scared you are. How do you make decisions? I'll also tell you that after a while you get less frieghtened and much smarter. That may be it's own problem. It's a good thing that I feel ready to fight. I'm getting the sbrt/gamma knife to my spine. And 2 more nivo infusions then scan. The radiation is mandatory. Neurosurgeon will do myelgram for mapping. Then it will be a one shot procedure. This is the second course thru my neck and the last. Risks we won't bring up here. I don't look forward to reliving last years struggle or worse. No options here. But I'm ready. Well, maybe more ready next week, or november, or never but I don't get to choose. I am playing my hand for extending quality of life. Cards are on the table.
Smart patients has a very interesting article with Q and A's at a symposium in San diego which validates your current plan and what I have learned about TKIs for my husband .
it was posted today and the symposium was this weekend.
Sarah
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Thinking about you, Foxy!Dave418 said:I'll wish you just one thing :
I'll wish you just one thing: May those cards on the table be a Royal Straight Flush!!
Good luck!!
Dave
Thinking about you, Foxy! Always! Don't flirt too much with those nurses....they don't need those distractions
Big hugs
Jojo
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WowEliezer2 said:cabo is new , from sutent family
not sure how much track recod there is
Damm sorry Fox will keep my fingers crossed hope u are still eating good and keeping your weight up
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Things can take so long
I guess I'm halfway there. First, if the nivo isn't working, how come I feel so good? My activity and health are great. Food is so damn good. But, upper extremity pain and weakness are a problem, so, I look forward to next week when I get the SBRT to my spine. I had a nivo infusion today and with it came a tumor flare up a couple hours later. I realize that I get many of these tumor flares. A month ago when I had my knee drained, it hemorraged because I was on coumadin. If I wasn't on coumadin, it would have just hurt. So we got a little misdirected because of the bleed. A couple days back I tossed some garbage and with it my shoulder. Same type of acute pain. So I may have this shoulder added to my radiation. Follow up scans won't be for 3-4 more weeks. Thats ok with me. One thing is for sure and that is that I don't really mind these acute episodes because otherwise I feel great. Not like the votrient where I was always sick. Pain has been manageable with a couple oxies a day and the occaisional trip to the dispensery.
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Also had a myelogramfoxhd said:Things can take so long
I guess I'm halfway there. First, if the nivo isn't working, how come I feel so good? My activity and health are great. Food is so damn good. But, upper extremity pain and weakness are a problem, so, I look forward to next week when I get the SBRT to my spine. I had a nivo infusion today and with it came a tumor flare up a couple hours later. I realize that I get many of these tumor flares. A month ago when I had my knee drained, it hemorraged because I was on coumadin. If I wasn't on coumadin, it would have just hurt. So we got a little misdirected because of the bleed. A couple days back I tossed some garbage and with it my shoulder. Same type of acute pain. So I may have this shoulder added to my radiation. Follow up scans won't be for 3-4 more weeks. Thats ok with me. One thing is for sure and that is that I don't really mind these acute episodes because otherwise I feel great. Not like the votrient where I was always sick. Pain has been manageable with a couple oxies a day and the occaisional trip to the dispensery.
last week to add to the mapping for my sbrt. Now as a therapist, I've seen hundreds and hundreds of patients post myelogram. But I never had one. It was an awesome experience. I am very impressed. The big lesson here is the same that we discuss regarding finding a doctor who does a lot of nephrectomies, not 2 or 3 a year. This Dr. Johnson must do hundreds and hundreds. Anyway, the entire process went flawlessly. Whatever drugs they used were perfect. Went home a couple hours later with only a tiny band aid on the procedure site. I even drove home. My biopsies a few years back should have been so easy.
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Always learning from you
Not sure what a myelogram is, so will look it all up. If you treated patients after one, it might be something that if not done perfectly, it leaves one in pain?
I am also holding well with the Nivo and feel SO good. I don't have anything but knee and shoulder pain a few days after, and although not really that awful, since I ordinarily feel SO good, it gives me something to complain about...
Isn't Cumadin the blood thinner you gotta get lots of blood test done often to keep the right dosage? I think I remember that from taking care of my Aunt. I am still taking twice a day Lovenox shots... bruises all over my middle are UGLY ugly... I want the PICC line out, but am told no because if there are clots attached, it would dislodge them. Sounds fishy to me... the blood thinner is supposed to disolve any clots... and after a month I think I should be clear. Oh well, what do I know... I'm just learning.
My scan resutls and Oncolgoy appointment are May 26th.... looking for good stuff... and for you too...
Be well Fox..... FLY
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