It's back
No surprise really, but frustrating that it's taken 2 months to figure out. Back in the bones again. Meet with the oncologist tomorrow to see what her plan is. Folfiri I think. She also wants to do a brain MRI to make sure there isn't anything else going on.
besides the perforation from the colonoscopy last week, he's been feeling okay. If not for the rise in CEA, we wouldn't have expected anything.
Comments
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Oh, damn, Jen, I'm sorry.
Oh, damn, Jen, I'm sorry. This has been such a roller coaster ride for your family. Prayers and wishes for a good plan and the strength to enter treatment again. You are an amazing supporter aand Mom and wife and.....so much on your plate.
hugs,
CM
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Jen, I'm so sorry
That is has once again showed up, but at least with the rising CEA you are no longer wondering where It is, but now onto how to fix it. This cancer sure isn't a walk in the park, it's more like walking through gang territory in a ghetto somewhere wondering when a bullet's going to hit you, it down right SUCKS big time, I think I'm in my pissed off at cancer mode right now, it's being pretty darn cruel to us all at the moment.
But... on the other hand, since we can't change what is, we might as well go forward kicking it's arse as we rid our bodies of it. Here's to the chemo attacking his cancer cells and tumors well, a good MRI and getting that CEA down once again and having a long break in the future from cancer.
Definitely sending hugs and an arm around the shoulder your way,
Winter Marie
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Sorry
There's radiation treatments for bone mets and luckily they're not fatal. Tumors in organs are but not the bones. A sensitive CEA is a good thing to have, it's a warning beacon so you can catch things early. Having said that it totally sucks that it's back for both of you. Modern medicine simply does not have a way of eradicating all tumor cells in us, the chemos are also ineffective much of the time. There's hope in more sophisticated targeted approaches like immunotherapy, gene mapping and cancer stem cell research but I sure wish they would hurry up! Keep the faith and good luck!
easyflip/Richard
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F cancer
I hate this disease and what it does to all of us. I, too, am still in the anger phase of grief. So many errors and bad treatment for my husband.
Recurrence is a word we all hate, but it is always lingering there in our minds. It's time for you to get back into fighting mode. My husband did pretty well on Folfiri, better than Folfox anyway.
Good luck with your next steps
Linda
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Just Relentless!
So sorry Jen! Hope he can get a good plan going and knock it out. He is young and strong, he can fight this off. I know this is scary for you, I will be thinking about you and hope for the best!
Sandy
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arrghMomof2plusteentwins said:Just Relentless!
So sorry Jen! Hope he can get a good plan going and knock it out. He is young and strong, he can fight this off. I know this is scary for you, I will be thinking about you and hope for the best!
Sandy
Just when you guys were ahead, one step backwards. Sorry about this. Hope they figure out an appropriate treatment plan for him.
atb
Karin
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Damn it. I am so, so sorry. I
Damn it. I am so, so sorry. I didn't even want to open the post. Cancer sucks. I hate it and am so sorry for you and your family.
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I was going to ask how your
I was going to ask how your husband is doing and saw your post. My husband's last CEA became 39.6, and the scan in the middle of Feb didn't show anything. I am sure cancer is somewhere, but I hope it is in a place where can be easily removed. I understand your frustration. We are in the same boat. Hang on there.
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Oh no...
I am so f'ing sorry, Jen. This is SO UNFAIR.
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Oh Jen!
Oh Jen,
I am so very, very sorry to hear this. I'll be thinking of both of you. I know how very difficult this news is. We will be here.
Aloha,
Kathleen
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Thank you all! You guys know
Thank you all! You guys know what to say, like no one else does.
Hoping the folfiri isn't too hard for him to handle. It's important for him to be able to work, do activities with the kids and his volunteer activities. I know it will be hard on him if he gets really wiped out. Hopefully the timing with spring will give him some extra energy. Mostly hoping it knocks out/down the cancer and we can continue with life hoping for a cure or really good trials.
So we went out last night to a fancy restaurant in town that he's never been to. I only recently went with friends. We've lived in this town for 19 years and have never been there because it's kind of pricey. He is very concerned about money, but I convinced him he needed to try it. We both thoroughly enjoyed ourselves. He even ordered dessert. I think we both needed it...we didn't even talk cancer - or the kids the whole time we were there
Thank you all. I appreciate you all so much.
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Have they done a colonoscopyFight for my love said:I was going to ask how your
I was going to ask how your husband is doing and saw your post. My husband's last CEA became 39.6, and the scan in the middle of Feb didn't show anything. I am sure cancer is somewhere, but I hope it is in a place where can be easily removed. I understand your frustration. We are in the same boat. Hang on there.
Have they done a colonoscopy or a brain MRI? It's so concerning and frustrating when they can't figure it out.
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You are right Richard - weEasyflip said:Sorry
There's radiation treatments for bone mets and luckily they're not fatal. Tumors in organs are but not the bones. A sensitive CEA is a good thing to have, it's a warning beacon so you can catch things early. Having said that it totally sucks that it's back for both of you. Modern medicine simply does not have a way of eradicating all tumor cells in us, the chemos are also ineffective much of the time. There's hope in more sophisticated targeted approaches like immunotherapy, gene mapping and cancer stem cell research but I sure wish they would hurry up! Keep the faith and good luck!
easyflip/Richard
You are right Richard - we are thankful it hasn't gotten to the organs yet (and hopefully won't). They are hesitant to use radiation as he's had it in the past for testicular cancer. Plus I think the bone mets are wide spread and they do seem to respond to the chemo.
Yes, hurry up with the damn cure already.
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Winter, I printed yourherdizziness said:Jen, I'm so sorry
That is has once again showed up, but at least with the rising CEA you are no longer wondering where It is, but now onto how to fix it. This cancer sure isn't a walk in the park, it's more like walking through gang territory in a ghetto somewhere wondering when a bullet's going to hit you, it down right SUCKS big time, I think I'm in my pissed off at cancer mode right now, it's being pretty darn cruel to us all at the moment.
But... on the other hand, since we can't change what is, we might as well go forward kicking it's arse as we rid our bodies of it. Here's to the chemo attacking his cancer cells and tumors well, a good MRI and getting that CEA down once again and having a long break in the future from cancer.
Definitely sending hugs and an arm around the shoulder your way,
Winter Marie
Winter, I printed your message on the other thread about how you decided to not sit and wait to die, you kept living. I also printed your entire history from your profile page. He's not a reader, but he read through the entire thing and really appreciated your insight and all you have been through.
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Oh one thing the oncologist
Oh one thing the oncologist mentioned. I don't think I asked about this yet, but she said his spleen is very enlarged. She seems to think it's holding onto his extra platelets and shooting them out when needed...or something like that. Anyone have any thoughts on that?
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I have a very enlarged spleenjen2012 said:Oh one thing the oncologist
Oh one thing the oncologist mentioned. I don't think I asked about this yet, but she said his spleen is very enlarged. She seems to think it's holding onto his extra platelets and shooting them out when needed...or something like that. Anyone have any thoughts on that?
I have a very enlarged spleen as well. My oncologist and interventional radiologist agree that it is holding my platelets giving me low counts. They think it is fromportal vein tension in my liver due to the surgeries which is causing the spleen to back up with the limited blood flow through my liver. My interventional radiologist said he can embolize the spleen to make it shrink but wants to wait until if and when my platelets drop to 50. I have a scan in 1 1/2 weeks so I am interested to see if the spleen grew more and how the ablations look 4 months later.
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