I got the answer to the question I never wanted to know the answer to
Comments
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Dang it!thready said:Not knowing what to say
Kathryn,
We started together it this ugly war, you went through a hell of a battle with cancer and with the chemo, it seems so unfair that you have to do it again. We will all be with you cyberly.
I hate this disease!
Jan
I am stage !V and have a very aggressive ONC, be sure you have one too!! You can do it!! Keep positive, smile and kick butt!0 -
....or even wanted to know the question!!!!
I'm sorry, dearheart, for the news...but knowing can be a power, also....
I haven't had mets, but 2 primary cancers...rectal, stage III, breast, stage II.
I really don't know which is worse...mets or multiple primary sites...I know what my insurance company thinks...if you are clean for 5 years from mets, you are insurable. If you have multiple primaries (like me), you are never insurable again...sigh...
Hugs, Kathi0 -
Kathryn , so sorry for the news but cheer up!KathiM said:....or even wanted to know the question!!!!
I'm sorry, dearheart, for the news...but knowing can be a power, also....
I haven't had mets, but 2 primary cancers...rectal, stage III, breast, stage II.
I really don't know which is worse...mets or multiple primary sites...I know what my insurance company thinks...if you are clean for 5 years from mets, you are insurable. If you have multiple primaries (like me), you are never insurable again...sigh...
Hugs, Kathi
You got a PM from me.0 -
I know
Hi Kathryn,
I feel for you & know how you feel- there was one point in time where I was told I was NED (this was before I joined CSN), but that NED status lasted only four months for me & I've been fighting the beast ever since. It will be hard, but then you get back into the "okay, now that I've digested and mourned this news, I'm now ready to give it all I've got and fight hard!". Folfiri can kick the cancer cell's butts!!
I'll be thinking about you and praying for you.
Take care,
Lisa0 -
My husband also
Kathryn,
My husband is also stage IV, he was diagnosed 3 years ago. He was put on the same chemo that you are going on for 6 months, and when they did his pet scan, the chemo had gotten everything, the Onc. took him off for 4 weeks and then did another pet scan, he had a small spot show up and she put him right back on chemo and took care of that. He is now cancer free and will be on chemo for the rest of his life - 3 days every 3 weeks. The onc. is good, she gives him breaks whenever he feels he needs them or wants to go on vacation or for holidays. But she limits him to 2 breaks a year - so he is careful when he chooses them. You will do great, that chemo will kill those little buggers and you will live a long live, and so what if you have to have chemo for the rest of your life, as my husband says, it's a small price to pay to be around for a long time; or until i get sick of him...LOL !!! Anyway, you will do great - i'm praying for you. Keep us informed.0 -
Kathryn,Sandi1 said:My husband also
Kathryn,
My husband is also stage IV, he was diagnosed 3 years ago. He was put on the same chemo that you are going on for 6 months, and when they did his pet scan, the chemo had gotten everything, the Onc. took him off for 4 weeks and then did another pet scan, he had a small spot show up and she put him right back on chemo and took care of that. He is now cancer free and will be on chemo for the rest of his life - 3 days every 3 weeks. The onc. is good, she gives him breaks whenever he feels he needs them or wants to go on vacation or for holidays. But she limits him to 2 breaks a year - so he is careful when he chooses them. You will do great, that chemo will kill those little buggers and you will live a long live, and so what if you have to have chemo for the rest of your life, as my husband says, it's a small price to pay to be around for a long time; or until i get sick of him...LOL !!! Anyway, you will do great - i'm praying for you. Keep us informed.
I am keeping you in
Kathryn,
I am keeping you in my prayers!
Kathy0 -
Two primaries for me tooKathiM said:....or even wanted to know the question!!!!
I'm sorry, dearheart, for the news...but knowing can be a power, also....
I haven't had mets, but 2 primary cancers...rectal, stage III, breast, stage II.
I really don't know which is worse...mets or multiple primary sites...I know what my insurance company thinks...if you are clean for 5 years from mets, you are insurable. If you have multiple primaries (like me), you are never insurable again...sigh...
Hugs, Kathi
This is my second primary. I fought cervical cancer for a couple years. I was NED for 5 years, then last fall my Pap was ASCUS. I didn't have a repeat check because chemo messes them up. I was going for the repeat the end of this month. But now it will be tomorrow before I start chemo again. I was just a stage IIa for cervical.
I'd take a dozen more primaries at stage II than one stage IV. But I'd prefer to have none of any kind, as we all would!0 -
AlthoughSundanceh said:Stage IV Club
Knowing the answers seldom makes it any easier, I have found throughout this trial. But, at least knowing is knowing and from there, we can move forward.
Your protocol sounds "sound." We'll absolutely hope that does the trick.
I'd say Welcome to the "club" but being a Stage IV doesn't make the ballons fall out of the ceiling, it just makes our road a little bit harder to hoe.
But knowing you, I know you can stand in there, Kathryn. I've got a bunch of stuff ahead myself with more chemo and radiation, so I understand how it was to hear what you already knew.
The road looks long now, but we've walked down this road together before, so we know the road markers ahead. I'll see you at the first "rest stop" - we'll chat:)
-Craig
Although you are a great role model, I'm not aspiring to be just like you. I'm not sure I'm up to dealing with robots.
Not just a bump in the road like first time around - now we just keep going over lots of bumps. But we've had practice, so while they might wear us down a bit more, we learn little tricks to deal with them better than before. And I don't see how Irinotecan can possibly attack me the way oxaliplatin did, with every weird side effect and the allergy. I'm going into the winter not having to worry about the cold issues with oxy either - another plus.
I hope you are getting enough rest to get you through your recovery right now. You've had a tough year. I'm pretty darn tough, but not sure if I'm put together quite as tough as you. I'll give it my best shot though!0 -
ThanksHollyID said:Kathryn,
This is a post that I never wanted to read from you. I am so sorry.
I am going to pray like mad that the FOLFIRI and Avastin kick it's butt.
Love and Hugs,
Holly
Thanks Holly - that is what I'm hoping. Oxy was hard on me - I expect Irinotecan and Avastin to be hard on the cancer!0 -
Thanksabmb said:Prayers
Thoughts & Prayers are with you. God Bless. Margaret
Thank you!0 -
ThanksAnneCan said:So sorry Kathryn
I am sorry to hear this news. Here's hoping Folfiri + avastin will do the trick + make those nasty buggars go away.
Thanks - me too!0 -
ThanksAnneCan said:So sorry Kathryn
I am sorry to hear this news. Here's hoping Folfiri + avastin will do the trick + make those nasty buggars go away.
Thanks - me too!0 -
ThanksAnneCan said:So sorry Kathryn
I am sorry to hear this news. Here's hoping Folfiri + avastin will do the trick + make those nasty buggars go away.
Thanks - me too!0 -
ThanksAnneCan said:So sorry Kathryn
I am sorry to hear this news. Here's hoping Folfiri + avastin will do the trick + make those nasty buggars go away.
Thanks - me too!0 -
ThanksAnneCan said:So sorry Kathryn
I am sorry to hear this news. Here's hoping Folfiri + avastin will do the trick + make those nasty buggars go away.
Thanks - me too!0 -
ThanksAnneCan said:So sorry Kathryn
I am sorry to hear this news. Here's hoping Folfiri + avastin will do the trick + make those nasty buggars go away.
Thank you - me too!0
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