Any long time liver metsters?
I just finished my 1st year anniversary with widespread mets to liver. Currently NEAD. Feeling hopeful
Any long time liver metsters still lurking on these boards? Just needing some support right now.
Comments
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Hi Sandi,
You may want to check out the How are people with liver mets doing? thread to find some inspirational members managing long-term liver mets. Make sure to say hi and share your story!
We hope this helps!
--The Mods
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Thanks!. I follow that thread. Was just hoping to get folks to respond who don't post there.
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I was diagnosed with liver mets 7/2010. I have been Ned since 2/11. I have been off all treatments for 3 years
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Thank you Lauriesh.
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I've wondered the same thing. Thanks for the post, SandiBeach
Lauriesh, your story is very encouraging. I hope you keep that going a long, long time!
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Hi there. Disregard my medical history below, as I started entering it and the dropdowns wouldn't work for me. It shows I am stage 0 - I am actually stage IV with mets to bones and liver. There is so much information I need to enter and decided to just do it later. I too, just finished up a year with mets to liver and am on Xeloda. Have been doing super and just had appointment this past Friday and markers are a tad up. I am not sure what meds you are on right now, but Xeloda hasn't really given me any terrible side effects. My oncologist is looking at Aromasin/Afinator for next treatment if Xeloda decides to stop working. There is another one he mentioned called Doce.... something. That would require a port again and I am just not feeling that!! I told him he would have to talk me into intravenous meds, because I said never again. We'll see.
A word of encouragement- we are all so different and people with mets to liver can do well and live well with faith and the rightmedication.
Eight years and three dx and this is my first post. Happy New Year to you and yours!
Jen
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I love to hear these stories. With all the new treatnents, I am hoping that liver mets will lose that dreaded feeling.
Thanks for posting. So looking forward to 2018. Afterall, we are still here and learning to live again!
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I was diagnosed with liver mets in June 2015. After chemo and the Y90 procedure I am currently NEAD. I hope to continue my good run for a long time!
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I was diagnosed with liver mets in 10/12, and became NEAD in 4/13. I did get a recurrence last November (16) but it is in just a couple lymph nodes near the liver. Tried faslodex/ibrance for 10 months, but recently changed due to minor progression (1 more lymph node, but some lighting up in liver though it wasn't an organized tumor). At least according to tumor markers, the exemestane/everolimus (Aromasin/Afinitor) seems to be working. We'll do a scan in a few months.
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Thanks everyone for posting. Hopefully these positive postings will help all of us who currently have or have NEAD liver mets.
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hey! Just adding myself to the long time liver metsters! Dx 9/12 and have been Ned since finishing up taxol 2/13! Only had 3 tumors in liver and they actually continued to shrink to nothing after finishing taxol. Thank God for good meds and good luck! May it continue for us all!
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