Bummed: Colon cancer has metastasized to my liver!
I’ve been cancer free for 4 years and now it has metastasized to my liver!!! Ugh! I’ve had the liver resection, stomach resection and gallbladder removed only to get news halfway through chemo (2nd time around) that there may be disease at the liver surgical site and chemo is not working. My blood work does not indicate any tumor activity but I’m scared and anxious that the cancer has in fact survived the chemo blast. I’m active, I eat well, I’m not over weight, I don’t have a family history of colon cancer, I haven’t had any polyps since the original one went haywire...I feel defeated by something that was never on my radar to being with! I want options.
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awww thank you - I do need to get my hands on uplifting stories like yours and the book suggestion. I'm a pragmatic accountant so I see statistics. I do try to visualize every cell being in my abdomen as being healthy. See it Believe it type of thing.
Hi @marshmallowjones, Thanks for sharing your story and what you are going through. You will notice that I moved your post to the conversation that you found as well about the same discussion. This way, the members in this group can see your experience and connect with you.
Can you give any detail about your resection being so hard?
@marshmallowjones I wanted to say hello. I don't have cancer and I can't share any medical advice, but I had an aunt with a bad lymphatic cancer and she should have only lived a year, but she got much more than that, somewhere around 10 years. She had a positive attitude that she was going to beat cancer. She had quality of life. Her first husband had passed away, and she got married again. I made her wedding cake. She believed with every part of her being that she could do it and she taught me a lesson about the power patients have over their health and healing if they embrace it, make intelligent choices, and believe in a positive outcome.
Have you heard of the book called "The Last Lecture" by Randy Pausch? He had terminal cancer and wrote this book about his journey. He also believed in his fight and got more years than his doctors promised. The premise of the book came from a college writing assignment to write a "last lecture" to say what is important to you and what has meaning to your life and to write it as if you were dying. His honesty about living is very uplifting.
I hope some other patients can share some relevant experience with you.
Stable scans sounds good. I believe you mentioned the disease is inoperable, are all the interventional radiology approaches (ablation, freezing) also out?. I'm sorry if that is the case. Are you tolerating Lonsurf well?
I’m now on Lonsurf since Folfox and Folfury did not stop or slow disease progression. The last 2 scans have shown disease is stable and no new disease but my oncologist says to be guarded about what scans indicate as the type of tumors could be hard to detect through imaging. I’ve also been taking Turmeric supplements and am choosing to believe that those are helping. I have scans this week so we’ll see if there’s any change.
How are you doing now @tinad? I'm in the same boat with diagnosis looking for answers
Hi I'm 2 months post liver resection surgery and trying to make sure I've researched all my options. 3C Cancer 2018 1.Colon Resection, 2. Folfox treatment, disease free until Sep20 (which is/was encouraging to me). 3. We tried an ablation and it came back. So 4. the big Liver Section surgery was rough. I am very hung up on my 5 year survival rate. I'm 53. No interesting markers, just TP53 which is common. Chemo is not being recommended - which I am OK with. Chemo was very difficult for me. So I'm told we wait....and we hope for 6 months clear and 2 months clear and at that point I could exhale. It's a 60% chance of returning apparently which stinks. Any advice? The NSK tumor test was send out but I don't understand the real value of that if doing a 2nd resection is what is recommended (if operable) Thank you for reading this
I’m doing my best to remain positive and have sent in a request for a consultation at the Rochester campus. Only option offerEd at this time from my doc is to switch from Folfox to Folfiery. I started that protocol yesterday. I saw an article about photoimmunotherapy trial that I’m interested in checking out since surgery is not an option for me. Does anyone know about this treatment?
I am so sorry to hear this. Do your best to stay positive and stay strong (I know it is easier said than done). I will pray for you
Doc was not in the office today so conversation on options has been pushed to Monday.