Liver cancer

[Kaitlinsmum]

For over a year my ovarian cancer cells have been sitting around on top of my liver. I recently found out that they have now gone inside my liver. I am experiencing pain in my right side and back.I had got to grips with the ovarian cancer and my body after surgery and treatments. Now I feel like I'm starting all over again. I'm feeling some of the same anxiety and fear that I originally felt on my primary diagnosis.

Would appreciate any guidance, positive words ect to help me get back on track with fighting this.

[A1r1t]

Hi kaitlinsmum, sorry to hear that you're a going through this horrible thing again. You are a strong lady, having been through it once and you can get through this thing again. Like all us ladies we keep pushing this thing back, I'm not even going to name it, it's a thing a bad thing but we can overcome it! 💖 There will be another plan of action for you I'm sure. I'm waiting for a scan to see if I'm on my first reacerance but trying not to over think it anyway I'm praying 🙏 for us all and sending you my best wishes. Please let us know how you go on love Ivy.

[Kjpip]

Hi Kaitlinsmum, so sorry to hear this. I guess you're back in that horrible in-between waiting phase where you have a diagnosis but not an action plan to fight it yet. I don't really have any words of wisdom I'm afraid but just wanted to let you know that I'll be thinking of you and sending you positive thoughts. Hopefully your oncology team will let you know the next steps really soon and that will help you get back into fighting mode - you've done that before and you can do it again!

Good luck, and let us know how you're getting on xx

[Tulips66]

Hi, you didnt mention in your post what plan your consultant has for you going forward. Is another op on the cards or just chemo? No matter what they decide you will get through it, just like I did & many more of the ladies on here. You are stronger than you think. I found it nearly harder to get my head around recurring so soon after my first diagnosis. I finished my first chemo July 2019 but continued on Avastin till Sept 2020. I recurred straight away, had surgery Dec 2020 & back on chemo March 2021. After chemo I continued on Gemcitabine as a maintenance till Nov 2022. I started on Niraparib middle of Jan 2023. Sometimes when I think of all I have gone through it upsets me but then I get myself together & put it aside. I realise that I am so lucky to be still here unlike some women who are not so lucky. Once my consultant keeps telling me he can treat me thats all that matters so try & turn your new diagnosis into a positive & it will help. Listening to loud music with earphones while walking really helps me to get rid of the bad thoughts that pop into my head now & again. You will be ok believe in yourself. We women are stronger together, so you know there is always someone on here who will give you encouragement, even if they are going through the same as you. All the best & keep us updated Xx

[delia2]

Hi. I’m sorry you’re dealing with this! You don’t mention any treatment or why the cells on your liver were left there? For the surface cells I think they can use ablation but now that hat they’ve invaded maybe surgery will be the plan? Keep us posted!

[tealblue1]

I am so sorry having thought that you were clear to now be dealing with this. Just remember that you have got through this before and you can again. You should already have access to your consultant from previously so your progress and decision for treatment I would hope will be swift. The in between time is always the worst. Keep your mind active with other things and try to look at the positive advancements that have been made. The liver is the only organ that regenerates if surgery to remove some of it is the option so there is hope. You are not alone. 🙏 💙 xx

[janers]

Hang in there! I just had some of my liver removed during my debulking surgery and the fatty layer around the liver. I guess the ovarian cancer cells love that fatty liver! You’ll be OK. Best wishes always, Julie

[FlowerRose]

I have nothing helpful to add other than a big, warm California hug.

[Pianoplayer731021]

I am saying what FlowerRose just mentioned. Just sending you a warm Michigan hug and praying that you will do well in your treatment for a recurrence. Donna xx 🙏💕

[Summergold2]

I have no answers either except it seems that it is slow? I am hoping they can find a treatment that will slow it down. I am in kind of the same situation nothing on liver for 3 years but in lymph nodes. Then in Feb spots and nodes now in April like someone kicked a dandelion it is all over. Going to a Hospital called City of Hope here in California as my doctor told me I have exhausted all standard of care practices. There is nothing for me but one trial they have there,

[Kaitlinsmum in reply to Summergold2]

I hope the trial works out well for you. Good luck 🤞