I saw my oncologist this morning and I am starting Gemcitabine and Carboplatin in the morning. My Ca125 has gone up to 374 from 166 in December and I have the new tumours. I am pleased that I can still have chemo although I'm slightly concerned by comments like "it's worth giving it a try" That doesn't exactly how inspire me with confidence.
The good news is that I saw the palliative care doctor at my local hospice yesterday who took time to listen to me, examined me, studied my ct pictures carefully and has some ideas about bowel issues and pain in my side and hip. She is liaising with my oncologist to prescribe medications which will work alongside my chemo. She gave me so much more hope if being in less pain.
Thank you ladies for your continued support. Sian xxxx
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Welshandproud
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Wishing you well with this combination Sian. This is what they gave me for a first recurrance. I found it very do able and a lot less troublesome than the carbo/taxel for the initial disease. Good luck and shall be thinking of you tomorrow. Sylvia x
I have everything crossed that this next line of treatment works for you & you can once again recover from this horrendous disease & get on with your life as you wish.
I’m about to have another major op ( Tuesday ) followed by more chemo after hearing about my first recurrence.
It’s all so daunting at times but there’s always hope.
Sian, I finished carbo/gem for 2nd recurrence in October 2019. It was by far my easiest chemo experience. My hair thinned a bit, but I got to keep most of it. Side effects were minimal. I felt tired. It did the job! CA in normal range. No visible disease on scan. I am now on Lynparza. I am 3C HGSE BRCA1 and HRD+. I feel better than I have for years. You can do this!!!❤
I am starting CarboGem today too. My CA125 is now over 1100, but my treatment was delayed by my looking at a trial. It’s good to hear that for many, this regime is manageable. My appointment is at 4:15 today, so I’m going to try to get my house reasonably tidy (we’ve had an amazing builder in doing our bathroom for about 10 weeks now!). I had a PICC line put in yesterday - another interesting experience, but I can’t have a shower until the waterproof sleeve arrives - possibly as late as Monday - euggg !!
I really hope this works for you - I will be with you in spirit all day.
This is my next line of treatment but I have decided to delay for a bit as just getting over the flu. Keep us posted on how it goes and good luck. I was originally diagnosed in 2013 and have just been on Zejula which, like many others, has not worked.
Good luck, Siam with the new chemo. Let’s hope it wipes out the cancer! It sounds like going to palliative care was an excellent idea. Let us know how it all works out. Xoxo
Wishing you well. I was on that combo for over a year. My doctor first put me on for 5 months and it came right back. Then he put me back on for a whole year. I went to NED almost right away and stayed that way. I have been in remission (on no chemo-just avastin) for 5 months. I think everyone tolerates different chemos differently. For me, by half way through my hair thinned. I suspect it activated my arthritis, because a few months after I got off, my arthritis abated. I hear from so many that one can do fine and be on chemo (or not) for at least 10 years and more. I keep hearing from people who do that. So please keep hope. Personally I try to feel that chemo for a decade or more won't be bad. I would love to have along remission, but I am worried about expecting too much and being disappointed.
Yes, really not bad for me. I try to stay positive mentally...remembering gratitude for what I have in life. Good luck to you. There's very many possibilities that things work out well for way longer than I thought when I was first diagnosed...even with chemo. Love and hugs!
Yes the same. The dexamethasone is certainly helping but you can't stay on them for too long. They also give me the munchies s I'll be having to widen the door frames soon lol xxxxx
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