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Hello and liver
Palmbeachprincess
Member Posts: 39 ✭
hi all
thought id introduce myself. 43 with 3 kids
I had bc 10 years ago. 2 years ago back pain and a scan showed Mets to sacrum. On xgeva and femara and in remission after radiation. Then most recent scan showed a met in my liver. Anyone else on a similar shitty path with the liver. I did a silly thing and looked at dr Google. Big mistake! Seeing my oncologist next Wednesday.
Xxxxxx
thought id introduce myself. 43 with 3 kids
I had bc 10 years ago. 2 years ago back pain and a scan showed Mets to sacrum. On xgeva and femara and in remission after radiation. Then most recent scan showed a met in my liver. Anyone else on a similar shitty path with the liver. I did a silly thing and looked at dr Google. Big mistake! Seeing my oncologist next Wednesday.
Xxxxxx
Tagged:
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Comments
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I'm not in the same situation but just wanted to say welcome. What shitty news. Dr Google is never a good place (but we all go there) - remember most of the stats are out of date.4
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Hi There.
I had bc 8yrs ago and last year found mets on spine and hips. I've had progression twice on my liver and have only just started my 3rd line of treatment (IV chemo Eribulin) to try and stablise it.
Good luck with your Onco appointment on Wednesday and I hope they can give you a treatment plan that will kick its ass.
Hugs to ya.
Rach4 -
Hi PBP yep I too have liver Mets in fact I have Mets in lungs, liver and bones - now when diagnosed stage 4 this completely freaked me out, however on reflection I try now not to worry to much about where the cancer is and focus on which systemic treatment is available to treat this nasty disease. Once this sucker learns how to travel it probably does not matter too much where it is, but whether it responds to treatment. I am currently doing ok and plan to live with the cancer thing including liver Mets for a few years yet. I understand the dr google thing I spend lots of time on the internet as I am a strong believer in looking my adversary in the eye - but it is not for all. I wish you well for your next appointment!! Cheers Al xx6
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Thanks for your reply. Are you having chemo? I’m dreading being told chemo is the plan and I ll loose my hair again0
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Rachey73 said:Hi There.
I had bc 8yrs ago and last year found mets on spine and hips. I've had progression twice on my liver and have only just started my 3rd line of treatment (IV chemo Eribulin) to try and stablise it.
Good luck with your Onco appointment on Wednesday and I hope they can give you a treatment plan that will kick its ass.
Hugs to ya.
Rach0 -
Thanks for your reply.
So good chatting to other members to this shitty club. I had an awful experience recently with my breast care. A charity spa day was offered, and the ladies with bc went in between 9 and 1 and ladies with mbc had the afternoon sessions. I could not make afternoon and asked if I could join morning, however basically told no, for fear of I guess putting the bc ladies on a negative path. Really felt alienated as if I was contagious 😷0 -
Somebody else spoke on the network about a similar experience. It seems a presumably well intentioned position of organisers rather than the consensus of participants. Don’t let it put you off attending, most of us find the determination and commitment of those with mbc inspiring.3
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Yes, @Palmbeachprincess, I had the same reaction when I went to participate in an Encore program. I was told that I would frighten those with early stage breast cancer. Their loss!1
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That's sad and extremely ignorant!
My Exmed Cancer group was a combination of different cancers and different stages.
We had an afternoon tea together where we could talk about our treatment if we wanted. I was fascinated to learn one lady, a little younger than me, had been diagnosed triple neg in one breast and HR positive in the other breast. A couple were stage 4 but very relaxed and giving. One was BC and the other Hodgkin's Lymphoma.
Don't let their ignorance spoil it for you!
Take care and best wishes with ongoing treatment
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Disgraceful discrimination0
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Hi @Palmbeachprincess, it’s different for everyone, but I was diagnosed stage 4 bc with liver Mets June 2015 and post-chemo I’ve had no trouble with my liver at all. No symptoms and liver function is normal. I credit all the wine and G&Ts for awesome liver fitness 😱😉 . Wishing you all the best xx4