Hello and liver

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 xx

Disgraceful discrimination 

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

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!

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. 

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 😷 

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.

Rach 

Thanks for your reply. Are you having chemo? I’m dreading being told chemo is the plan and I ll loose my hair again 

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 xx

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.

Rach