Hi Linda, I was dx 2 year ago but I know I definitely had it a year at least before that because of rib pain, docs kept fobbing me off so I phoned the bcn myself. Got a scan within about a week. Hate waiting for results, I've waited 2 months before.
So did you not have bc previously before that? You are doing really well 10 years and still going strong I hope. I've had all them treatments you've had. I was on letrozole for a few years when I found my primary, I had a full mastectomy and 20 lymph nodes removed, think about 10 had cancer in them. The longest one that's worked for me since I've had secondary's is capcitabine. Worked for just over a year. I hope they find something else be gutted if they don't. Thanks for replying and wish you all the best and good luck Linda.
Did not realise it was 10 years for your primary breast cancer. Have you just been diagnosed with secondary breast cancer?
It is a worry when we have CT scans waiting for results . I quite often have to wait upto 5 weeks for results .
I was diagnosed with breast cancer and bone mets at same time com ing upto 10 years 2 years liver mets. Over the years I have had various treatments. 6 chemo back on 2009 then Letrozole for 4 years then Everolimus and extermestane. Capecebine for 10 months then 10 pacitaxil . I am sure there must be something out there you can try if pacitaxil does not work. Don't give up.
Glad the chemo worked for you but shame it had to be stopped because of neuropathy. I've had tomoxifen for my primary was on it for years. Then they tried it again when I got dx with secondaries but it didn't work. Hope the chemo your on now keeps working for you, fingers crosses.
it wasn't a nice feeling to be told nothing more they can do. If it does come to that I will be asking for something else or a second opinion. There are 100's of different chemo so don't believe they can't find me one.anyway, good luck with everything and thank you very much for replying to my post.
Hi Sarah, thanks for replying. You haven't done to bad on chemo then, apart from your nails and neuropathy, I had that with last chemo, so I'm bound to get it again. I shaved my hair of when I was on last chemo, they said it will only thin but it was coming out in clumps and looked a mess.. I don't mind as I lost my hair 10 years ago when I was first dx, I was gutted then, not to bothered now. I just wear scarves and tie them in different ways, they look nice. Sorry to hear about your liver mets. I'm waiting for my scan results too but my onc is on holiday for 2 weeks now, so will have to wait a while.
Let me know what chemo they put you on. Good luck with everything, fingers crossed for you. Thank you so much for your kind words.
Hi Shelley 10,
I have just completed 24 rounds of weekly pacitaxol and have tolerated it incredibly well.
The only slight side effects I have suffered with are minor neuropathy in the feet and my finger nails have also suffered. I have cold caped throughout and my hair has improved since being on letrozol which sadly didn't work for me although I have lost all other body hair.
All in all I have found it very manageable and have carried on life as normal, the treatment had been very effective for me and all my liver tumours had responded well, unfortunately following my latest CT scan whilst all my other tumours have still responded well I have a new one to the liver so it is back to the drawing board to see what treatment options are still available to me.
I wish you every luck with your treatment.
Just noticed your post about pacitaxil . I was on it for 10 weeks backend of last year. I should have had 12 but started to get neopathy in fingers so it was stopped. It did work really well though. Was put on tamoxifen which worked for 9 months. I am now on Navelbine . 2 tablets per week. It must have been a shock to be told no more treatments after this chemo.
I’m wishing you lots of luck for your results. Xx
Im still waiting for my date for scan
Hi Shelly sorry it’s taken a while for me to reply.
I really don’t know much to help with what the lump would be.
I went straight to sbc with mets in spine and my lung
Hi Chrystal, I didn't get my scan results, my onc thought she would be able to read them but she couldn't. Will have to wait for them to be read properly. I'm no longer on eribulin it has stopped working. She is putting me on paclitaxel, start in 3 weeks. She also told me there's no more options for me after this one, so not a happy bunny. Not looking forward to paclitaxel as I've read lots of bad reviews. People saying you get neuropathy and really bad pains in your leg, also bad diarrhoea. So wish me luck. Hope your scan results are good, fingers crossed for you.xxx
Hi Chrystal, I absolutely love this forum, so glad I found it, it really helps to talk to people going through the same thing as yourself. Bit nervous about scan results. I've developed a huge lump in my breast, the opposite one to where my primary was. Do you think this could be secondary or another primary. What are you dx with. Thank you for replying to my post.xx
Hi Shelly. Wow you’ve had a lot to cope with.
I hope you find being on here a help as I did especially at the beginning . Fingers crossed for your scan results. I’m waiting for my date to come through for my next scan .
Anxious times but good to chat to people who understand.x
Thank you so much Annie for replying to my post. Definitely been through the mill lol. I've been fine on eribulin apart from at the start. Was just tired all the time and just generally felt unwell. They reduced my dose and I've been great on it. Still suffer with fatigue but that could also be the cancer. Anyway thank you for your support and good luck to you too.xx
Hi Shelley, and welcome to the group. Thank you so much for sharing your story. It has been quite a journey for you, hasn’t it? I’m so sorry it took so long to discover the source of your pain. I think we know our bodies and when things aren’t right, and I admire you for fighting the system to get your diagnosis. I’ve been on Erubilin and it’s a bit harsh, so well done you fir getting on with it. I have my fingers and toes crossed for a good result fir you. Best wishes. 🍀🤞 x
Hi ladies, my names Michelle or Shelly, I had bc 10 year ago, had mastectomy and reconstruction. Ovaries removed, so shot straight into the menopause. Then nothing for 7 years. 3 year ago I was getting really bad pain in my ribs, for a year I went back and forth to the docs only to be told every time it was costacondritis. In the end I phoned my breast care nurse and she got me in the same week for a scan. Went week later for results to be told I had stage 4 secondary bc which had spread to my ribs, spine, shoulders and long bones in the arms and legs. They started me on a few different hormone therapies which all stopped working. The cancer spread to my liver and omental layer, which is apparently rare. Then I've had a few different types of chemo, capcitabine, everolimus, can't remember the one I was on before the one I'm on now, which is Eribulin. Get scan results next week to see if it's spread. Fingers crossed. Sorry about the long post lol.x