26-07-2010 06:00 PM
Marychris: I was diagnosed with bc 4 years ago, bone mets found 3 weeks later. Treatment for the first 3 years was hormonal (Femara) and pamidronate, which was changed first to Zometa and then Bondronat tablets, which I'm still taking. Bone mets in several places, the hip met is the only one that has been troublesome.
Unfortunately a year ago I was dx with liver mets so needed my first chemo (EC). I've been reluctant to post on bone mets threads since then, but the chemo did a good job and I'm now feeling well, currently on another hormonal, exemestane.
Am negative for herceptin so haven't had that treatment.
Anyone on Zometa, make sure you take a calcium supplement.
26-07-2010 05:33 PM
I have a met in my lung and one on T12 in the spine!
I had rads to the spine and have been on herceptin, femara,zometa and zoladex for 27 months. I am due for more scans but have been stable for this time (not sure about the moment though having a wobble)
I was told stable was good and chemo would be kept in reserve until there was any change.
I was also told that my treatment would have been the same if I had had multiple bone mets (although not lung).
26-07-2010 05:24 PM
I was dx with bone mets in April, My pain was ignored for about three months,until I insisted on having a scan, by that time I had extensive mets, in my ribs, spine, skull, and leg! I was in a lot of pain, and started Zometa in May, and hormone was changed to Tamoxifen. My pains have settled, and my tumour markers have gone down. What I don't understand is why my onc didn't suggest chemo for me! I saw him on Wednesday, and asked about another scan to see if anything had changed, but he said no, as all the signs were good, and I felt well. To be honest after a series of things going wrong, I have lost confidence. Is there anyone else who was just treated with hormone and Zometa?
26-07-2010 04:54 PM
My mets were originally to spine, ribs and sternum but I had chemo first and the next scan showed the sternum one and part of the spine ones had gone so that was good. In June last year I had a small new area towards my upper ribs on left hand side but part of my spine had improved a bit too so it wasn't all bad. I have since had scans last Dec and this June and they have all looked the same as the one from June 09.
At the mo, I'm on zoladex with arimidex as I'm 100% er and pr+, and then zometa every 4 weeks and a daily calcium tablet. Fingers crossed they all keep working as long as poss. I have been told that at some point in the future when they worsen, I'll need chemo/rads or whatever but I'll cross that bridge at that time.
26-07-2010 04:47 PM
i was dx with bone met on 6th July,my breast cancer was back in 2005
it would have been the 5 year NED for me in October this year,
unfortunately i never reached it.
my cancer has returned in my sternum, and after numerous scans
inc a PET scan they have told me that I'm unusual as it is only
in one area of my sternum, close to heart I've been told.
i started on chemo a week ago,I'm on Taxotere & herceptin
the Tax is till end Sept & the herceptin is indefinitely.
Any info on bone mets would be great for me, as I'm not fully up to speed on it all yet, and anything that i should be asking my oncologist i will!
when i was 1st dx i just wanted them to treat me and i did not really want to know any details however now i like to know everything!!
26-07-2010 03:29 PM
Hi Daffy - I remember reading your story and was so shocked at how you had been treated. I'm glad you are now getting what you need, but it must be very difficult for you to put the mistakes behind you. So glad the pain has reduced for you and hope the bone strengthener can undo some of the damage.
Hi Liz - I agree, Belinda and Dawn have been a great source of inspiration, and Scottishlass too. It's great that your mets are stable - have you been like that since dx? What meds are you on? As my single met is quite small I am hoping I will be as lucky as you, but there doesn't seem to be any way of predicting how it will progress.
26-07-2010 02:05 PM
Hi Finty, I have bone mets. Diagnosed in June 2009 with a spinal met to L1.Due to a clerical error where new mets were not added to my file, from a scan in Nov 2009 - so was considered stable and no treatment apart from hormone given. Which obviously was an error. I now have widespread spinal mets and a few rib, difficult to differentiate as I have developed osteoporosis. I am sure errors are not common but I would say to anyone, ask for copies of reports to be copied to yourself, keep an diary of appointments and outcomes from those appointments.
I have just started Capecitabine, had one cycle. Herceptin and Pamidronate. Had a port fitted last Friday. I was in a fair amount of pain but a month ago had a second radiotherapy session to a large area of my spine and only have discomfort from L1 now. I was considered for surgery as the body of L1 has crumbled but bone shards are too near the spinal cord and its considered too risky.
I have found this forum so helpful. It was reading other ladies experiences with bone mets and treatments that started me questioning my treatment and hence the error being spotted.
Wish you well
26-07-2010 01:52 PM
Great idea ! I was diagnosed with bone mets at diagnosis 3 yrs ago and have benefited greatly from the words of wisdom from ladies on here. Not to mention their stories of hope etc - thinking esp. of Belinda and Dawn here. Would love to be your onc getting loads of questions from you next visit !!!
Fortunately my mets seem to be remaining stable and there's only in a bit of the spine and ribs at the mo. I feel great and am making the most of retirement from work - Amsterdam calls next week for a few days....I do try and go on live chat on Tues evenings when I'm around and remember and there are a few on there with bone mets.
26-07-2010 01:44 PM
I was dx with a bone met at original dx in Oct 09. Recently I have been shamelessly picking the brains of other ladies with bone mets wherever I find them, and have found the process very helpful and often encouraging. It has enabled me to be less panicked about my prognosis, and given me a much better understanding of my condition. I now have a whole new set of questions to ask at my next consult - bet my onc can't wait!
I know I would find it very useful to have a designated thread where experiences can be shared, and advice sought - so if you agree and also have bone mets perhaps you could check in here and we could get the process started. I know it's a bit quiet at the moment, with many away on holiday - but here goes .....