Hallo Ladies
My bone mets (and lung) were discovered in August this year after I broke a rib back in Dec and it wouldn't heal. Eventually a nuclear scan showed up the secondaries ! I had BC in 2002 and in the other breast in 2014 and am now devestated that this has now happened. My treatment for the last 3 months has been Denos umab injections, Exemestane and Everolimus which I've found nearly as tough as the chemo back in May 2014. I had a ct with contrast scan today and see the consultant next Tues for a comparison to see if the treatment is doing anything positive. I found the BCC forums really supportive before and although I never wanted to be back here it's a relief to read your threads and understand I'm not alone !
Cheers, Gill
My bone mets were found accidentally after another unrelated procedure. You are so lucky you're getting scanned. I had gone to doctors severat times complaining of various pains but at no point did anyone suggest it might have anything to do with the breast cancer I had years ago. My pains are quite sharp - like being stabbed repeatedly rather than dull aches.
Hi Flora
Some ladies have not known they have got bone mets, I was one of them. A routine mammogram showed a local recurrence then a subsequent bone scan picked up a couple of mets in my spine. I now have quite extensive bone mets but that was because I was doing so well a few years back that my regular scans got spread out too much so the changes weren't spotted as quickly as they should have been. On that occasion I did have a ache in my thigh which felt more muscular than anything but it turned out to be more bone mets. Some ladies have had a spontaneous fracture, others have reported having aches which were then checked with scans. It's not always obvious and unfortunately some GPs dismiss a lot of our concerns whereas they should take them seriously especially where there is a history of BC.
I hope your scans do give you the answers you need and that it isnt bone mets. However you have found the right place to come should you need further support.
Nicky x
Hi Flora
You may get many different replies to your question, but they are slow coming in. I limped a bit but have limped a long time since an old injury. After the first primary it was assumed to be the tamoxifen. At the second primary I had a CT scan and bone mets were diagnosed then and apparently were from the first primary.
Your scan will hopefully be reassurring.
Pippin
Hello everyone
I was diagnosed with bone mets almost 6 years ago just 7 weeks after my primary diagnosis. Also had shadows in my peritoneum . I went onto Letrozole and Zometa which kept me stable for about 5 years then my TMs started to increase - scans showed more obvious infiltration in the peritoneum but my last scan also showed some differences in my lower back and the Onc told me that he suspected infiltration in my bone marrow.
I was put on cape and have just started my third cycle and my blood results have been very encouraging. I didn’t ask much about the bone marrow suspicions and am wondering if anyone here has any experience of this....or can point me to a site that has some information.
I am finding that I have lower back pain and am wondering if that is the cause. Have an appt with my GP next week to ask about pain killers.
xx
Mrs timps, sorry you've had to join us but you will find this forum amazing. i can only tell you that when my scans are looked at and there is any progression at all my treatment is changed. Do you have a sympathetic gp or a breast nurse you can talk to?
big hugs
Ramade
Mrstimps, Some drs are more aggressive than others. They also go by how you feel. My oncologist will go and look at the scans herself if she isn't sure. If you aren't comfortable with this maybe a second opinion would be good. FF
Hi Linda so pleased for you that is great news. last time we talked we had both started on e/e,didn't work for me but glad you had a fair time with it. i imagine taxol is chemo, i recognise the name as a heavy 6 month dose years ago after my primary.Hope things keep going in the right direction for you.
love and hugs
Ramade x
That's great news Linda! Very excited for you. Go celebrate! FF
Following a meeting wth the surgeon yesterday, it now seems that she would definitely like to do surgery in the New Year! Am currently gettng herceptin injections which are working very well, but she doesn't want to leave me undefended should I need to stop the herceptin for any reason. Surgeon and oncologist seem to have different opinions
Wonderful news Linda. It makes the harsh SEs we have to put up with whilst on chemo all the more worth it doesn’t it? Thanks for sharing.
Nicky xx
Hi Leigh
It is a lot to take in right now but we seem to learn and adjust along the way. In my own experience and after reading the experiences of many ladies on here over the years surgery is not given very often.
The reasoning behind this seems to be if you have a major operation, such as breast surgery, your immune system can be compromised which in turn can compromise your metastases. Most oncologists also like to have a reasonably time of stability, after initial treatment, to see how your particular BC, and SBC, reacts. If it is more aggressive they might not want to rock the boat so to speak. Their main aim is to prevent the mets spreading any further for as long as possible. By having chemo which will have been targeted to your type of BC it will have treated you systemically. Your original BC lump should have reacted to it as well. Also, from something that an oncologist said to me once, they can monitor the lump easier than bone mets etc which involve far more intrusive scans. My bone mets were found after a routine mammogram some 4-5 years after my primary. I had a local recurrence and was due a mastectomy but once the one mets were found it was straight into chemo nd then hormone treatments nd no surgery. I did ask over the years if I could have a biopsy or surgery and they said that on every CT scan I’d had there was no evidence of disease in the breast so it would have been pointless to have gone through surgery to have found nothing. By the way that was over 10 years ago and I’m still here! Over the years there’s been a lot of debate on this but there definitely doesn’t seem to be any pattern as to survival rates between those who didn’t have surgery for their primary (when they were diagnosed with secondaries at a similar time) to those that did, and very few (on the forum) have had the primary removed
Hope this helps or gives you some questions you may want to ask your oncologist.
Nicky x
Hi all, this is my first post so this is all new to me. Haven't read through all the posts and am a bit worried about sounding stupid! I was diagnosed in February and early on my oncologist had suspicions of a boney met in my sternum. All along surgery had been discussed following initial chemotherapy. However following chemotherapy there seems to be a turnaround where my onc. and the surgeon are both now thinking no surgery. Scans don't show any other secondaries bar the localised bone met. Any one else been in a similar situation and are wondering if it is best to get rid of the primary in the breast? Tks x
Good luck Bon, thinking of you today and thanks for the info you've put on line, interesting.
ramade x
ff, absolutely! no options should get thrown out of the window. Different things work for different people simply because everybody responds differently, if this wasn't the case a cure would have been found. it is a highly complicated and very individual disease, well done, stay strong,
love and hugs
Ramade xx
Ramade, Thanks for that info on tamoxifen. I have never taken tamoxifen and talked to my oncologist about it. That as after ibrance and letrozole but before E & E. She told me since I had used a double agent that a single agent wouldn't work. That tamoxifen wasn't an option. I will be telling her no options get thrown out the window until I try them and they fail! My original oncologist threw all hormonals out til I pushed for them. He told me they would never work for me bc lupron injections did nothing as my first treatment. I've been on hormonal for 3 years now. If my oncologist won't try tamoxifen, I will go elsewhere.
I'm glad it's working for you. How long have you been doing metastatic BC now? I'm tired too. This year has been my worse for tiredness!
Take care, FF
Hello feel the fear,
I don't pop in here that often....how are you keeping? I really enjoy the autumn and I'm busy doing my X'mas shopping for family and friends.
You could not be more right about oncologists and pain. They should learn to be more supportive. Bad pain is bad pain. I've found myself a really decent Pain consultant and we are tinkering with my ongoing analgesia...
take eXtra special care of u.....xx..hugggs
Hi ff so glad to hear you are doing well, we really appreciate our granchildren as we have this darn cancer. e/e i started same time as you but didn't work unfortunately so i then had another 6 months of chemo, horrendous and didn't change a thing with the cancer so now i'm on tamoxifen which seems to be working, been on it 2 months, it makes me feel exhausted but i will just carry on with it and thankful that it makes me better. i just keep making too much estrogen maybe. Anyway love to you and hope your scan brings continued good results in November
hugs Ramade
Ramada, I'm OK. I've been on E & E for 17 months. I'm still working PT. I have scan and check up in Nov. I hope I'm able to stay on this treatment longer. It messes with my diabetes and this is the most tired I have been, but I'm enjoying my granddaughter. Nov. will be the my 13 year mark of mets!
How have you been doing? You have been at this awhile now too. I forget what treatment you are on. Wishing you the best! FF
hello sammycat......x
one of my relative is just diagonesed with MBC , originally it was discovered in 2005 ER+ pr - her-, grade II, now in 2018 she has been diagnosed as per ct scan + pet scan
1) bone mets
2) general haziness of omental & mesentric
Currently the medication is letrozole + ibrance + monthly injection
intially on songraphy mild ascites was deducted,
3) is general haziness is a definately indication the mets is in omental region or is it early stage
i can see you are having it since last 4 years, as on net it says the progonis is poor, currently what options we have and can it be change to chronic disease
Regards,
one of my relative is just diagonesed with MBC , originally it was discovered in 2005 ER+ pr - her-, grade II, now in 2018 she has been diagnosed as per ct scan + pet scan
1) bone mets
2) general haziness of omental & mesentric
Currently the medication is letrozole + ibrance + monthly injection
intially on songraphy mild ascites was deducted,
3) is general haziness is a definately indication the mets is in omental region or is it early stage
i can see you are having it since last 4 years, as on net it says the progonis is poor, currently what options we have and can it be change to chronic disease
Regards,
How are you doing these days ff, are you still working?
ramade xx
I haven't been on much the last few days. Just saw all the posts about Moijan. Sending thoughts and prayers to her family and friends. May you have many memories. FF
P.S.....& yes, I'm a glass 1/2 full type of gal and my sense of humour is my armour...xx
Hello sammy/c & how do you do...,
Oh, its actually appalling..my pain left groin, under LH rib cage, upper back & lower back. I'm on 10mls morphine sulphate and 1200 mgs Gabapentin a day with a lil' relief but my pain man is overseeing futher increases in Gabapentin. I know 'that' look from my oncologist...I feel like saying walk just one day in 'my' shoes!!!....MRIs & PETs are expensive. so not used regularly.....its terrible to be in such pain in this day and age.....do KIT.....very gentle huggggs to you.....I'm seeing my G.P. on Wed......it just 'hurts'!!
HI Silverlining
I also have intense pain in back and chest. I find sitting torture!! I recently had the same scans as you and I was told at the moment everything is very stable!! If this is true why all the dreadful pain??? I just feel no one understands and my Onco looks at me as though it's all in my head. I'm so reluctant to go on morphine as it makes me feel so sick and weird. I just have 10 mgs of amytriptyline when I go to bed and then paracetemol in the day. Have you found any meds that actually work? I am trying to work but feel I will have to go off sick again soon. What a dreadful thing this is!!! Sorry to sound so gloomy. I am actually a very happy positive person most of the time!!
So sorry to hear about Moijan. We’ve ‘spoken’ a lot since March when we both started a course of chemo at the same time. Can’t believe she’s gone, as others have said I did notice that she was very quiet. RIP.
feel so choked up to hear about Moijan, had missed her recently. She was a lovely friend and pm friend. i do hope and pray we can find a cure for this dreadful life robbing disease.
hugs to all of you dear people.
Ramade
I am another that is so saddened to hear of Moijan's passing. We shared the same hospital and she always gave good advice and was a friend to so many. Fly high lovely lady. Hugs to her family and friends xx