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Bone mets - please join in

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Re: Bone mets - please join in

Hi becket I am sure everyone is different but my bone pain came and went, one night I had a pain in my chest like I’d been kicked by a horse, that was when I went to the gp, but I’d also had smaller pains I had ignored as just aches and pains, which may or may not have been early signs. I am where I am, I try not to think about it. X rusty 

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Re: Bone mets - please join in

Hi ladies

I finish 5 months chemo at the end of Nov 18 and had right mastectomy on New Years Eve. It was a grade 3 triple negative tumour.

All was good but I'm sufferring with heavy aching in my right shoulder. BN is arranging a bone scan but really worried.

What does it feel like if it has returned? Am I worrying over nothing?

Becks x

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Re: Bone mets - please join in

Hi rustyharas

Sorry you have to find yoiurself in the place that none of us want to be in.  Unfortunartely breast cancer is a crafty little bugger and can come back even when you've been given an excellent prognosis after treatment for primary BC. The same thing happened to me. Great prognosis with primary, low grade, found early, no lymph node involvement.  Hey presto nearly 5 years on from that I found I had bone mets.  I just wanted to add some support as it is a horrible time that you are going through, waiting to find out what happens next.

You will find on this part of the forum that many of us are living well with bone mets, I'm currently coming up to 11 years with them (as well as now having liver mets although they are a different story).  I think this thread has gone so quiet due to the change in the forum - no one can find it! And when they do our posts get lost, grrrrr.  There are many of us out there with bone mets and another reason this can go quiet is that unkess things have progressed or changed we often are not posting, and tend to do so more when a change int reatment is needed.

One thing you will find out is we do not seem to all have the same treatment on initial diagnosis of mets. This will be down to our receptor status and also sometimes down to our oncologists view.  It can be chemo or 'just' hormone treatment (if we are hormone positive) or a Herceptin based treatment if we are HER2 +. Sometimes targetted radiotherapy is also used but this tends to be when there is significant pain.  Most of us have had a bone scan which does give a clearer 'picture' of our bone mets but quite often this isnt repeated and can be used for diagnostic ourposes only. You're right about CT scans not picking up very small mets, MRI's are more accurate and I'm not sure about PET scans as my hospital doesn't use them.  Most often, along with your chemo/hormone/herceptin you will also be given a bone strengthening treatment.  Most of us are on the newest drug, Denosumab, but others are on infusions or even tablets, agsin, this will depend on your oncologists choice to some extent.  Also, as this is your first diagnosis of mets (and therefore first line treatment for mets) you may be given additional, newer drugs alongside whatever treatment you go onto.

Almost all of us found that once we had a treatment plan in place we were more able to adjust and cope with our secondary diagnosis.  Take your time it is a huge shock for you and your family.  Please come back on here with any questions you may have and to get support from fellow SBC ladies.  Hopefully some of the other longer term members will come along to offer their advice as well.

Good luck

Nicky x

 

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Thank you gaybar,  on way to see oncologist now.  Feel sick.  Husband is worrying about parking... 

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Just to add. I can eat normally but have to drink plenty of water.

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Hello,

Yes I have thorax and abdomen CT scan every three months with contrast. Along with full blood count for, bone profile, liver and rental. Wishing you all the best.

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Thank you people.  So you both had CT scans, all good information, thanks

and no i don’t think I did anything wrong, lovemama, in fact pre the original diagnosis my friends would say I was the healthiest person they knew.  Vegetarian for years, bit of a health food nut in fact, exercised, didn’t smoke..  even more so after diagnosis.  

 

(I did forget that I wasn’t supposed to eat , on the morning of the CT I went and made myself a piece of toast on autopilot... and then had an hour’s agonising about whether they were going to tell me I couldn’t have the scan.  But it was ok.)

 

I havent told my husband yet but it’s going to be no sugar, no alcohol, and even less processed food in this house... at least that is something I can control.  He already has to get his meat fix in on business trips, now it’s going to be chocolates and crisps too, haha.

 

Just realisised that sounds terrible.  No I don’t forbid meat in the house, just how we’ve always managed it.

 

Rusty

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Re: Bone mets - please join in

This is my second time trying to post. The last one was lost. 8-(

Hi Rustyhares.  I was dxed bone met in Aug last year. A dot shown on chest x-ray. A leison shown on bone scan. A leison with ~1.5cm (forgot the exact figure) desruptive on both vertex shown on chest CT scan. Having 8 cycles chemo. CT scan after 4th cycle, 2 leisons on adominal linings disappeared and sternum is healing. Requested radiation and was rejected. My current oncologist told me my previous oncologist (left the hospital after my 5th cycle) believe the chemo is able to clear my last leison on sternum. No sharp pain but  dull shoulder pain and come-and-go chest pain. By the way, did you do something wrong (like me, took high dose bee propolis+soy milk for 1 month) before the CT scan 

My first diagnosis was in 2011. At that time, my oncologist told me  tumor marker test was showing ZERO.  

PS. in Hong kong , one oncologist consider cure if no recurrence in two years for triple negative, 5 years for ER+ HER-, 10 years for ER+ HER2+.

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Re: Bone mets - please join in

Hello,

I come on here from time to time for a look or when something is bothering me. I was first DX in 2009 age 40 stage and grade one. It came back in 2016. Ultra sound, biopsy, CT scan, MRI and bone scan found out it had come back. A huge mass at the back of the sternum, one in my neck and in-between the 5th and 6th rib. Inoperable but treatable. Six months of chemo and the huge one at the back of the sternum and neck NED and the one inbetween my 5th and 6th rib has shrunk and stable. CT scans and blood every 3 months show all is stable and letrozole is doing it's job. I'm nearly 3 years on from secondary DX. Hope some of this is useful. Wishing you all the best.

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 Doesn’t seem like much activity recently,  anybody still on here?  Just been told today results of chest CT that I have bone mets in my sternum (went to my gp with sharp  pain in chest, had it a few times, in various places, came and went.  Didn’t believe it could be cancer) 

appointment with oncologist tomorrow, I’d like to know what scans people have had to start off with  and why - I read that CT scans don’t show tumours smaller than 2cm, is that right?  Does  a PET  scan show up more?  

 

I want to make the most of my appointment and I’m the sort of person who feels better the more information she has.  

 

Oh and I’m 54, diagnosed with BC originally 2010, chemo, rads, tamoxifen.  Told me I was lucky, I’d found it early.  My breast surgeon said I’d still be here when I was 80.  (This is maybe one question I don’t want answered at the moment.)

 

And I haven’t even begun to think about how I can tell my children, my eighty year old mother and my two siblings.... my best friend who was a fabulous support last time is dealing with her sister having terminal (secondary bone) cancer at the moment.  I do feel a bit alone...

 

 

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Please, i have one more question. Do you know, why meta was not seen on normal lung RTG, but PET/CT show something on lungs?
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Thank you soooo much bonareinsis!!!!! I tried look internet, but i didnt manage to find so great picture.
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There are two sciatic nerves, one on each side which run down into each leg

 

sciatica.jpg

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Re: Bone mets - please join in

Hi

Just another thought, late at night for me as I usually read the forum earlier in the day! One of the nurses who have me my injection the other month mentioned the sciatic nerve and how she dreads hitting it when she gives the injection so makes sure she gives it quite high up. Maybe your pain is related to this? I seem to think the sciatic nerve is on the right hand side but don’t actually know for certain.

Nicky x

 

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Re: Bone mets - please join in

Thank you Nicki and Marmeid, we try it, sides effects is also muscle pain, but funny is that is only on one side(injection both sides) and roughly week after injection for 3 days. I def check it up with onc and let you know.
Thank you all for replais, mean much and help much🍀🍀🍀
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Re: Bone mets - please join in

Hi

The injection is put into the muscle at the top part of your bottom and when I have the right side done I feel nothing but when she injects the left side It always hurts a little. I would mention it to your nurse. It may be that you need to massage the area for a while after the injection. Maybe a hot water bottle on the area the night yiu have the treatment? We are all different, I hope you find a solution.

xx

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As us like you go fitness and you pull your muscles. I will check it up with onc , but it is only one week after injections and it last cca 3 days and only on right side. Keft side is goid after injection. The pain always sort out 1 tablet of common painkillers, so hope thats not something bad, anyway i am curious
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Hi Majck 

Ive been having faslodex injections for nearly a year now and don’t get any pain from them. I do get localised itching and redness where the injection goes under the skin but nothing I could say was ‘pain’. As mermaids has said, where is the pain? It could be listed in the side effects which you can look up online (as you might not have been given an info sheet about them)

Alternatively speak with your onc team who may be able to help?

Nicky x

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Hello Majick,

I haven’t experienced any pain from Faslodex, where are you getting the pain? X

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Re: Bone mets - please join in

Nice evening all,
May i ask someone please, Faslodex, 1 dose, 2 dose two weeks later and now monthly. Each time it was injected 250ml in bottom, and pain came always 5.6.7th day afterwods. And ONLY on right side, left is good. Any experience?
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Re: Bone mets - please join in

I am sorry that you have to join us! There is a lot of advice and support on offer here. I was diagnosed with bone mets in April at the same time as my breast cancer diagnosis. I was very shocked and cried a lot. I'm on Ibrance Anastrozole and Zometa. Scans have been encouraging and I am working full time and feeling fine. It's not easy but I have got used to the regime and I manage not to think about it all the time. Best wishes 

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Re: Bone mets - please join in

Morning all

I am new to this..  was told yesterday that I have some spots on my liver and on my spine and pelvis.  I hurt my leg  back in Oct which they said was a muscle strain, I then fell 3 times in the next few months and the pain increased.  They suspected a fracture of pelvis which turns out was true but only because a spot of cancer was on the bone and had weakened it. I was on tamoxifen although was having a few weeks off.

 

I only finished Herceptin last Feb (I am triple positive) after single mastectomy , chemo FECT and radio and petumazab.  They think perhaps it was there all time but so small no one could see it on scans but since treatment ended its started to grow. I started to feel a little bloated on and off the week before xmas but have had IBS in past so just presumed it was an attack.

 

Not sure what to expect - v scared .  any positive experiences out there please .

thanks

x

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Re: Bone mets - please join in

My hospital decided to try getting patients to do their own denosumab injections at home, it was to be delivered to my home. I was not keen and asked if my GP practice could do it but was told they were not licensed to do it. So much for care in the community! Have not heard any more. Usually it doesn't take very long and when my hospital appointments were quite spaced out it was quite reassuring to see a nurse regularly. I am going onto 6 weekly injections now to coincide with capecitabine appointments.. Had a lot of bone pain after last injection so am pleased they will be less frequent.

 

 

 

 

 

 

 

 

 

 

 

 

 

pea
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Re: Bone mets - please join in

Thanks so much Nicky. Your reply has been really helpful and reassuring. I will keep you updated on how I get on. 😀 Phoebe xx
Community Champion

Re: Bone mets - please join in

Hi pea

Sorry you have to join us but you have definitely come to the right place for support and to ask questions.

I have been an active member of the secondary forum for over 10years now and I must say in all that time I’ve not heard of anyone having their sternum removed. There have been other surgical bone procedures such as hip replacements but not the whole sternum. Obviously there must be someone out there who has had it done but no-one has posted on the forum as far as I can remember. Therefore you may not get any advice as we tend to give it if we have experienced the same.

I would get a second opinion, you’ve got nothing to lose and maybe find out if there’s a specialist surgeon who has done this before. I recently had liver surgery and was very grateful for the fact that my surgeon (at my local hosptial) is one of the leading abdominal cancer surgeons in the county. It gave me great faith in his abilities and trusted him with his opinion about my particular case and recovery times etc as he has done the same surgery many times.

In terms of survival rates whether you have surgery or not it is of course impossible to answer. Having said that I have had no surgery or radiotherapy to my bone mets in the time I’ve had them and although they are now more wide spread than they were they have never caused me any issues or pain - and I’m still here!

Sorry I can’t be of more help, maybe someone else can. Good luck though with your decision and let us know how you get on.

Nicky xx

pea
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Re: Bone mets - please join in

Hi All - I'm new to this and would like to pick the brains of all of you amazing ladies.

I was dx with BC in April 2018 and two weeks later an MRI scan and PET CT scan showed I had a solitary secondary bone met lesion in my sternum. I had chemo (FEC-T) followed by lumpectomy (x2) to remove primary. I am currently on anastrazole and zoladex (goserelin).

I have been told by the relevant surgeons that I am a good candidate for sternum removal (and rebuilding) but my oncologist is not keen. I still have to have RT and my oncologist said palbociclib is the next stage of treatment. I am at a cross-roads because the option to have the surgery is purely down to me and as I am a rare case there is no literature to support whether removal slows down progression of the disease. I am 47 and want to give myself the best shot but it's a massive surgery and will take months to recover from.

I'm going to ask for a second opinion on this from other oncologists.

Has anyone else been in this situation? I would love to hear from you. Yikes! What do I do?

xxx

 

 

 

 

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Riversidedawn, my hospital recently changed to giving Denosumab 3 monthly, saying it stays active in the body for such a long time, the Maxillo Facial team I see also agree with this, obviously they are concerned re jaw issues. Both teams say it stays in the body beyond 3 months and my dentist says he’d be surprised if it didn’t stay way beyond that! I was told later results agree with this and extending the time between doses reduces the risks of onj. When my hospital protocol was monthly my Oncologist always said not to worry if I went 6 weekly or even missed a dose, so assume they have always known how it stays in our systems.

Could you ask to adjust the frequency to fit in with your other visits? Kate x

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Wow, Riversidedawn, that is a long time for just a quick injection. As the other ladies have said you could ask if your GP will administer it but unless the nurses are trained I don’t think they can. I have had Denosumab for nearly 6 years now and have had it at varying intervals depending on the other treatment I’m on. At present I have it 4 weekly along with my fulvestrant but have had it 6 weekly. If I’m continuing on fulvestrant (after I find out my recent scan results) I am going to ask if it can be 8 weekly. Each time I go for my injections and port a cath ‘flush’ I’m in and out within 30 mins give or take 10 mins, waiting around for 3 hours is awful so I don’t blame you trying to find out how you can get it done more quickly. I don’t think oncologists, or chemo nurses, understand that once we have secondary BC we are spending too much of our valuable time in a hospital so want to get out ASAP!

Nicky x 

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Next Christmas it WILL be better!! Jayrand56!
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Next Christmas it WILL be better!!
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Yes I wish everyone here a happy new year with good results from whatever scans/ tests and good responses to whatever treatment. May this be a year of success for all.
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Correction! Been on Denosumab for 6 years not 5!
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Hi Riversidedawn
I have been on Denosumab for 5 years, it was licensed in late 2012 & I was put on it when diagnosed Dec 2012 so GP saying it's a new drug isn't quite true. GPs don't tend to administer it because it costs too much, I was told £150+ per injection back in 2012!! Having said that, my local hospice will give it & I know someone on this forum who self administers at home. My chemo unit & onc are very flexible as to when I get Denosumab-they tend to tie it in with whichever chemo I happen to be on so I have had 4 weekly, 6 weekly , 8 & 12 weekly. All the best with your treatment.
Helen x
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Lovely good evening,
I wish you all clean scans, good fight, stay strong and positive in the upcoming 2019.
Hugs🎉🎉🎉
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Just joining in for a bit of support. I was admitted onto the oncology ward on Boxing Day with a chest infection; I already had breathlessness which had been exacerbated by the Paclitaxel so not good!
I’m having IV antibiotics and steroids and feeling much better, in fact there is some suggestion from the CT that there has been an underlying infection for a while.
Not sure if I will be allowed home today as there is talk of a chest drain, despite my consultant saying it wasn’t necessary last time I saw her.
Feeling a bit fed up, and trying to convince myself that next Christmas will be better..
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Re: Bone mets - please join in

Hi. I am on denosumab. I get my injection every four weeks at hospital when I am picking up my palbociclib. I can be in and out in 20 minutes but sometimes there is a glitch with the prescription or no room available. I have asked if I could have it done at the GP but was told as it was a relatively new drug it was to be administered at the hospital.  I don't always see my onc when I am in. If my bloods are OK I get a phone call the evening before to ask how I am doing. I have the option to see him if I want to but much as he is lovely and very approachable I prefer not. I find it is the best approach for me at the moment. 

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Hi

I have Denosumab every 4 weeks at my dr's surgery. You should ring them and see if there is a nurse trained to give the injection. 

 

Vicky

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I am on Ibrance and Zometa and Anastrosole. I have Zometa every four weeks and also have to see the oncologist every four weeks to get the Ibrance. I’m one a low dose and one week on one week off as my white cell counts are low. Often the appointments don’t work out to be on the same day so I have to go consequtive weeks. It is time consuming but the hospital is near my work so it’s okay. I haven’t heard of anyone having it at home but this is the right place to ask. Could you try and have both on the same day? I sometimes can which is good. Best wishes Anne
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Hi is anyone on denosumab? I have to see onc every four weeks to pick up ibrance (palbociclib) and also return every 6 weeks for denosumab. Never get out in anything under 3 hours even when it's just a quick injection.
My GP won't fund ibrance so that's fair enough but I wondered if GPs will do denosumab or if anyone is trusted to do it at home? Really don't want fortnightly hospital trips.
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Merry Christmas! Relax and enjoy the festivities with your family and friends! FF

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A Happy Christmas from me as well 🎄🎅🏻Wishing you a lovely time with your family and friends.

Nicky xx

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Happy Christmas to everyone and thank you for all the support and encouragement. Here’s to strength and peace in 2019 x
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Christmas wishes and good luck to all . Here’s to a great 2019xxxx

Wendy x
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Hello, i just wanted to wish you all a happy Christmas and positive scan results for the new year

Big hugs to all

Ramade

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Thank you for your replies. I hit a wall yesterday when the onc told me I may not be able to tolerate the Paclitaxel; overtired, oversthinking and just plain fed up!
Today I have pulled up my Big Girl Pants and decided to look forward to seeing my gorgeous pocket rocket grandson tomorrow!
In the meantime I am working to manage my breathing and bought a v shaped pillow to help at night. Part of the problem is that my husband works away Mon to Fri, so the nights alone can be scary. He is now home until New Year. I understand now that there are alternative chemos I can try if this isn’t possible. Thank you all, you are a lifeline.
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Hi Jayrand56

Some people have an allergic reaction to one type of chemo but not necessarily another. There is another taxane, docetaxel, which works in a similar way but doesn’t necessarily mean you would react to it in such a bad way. There’s also Eribulin which is completely different and is well tolerated plus of course Capecitabine. Some of these other chemos can’t be given until after another one has been tried. I’m sure there is one (there are more than these I’ve mentioned) that will work effectively without the distressing side effects.

Good luck

Nicky xx

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Jayrand56, About 4 1/2 years ago I had been on gemcitibine for about 10 months. Hubby and I HD gone away camping for the weekend. I was fine Friday when we left. I woke up Saturday morning extremely short of breath. I couldn't even walk a few feet to the outhouse. I was out of breath even putting socks on. We were due to go home Sunday. We packed up to go home and when I went to hug our friends bye we were all crying. Everyone thought I had taken a turn for the worse and that this was it, including me! I had never been that SOB with my lung mets. Monday morning I called my oncologist and he had me come in right away. They scanned me and there was no change in my cancer. I had pneumonitis. Which is inflammation all the lobes of the lungs. He took me off gemcitibine and all treatments for a month. I had to go on O2. In about 3 weeks I was fine, but my run with gemcitibine was over. FF

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I’ve just started weekly a Paclitaxol and also will have bone strengthening injections monthly
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Hi. What medication are you on to stabilize your lung tumors?
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I don’t know if this is the right thread to ask, but does anyone else have experience of a bad reaction to Paclitaxol? I have only had 2 weekly doses, but each time my breathlessness has worsened. Onc thinks it may be the chemo side effect.
I am currently house bound as any exertion sets me off. It is possible that they will bring me in to the ward this weekend to scan for possible clots.
If I have to stop the Paclitaxol, I’m worried that there won’t be anything else for me. I have lungs mets and bone mets on my sternum