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Bone mets - please join in

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Re: Bone mets - please join in

Ladies I need your advice...

brief history.... breast cancer 1999 chemo radio tamoxifen 5 years letrozole 5 years.

Dec 2014 extensive bone mets had Radiotherapy and been on exemestane sine then with monthly Denosumab. I scored 8 on estrogen level. Recent MRI has show new lesions the only thing my oncologist can offer is chemo!!! I asked about Faslodex she said it’s not funded by the hospital ( Dudley) or ( Wolverhampton) she will ask for funding but isn’t hopeful. Ibrance also not funded which I think is the case for many. She will look for any trials that might be suitable.

I asked if I should revisit Letrozole but she said if Exemestane has stopped working, and it’s the same category as Letrozole but stronger, then Letrozole unlikely to work.

She is at the mercy of funding I know but can the ladies on here give me anything from experience.... is there anything else? Would you think Faslodex should be my next ammunition? Would you have expected Exemestane to have worked for longer? I really wanted chemo to be the last resort.

Thanks for listening and you are all awesome, sorry I have rambled on a bit.

xxx

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Re: Bone mets - please join in

Hi f-the-f,

 

Ooopsie.....I do actually realise that there is a time & place for stats. Those European figs. enlightened me....& we are all very special individuals on our own individual journeys.....Positivity abounds....xx...take good care..

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Re: Bone mets - please join in

Morning ladies.
Zana, sorry you’re joining us. I’ve only been here a month myself so understand what you’re going through. Having only one bone met has to be a good thing. I mean I’m sure you’d rather have none, but one is the next best outcome.
If your ct scan didn’t show any spread elsewhere then there probably isn’t any I’d think.
My liver mets showed up very clearly on the ct with contrast and they’re tiny.
People live for a very very long time with bone mets.
Hopefully one of these clinical trials will zap the one you’ve got and get you into NED very soon.

They say these new immunotherapy drugs should be available more widely in around five years time. There are clinical trials taking place in America as we speak.

Silver, talking about statistics. Last night I read ‘the median isn’t the message’ by Stephen jay Gould. Interesting stuff.
Just reminded me why I should feel very positive about my future. After feeling like I was slipping into a bit of a hole (thanks to the meds) this has really picked me back up and set me back on the right track for me. It’s worth a read I think. Xx
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Re: Bone mets - please join in

Not sure what happened there! 

 

Just to add, the other thing which was unusual in my case was I’d only had 5 Denosumab injections when I stopped them prior to having the work done, my dentist etc all said as I’d been on treatment for such a short time what happened to me was even more strange, and this fit with my research, maybe I was just unlucky!! Kxx

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Re: Bone mets - please join in

You’re welcome, anytime, please let me know how you get on xx


@silverlining wrote:

dear kate,

 

I cannot thank you enough. I'm going to look closely into this......many thx for your time and kind consideration.....

huggs,

silver..xx


Member

Re: Bone mets - please join in

dear kate,

 

I cannot thank you enough. I'm going to look closely into this......many thx for your time and kind consideration.....

huggs,

silver..xx

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Re: Bone mets - please join in

I can only speak from my personal experience Silver and I’m sure the oncology nurses have seen more people having dental work done, but I personally would not have any done on that time frame. I missed three monthly injections prior and four afterwards. As I said initially mine appeared to have fully healed but the Max Fax team said it’s where you can’t see that problems tend to arise, and again he was right in my case. He said it can take six months for things to fully settle down, yet in all my research, and I did a lot, I never once read that length of time. That said, my dentist, the dental surgeon and my Oncologist all said my case baffled them as to why I’d had problems after it had healed so well as usually it was only when the jaw didn’t heal afterwards, only Mr Max Fax said differently. If I need more dental work I will go and see a biological dentist before I get anything done, I would’ve done this last time but because I had a holiday to California booked I wanted to get the dental work completed and all healed before my flight, and at that point it was, it was much later that problems arose. In fact on that holiday I fell over a raised paving flag, went face down so automatically put my hands out to break my fall, I dislocated a finger (my bag handle got caught around it as my knee fell onto the bag itself and that pulled my finger out) but didn’t break anything or injure my mouth. I was taken to Cedar Sinai who commented in the report that from the state of me after falling, and with my medical history, they were surprised I hadn’t broken anything and I hadn’t had a Denosumab injection for five months at that stage. That hospital belongs, I believe, to a non profit making group yet it was around £11,000 for the manipulation, a few X-rays and a pain killer...the prescription was extra!! Thank goodness I had health insurance and because it wasn’t due to cancer in any way the company have said they will insure me again, phew!

If it was me I’d do lots of research and definitely get another opinion and at least speak to a biological dentist. Kxx

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Re: Bone mets - please join in

hi kate,

 

I've been on monthly Denosumab injections for 2 years & 7 months.

 

The onco. nurse today said 8 weeks prior and after dental work...no Denosumab.

 

Is this not careful enough?

 

silver..xx

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Re: Bone mets - please join in

Hi Silver,

 

Can I ask you how many doses of Denosumab you’ve had?

 

I ended up at the Maxillo Facial department after my dental work, if they hadn’t been so fantastic I dread to think! I had my work done at the dental hospital and all went well, healed quickly and both my dentist and the dental surgeon were happy, then I got an infection and things deteriorated from there. That said I mainly blame my dental practice for the resulting problems because my dentist was on holiday and the other one was useless, and that’s putting it mildly! The Max Fax surgeon said Oncologists and dentists generally don’t give a long enough recovery time before re starting Denosumab, he advised leaving it six months afterwards, if the gum is involved, both my dentist and dental surgeon said three, also read that on line and my Onc agreed, Mr Max Fax was adamant that wasn’t long enough and on reflection I agree with him. I ended up leaving it four anyway but still had problems. Obviously I didn’t see the Max Fax team until the problems had arisen but if I’d known then what I know now I would have asked for a referral, or at least what time frames they advise. I may sound ott about this but if you develop osteonecrosis of the jaw then you cannot have Denosumab full stop.

I would also advise taking probiotics and/or something like kefir, as I’m sure you’ll be given antibiotics to take especially if you’re having an extraction. Supermarket bought kefir may help but generally isn’t potent enough on it’s own!

 

Kate x

 

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JWD
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Re: Bone mets - please join in

Silver lining you have done so well with treatment and surgery such a brave lady and so glad you have support from Macmillan..My onc said I fell in the small % bracket with it coming back because it was low grade first time and caught very early. I've only got to ring my oncologist Secretary on Thursday she will tell me if bone scan has been looked at. The worry will be if I have to go to Friday's surgery to discuss results because with ct results she told me over phone that they were clear. I had my pre op test on Monday and I'm booked to have lumpectomy on 30th July so it just depends on results. I never asked my onc what the plan b was if bone scan showed Mets. It could be that I still have op. My husband and family are very support. My husband is very understanding as he had oesophageal cancer last year and had surgery to remove 2 parts oesophagas and 2 parts stomach plus chemo before and after. We keep each other going and have a good sense of humour which helps😄 this forum is really good because like you say knowledge is good and you realise your not on your own. I will let you how I get on. Stay strong silverlining and thanks.xx
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hi funnyface,

 

Firstly you are just amazing!

 

My only life's link with the U.S. is that my favourite Uncle lived in Sacramento. Strangely enough he was a physician. I really miss our chats.....

Take care,

silver xx

 

P.S. the problem here is that there is simply no rain and its far too hot for me. Spring & autumn are my favourites....my rain dances aren't working...te,he,he

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Re: Bone mets - please join in

Hi Kate 21,

 

Uncanny.....I found out yesterday that I need a molar extracted so I've been finding out what I need to do wrt Denosumab.

 

So very many thx as I'm on the road to the dental hospital in August as my dentist does not want to do it himself.

 

I simply hate dentistry!!!

xx....how very timely....

 

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Re: Bone mets - please join in

@ JWD,

 

I could not agree more...knowledge is empowering in this journey.

 

3+ years ago.....I was one of the10/15% found to be stage 4, on discovery. It was such a jolt...I'd no idea. So I had 6 months FEC and a month of daily radio. after a lumpectomy & axilliary clearance 2 weeks later. I just did as i was told.I'm now on Denosumab injections & Letrozole. I've mets on both hips......

 

I only recently found this forum & I'm learning a gr8 deal......will someone be coming with u on Thursday?

 

It was after my initial treatment that I was assigned a Macmillan befriender & he helps so very much.

hugs,

silver..xx

Community Champion

Re: Bone mets - please join in

Silver, I've been on my Mets journey for almost 13 years! It was in my lungs and some lymph nodes in my chest. My mets started 10 years after my primary.

 

I live in Pennsylvania about a hour west of Philadelphia. It is stinking hot plus we had 5to 8 inches of rain in a couple hours. We have had about another 4 since yesterday. Supposed to rain for days!! 

JWD
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Re: Bone mets - please join in

Thank you silver lining. It was a shock but I think it's the not knowing that's a killer and once it's confirmed you get this inner strength.. And yes its the scan-ixety which is the worst part. Thanks for kind thoughts.xxx what treatment are you having?? Hope it is going well..Take care xx
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Hi Silver,

just to say I had quite a detailed chat with my Onc about Denosumab last year when I had to stop it for 7-8 months due to some dental work (initially thought it would be 6 but ended up longer) and she was very confident it wouldn’t make any difference, and it didn’t. She explained it stays in the system for a very long time, hence why you have to stop before and after dental work (not basic fillings). I asked her why then did we have it monthly and she said if I wanted it less frequently she had no issue with that. I think sometimes it’s just to keep a plan or routine in place, which seems crazy I know but it appears that way at times. She also said  Denosumab hadn’t been used in cancer treatment for that long, although it has been used longer for osteoporosis, so maybe new information is still coming to light about it’s half life etc. Kate x

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Just a wee update, I seen the specialist doctor today and because I have only one bone met on my spine I have to have a pet scan to check it’s nowhere else, if this is the case he says I am a good candidate for clinical trials, I did mention in particular the immunotherapy trials, he said they haven’t tried it on bc yet but he will definitely talk to his colleagues about me. I came away today feeling a wee bit more positive today 😁

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hello JWD,

 

Many thx for sharing your journey. It must have been a shock to find the new 'lump'.

 

As with us all, the phrase scan-xiety is just the pits. Trying distraction techniques is what i do, but it does not always work! Thinking of u.....not long now...

hugggs,

silver..x

JWD
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Re: Bone mets - please join in

Hi silverlining
Yes basically I had mastectomy 9 years ago. Grade 1 estrogen poss no lymph node involvement. I had 2 years zoladex and was on tamoxafin for 5 years.i had a saline expander implant fitted. At the beginning of this year I felt a hard lump almost like a piece of plastic along my mastectomy scar near to were I had breast dimpleing last time. I didn't even panic as I thought I've had mastectomy.How naive was I? I'd got my routine appointment the next month so I thought I'll mention it then. The breast nurse reassured me and said she thought my implant had ruptured.So then the scans started ultrasound which showed nothing then Mri which my onc confirmed rupture but was still unsure about lump I asked if she thought it was cancer she said she was unsure and it could be a crack in implant..Im convinced she knew there and then but didn't want to worry me. She did a biopsy and I had results a week later which confirmed grade 1 and estrogen positive exactly the same as before. She did a blood test which confirmed post menopause so started me on Anastrazole. She requested ct and bone scan to rule out Mets. Ct was clear but I'm still waiting for bone results should no more on Thurs. I'm booked to have lumpectomy on 30th July and my implant exchanged then she said definitely radiotherapy but unsure about chemo about chemo. Xx
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dear funny face,

 

That must cause so much pressure at a time when you least need it......

 

How long have you been on your 'secondaries' journey?

 

I'd no idea that you were from across the pond......is it very hot there, too?

hugs,

silver..xx

Community Champion

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Moijan, Not all USA ladies get these drugs ! Yes some insurance companies pay. Others have a huge copay. I'm on Medicare which covers 80% of infusion drugs. You pay for Medicare and then you need a secondary insurance to cover the 20%. Prescriptions fall under your prescription plan which you pay for too. All of this coverage cost me $450 a month for me and $450 for hubby. For prescriptions there is a copay. To get palbociclibthe copay for my first month was $3500. Then $800 a month after that. I was able to obtain a grant to pay my copay. When my grant ran out I had to apply again. There was no money left for any grants for metastatic breast cancer. All the funds were used up. I had to apply to the manufacturer "Pfizer" for assistance.Luckily Pfizer agreed to sponsor me for one year. Sadly then the drugs quit working , I only used 5 months of my assistance. Then it was onto the combo I'm on now. This sent me back to finding a grant again. Luckily there was some funding open for metastatic breast cancer again. I was given a $8000 dollar grant for my compacts. I only have enough money until August or Sept. Then I have to reapply for another grant, if no funds available we will try the manufacturer. If they won't give it to me then I will have to switch drugs. I can't afford $700 dollar copay plus the copays on my other medications plus hubby 's copays and the insurance premiums. Very few people here get these drugs completely covered by insurance. FF

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I already know that some of you have a very negative opinion on stats. but these are relevant to the current chat:-

 

I can't share the Guardian article but it states that the UK cancer survival rates trail 10 years behind European countries...x

 

 

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Hi JWD,

 

I like to form a 'picture' in my mind. am I right in thinking that 'these' are your first secondaries after 9 years? Hoping you have love and support around u....xx

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Thanks for the info moijan.

I’m really fuming about this. I’m brand new to secondaries so I’m probably being naive, but is there nothing that can be done?
Has anyone ever started a petition? There seem to be petitions for everything now.

What about support from local MPs?
Surely this just can’t be right.
I had fec-t chemo last year and I’m eligible. It’s just ridiculous.

In my opinion, there is a lot of wasted money that should be redirected into healthcare.

I watched a prominent UK liver mets doctor on Twitter talking about some life saving/extending treatments that our government won’t pay for, so most of his patients are either wealthy or traveling from countries like Germany, where their governments are happy to pay.

He has to turn people from England away, even though he could help them. He works for the NHS but these treatments, such as SIRT and chemosaturation, he carries out privately.

If we can’t have the same standard of care as other places in Europe, then I believe the government has a responsibility to be honest and let people know that their lives are only worth a certain amount.
That if you want to be sure of receiving any treatment you might need, then you need to take out private insurance.
Because if their lives depend on being able to access life saving treatments on the NHS the answer could very likely be NO 😡
I was definitely naive when it comes to this. I thought private healthcare was more about waiting times.
In hindsight, I obviously very much regret not taking any out.
Xx
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Ftf

 

i have battled with Nice about these drugs....they told me that the trials showed no evidence that they worked with people who had had chemo before.that was because chemo treated ladies were excluded from the trials!)

 

 

actually there IS  evidence now that they do  (in. The USA).

 

Publicising the drugs initially,  said that they were sooo pleased to be able to spare future bc sufferers from going through chemo...and giving extra years to these people, So they  can see their kids, grandkids grownup.

 

I wrote and said that there are thousands of us ladies, who now felt disadvantaged...who’s drugs eventually. Run out and prospects were poorer. That’s when they wrote and said there is no evidence they work for Us!

 

You can read all about their decision making on the Nice website.

 

i am afraid it’s all down to money. The USA ladies get them as their insurance pays!

 

much love to you

 

Moijan..

JWD
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Thanks silver lining will keep you posted.xx
JWD
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Thanks Feel the fear for your support and advice hopefully bone scan will be clear. I was on zoladex injections after my mastectomy and I could get quite weepy and very fatigued but you just put it down to everything you have been through.My emotions were all over the place at times with highs and lows.xx
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Weird....I've just been reliably informed that my oncology's department protocol will be changing...Denosumab will be administered 1 x every 3  months! Not sure i rest easy with this cut back......Any thoughts...x???

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Hi JWD,

 

Snap!....being very new to the forum. There is a wealth of knowledge here...best of luck with your bone scan...do let us know.....x

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Thanks for all of this Nicky. I appreciate it so much. I’m building up a folder. My oncology appointments are very long. 🙄
I’ve sent emails off to a couple of renowned liver met specialists and have had replies stating that they agree with my current line of treatment.
Im very keen on the idea of surgery of some sort or radio ablation maybe. I’m terrified about this lesion that’s next to my portal vein. I’m obsessed with it. It’s tiny now but if this treatment doesn’t stop the growth it could end up being a huge danger to me I think.
Although my oncologist hasn’t mentioned anything about it.
How absolutely terrible that chemo gave you heart failure. I can’t imagine what you went through. You’re obviously made of tough stuff.

I’m confused about my pathology report too. That’s something else I need to clear up at my next appointment.

Angela xx
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Hi 

FtF, I really hope you don’t have to battle to get the right treatments although what you have had to deal with for your sone might help you. A good friend of mine, who has had bone mets for over 15 years, also has a disabled sone and has the bit between her teeth for her own treatment as well. All I’d say is make sure you educate yourself about what treatment is right for your type of BC and be prepared to challenge any decisions you don’t think are the right ones. Also be prepared to ask for a second opinion if you don’t agree with the decisions by your own oncologist, a major research hospital will have a wealth of experience that some more local hospitals don’t. All I have done is make sure I know what the next step will be and that has helped me take some form of control, which is what we all lose when we’re plunged into this nightmare. I was like FF with my primary, as most ladies are, you don’t seem to have the time to consider what might be right or wrong and you accept every word your oncologist tells you as you just want to get the cancer out of your body and move on. With secondaries it isn’t going to be gone, it’s with you and you will have more than one treatment over the years so I learnt to know what was coming next.  In fact with my original secondaries diagnosis I probably got it wrong and shouldn’t have had chemo but stuck to hormonal treatments but the thought of the hormonal taking longer to work than chemo was enough to convince me I should go the chemo route. Great news it stabilised the bone mets and got rid of the local recurrence but absolutely bad news it gave me heart failure! This then compromised my treatment options 5 years later when liver mets were also diagnosed. Luckily I was able to get excellent help with the heart failure and get it back to full working order but at the time I thought I was a goner, stress and anxiety doesn’t even cover how I felt. As to why us long term survivors can’t have the new drugs through the NHS it is unfortunately down to cost. Obviously if you have private health cover, like is needed in the US, you can get them but their cost effectiveness isn’t proven yet so NICE won’t put them on the accepted list for all patients. However the new drugs are always given in addition to a hormonal drug (correct me anyone if I’m wrong) so it is difficult to prove how much they enhance the effect of the hormonal in patients who have had more treatments as the drug trials have so far only taken place on 1st line patients, but hopefully in future they will be introduced as a standard for all long term survivors. Even without the newer drugs I have had 5 years out of arimidex originally and about 18 months out of letrozole (which was by then my 4th line of treatment). With your pathology report it sounds like to are hormone positive but I’m not sure about the percentages that are quoted. Usually ER and PR are marked out of 8 so 7/8 is highly positive, maybe the percentages are working out something else as 7/8 in my mind would be between 75% and 88%? Tamoxifen does work in a different way to the AIs (aromatase innibitors). I don’t think tamoxifen worked for me after my primary, but I could be wrong, after all my recurrence wasn’t for 5 years but by then I had my periods back which I’m sure didn’t help.

Hope all this helps with information gathering 😊this is what I’ve done over the years, find out from here as it’s far more up to date with opinions from oncologists all around the country (as we are all around the country ) so instead of getting a second opinion I’ve often had 10 opinions when I’ve asked a question which is great. Long make we continue to share and help others.

Nicky xx

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Hi JWD.
Sorry that you’re in the waiting game. It’s the worst of feelings isn’t it, and we over think every single thing anyone who works in a hospital says to us.
It’s impossible not to.
I’d think your scan has probably been marked as urgent just because of your recurrence. I don’t think they could be keeping anything from you if no one has even looked at it yet.
I know it’s much much easier said than done, but do try not to worry. I’d say they’re just being cautious giving you the bone scan. If your ct scan is clear I’d say it’s looking very positive for you. X
JWD
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Hello I'm new to this forum too. You have every right to be emotionally worried. It must be hell for you. Could you ask for more scans to put your mind at ease. I had mastectomy 9 years ago estrogen positive and had zoladex injections and tamoxafin. Recently been diagnosed with local reoccurrance I had a lump along scar.its still estrogen positive and ct scan clear. I've started taking anastrazole but I'm waiting for bone scan results I rang yesterday and nurse said the results are marked urgent to be looked at as they hav'nt been reported on yet. So I've gone into complete panic. I'm due to have lumpectomy and implant removed on 30th July but unsure of the plan depending on bone scan results. I've got to ring oncologist Secretary on Thursday. I'm usually really good at appointments and ask everything but I failed to ask would the operation still go ahead if the bone scan showed mets. I did ask nurse yesterday and she said she wasn't sure about other options but you know that feeling when you think they are keeping things from you! or is it just me and my mind working overtime.
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FtF, I take the blame for it all! I was too trusting and naive! I was raised that you say Yes Dr., thank you Dr. Never that naive again! FF

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FF, that’s a very shocking story. We’re brought up believing that doctors know best. Most of us just trust them, especially when we’re in a life or death situation.
I was very worried my periods didn’t stop until after chemo 5 and continued on tamoxifen. I was told not to worry. 🙄
And now I’m still worried. I’ve just had another heavy period. I’ve only had one zoladex injection, but it obviously hasn’t worked straight away.

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Nicky and FtF, When I first started with mets I had lupron injections to shut down my ovaries. At 4 months tumors were still growing. Oncologist decided I wasn't hormone positive enough and that no hormonal would work for me. I went for a 2nd opinion and that oncologist felt lupron wasn't enough bc it only shuts down your ovaries and not your adrenal glands. He said if I ever wanted to try hormonal and my Inc wouldn't do them to come see him. Take a big leap over 10 years of chemo and palbociclib came on the market. I wanted to try it. My onc said, NO! He said he would only give it to me if I had my lung tumors biopsies again. He said we needed more evidence it might work. We got in a big argument. I said I wasn't risking having my lungs biopsied again. They were in great jeopardy of collapsing 10 years before, so I wasn't risking it. I said when you give me chemo it's a game. You don't know if it will work so I want to take a chance and see if this works. He finally agreed I could try it, but with a big attitude! Also proclaiming it would never work. Well in  Oct I had a scan and was stable so we continued. In Dec he quit. In April was when the scan told me how great it was doing. He never got to know! Now I'm on E & E, another hormonal and its working too. Pablociclib was my 6th line of treatment. I look back now since I'm doing so good on hormonal and wish I had tamoxifen after my primary. At the 7 year Mark I asked him why I didn't have it and he said bc you weren't ER positive. Then he looked it up and said OH, yes you were. Then he said it was bc he decided it wasn't protocal for my age and no lymph nodes. My surgeon was furious when I told her all this when I had my port placed. She said I should have had tamoxifen and I probably wouldn't have mets. She said but no sense crying over spilt milk! So please fight for whatever you think you need. I thought he was doing whatever I needed. Obviously he wasn't!!

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Thanks for that Nikki, my original diagnosis was a small lump at side of my breast, cancer in 5 of 7 lymph nodes and sentinel node, as you say hopefully more answers tomorrow x
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By the way no one has ever mentioned how strongly ER I am. Last week I requested my original pathology report from last year’s mastectomy and it seems I’m 7/8: 34 to 66%/ strong. Whatever that means.
I know the tamoxifen clearly wasn’t working. 🤔
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Thank you for taking the time to explain HER2 for me Nicky. There’s so much to get my head around in a short space of time. My oncologist probably shouldn’t of suggested HER+ would be the best outcome.
Thank goodness for this forum. 😳 imagine the state I could of got myself into without you ladies. It’s slightly worrying that I need to come here for fact checking, but I’m extremely grateful that I can.

I think it’s absolutely disgusting that you can’t have access to these new drugs. Why won’t they allow you to have them? They worked for FF for 21 months. I can’t see how they can justify not allowing them.
I’ve had to battle for my disabled son for the past 27 years. I’ve got a feeling getting access to the treatments I might need over the coming years is also going to turn into a battle. At least I’ve got practice. I just hope I’m as good at fighting for myself as I am for him.
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Hi FtF

I agree with what FF has said.  I am also HER2 negative and have been living with mets for over 10 years now.  After one of my liver biopsies it was decided I was HER2+ but in hindsight we all realised that it was so marginal I wasn't benefitting from any treatment that was specific for HER+. I have however always benefitted from hormone treatments (as well as chemo when I've had to have it)  There's alot to take in when you are first diagnosed with secondaries, far more than with primaries as other treatments are more appropriate and of course it is long term rather than a set amount of cycles.  I only understood what HER2 meant when I was investigating it for myself.  From what I understand we all have HER2 receptors on our BC cells.  However it is only when these are over-expressed (ie there's too many of them) that you are treated with a Herceptin related drug.  In the same way if you do not have a high level of ER or PR receptors you are unlikely to benefit from hormone blocking treatments.  In my case my test results came back as possibly HER2+ so they conducted another set of tests at gene level and this still came back as marginally over the cut off point between what is HER2- and what is HER2+.  I hope this explains it a bit and may make you realise that you don't need to be HER2+ to get excellent treatment.  Being HER2+ means you have another set of receptors that need blocking.  In fact the press always seem to pick up on Herceptin/HER2+ as alot of research has been done to level the playing field between HER2- and HER2+ however there has been more recent drugs that are now being used to boost the effectiveness of hormone treatment.  I, along with other long term secondary BC survivors, can't actually have these newer drugs (in the UK/on the NHS) as they are only for the first line of treatment (ie the first hormone treatment you have after your mets are diagnosed) so we haven't benefitted from the enhanced performance they give.

As to how you are feeling emotionally as I said earlier there's alot to take in and suddenly being plunged into the menopause doesnt help!  I had zoladex injections for 2 years after my primary diagnosis and I do know its not much fun! For ovaries to be shut down almost immediately is difficult especially with all the other emotions going through your head.

 

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I think my emotional state might have something to do with the zoladex injections I’m on. I wonder if anyone else has experienced this?
I know I’m going through a difficult time but I’m genuinely not one for crying. Since I started the injections I seem to be on the verge of tears constantly.
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Thanks for the advice and tips FF.

I started running about 8 weeks ago so I’m hoping this helps. It’s an nhs thing called couch to 5k. I can manage about half an hour running every other day now. I started this before my secondary diagnosis just to get a bit fitter. Who’d of known how important it would turn out to be.

I’m feeling optimistic about the meds, improvements at 6 months would be wonderful. Maybe I’d be eligible for surgery then.
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Feel the Fear, I was on letrozole/palbociclib for 21 months. My first scan at 3 months was stable. The second scan at the 6 month mark showed lots of improvement. Letrozole killed my knees with pain. Palbociclib made my leg muscles weak. I had some friends this happened to, too. I would suggest doing some leg strengthening exercises. My legs have gained some strength back, but not all. This combo worked 21 months for me. FF

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You are welcome. I was hoping you would log back in soon. I wanted to ease your mind some! FF

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Ahh FF, you’ve got no idea how you’ve brought me to my senses. That’s exactly what I needed to hear. I thought you were her positive as well.
Thank you so much for letting me know. 😀

I think my oncologist was referring to me being able to have herceptin if I’d been positive.
You’re obviously doing very well without it. Especially with your recent good news.
Thanks again FF. I might get my appetite back enough to have a late lunch now. 👍
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Feel the Fear, I was told ER+, PR+ and HER 2- is the least aggressive. Then ER+, PR -, HER2-.

 

I was told I was ER+, PR- and HER2-.  Then my new oncologist wrote on a letter I needed that I was PR+. I questioned her about it and she said that there was no difference in treatment and that being PR+ would actually be better. Lol still never gave me an answer on it. 

 

I have had mets for almost 13 years and I am HER 2 negative!!!

 

FF

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Thanks for the support ladies.
Annie, it’s brilliant that your mets are shrinking.
I would love to have surgery at some point. My biggest lesion is just over 1cm. My oncologist said it was over 2 but the radiologist said no, much smaller. I have 7 or 8 in total. Most are that small they’re barely visible.

Oncologist wants me to try these meds before considering surgery. I noticed looking at my scan that there’s one lesion quite close to a portal vein. 😳 that’s giving me sleepless nights.
I think I just need to give my head a shake. I’m usually so positive. I’ve even cried on the phone to my Mam this afternoon and now I feel terribly guilty, she’ll be worried sick. 🙄
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Ftf, sorry it wasn't the news you wanted. Try to focus on the positive- you may be her-neg, but you are still er+, which from what I've read is probably the most important element in terms of possible treatments. Totally understand your wobble, I have them frequently and they come in every shape and size! Sending hugs and best wishes for when you start treatment.xx
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FTf ,

 

fingers crossed for the ibrance, seems to be getting really good resultsxx Sorry I have no real knowledge of herceptin, but Ibrance hopefully will work well for you.

 

Moijan

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