Rosie/Janette, Happy to see you posting. I'm pleased but very cautious. I really don't believe or can't allow myself to believe it's dead! I haven't told anyone but you girls and my family.Time will tell. Thanks for the well wishes. FF
oh....with me & gardens...the bigger the better but they are hard work, but always, always worth it. My forever garden is very small...a tiny patch in the front and a small area in the back where I have my beloved African hut!! Its sheer delight...
I know so lil' about all these drugs..is 'P' a tablet?
Owing to my tooth, I'll be coming off Denosumab for 8 weeks/more.....methinks this is a tad scary!!
Just popping in to say a lil' hello...I'm really enjoying this rain and my garden is loving it and perking up....have a good Monday....x
It's lovely to read the kind messages to Carolyn in this thread. Sending you our best wishes too Carolyn.
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It always amazes me how readily 'they' whisk us out of hosp. these days....
Thank goodness for the rain!
Bestest of luck to u....xx
I'm delighted to read your news.....& I'm wishing you all the very best for your op. on Monday. How long will u be in hosp.? Hugs.....
oh....& please call me silver....xx
Dearest Carolyn, I can't say any more than Nicky's words, thank you to the funniest, most upbeat and caring person on the forum, you and your family will be in my thoughts and prayers xxxx
Dear Carolyn, what a shock to read your latest post, my heart goes out to you. I had thought you had been a bit quiet on the forum over the past few weeks but put it down to being busy elsewhere, in the real world. As the other ladies have said you have been such a wonderful friend on here to so many of us, we will miss your ‘as useful as a chocolate teapot’ expression. You have always brought a cheery start to the day (we log on and read at a similar time) which we will all miss. If you feel it is right please do come back on here, even if it’s only to read the messages of support. You will know that we, your friends, are holding you close. Now make sure you get on and spend that time with your family as they are the most important people for you.
I put my thinking cap on.....I've inflammatory arthritis so I'm also under a Consultant rheumatologist. There are 2 ways to attack pain of this sort....anti-inflammatories like Etiricoxib/ neuropathic drugs like Gabapentin...We should not have to suffer pain. I'm in flare at the mo' so u have my heartfelt sympathy....please seek professional advice...& take care..x
I'm sorry you are in so much pain. Having had severe back pain quite unconnected with cancer, I know how awful it can be. The fact that you recently had a bone scan and a ct scan should be reassuring, I have never had a lot of pain from the mets in my pelvis but I did have acute pain a while back because of too much strenuous gardening. I got some painkillers from my GP - that might be a good thing to do - and had arranged to see the onc but it began to improve before I got there so I never went. There's no harm in getting some painkillers and speaking to your bcn. She should be able to advise you what's best to do. It's lucky you have an onc appointment soon so will be able to talk to him/her.
Hope the pain eases.
I have been lucky enough to meet Carolyn once or twice and she's just the same face to face as she is in her posts. I am sad that i won't be reading them any more.
We will all miss you and your support and will carry on holding you in our hearts and remembering how you brightened up our days.
Oh Carolyn, my heart goes out to you. Wishing you all the best - it doesn't matter how long we get - we always need more time.
I hope the dreaded C is gentle with you.
All my love to you and your family
Carolyn.........we’ll miss you. But we are all still holding hands so maybe you will be dropping by to keep an eye on everyone!
Always thinking of you, Carolyn. You’ve given me a lot of laughs! But now it’s time to concentrate on Carolyn for a while.
Carolyn, We are here if you need us! Thanks for always finding a way to make us laugh! You always put a smile on my face! Your advice and humor will be missed. FF
I am very sorry to read your post Carolyn. I know you have been supportive to, and appreciated by, many ladies on here and believe from reading your posts that you will have that support from your family and friends. I wish you, and your loved ones, well. Kate x
I can give you his answer to that one now...his opinion will definitely be no, but to check with your Oncologist. I think because the Onc is sort of in overall charge of us they kind of have to say that! That said my Onc says what did Max Fax say!!
..just to add, I will ask again even though in the past has said longer x
Actually I do have one question. Is 8 weeks off Denosumab either side of extraction sufficient? Many thx for your kindness....
Hi Silver, my dentist wouldn’t do the work on mine so I was referred to the dental surgeons, I was referring to when I had the first signs of infection when I said my dentist was useless, the dental surgeon was excellent. I have my Max Fax check up next week, and if it’s still the same surgeon he is lovely so if there’s anything you’d like me to ask him let me know and I will run it past him...he can only say no! Kate x
When I was Dxed I had mets in L&R pelvis but I was asymptomatic.....guess that's not really helpful.....x
I just could not read & leave. Although I do not know you, I am sad to read your news, Take good care....xx
Hi mermaid, and welcome.
Sounds like you have done incredibly well on the hormone treatments and so far avoiding chemo. In my experience (10+ years with bone mets) I have found 5 years seems to be about the maximum you might get out of one type of hormone treatment and quite often they all become less effective when they are 2nd, 3rd or further line treatments. You don’t mention anastrozole, I’m assuming you’ve not had it and although it is similar to letrozole I have managed to get a good few years out of both of these treatments, initially anastrozole for nearly 5 years and then a few years later about 18 months from letrozole. A lot of us hormone positive ladies seem to have a couple of hormone treatments then have to go onto chemo to knock everything back a bit if progression is shown on scans, although this isn’t the case with everyone especially if you ‘only’ have bone mets. It may be worth asking about anastrozole? Btw because you have already had exemestane on its own you wouldn’t be eligible to get evermolimus on the NHS, The NICE guidelines include it only if you have not had exemestane. Also if exemestane has stopped being effective I don’t hink your oncologist would expect it to work for any longer if you were able to add evermolimus into the mix ie if you funded it yourself. It is worth getting your oncologist to ask about getting funding for faslodex, I’m currently on it and luckily my hospital trust had already agreed to fund it themselves before I had to ask about it. Possibly you could ask if you can fund it yourself and find out the costs, obviously this would depend on whether you could afford it or not but as it’s a long established treatment the costs aren’t as high as some of the newer drugs. As to having chemo there are options that aren’t as harsh as you might think. Capecitabine is tablet form and is very effective, and Eribulin seems to be very effective for hormone positive BC although I seem to remember that you may not be able to have either if you haven’t had any form of chemo before, but the ‘rules’ may have changed.
Sorry I’m not much help but just wanted to mention anastrozole in particular.
Mermaid, How about a combo of exemestane and evermolimus. You might need to move up to double agent rather than a single. I'm from the States and don't know much about your medical system, so can't help you there. I would suggest looking for the thread about palbociclib and ask those ladies how and where they got it? Also, you might want to ask your oncologist if you need chemo to knock it back! Every oncologist seems to have their own plan of action. Good luck! FF
Oh no!!! not hot flushes..u poor thing....I left 'all' that behind me a ways back.
TBQH, I loathe the heat & my inflammatory arthritis is in flare so losing my innate sense of bonhomie.....literally praying for rain...for me & my forever garden....
cool huggs for u,
That really was a piece of very bad luck....
My dentist refuses to do the extraction...I'm being referred to a dental hospital....but to be very honest, I'm very EEEK about the whole shebang....thx for being there...xx
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.
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..