Best Of
Re: 7 year diagnosis anniversary is today ..... how time flies!
Dear @arpie, I am so grateful for all your support throughout my journey. I hate saying this because I wish no one ever needed to join this network but having you here has been incredibly important to so many of us. I’m glad to hear that you’ve reached your 7th anniversary, and I wish you and others many more anniversaries ahead.
GorgyS
2
Re: Feeling scared and just a bit angry
Hi @Kaz27
Sorry to see you here but as others have said we are a wealth of information between us, those that have gone before us, us and those, like you, starting out!
I am a firm believer that stress has a lot to do with the state we find ourselves in - my life was extremely stressful leading up to the BC diagnosis. I had to reassess what I was doing volunteer and workwise, snub the bullies, and more importantly always smiled and said hello to the bullies when I came across them, to prove their crap may have sat heavy but I have risen up above it and never let on about my cancer diagnosis to them!
For me personally I am fortunate to have been married for a very long time and my hubby is as supportive as he was from the first time, we went out together! My stresses are a little different now as I am a full-time carer for a younger sister with Dementia! It's watching someone you love to deteriorate, and you can only nurture and accept and repeat the answer to a question asked over and over!
I agree with others advice, please seek some counselling - your personal life sounds in turmoil but at present you need all your emotional and physical energy to cope with and beat this, Cancer! Counselling hopefully will give you some coping mechanisms. Both on a personal level and on the Cancer level. I was put with a Counsellor the day of diagnosis and her advice was if you feel yourself starting to stress out then pat your legs saying this is me, this is now and true enough it works, as your thoughts are concentrating on the patting and yourself, it brings you into the now!
Lots of help here, just please don't belt yourself up over the diagnosis, it is what it is and there's plans in place to hopefully beat it!
Sad to read of the plight of your son and daughter in law.
Best wishes
Take care
Sorry to see you here but as others have said we are a wealth of information between us, those that have gone before us, us and those, like you, starting out!
I am a firm believer that stress has a lot to do with the state we find ourselves in - my life was extremely stressful leading up to the BC diagnosis. I had to reassess what I was doing volunteer and workwise, snub the bullies, and more importantly always smiled and said hello to the bullies when I came across them, to prove their crap may have sat heavy but I have risen up above it and never let on about my cancer diagnosis to them!
For me personally I am fortunate to have been married for a very long time and my hubby is as supportive as he was from the first time, we went out together! My stresses are a little different now as I am a full-time carer for a younger sister with Dementia! It's watching someone you love to deteriorate, and you can only nurture and accept and repeat the answer to a question asked over and over!
I agree with others advice, please seek some counselling - your personal life sounds in turmoil but at present you need all your emotional and physical energy to cope with and beat this, Cancer! Counselling hopefully will give you some coping mechanisms. Both on a personal level and on the Cancer level. I was put with a Counsellor the day of diagnosis and her advice was if you feel yourself starting to stress out then pat your legs saying this is me, this is now and true enough it works, as your thoughts are concentrating on the patting and yourself, it brings you into the now!
Lots of help here, just please don't belt yourself up over the diagnosis, it is what it is and there's plans in place to hopefully beat it!
Sad to read of the plight of your son and daughter in law.
Best wishes
Take care
Re: 5 Years on...
Congrats @Harvey1903 on your 5 years clear xx Great news.
My diagnosis Anniversary is 7 years on 5th January 2025 .... still going strong xx
take care & all the best
My diagnosis Anniversary is 7 years on 5th January 2025 .... still going strong xx
take care & all the best
arpie
3
Re: 7 year diagnosis anniversary is today ..... how time flies!
@arpie wow that is great 🙌🏽 woohoo.
Thanks you advice and feedback on our posts, you are valuable on this forum
Thanks you advice and feedback on our posts, you are valuable on this forum
Cheri
3
Re: 7 year diagnosis anniversary is today ..... how time flies!
@arpie This is wonderful news. Congratulations. Thank you for being here for all of us. Sending big hugs
Re: Recovery times and support required following mastectomy and chemo
Hi @Shenners
I'm sorry to hear of your diagnosis and that you've been through a tough few years.
I had a bilateral skin sparing mastectomy (ie nipples removed) and direct to implant surgery in May 2024 for invasive ductal cancer, with a sentinel node biopsy at the same time. I saw an oncoplastic surgeon who could complete both the breast removal and the implant insertion in one go (to limit the number of surgeries required). Implants were recommended due to not enough of my own flesh being available for a DIEP flap recon.
I went through the private system and was out of pocket approx. $6,500 for the surgeon and anesthetist after private health and Medicare.
Surgery took approx 4 hours (less than DIEP flap) and I was in hospital for 5 days. I stayed in until my surgical drains came out, but a home nurse was available if I wanted to discharge with the drains in. Managing a drain on each side can be tricky and uncomfortable.
Pain was manageable and I stopped taking the pain killers on my return home. Movement was restricted for a few weeks (and no driving for two weeks), but I was provided with physio exercises to do straight away and these helped gain mobility back.
Before heading to hospital, I purchased a reclining camping chair (as this was cheap and we didn't have a proper recliner) which helped me to sleep on my back at home - I slept in it for the first week home and then went back to a normal bed, but still on my back. To avoid any arm extension, I moved my favourite kitchen items (ie coffee cup etc) to a lower cupboard and made sure I didn't carry any heavy things (ie shopping bags, full washing baskets) for approx. 1 month. You also may not be able to hang washing on the line, so I recommend getting a metal rack thing and doing light loads only.
I am happy with my implants, although they will need to be changed out in 10-15 years. I don't need mammograms, but do have a yearly ultrasound.
All the best and feel free to ask any questions xx
I'm sorry to hear of your diagnosis and that you've been through a tough few years.
I had a bilateral skin sparing mastectomy (ie nipples removed) and direct to implant surgery in May 2024 for invasive ductal cancer, with a sentinel node biopsy at the same time. I saw an oncoplastic surgeon who could complete both the breast removal and the implant insertion in one go (to limit the number of surgeries required). Implants were recommended due to not enough of my own flesh being available for a DIEP flap recon.
I went through the private system and was out of pocket approx. $6,500 for the surgeon and anesthetist after private health and Medicare.
Surgery took approx 4 hours (less than DIEP flap) and I was in hospital for 5 days. I stayed in until my surgical drains came out, but a home nurse was available if I wanted to discharge with the drains in. Managing a drain on each side can be tricky and uncomfortable.
Pain was manageable and I stopped taking the pain killers on my return home. Movement was restricted for a few weeks (and no driving for two weeks), but I was provided with physio exercises to do straight away and these helped gain mobility back.
Before heading to hospital, I purchased a reclining camping chair (as this was cheap and we didn't have a proper recliner) which helped me to sleep on my back at home - I slept in it for the first week home and then went back to a normal bed, but still on my back. To avoid any arm extension, I moved my favourite kitchen items (ie coffee cup etc) to a lower cupboard and made sure I didn't carry any heavy things (ie shopping bags, full washing baskets) for approx. 1 month. You also may not be able to hang washing on the line, so I recommend getting a metal rack thing and doing light loads only.
I am happy with my implants, although they will need to be changed out in 10-15 years. I don't need mammograms, but do have a yearly ultrasound.
All the best and feel free to ask any questions xx
Suki
2
Re: Recovery times and support required following mastectomy and chemo
Gosh, you've had an extremely hard time of it in the lead up to your diagnosis, @Shenners xx.
Sending you big hugs xx. I lost my husband to cancer 2.5 years ago & know just how heart breaking it is to lose your wonderful partner xx. I saw a grief counselor up here - I hope you'll be able to see someone soon (or ring our helpline, info below, in the meantime.) xx Make sure you ask your medical team to point you to some counseling too xx In the meantime, have a listen to Charlotte Tottman's Podcasts, as she covers an awful lot of topics, having been diagnosed with BC herself & having a double mastectomy & remaining flat. She is very easy to listen to & very much 'common sense' & calming xx
http://www.drcharlottetottman.com.au/my-podcast.html
Have you been assigned a Breast Care Nurse yet? They should be a wonderful support for you as well. And if you want to speak to someone here, ring our helpline 1800 500 258 Mon-Fri, 9-5 xx They've come back 'on line' today, after the Xmas break.
I have no doubt that your family & friends will muck in together to help you out with meals & stuff (mowing, gardening, helping with the kids when you are not able) so make sure you take them up on any offer xx Even work out a roster, maybe? In the mean time, consider cooking & freezing some meals now if you can - to make it a bit easier later one when you are home again.
Having fairly young kids too, There are also various organisations (like Canteen and Red Kite and Camp Quality) where they give kids (who's parent has cancer) the chance to meet up with other kids in the same boat & just have fun together. Your hospital Social Worker should be able to point you to local organisations who may be able to help too. Your Breast Care Nurse may also be able to point you to relevant organisations, too. xx
Re your surgery - I only had a lumpectomy - your surgeon will be able to fill you in on the recovery - as it depends on whether you are having immediate reconstruction, or have to wait for it! We have 2 groups here that you may like to join today (so you can read up tonight before seeing the surgeon tomorrow! Maybe call the Helpline, for that??) Reconstruction & those who choose to remain flat.
https://onlinenetwork.bcna.org.au/group/1-choosing-breast-reconstruction
https://onlinenetwork.bcna.org.au/group/29-flat-chat-no-breast-reconstruction
You can also read up on other areas of the forum that may interest you, here (including some tick sheets on your mental & physical recovery, post op.)
https://onlinenetwork.bcna.org.au/discussion/23477/a-big-welcome-to-all-new-online-network-members#latest
take care, be kind to yourself, you are being a superwoman just now xx Take things one day at a time, one hour at a time, if needs be xx Wishing you all the best for tomorrow xx
Sending you big hugs xx. I lost my husband to cancer 2.5 years ago & know just how heart breaking it is to lose your wonderful partner xx. I saw a grief counselor up here - I hope you'll be able to see someone soon (or ring our helpline, info below, in the meantime.) xx Make sure you ask your medical team to point you to some counseling too xx In the meantime, have a listen to Charlotte Tottman's Podcasts, as she covers an awful lot of topics, having been diagnosed with BC herself & having a double mastectomy & remaining flat. She is very easy to listen to & very much 'common sense' & calming xx
http://www.drcharlottetottman.com.au/my-podcast.html
Have you been assigned a Breast Care Nurse yet? They should be a wonderful support for you as well. And if you want to speak to someone here, ring our helpline 1800 500 258 Mon-Fri, 9-5 xx They've come back 'on line' today, after the Xmas break.
I have no doubt that your family & friends will muck in together to help you out with meals & stuff (mowing, gardening, helping with the kids when you are not able) so make sure you take them up on any offer xx Even work out a roster, maybe? In the mean time, consider cooking & freezing some meals now if you can - to make it a bit easier later one when you are home again.
Having fairly young kids too, There are also various organisations (like Canteen and Red Kite and Camp Quality) where they give kids (who's parent has cancer) the chance to meet up with other kids in the same boat & just have fun together. Your hospital Social Worker should be able to point you to local organisations who may be able to help too. Your Breast Care Nurse may also be able to point you to relevant organisations, too. xx
Re your surgery - I only had a lumpectomy - your surgeon will be able to fill you in on the recovery - as it depends on whether you are having immediate reconstruction, or have to wait for it! We have 2 groups here that you may like to join today (so you can read up tonight before seeing the surgeon tomorrow! Maybe call the Helpline, for that??) Reconstruction & those who choose to remain flat.
https://onlinenetwork.bcna.org.au/group/1-choosing-breast-reconstruction
https://onlinenetwork.bcna.org.au/group/29-flat-chat-no-breast-reconstruction
You can also read up on other areas of the forum that may interest you, here (including some tick sheets on your mental & physical recovery, post op.)
https://onlinenetwork.bcna.org.au/discussion/23477/a-big-welcome-to-all-new-online-network-members#latest
take care, be kind to yourself, you are being a superwoman just now xx Take things one day at a time, one hour at a time, if needs be xx Wishing you all the best for tomorrow xx
arpie
2
Re: Recovery times and support required following mastectomy and chemo
Dear @Shenners
No-one ‘deserves’ cancer but you have been through quite enough without this. Your practical approach and resilience is outstanding. I’m sure you have moments when it’s not so good but under the circumstances you are to be utterly commended.
I had a single mastectomy and no reconstruction so I can’t advise on bilateral
surgery or reconstruction. But the latter can be time intensive and possibly expensive depending on your circumstances. In due course your surgeon can give you more details.
No-one ‘deserves’ cancer but you have been through quite enough without this. Your practical approach and resilience is outstanding. I’m sure you have moments when it’s not so good but under the circumstances you are to be utterly commended.
I had a single mastectomy and no reconstruction so I can’t advise on bilateral
surgery or reconstruction. But the latter can be time intensive and possibly expensive depending on your circumstances. In due course your surgeon can give you more details.
Your wish not to live in perpetual fear of breast cancer is completely understandable but again, may depend on circumstances. My oncologist believed that I had a possibly greater chance of cancer elsewhere in the body than in my (so far) unaffected breast. So far, so good, 12 years! My surgeon preferred to wait rather than immediate reconstruction, which suited me fine as I wasn’t sure about it. Some people hate being lop sided, I’m large breasted, use a prosthesis and find it fine.
So…among all the other options, there is also the one of a single mastectomy (which is usually remarkably painless and a quick recovery) and take some time to consider and make longer term decisions. That may alter your reconstructive options so needs to be discussed with your surgeon. But it may also give you some time to fully absorb the losses you have experienced, help your children in their own demanding year and breathe a bit!
Can’t recommend too highly a good counsellor. This is ‘mess with your brain’ stuff. All of it. I spent a remarkably short time with an excellent counsellor - she gently but firmly questioned some of my long held practices (very little of her concerns were about how I was dealing with cancer!) that were not productive in a balanced life - she didn’t tell me what to fix, she just encouraged ‘the examined life’. Her exercises led me to a better life/work balance, and a sane and productive attitude towards death. I still use many of them. Knowing that cancer is often the first brush with that intrusive concept is a step in the right direction all by itself. My counsellor no longer consults in Melbourne, but your GP may be able to recommend practitioners suited to cancer patients.
So many decisions. My very best wishes for your health and happiness whatever you choose.
Can’t recommend too highly a good counsellor. This is ‘mess with your brain’ stuff. All of it. I spent a remarkably short time with an excellent counsellor - she gently but firmly questioned some of my long held practices (very little of her concerns were about how I was dealing with cancer!) that were not productive in a balanced life - she didn’t tell me what to fix, she just encouraged ‘the examined life’. Her exercises led me to a better life/work balance, and a sane and productive attitude towards death. I still use many of them. Knowing that cancer is often the first brush with that intrusive concept is a step in the right direction all by itself. My counsellor no longer consults in Melbourne, but your GP may be able to recommend practitioners suited to cancer patients.
So many decisions. My very best wishes for your health and happiness whatever you choose.
Afraser
3