The information available on the Breast Cancer Network Australia website is not medical advice and is provided for information purposes only. It should not be viewed as a replacement for a consultation with a qualified medical professional. Our website is designed to offer information and support to the general public. Be aware that we do not provide any medical advice, and for medical advice we recommend you speak to a qualified medical professional or doctor. 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Changers Living with Advanced Breast Cancer","id":"message:55531","revisionNum":1,"repliesCount":10,"author":{"__ref":"User:user:14227"},"depth":0,"hasGivenKudo":false,"board":{"__ref":"Forum:board:living-with-metastatic-breast-cancer"},"conversation":{"__ref":"Conversation:conversation:55531"},"readOnly":false,"editFrozen":false,"moderationData":{"__ref":"ModerationData:moderation_data:55531"},"body@stripHtml({\"truncateLength\":200})":"Hi everyone, here is a story I wrote a couple of years ago. m I feel it is still very relevant and seeing its Advanced Breast Cancer day on Sunday I felt it appropriate to post it again. I am sure ma...","body@stringLength":"14500","rawBody":"Hi everyone, here is a story I wrote a couple of years ago. m I feel it is still very relevant and seeing its Advanced Breast Cancer day on Sunday I felt it appropriate to post it again. I am sure many of you can relate to parts if not all of the content. I am grateful that I am able to post this again because I still have good quality of life and hope to continue to do so. I wish you all health and happiness.
Hi, my name is\nKaren, I am 61 years old, married and mother of 2 adult boys and have lived\nwith HER2 Advanced Breast Cancer for 13 years. As we are acknowledging\npeople with Advanced Breast Cancer on the 13th of this month, I thought I'd put\ndown some thoughts.
\n\n
Here under are my\nmusings with regards to events during my journey that have had a profound\neffect on my emotional being and the way I live. I hope what I have said\nresonates with some of you living with Advanced Breast Cancer. Sometimes\nwe find it hard to express our game changes and I hope you find what I have\nwritten interesting.
1. \nBeing diagnosed in 2007\nwith Metastatic bone disease - mortality really kicks in!
\n\n
\n\n
I’d thought I was going to\ndie in a matter of months. I asked my\ndoctors what my life expectancy would\nbe. Based on the average, I was told 4\nyears and I already had one! My life was now\nin a holding pattern as I was dictated by a new entity “cancer”.
\n\n
Despite this news, I was determined to keep life as\nnormal as possible for self preservation and the well being of my two young\nadult boys and husband and bills had to be paid. I worked for 6 years living with cancer. There\nwere periods during those years when I had to draw on my annual leave, sick\nleave and long service leave due to surgery, radiotherapy and regular\nchemotherapy. Despite my chronic\nillness, I was nonetheless still able execute my position well, and those not\naware of my personal health challenge were none the wiser. However, in the end, it did become too hard\nto work full time as years of chemotherapy and the disease not being stable had\ndebilitated my body and energy.
\n\n
There were many times when I had to rise above my\nlimitations and living with permanent fatigue made me irritable which I vented\nat home. I was not always nice to be\naround.
\n\n
On a positive side, my disease has made me take\nnothing for granted and I have become more tolerant of people and much less\njudgmental. I now stop and smell the\nroses and give time to myself. I have a\ndeeper connection with my family and friends that I hold dearly in my heart and\nfeel blessed to have them.
\n\n
2. \nGiving up work.
\n\n
\n\n
I gave up work prematurely because my employer agreed for\nme to go part-time but this did not materialise, forcing me to take my Income\nInsurance. At that time I advised my\ncompany in writing I was taking unpaid sick leave and believed this to be so as\nI was not told otherwise. I kept in\ncontact with my immediate boss however when I paid a visit to Human Resources\nsome 21 months after I left work to discuss my return, I was told I had been struck\noff the books. The explanation given was\n“company policy”. This was not a proper\nexplanation, nor grounds for dismissal. No-one bothered to advise me that my services\nwere no longer required and I had not resigned. Due to my employer’s actions, despite being\na skilled person, competent in business and marketing, my continuity in the\nworkforce had been broken. Given my age\nand illness, finding new employment has proved problematic.
\n\n
This was extremely upsetting to me. I worked in this organisation for 22 years. I had a career which I identified as a big\npart of me. To have this taken away was\nmortifying and has taken me a long time to accept that I am no longer in the\nworkforce.
\n\n
Through my own experience and talking to fellow cancer\nsurvivors, I am aware problems are not uncommon where people with cancer are\nencouraged to leave their jobs, or having their terms and conditions altered,\nto their detriment, upon their return. In\nmy case I got lip service and was dismissed surreptitiously.
\n\n
Currently cancer is considered to be a disability\nunder anti-discrimination laws, which means that reasonable adjustments are\nmade so people living with cancer are not disadvantaged at work. I don’t believe this is understood by\nemployers.
\n\n
3. \nCashing in my\nsuperannuation
\n\n
\n\n
As I was no longer working and had\nterminal cancer, I cashed in my superannuation because as a family we had to\nreduce our household debt in order to live off one wage, pay medical and other\nbills. When I cashed in I was\ndiagnosed with metastatic brain disease and indications were that I only had months to live. Now I have lived on for another 5\nyears. What this means, my husband and\nI no longer have a retirement plan and will have to rely on pensions that has\nalready started with me being on a disability pension. I was the main income earner so our standard\nof living has dropped and keeps doing so whilst I keep living. Living with cancer brings everything\nforward making it much harder to make ends meet whilst living and coping with a\ndisease and its associated costs.
\n\n
\n\n
To access my income insurance then my\nsuperannuation, entailed extensive paperwork that had to be completed by my\noncologist, GP and myself. As I have terminal cancer, my applications\nwere accepted but the process was arduous and I can understand it being\noverwhelming for some. To add salt to\nthe wound, in the early days of receiving my income insurance, I had to chase\nthe insurance company every month with monthly telephone interviews regarding\nmy health. Not nice when you have an\nincurable disease and are asked to justify why you qualify to get your next\npayment!
I was terrified that I was going to die very soon. I couldn’t believe it, I had no symptoms. The lesions were picked on my regular\nscans. My mortality was very much front\nof mind and I was deeply concerned how this diagnosis was going to affect my\nquality of life and how quickly I would deteriorate. I had three tumours in my brain as well as\none in my spinal cord. The one in the\nspinal cord was troublesome as I already had extensive radiotherapy on my neck\ndue to bone mets and it was touch and go if they would give me another dose to\ntreat this new threat which could render me a quadriplegic. Very dark times. Radiotherapy eradicated this threat and has\ndisappeared (a miracle).
\n\n
\n\n
5. \nAcceptance that cancer\nis a part of me.
\n\n
\n\n
Cancer is my reality which I now embrace as part of me\nand consequently I try to make the most of every day and moment. It\nhas taken a long time to accept that Cancer is part of my body. When I was first diagnosed, it was a foreign\nentity that had to be conquered.
\n\n
Sure, I am now\nexperiencing some long term problems such as nerve damage in the form of\nneuropathy in feet and hands which affects my mobility due to the disease and years\nof chemotherapy, radiotherapy and surgery has affected my balance, but for the\nmost part, I take it in my stride. My\nnormal is changing because of my physical limitations but I have a good quality\nof life.
\n\n
I am living with advanced Breast Cancer, however\nincurable does not mean untreatable. 5\nyears ago treatment options were drying up until Kadcyla became available. I have had 70 doses and I am still\nhere! New technology brings hope.
\n\n
6. \nGoing on a disability\npension.
\n\n
\n\n
I am now on a disability pension, which\ndoesn’t sit easy with me. I have always been independent, I have exhausted my\nown personal avenues for income to pay the bills, and a pension was my last\noption.
\n\n
Once I went on the pension and my health\nimproved I sought part-time work through employment agencies that place people\non a Disability Support Pension. I\nsoon discovered that although the government pigeon hole people living well\nwith cancer as Disability Pensioners, they are discriminated against because\novertly they appear normal. In my case\nI am skilled and articulate and found they are either not set up or aren’t\ninterested in people like myself. Naively\nI thought this avenue of employment would work as having cancer, one is not\nsure what is around the corner and this system would be able to accommodate any\nchanges. I was wrong.
\n\n
How I feel about this, I am now 61 and invisible. It’s had a profound effect on my self-worth\nbeen as I have not been able to contribute to my family\nfinancially. Those living well with\ncancer should be encouraged to work and be part of mainstream society. It’s a win/win for the people living with\ncancer and their families and the economy. \n
\n\n
\n\n
7. \nAdjusting to early\nretirement
\n\n
\n\n
For me this is a new\nrealisation. I am now not so angry that\nI cannot work and have become quite the domestic queen. Mind you I don’t find it fulfilling but at\nleast its filling my days. Fortunately,\nI was well enough to do a bit of travelling with my husband in 2014. I am not complaining, but it’s probably our\none and only opportunity. My husband\nworks very hard but is unable to earn enough to pay our bills. Our quality of living has dropped and will\ncontinue to do so. We have cut down\nour debts as best we could but now find we will need to go back into debt due\nto cost of living. Not an ideal\nprospect.
\n\n
\n\n
8. \nFinancial Impact having\nABC
\n\n
Having lived with ABC and having a husband who has his own health\nchallenges, our medical out-of-pockets have been significant, in the vicinity\nof $55K which are over and above even with top medical cover. I have also paid $15,000 for a life saving\ndrug prior to it becoming available on the PBS. \nWe have now made the decision to downsize, to be close to a medical\nprecinct, shops and public transport. I\nam not allowed to drive presently which has affected my independence\ndramatically as nothing is walking distance from my home.
Latest change in my health is due to\nside effects from long term treatment. \nMy disease is mostly under control, but your body can only take so much.\n
\n\n
\n\n
In 2016, I had fractured in both\nfemurs due to a drug ironically was given to strengthen my bones but did the\nopposite. This has been my “biggest”\nhealth and lifestyle challenge. It took\n12 months to get over. At times I was\nbed ridden and in a wheelchair. Through\nextensive rehab, physiotherapy and exercise physiology, I am back on both\nfeet. During that time, I sought\nexternal help and quickly discovered there was a real disconnect for patients\nand services on offer. This needs to\nimprove. I discovered pallative care which\ndid have services that could have helped, but I learnt about them too late. As I now have no income I resorted to\nseeking out services available through my community centre and the Council. Quickly discovered you had to be “65” for the\ncouncil to help you even though I am on a disability pension. Had to pay for a cleaner myself.
\n\n
\n\n
18 months go I underwent brain\nsurgery to remove a 5cm cyst attached to necrotic tissue which is what remained\nfrom a lesion that was treated through radio stereo surgery.
\n\n
Another setback. This part and parcel of my existence. The outcome because of small visual\ninterruptions which are deemed seizures, I am not allowed to drive, taking away\nmy independence.
\n\n
Having said this, I\ndo believe I have never lost myself. \n“Cancer” has challenged who I am but through it there has been a lot of self-discovery\nalong the way. Some of it good some of\nit bad. My circumstance has not allowed\nme to forget “cancer”. Living with\ncancer, you overcome one hurdle, feel good for a while, then it’s back again. Because of this, I have lost my personal sense\nof safety and health.
\n\n
I hope what I\nhave said resonates with some of you living with Advanced Breast Cancer. I decided to put pen to paper as sometimes\nwe find it hard to express our game changers and I think it’s helpful to open\nup, break down emotional walls and realise you are not alone in dealing with these\nchanges. Advanced Breast Cancer\npresents a myriad of challenges as everyone’s journey is different.
\n\n
\n\n
Bye for now.
\n\n
Karen C
\n\n
BCNA Consumer Representative
\n\n
Living with Cancer for 13 Years
","kudosSumWeight":3,"postTime":"2019-10-11T03:14:45.000-07:00","images":{"__typename":"AssociatedImageConnection","edges":[],"totalCount":0,"pageInfo":{"__typename":"PageInfo","hasNextPage":false,"endCursor":null,"hasPreviousPage":false,"startCursor":null}},"attachments":{"__typename":"AttachmentConnection","pageInfo":{"__typename":"PageInfo","hasNextPage":false,"endCursor":null,"hasPreviousPage":false,"startCursor":null},"edges":[]},"tags":{"__typename":"TagConnection","pageInfo":{"__typename":"PageInfo","hasNextPage":false,"endCursor":null,"hasPreviousPage":false,"startCursor":null},"edges":[{"__typename":"TagEdge","cursor":"MjUuMnwyLjF8b3wxMHxfTlZffDE","node":{"__typename":"Tag","id":"tag:metastatic-breast-cancer","text":"metastatic-breast-cancer","time":"2025-03-25T05:02:15.378-07:00","lastActivityTime":null,"messagesCount":null,"followersCount":null}}]},"timeToRead":9,"currentRevision":{"__ref":"Revision:revision:55531_1"},"latestVersion":null,"metrics":{"__typename":"MessageMetrics","views":592},"visibilityScope":"PUBLIC","canonicalUrl":null,"seoTitle":null,"seoDescription":null,"isEscalated":null,"placeholder":false,"originalMessageForPlaceholder":null,"messagePolicies":{"__typename":"MessagePolicies","canModerateSpamMessage":{"__typename":"PolicyResult","failureReason":{"__typename":"FailureReason","message":"error.lithium.policies.feature.moderation_spam.action.moderate_entity.allowed.accessDenied","key":"error.lithium.policies.feature.moderation_spam.action.moderate_entity.allowed.accessDenied","args":[]}}},"archivalData":null,"customFields":[],"body":"Hi everyone, here is a story I wrote a couple of years ago. m I feel it is still very relevant and seeing its Advanced Breast Cancer day on Sunday I felt it appropriate to post it again. I am sure many of you can relate to parts if not all of the content. I am grateful that I am able to post this again because I still have good quality of life and hope to continue to do so. I wish you all health and happiness.
Hi, my name is\nKaren, I am 61 years old, married and mother of 2 adult boys and have lived\nwith HER2 Advanced Breast Cancer for 13 years. As we are acknowledging\npeople with Advanced Breast Cancer on the 13th of this month, I thought I'd put\ndown some thoughts.
\n\n
Here under are my\nmusings with regards to events during my journey that have had a profound\neffect on my emotional being and the way I live. I hope what I have said\nresonates with some of you living with Advanced Breast Cancer. Sometimes\nwe find it hard to express our game changes and I hope you find what I have\nwritten interesting.
1. \nBeing diagnosed in 2007\nwith Metastatic bone disease - mortality really kicks in!
\n\n
\n\n
I’d thought I was going to\ndie in a matter of months. I asked my\ndoctors what my life expectancy would\nbe. Based on the average, I was told 4\nyears and I already had one! My life was now\nin a holding pattern as I was dictated by a new entity “cancer”.
\n\n
Despite this news, I was determined to keep life as\nnormal as possible for self preservation and the well being of my two young\nadult boys and husband and bills had to be paid. I worked for 6 years living with cancer. There\nwere periods during those years when I had to draw on my annual leave, sick\nleave and long service leave due to surgery, radiotherapy and regular\nchemotherapy. Despite my chronic\nillness, I was nonetheless still able execute my position well, and those not\naware of my personal health challenge were none the wiser. However, in the end, it did become too hard\nto work full time as years of chemotherapy and the disease not being stable had\ndebilitated my body and energy.
\n\n
There were many times when I had to rise above my\nlimitations and living with permanent fatigue made me irritable which I vented\nat home. I was not always nice to be\naround.
\n\n
On a positive side, my disease has made me take\nnothing for granted and I have become more tolerant of people and much less\njudgmental. I now stop and smell the\nroses and give time to myself. I have a\ndeeper connection with my family and friends that I hold dearly in my heart and\nfeel blessed to have them.
\n\n
2. \nGiving up work.
\n\n
\n\n
I gave up work prematurely because my employer agreed for\nme to go part-time but this did not materialise, forcing me to take my Income\nInsurance. At that time I advised my\ncompany in writing I was taking unpaid sick leave and believed this to be so as\nI was not told otherwise. I kept in\ncontact with my immediate boss however when I paid a visit to Human Resources\nsome 21 months after I left work to discuss my return, I was told I had been struck\noff the books. The explanation given was\n“company policy”. This was not a proper\nexplanation, nor grounds for dismissal. No-one bothered to advise me that my services\nwere no longer required and I had not resigned. Due to my employer’s actions, despite being\na skilled person, competent in business and marketing, my continuity in the\nworkforce had been broken. Given my age\nand illness, finding new employment has proved problematic.
\n\n
This was extremely upsetting to me. I worked in this organisation for 22 years. I had a career which I identified as a big\npart of me. To have this taken away was\nmortifying and has taken me a long time to accept that I am no longer in the\nworkforce.
\n\n
Through my own experience and talking to fellow cancer\nsurvivors, I am aware problems are not uncommon where people with cancer are\nencouraged to leave their jobs, or having their terms and conditions altered,\nto their detriment, upon their return. In\nmy case I got lip service and was dismissed surreptitiously.
\n\n
Currently cancer is considered to be a disability\nunder anti-discrimination laws, which means that reasonable adjustments are\nmade so people living with cancer are not disadvantaged at work. I don’t believe this is understood by\nemployers.
\n\n
3. \nCashing in my\nsuperannuation
\n\n
\n\n
As I was no longer working and had\nterminal cancer, I cashed in my superannuation because as a family we had to\nreduce our household debt in order to live off one wage, pay medical and other\nbills. When I cashed in I was\ndiagnosed with metastatic brain disease and indications were that I only had months to live. Now I have lived on for another 5\nyears. What this means, my husband and\nI no longer have a retirement plan and will have to rely on pensions that has\nalready started with me being on a disability pension. I was the main income earner so our standard\nof living has dropped and keeps doing so whilst I keep living. Living with cancer brings everything\nforward making it much harder to make ends meet whilst living and coping with a\ndisease and its associated costs.
\n\n
\n\n
To access my income insurance then my\nsuperannuation, entailed extensive paperwork that had to be completed by my\noncologist, GP and myself. As I have terminal cancer, my applications\nwere accepted but the process was arduous and I can understand it being\noverwhelming for some. To add salt to\nthe wound, in the early days of receiving my income insurance, I had to chase\nthe insurance company every month with monthly telephone interviews regarding\nmy health. Not nice when you have an\nincurable disease and are asked to justify why you qualify to get your next\npayment!
I was terrified that I was going to die very soon. I couldn’t believe it, I had no symptoms. The lesions were picked on my regular\nscans. My mortality was very much front\nof mind and I was deeply concerned how this diagnosis was going to affect my\nquality of life and how quickly I would deteriorate. I had three tumours in my brain as well as\none in my spinal cord. The one in the\nspinal cord was troublesome as I already had extensive radiotherapy on my neck\ndue to bone mets and it was touch and go if they would give me another dose to\ntreat this new threat which could render me a quadriplegic. Very dark times. Radiotherapy eradicated this threat and has\ndisappeared (a miracle).
\n\n
\n\n
5. \nAcceptance that cancer\nis a part of me.
\n\n
\n\n
Cancer is my reality which I now embrace as part of me\nand consequently I try to make the most of every day and moment. It\nhas taken a long time to accept that Cancer is part of my body. When I was first diagnosed, it was a foreign\nentity that had to be conquered.
\n\n
Sure, I am now\nexperiencing some long term problems such as nerve damage in the form of\nneuropathy in feet and hands which affects my mobility due to the disease and years\nof chemotherapy, radiotherapy and surgery has affected my balance, but for the\nmost part, I take it in my stride. My\nnormal is changing because of my physical limitations but I have a good quality\nof life.
\n\n
I am living with advanced Breast Cancer, however\nincurable does not mean untreatable. 5\nyears ago treatment options were drying up until Kadcyla became available. I have had 70 doses and I am still\nhere! New technology brings hope.
\n\n
6. \nGoing on a disability\npension.
\n\n
\n\n
I am now on a disability pension, which\ndoesn’t sit easy with me. I have always been independent, I have exhausted my\nown personal avenues for income to pay the bills, and a pension was my last\noption.
\n\n
Once I went on the pension and my health\nimproved I sought part-time work through employment agencies that place people\non a Disability Support Pension. I\nsoon discovered that although the government pigeon hole people living well\nwith cancer as Disability Pensioners, they are discriminated against because\novertly they appear normal. In my case\nI am skilled and articulate and found they are either not set up or aren’t\ninterested in people like myself. Naively\nI thought this avenue of employment would work as having cancer, one is not\nsure what is around the corner and this system would be able to accommodate any\nchanges. I was wrong.
\n\n
How I feel about this, I am now 61 and invisible. It’s had a profound effect on my self-worth\nbeen as I have not been able to contribute to my family\nfinancially. Those living well with\ncancer should be encouraged to work and be part of mainstream society. It’s a win/win for the people living with\ncancer and their families and the economy. \n
\n\n
\n\n
7. \nAdjusting to early\nretirement
\n\n
\n\n
For me this is a new\nrealisation. I am now not so angry that\nI cannot work and have become quite the domestic queen. Mind you I don’t find it fulfilling but at\nleast its filling my days. Fortunately,\nI was well enough to do a bit of travelling with my husband in 2014. I am not complaining, but it’s probably our\none and only opportunity. My husband\nworks very hard but is unable to earn enough to pay our bills. Our quality of living has dropped and will\ncontinue to do so. We have cut down\nour debts as best we could but now find we will need to go back into debt due\nto cost of living. Not an ideal\nprospect.
\n\n
\n\n
8. \nFinancial Impact having\nABC
\n\n
Having lived with ABC and having a husband who has his own health\nchallenges, our medical out-of-pockets have been significant, in the vicinity\nof $55K which are over and above even with top medical cover. I have also paid $15,000 for a life saving\ndrug prior to it becoming available on the PBS. \nWe have now made the decision to downsize, to be close to a medical\nprecinct, shops and public transport. I\nam not allowed to drive presently which has affected my independence\ndramatically as nothing is walking distance from my home.
Latest change in my health is due to\nside effects from long term treatment. \nMy disease is mostly under control, but your body can only take so much.\n
\n\n
\n\n
In 2016, I had fractured in both\nfemurs due to a drug ironically was given to strengthen my bones but did the\nopposite. This has been my “biggest”\nhealth and lifestyle challenge. It took\n12 months to get over. At times I was\nbed ridden and in a wheelchair. Through\nextensive rehab, physiotherapy and exercise physiology, I am back on both\nfeet. During that time, I sought\nexternal help and quickly discovered there was a real disconnect for patients\nand services on offer. This needs to\nimprove. I discovered pallative care which\ndid have services that could have helped, but I learnt about them too late. As I now have no income I resorted to\nseeking out services available through my community centre and the Council. Quickly discovered you had to be “65” for the\ncouncil to help you even though I am on a disability pension. Had to pay for a cleaner myself.
\n\n
\n\n
18 months go I underwent brain\nsurgery to remove a 5cm cyst attached to necrotic tissue which is what remained\nfrom a lesion that was treated through radio stereo surgery.
\n\n
Another setback. This part and parcel of my existence. The outcome because of small visual\ninterruptions which are deemed seizures, I am not allowed to drive, taking away\nmy independence.
\n\n
Having said this, I\ndo believe I have never lost myself. \n“Cancer” has challenged who I am but through it there has been a lot of self-discovery\nalong the way. Some of it good some of\nit bad. My circumstance has not allowed\nme to forget “cancer”. Living with\ncancer, you overcome one hurdle, feel good for a while, then it’s back again. Because of this, I have lost my personal sense\nof safety and health.
\n\n
I hope what I\nhave said resonates with some of you living with Advanced Breast Cancer. I decided to put pen to paper as sometimes\nwe find it hard to express our game changers and I think it’s helpful to open\nup, break down emotional walls and realise you are not alone in dealing with these\nchanges. Advanced Breast Cancer\npresents a myriad of challenges as everyone’s journey is different.
\n\n
\n\n
Bye for now.
\n\n
Karen C
\n\n
BCNA Consumer Representative
\n\n
Living with Cancer for 13 Years
"},"Conversation:conversation:55531":{"__typename":"Conversation","id":"conversation:55531","solved":false,"topic":{"__ref":"ForumTopicMessage:message:55531"},"lastPostingActivityTime":"2019-10-18T02:58:28.000-07:00","lastPostTime":"2019-10-18T02:58:28.000-07:00","unreadReplyCount":10,"isSubscribed":false},"ModerationData:moderation_data:55531":{"__typename":"ModerationData","id":"moderation_data:55531","status":"APPROVED","rejectReason":null,"isReportedAbuse":false,"rejectUser":null,"rejectTime":null,"rejectActorType":null},"Revision:revision:55531_1":{"__typename":"Revision","id":"revision:55531_1","lastEditTime":"2019-10-11T03:14:45.000-07:00"},"ForumReplyMessage:message:55533":{"__typename":"ForumReplyMessage","id":"message:55533","conversation":{"__ref":"Conversation:conversation:55531"},"author":{"__ref":"User:user:14227"},"revisionNum":1,"uid":55533,"depth":1,"hasGivenKudo":false,"subscribed":false,"board":{"__ref":"Forum:board:living-with-metastatic-breast-cancer"},"subject":"Re: Game Changers Living with Advanced Breast Cancer","readOnly":false,"editFrozen":false,"moderationData":{"__ref":"ModerationData:moderation_data:55533"},"parent":{"__ref":"ForumTopicMessage:message:55531"},"body":"Hi Sister, Hopefully in the future breast cancer will be a \"cold\". Wouldn't that be great. Enjoy your day. Karen C","body@stringLength":"135","rawBody":"Hi Sister, Hopefully in the future breast cancer will be a \"cold\". Wouldn't that be great. Enjoy your day. Karen C","kudosSumWeight":0,"repliesCount":0,"postTime":"2019-10-11T14:17:36.000-07:00","images":{"__typename":"AssociatedImageConnection","edges":[],"totalCount":0,"pageInfo":{"__typename":"PageInfo","hasNextPage":false,"endCursor":null,"hasPreviousPage":false,"startCursor":null}},"attachments":{"__typename":"AttachmentConnection","pageInfo":{"__typename":"PageInfo","hasNextPage":false,"endCursor":null,"hasPreviousPage":false,"startCursor":null},"edges":[]},"timeToRead":1,"currentRevision":{"__ref":"Revision:revision:55533_1"},"latestVersion":null,"metrics":{"__typename":"MessageMetrics","views":1},"visibilityScope":"PUBLIC","isEscalated":null,"placeholder":false,"originalMessageForPlaceholder":null,"messagePolicies":{"__typename":"MessagePolicies","canModerateSpamMessage":{"__typename":"PolicyResult","failureReason":{"__typename":"FailureReason","message":"error.lithium.policies.feature.moderation_spam.action.moderate_entity.allowed.accessDenied","key":"error.lithium.policies.feature.moderation_spam.action.moderate_entity.allowed.accessDenied","args":[]}}},"customFields":[],"replies":{"__typename":"MessageConnection","edges":[],"pageInfo":{"__typename":"PageInfo","hasNextPage":false,"endCursor":null,"hasPreviousPage":false,"startCursor":null}}},"CachedAsset:theme:customTheme1-1744167669796":{"__typename":"CachedAsset","id":"theme:customTheme1-1744167669796","value":{"id":"customTheme1","animation":{"fast":"150ms","normal":"250ms","slow":"500ms","slowest":"750ms","function":"cubic-bezier(0.07, 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