WHY would I put myself through this?
Comments
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We've been through this all before when wornoutmom was looking for survivors who used alternative treatments only - there were none. In fact there were several people who had tried alternative only and ended up in a mess. I will never say that choosing chemo/herceptin has a guaranteed outcome but it is safer than trying an alternative method like the Gerson Diet which has been proven not to work.
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I very much appreciate all points of view and think there is enormous value in this debate - muffling either side does us all a disservice.
That said, I value kindness above all character traits.I understand the visceral need to persuade that ones chosen course of action is Right - dear God, we are not only dealing with our own lives, but the mothers amongst us with the lives of our children. I daresay there are few mothers here who haven't eyed the calendar thinking "would love to see the grand kids but I need X number of years to get my kid to Y point."
Sharing our experience, and I don't know about you but so far for me it all sucks, may lead us to compromise thinking that will serve everyone well - hey, I bought a bottle of Fish Oil and Vitamin D today, an event those who know me would have voted as likely as the sun rising in the east. Ok, they are just sitting there and it is entirely possible they will never be opened - however, but for reading on the alternative forum, I would never have done that, nor would I have decided in a quite vehement way that my 22 year old daughter must avoid hormone laden meat and dairy like the plague.
Don't be trying to make me drink that green stuff though...ain't happening. -
You'll be surprised at some of the things you'll change in your life to ward off cancer. They may not be the sucker-punch you really want (or need), but I can guarantee you they'll be good changes. I eat better now than I use to (hey, brussels sprouts are pretty darned tasty, who knew), I take supplements and vitamins religiously, and I have learned to make serious shifts at work to minimize stress. My ambitions in life have changed, because my desires have changed - to see my 5-year-old grow up. Who cares if I'm not the Director Over Everybody Else in the Department anymore? I play games with my son and make sure I hold him on my lap with the tightest hugs possible every night. That's my idea of making my life meaningful.
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LadyGrey, it sounds like you are regaining your sense of humor, something that will serve you well on this journey.
My thought has always been that I wanted to do everything I could medically to beat it, plus everything I could do in the complimentary/life style way....combining those would give me the best shot.....it isn't an either/or type of thing to me.
Remember we are all lay-people here. We can give you our experiences, our points of view, our biases; but you need find a really good medical team whom you trust and who knows all the particulars of your unique health situation....ask questions from what you read here; but don't do, or not do anything, solely based on what you read here.
I can't stand green tea either!
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Grean tea isn't so bad with a bit of honey.
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What if you just eat the honey and skip the tea altogether?
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LadyGrey - I take lots of supplements including Vit D and fish oil - that is not the same as using alternative treatments - look at the Complementary forum - a lot of us had chemo and use supplements and none of us would expect taking vitamins would keep cancer at bay. There is a definition of Alternative Treatment on the Alternative page I think - those that believe in it refuse conventional treatment totally (apart from surgery).
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LadyGray,
I thought I couldn't go through the chemo, mastectomy and radiation I was originally prescribed.
And then it turned out I was stage IV and didn't have to do any of those things.
Now when I think back, I think how lucky I would have been to be able to go through all this and be cured in the end.
So, beware what you wish for.
Things could be much much worse that a chemo. Don't procrastinate starting your treatment because with this desease time is of the essence and the clock cannot be turned back.
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Mary - my heart goes out to you. That is the one thing that really upsets me - people like yourself that never had the opportunity.
((((((((((((HUGS))))))))))))
Sue
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Mary, I'm saddened to hear your story - it must be frustrating to read about people who have choices that aren't available to you at this point.
I question the wisdom of going forward with treatment for me. I will regret my choice if I go forward and suffer permanent side effects. I will regret my choice if I don't go forward and have a recurrence.
My choice architecture is a big Venn diagram. At this point, it is highly unlikely I will have further treatment. I will consider what the oncologist has to say - perhaps she will provide additional information that would make her recommendations more persuasive. However, in my opinion, it is far more likely she will give me the trifecta in the "Doctors Who Cut/Poison You Without Asking How You Are" competition.
Honestly, I think I am a shoe in. Place your bets accordingly.
Susie - the alternative forum description clearly invites anyone who is interested, whether they are receiving conventional treatment or not.
One thing I find very troubling is I think there are women here who eschew conventional treatment based upon their conviction that they have no insurance, no money and no job security. When one has no way to pay for conventional treatment, alternative treatment is it. Perhaps we should be slow to assume that everyone has the same treatment choices - it might be hurtful to hear a subtext of "you are a moron for pursuing alternative treatment" when one can't afford to go the conventional route, which in addition to out of pocket, carries the threat of debilitating side effects that make working impossible and may result in job loss. Not everyone is going to be willing to say their choices are limited by finances, that their kid's asthma has taken all the sick leave, XH pays child support only sporadically, and the boss is a total jerk who will fire her if she misses too many days because of chemo. That carries its on shame burden, however unmerited. I'm not suggesting most women who choose alternative treatment are driven by job considerations and finances - but some are for sure.
I think it would be lovely if some of those pink dollars were devoted to ensuring that all women have equal access to treatments. I'm sure Komen would be all over that but for the "Meander for the Cure". -
LadyGrey - the chance of you suffering permanent side effects is a lot slimmer than progression if you don't have treatment. I'm sorry to be so blunt about it, but I am SO grateful that treatment was available to me.
I stay away from the Alternative forum - we have already had a huge fight which resulted in the Complementary and Alternative split - life is a lot more peaceful now.
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LadyGray,
I made my choices when I procrastinated and didn't get checked on time. I was sure cancer couldn't happen to me and the thought of metastases didn't even cross my mind.
I don't find other people's choices frustrating.
What I find frustrating is that yet another person can get themselves in a bad situation because they don't understand the seriousness of the consequences.
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One goes to an oncologist for his/her expertise in treating cancer. While a "caring" oncologist is an extra bonus, whether s/he delves into your feelings will have little to no influence on how effective the medications they administer to you will be on the cancer. If you need someone to address your feelings, go to someone who has expertise in that field (as you are doing).
I went through chemo and BMX and am taking Arimidex. I have no permanent side effects from the chemo (completed it a year and a half ago) and minimal side effects from the Arimidex. The "side effects" from a progression of the cancer are devastating (having witnessed what my friend is going through).
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LadyGrey: I've been following this thread with interest, as I understand your quandary. I had a mastectomy, after no clear margins were achieved with a lumpectomy. I hasten to add that my surgeon would have performed a re-excision, but I knew that my boobs would be so mismatched (!) anyhow, so I opted for a mastectomy. I was clueless as to what prosthetics were available to me.....
Then the time came to decide on chemo -- to do or not to do. Yes, my onc gave me a choice. Based on "statistics" (I live in Canada and the oncotype DX was not available to me), the difference was not terribly significant and I initially said "Nope, not gonna do it".
Ultimately, I decided to have chemo, followed up by an aromatase inhibitor (Femara) for five years. For me, there was always that "What if I didn't, and the cancer came back?" question in the back of my head. How would I feel about that? But that's just me -- always doubting myself.
Will the surgery, the chemo and the AI be enough to keep the beast from recurring? I don't know, nor does anyone on these boards know. My onc doesn't know, the bc researchers don't know. All I (or they) can do is hope that cancer doesn't recur. Statistics say I have a good chance of dying from something else, or even maybe old age! But, as one famous person (can't remember who) has said "there are lies, damn lies, and statistics"......
What I'm saying is that you have to do what feels right, and what you feel (currently) will have been the right decision a year, two years, five years from now. I wish you only the best, along with the knowledge that what you did was the right thing for you. Because, believe me, none of US knows what is the right thing for you.
Hugs, Linda
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It was not my intent to muffle this conversation rather to redirect it elsewhere. I just hate to see a battle on this thread as found on the alternative and holistic threads. The her2+ threads deals mostly with questions, and treatments that deal with her2+. I have tried to respect women who post on different threads by not pushing my alternative views. This is why the mods gave us our own board, which I am happy about. Lady Gray, you haven't been around long enough to see how mean people can get when it comes to conventional vs alternative. I don't want to get involved in that kind of discussion.
In defense of impositive, she was dx exactly 2 years ago with idc, 1 C, her2+++. As I recall she did not have clean margins after her lumpectomy. She decided not to do more surgery, and do it all alternative. She then put her head to the books and began studying natural ways to fight cancer. Before her dx, I believe she had melanoma, skin cancer. It seems earlier this fall her melonoma returned. It was cut out, and she had a pet scan that showed that it had spread to her lymph nodes. She is now at an alternative cancer center to treat her skin cancer. I am following her treatment as this too looks very promising without all the potential side effects.
What is encouraging to me about impositive is that 2 yrs ago she was dx with idc, 1 c, without clean margins, and the recent pet scan showed no recurrence other than the skin cancer that she had had before bc. Two Years! I would had figured that such an aggressive cancer with the her2+++ gene it would had pretty much spread to her liver, bones or lungs by now.
I'm also in contact with wornoutmom. Her cancer had moved into stage IV and then decided to go to a smiliar cancer center with the same kind of treatment that impositive is now getting. Her numbers since being at this alternative cancer center has drastically dropped, and she is doing great.
As I said, I have a recurrence... idc, 2 C, with the her2+++ and proliferation rate H. This new dx is shocking, and it is something I now am facing as well. I haven't had my mx yet. I've been told that I will have a pet scan and tumor markers checked. For me the past few years, I've been trying to find out what went wrong the first place. I believe there is a cause and effect for everything that happens. With what I know, I would not do chemo. I respect those who choose otherwise. There are a lot of brave women who choose these tough treatments...and impositive is brave as well to choose her path.
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Eve - not what I wanted to hear about wornoutmom - maybe if she hadn't procrastinated with treatment she wouldn't be in this situation. I'm very sorry to hear this news, very sorry.
Sue
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susieq...not to get into tit for tat here....but it is not implausible that the risk of progression is less than or equal to the chemo benefit.
For example the risk of complications is 3-4 percent
while my risk of recurrence is 14%, with chemo it was still 10-12%
my risk of complications was possibly greater than my chemo benefit
I am NOT saying that is the case for TLG... I guess someone could go plug her stats into lifemath...but with such a small tumor there may be some grey area.
I have a question...I thought I read that many more cases of DCIS were her+ than IDC. How long does it take the IDC to "shed" the Her2? Is it possible some of these tiny tumors would have lost their Her2+ status.
Paging Bessie
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We each have to make decisions as to what we feel is best for ourselves. I hope for those who decline traditional treatment, that they never see this ugly disease again. I just want to say this....once it goes to stage 4...there are no more stages and it is no longer curable. Is it so wrong to treat the cancer you now have with drugs etc and do the natural stuff to hopefully ward it off from returning? The natural may very well prevent cancer but what about the cancer you already have? With great respect to all, Mazy
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Lady Gray
It sounds as though you may be back on your feet from the initial blow. Glad to hear this. If you want to hear my story you can PM me and I will share it. What ever you do, you must give it your all. There are lots of things to choose from. I believe there is a strong spiritual side, as well as physical and mental issues to work through. Sorry you had to join the OH SHIT club at all, but also glad to hear you have your chin up today. Keep walking forward and you will find yourself at least out of the quagmire that we all feel at first. Once you have a plan ( no matter what you put together for yourself) you will feel better I promise.
Love, hugs, and healing light to you my dear. I lit another candle for you along side mine this morning.
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CookieGal - the risk of node negative HER2 recurring is 23% - chemo/herceptin halves that - big benefit IMHO. If I hadn't been HER2 - chemo/herceptin would not have been on the cards.
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Merilee everything you typed is spot on .
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LadyGray, I was lst diagnosed in 1990. I am not going to bore you with details of my years with cancer and treatments, but I was one who was never going to do chemo. And I was fortunate enough to be able to avoid it for many years ( at least 8 or 9 forget now) since I was ER+, PR+ and responded favorably to hormonal treatments. Then my onco sort of eased me into chemo because by that time I had found that even though I was Stage lV, I could live with cancer with a good quality of life.....lst we did oral and then moved on to the infusions. I did have the oozy smelly nails you mentioned, but that was only with one chemo....I also had constantly tearing eyes and neuropathy and edema and a bunch of other stuff, .....but when the side effects got too bad, I told my onco I was done with that treatment and we moved on to another one....and I am fortunate in that none of my side effects have really stayed with me. I do have some neuropathy, but it doesnt keep me from doing things and I still am able to work. I had a very strage SE with my eyelashes in that they now grow toward my eye and scratch my cornea if I don't have them plucked out about every three weeks in this one area, but that is NOT a normal SE.....it's a PIA, but a small price to pay for life when you look at the big picture. As I said earlier, I do not want to bore you with my treatment history, but the point is I found that chemo, the thing I said I would NEVER do has kept me alive. Is it fun, NO.....is it worth it?....well, that all depends on you I guess. I am still here after almost 14 years of being Stage lV and I am still enjoying my life so it has been worth it for me. Right now I am waiting for them to come up with a new treatment plan for me and I am hoping it doesn't interfere with the Xmas parties I plan on having.....If it does, I have understanding friends and they will help me with the party or maybe I will have to put them off until after the lst of the year.....however, I do plan on being here next year and that is a good thing. I always have things planned ahead and that gives me something to look forward to and keeps me going.
Hearing you have cancer is overwhelming and not too many positive things go through your head in the beginning (at least they did not with me), but I am of the opinion that it is doable....and this is coming from one who was never going to do chemo.
So far as alternative treatments, I know nothing about them as I have not done any. I really have not even altered my diet other than the fact I seldom ever have a drink, but that is because the desire is no longer there for some reason. I did quit smoking, but that was something I needed to do anyway.
I am not telling you what you should or should not do, that is your decision, but I just wanted you to know that for me treatment was worth it and the reason I put myself through it was because I just was not ready to give up living yet. Tell your onco exactly what your feelings are and hopefully they will have some options for you that will not have devestating side effects.
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eve
I just thought you should know that with Herceptin I am almost 5years out from a diagnosis of idc that was HER2++. My tumor was .8cm. So two years out may be god on alternatives, I don't know but I do know that Herceptin is a wonder drug for Her2+ cancer. So much so that the chemo regimens used with it become milder all the time. That step is taken only after there is evidence that the milder chemo will work
Lady Grey alternatives do not have evidence that they work. There are statitics that show the efficacy of each chemo treatment. You need to do what your heart and head tell you is right.
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I received a PM from another BCO member, and I wanted to post my response to her. Yes, my posts can be confrontational on this issue, of extolling natural alternatives that are supposedly just as efficacious as conventional treatment, but I really do have no intention of ceasing from calling other members out on lies that they may propagate. Yes, of course everyone has a choice, everyone is in ultimate control of their own bodies. It would be absurd for anyone to think that they can be forced into a treatment they don't want. But it is equally important to understand that all choices have implications, no matter what they are. Pretending that these choices are all equal is just sticking your head in the sand.
Here's my response to the other member:
I appreciate your comments, I really do. But when there are blatant lies, such as there are natural alternatives to chemo which are just as effective or that all cancer has been growing in one's bodies for years (these are just the most recent flat out lies posted by a member), I really have no intention of not continuing to call them out. We're not playing a little dance here, it's not this sweet "educate before I medicate" and all choices are equal kind of game. For both impositive, and the poor woman that eve mentioned most recently (who played the natural game and is now stage IV), cancer marches on. And yes, time is an issue. It would be naive to also say that I'll do this one choice now and then if it gets worse later, then I'll consider something else. I wish that's how it worked, but it doesn't. When you've got to later stages, you've lost most of your opportunity. While it sounds really nice that all choices are created equal and we must at all times maintain control of our bodies at all times, the horse is already out of the barn when you've been diagnosed with cancer. To maintain that it isn't and then try to persuade other women that there are better, more "natural" alternatives out there, is deadly, to me. Sure, everyone has a choice. But members also have the same right to outline the implications of both choices, conventional or totally alternative. Foregoing conventional treatment (in this case Herceptin) and pretending that you're fine with that and will just deal with the cancer later if you have to, is totally naive. Dealing with the later stages of cancer is tortuous, painful, a really dreadful way to go. To pretend that one is just going to ride off into the sunset and die this nice peaceful death is an outright lie. I wish it weren't, and these are all absurd choices that one has to make, but I have no interest in watching as another member perpetuates a lie. No treatment, or totally alternative treatment, has consequences as well.
By the way, if one were to do a full search of my posts on BCO, one would find that I actually have a very nice, non-confrontational personality when it comes to other topics. But no, I'm not going to just sit by while lies are perpetuated on this one issue.
With regard to how my post here relates to the original poster's comments, I will again say that I'm just calling people out if there are blatant lies. She is obviously entitled to her own choices, of course! But again, to think that you're going to just ride off into the sunset is also an illusion. All these choices suck, but they all have implications. She has a right to at least be entitled to the facts for whichever choice she chooses.
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Just want to chime in and say, the DH has a rare orphan illness. He is under the care of the most brilliant of brilliant physicians AND researchers. When it comes time to making decisions about his care, there is NOTHING conventional about his treatment because his disorder is so rare. Even so, the doctors design clinical trials for him and the handful of folks who have his disorder and are followed closely by the FDA. Everything they do is evidence based. The doctors who study and treat people like my husband are at the mercy of the NIH for what little money they can poney up to do their research. The bottom line is, while we are FORCED to do ALTERNATIVE treatment, there are STILL strict rules to follow and everything they do to help him is based on evidence based medicine. Rarely does Pharma participate in these types of clinical trials, because they can't make money on creating a treatment that will only help a handful of people. So, what I'm trying to tell EVERYONE is that if anyone has an ALTERNATIVE treatment for breast cancer, they should step up to the plate and follow the protocol that doctors and researchers like my husband's do AND then get their research published in one of the MAJOR peer reviewed journals for EVERYONE to see and consider. My husband has been written up in the MAJOR medical journals for over a dozen years. It's NOT that hard to get published. Really.
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Ladygrey,
I dont know all the stuff on my pathology report, but I can definitely relate to your quandries. Why put mysel through horrible stuff if I will live 5 years and if I dont put myself through it live 5 years? at least those 5 years wouldnt be quiteso bad.......fought with it alot- almost decided not to, but I have a 15 yr old and a 20 yr old that love me dearly, my 22 year old and 3 grandkids would be great reasons to keep going, but my oldest hates me dues to past transgressions. (Long story- lets just say battles won and not a issue now) I havealready started my first round of chemo, so i guess im gonna try to fight this crap. Good luck to you and hugs. lots and lots- I hope you have strong friends and family to support you.in whichever decision u make (beach sounds good lol))
Connie
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To each his/her own and I wish you the best. Me, I'm gonna fight like hell to LIVE!
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Voraciousreader made me remember this website which I found very helpful when I was learning about breast cancer - LINK - it reviews much of the information that has been published about hormone therapy, chemotherapy, radiotherapy, surgery and much more. The chemotherapy section for early breast cancer starts about half way down the page.
It was compiled by Constantine Kaniklidis who did a superb job in reviewing the information out there. She also has a page about drug interactions - LINK
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TLG - my onc had the personality and warmth of a clam. Awful. I decided not to switch oncs until active treatment was over (which I have since done and the new one is AWESOME). But the way I coped was to say "He is in charge of my cells, not my soul." I saw the cancer psychologist monthly during treatment - she handled cancer patients only and was a huge benefit. If your cancer center has one, it might be worth seeing him/her.
I sense that beneath your sarcasm and quick repartee, you are one terrified lady. The loss of control when you enter the 'medical system' is huge. It was what terrified me more than anything. People write all the time to 'listen to your gut,' but there is a narrow line between what your instincts are telling you, and letting fear guide you. it is a huge challenge to make thoughtful and wise decisions at a time when this is all so new, overwhelming and frightening. I wish you peace of heart and mind to make good choices.
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AmyIsStrong - It is so true - there is so much fear on both sides - fear of cancer and fear of treatment.
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