Conventional vs. Alternative vs. Complimentary Treatment
Comments
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ladies,
Let's not devolve into the same arguments. The op asked a question regarding head to head stats for conventional vs. alternative tx. He also made the same post o
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Ladies,
Let's not devolve into the same arguments. The op was asking about stats for a head to head comparison of conventional vs. alternative tx. He also started an almost identical thread under the "Help me get through tx" area. I was the one who suggested he post in complementary or alternative, because I knew of no such studies (nor did anyone else who responded to that thread). If such a study does exist, I thought someone else might know. Also, this is the complementary forum, so questioning is allowed.
Juneping,
I am stage IV and have never "suffered from chemo". I was given the choice and chose a different path. I have never been admonished for it and I think many (but not all:) do worry and care about me. On the flip side, I worry about all the women on bco, regardless of their tx choices, because it's not a cakewalk for any of us
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June, get that feeling from my onc sometimes. If I am nervous about SEs or if I ask about a certain non-standard treatment he will do this chuckle that sounds like "there you go again, trying to cheat". I want to do VERO radiation in FL and they think may be elligible but just need an MRI to make the final determination. I emailed my onc and his reply was not simply for an experimental treatment and not without speaking with this person who allegedly wants hm to order it. there was more to it than that and it read as though he was really pissed at me! I am used to his attitude towards alt/complimentary and even standard stuff in a dfferent order, but the whole rest of it was just really strange and disappointing. I am still not sure what to think about it.
Sorry that was unrelated but what June said struck a chord and don't think Ben is coming back anyway. just to clarify, have not had that feeling from any of you here, just the dr.
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Oncs are good little soldiers following orders of their teachers. Asking them to listen to anything about alternative or even complementary sometimes would be like asking your postal carrier to give you a haircut.
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Perhaps this is true of some oncologists, but not all. The key is to find one who is more open to complementary options. Of course, this is not easy if you live in an area with few choices, so traveling can be worth it. My first mo, would not have strayed even a millimeter from protocol but my current mo is wonderful. Both she and my second opinion mo laid out two tx paths, one with chemo, one without. I was the ultimate decision maker and they patiently answered my questions and provided me with whatever data/stats were pertinent to my situation. My mo knows about the supplements I take without poo pooing them. My medical center offers yoga for cancer patients, nutrition classes, a weekly farmers market etc. So, not all are "good soldiers".
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My medical centre offers those things as well. They are not mentioned by the oncologist and in fact he shrugged when I asked about diet....like it would make no difference. I think most cancer centres are up to date but many oncologists are not. I actually don't blame them for providing a service they were trained to provide. It is what it is. I like my oncologist but would not approach him about certain things that are outside his area of concern.
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Thanks to Momine for reminding us that, at the heart of Ben's long post, was a request for statistics that show the efficacy of alternative treatment.
Unfortunately there are are no reliable stats because patients whose medical treatment fails end up at alternative practitioners hoping for a cure. And oncologists like mine see new patients regularly who've started with alternative treatments and now require the full oncological regime if they are to have any chance of survival. I'm not aware of a study that examines these common situations.
What is clear is that, depending on our BC types, stages and grades, statistics show that varying percentages of us who go down the medical road will be around in X number of years. These stats can be found on this site.
If someone can point to the statistics on the various alternative treatment efficacy rates, please post them.
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Brnxgirl, you are a very good example of someone who got "proper" and successful (yay!) treatment that did not involve chemo.
HLB, that is terrible. I have differences with my onc, but in other areas. Besides, when he gets out of line, I simply tell him off, which he accepts. He will answer seriously if asked about complementary and alternative strategies. He knows that conventional treatment is not a cure and is always on the lookout for things that can be added to improve outcomes.
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I pray one day soon we won't have to make difficult treatment decisions. Chemotherapy/hormone therapy, Radiation, Mastectomy will be history and treatment will be simple and safe. No more statistics and debating.
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Meow, same here.
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Thanks Momine, I am lucky I was able to find a holistic doc who is also a peds oncologist and he has helped me to come up with some strategies. I really like him and he explains everything to me and draws pictures to explain how things work, mechanism of action etc. It is self pay but I think it's worth it because my onc is so rigid. They both work for the same hospital so I am not sure yet how that will work out but so far it's ok. I am finding that I have a really hard time making treatment decisions and when I try to get opinions it's extremely frustrating because they are either like my onc where the answer to everything is no, or they are wishy washy and say it's up to me, or they wll say "what do you think?" and then only after I make the decision will they say "I think that's agood idea". geez it's like pulling teeth and I get s mentally exhausted! I do understand the reason behind it being liabilty but it's not right that a doctor is not even allowed to give you an opinion. When the onc wrote that email reply to mhe copied the holistic doc and the radonc that I had seen once. saw her yesterday and wanted to see what she thought about the VERO ad she said that even though it would treeat the lesions there is no guarantee that there might not still be cancer cells elsewhere that did not show up yet. OMG NO KIDDING! I have told them both in person and in reply to the email that I had no intention of stopping the systemic therapy. Complete waste of time. I am finally realizing that wrenn is right, no point talking to them about anything they do not do themselves. I will just have to do my appointments and then research exhaustively.
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HBL, that does sound really frustrating. Lots of docs could use better communication and people skills. I do feel sort of lucky to be in Greece. We do not have the malpractice suit culture of the US, so docs tend to be more willing to offer opinions, for better or worse. I really like my surgeon, because every time I ask him something, he can cite me numbers nad specifics, which shows that he reads all the relevant studies and remembers them. The onc is not quite as much of a human encyclopedia, and his people skills are pretty sad, but he is curious and openminded. So I take from each what I can get. In the end, they are just people, like the rest of us and you can't get blood from a stone
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Well, if we haven't scared Ben away, my advise to him is to be supportive no matter what kind of therapy his girlfriend chooses, to respect her choices-and they have to be and will be her choices, not his, despite his best intentions.
One of the most important things we can do is to believe in our treatment choices and one of the most important things our partners can do is be supportive of our choices.
While it is admirable for Ben to seek advice here and support (our partners need support), his girlfriend will need to do the research on her own, as many of us, those who don't just do whatever the doctor says, have done. He writes his girlfriend is very smart and determined to figure out the best treatments for herself. His job, as I see it, is to support her.
Personally, I think it's a horrible and hard thing to do. I don't envy my spouse for the position he's found himself in since my diagnosis, but I am so grateful for his willingness to support my choices, even when he's not always sure they are the right ones. This is my advice to Ben, support your partner's choices, don't blow holes in them, remind yourself she is smart and competent and the most important thing you can actually DO for her is to be supportive.
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I wouldnworry that you all scared Ben away. Saw him on another forum where he asked a similar question and I answered but he never came back there either. I think he's just very upset and looking for answers but doesn't like them and can't say I blame him--there are no answers you want to hear with this.
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Kayb, that does seem to be to the best "evidence" one can hope for in this area: "I can't find anything I think is reliable enough to say it will help, but I don't think it will hurt you so go ahead and try it." This does, of course, pose a problem, because anything that actually does anything is also likely to have some sort of SEs. In other words, if there is no potential harm or downside at all, it is unlikely that the substance, whatever it is, does much of anything.
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I can say from experience that though I cannot measure with certainty the active role my supplements have had on the cancer as only time will tell, I can with most certainty say that my quality of life has improved with the immune boosters, in addition to anticancer and immune boosting diet changes. Fully having, and fulling living my life that I have today, is that important to me. I could not tolerate the Aromatase inhibitors. I just couldn't. After 1 1/2 yrs, I had to start getting honest with myself. The honesty was that I would rather die of cancer than live that way with those side effects from the AI any longer. I would rather die of natural causes than die at the hands of man. It is harsh, but for me it was true. That was my subjective reality that no one can deny was the truth. I also knew with clear evidence they were destroying my health, and my life. I made some changes to go natural, in my efforts to avoid a recurrence that I don't regret. I won't regret them no matter what, because I am truly living my life that I have now. With the scientific backing esp in regards to the med mushrooms, I really doubt the supplements I take will harm in terms of cancer, especially how I take them, and what evidence there is, points to some potential that they may help. Some of the scientific studies actually say that. I feel as though they are supporting my health and I have improved bloodwork to prove it. I am grateful to have discovered them because they have improved my health and quality of life overall. There is a world of things one can do in response to their breast cancer. I believe that each person's own diligent, and never ending study about options, along with their subjective experience, and ongoing bloodwork from their physcians as a compass, will guide them about what to do, and also about what they physically can do, and are willing to do in terms of those options.
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Kayb, I agree that it is great that your doctor will take the question seriously and do the research. It is also great that you have improved your health and well-being with these approaches.
I do not mean that something HAS to have bad SEs to be useful. I mean that, usually, if a supplement has real action in the body, there is also usually some potential for harm. Vitamin D, for example, can be toxic if you OD, so someone taking large doses should have vit D levels monitored.
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Kayb, oh, definitely. I am not saying things like vit D shouldn't be used. I am just saying that most things that have some definite action also do usually have some sort of potential for toxicity, harm or SEs. To my mind, this is all the more reason for docs to take a holistic and openminded approach.
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