Polite Explanations are Welcome....

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  • voraciousreader
    voraciousreader Member Posts: 7,496
    edited January 2012

    Kaara... My beloved 86 year old mother was the director of nursing at an impoverished New York City Hospital. While growing up, I visited her often at work. I often met her in the hospital's emergency room. When patients came in with cardiac arrest, gun shot wounds or in labor, I don't recall anyone, insured or not, getting anything less than the Standard of Care. The doctors and nurses performed MIRACLES every day in that emergency room! And, that's a fact too.

  • AlaskaAngel
    AlaskaAngel Member Posts: 1,836
    edited January 2012

    hillck,

    My experience is colored and is not what everyone experiences. I would never had been so inclined to give the onc the benefit of the doubt had I not already had one bad experience, and thought it was just a fluke.

    The female surgeon I saw (not the one who did my surgery, but the one who did my biopsy) did her own ultrasound in her office, said it was fine, and wanted to compare it to the one the hospital, and recommended a follow up U/S at the hospital.

    I called to request a copy of the rads report from the hospital. They said I would have to come by in person with my ID to get a copy. I was working 2 jobs some distance from the hospital but finally I went to pick it up on my lunch hour. The staff person on duty at lunch said the person who could provide it would not be back until after I had to be back at work. She said they would mail it to me. Two weeks went by and I finally received their envelope in the mail.  They had sent the wrong rads report to me. By then my next ultrasound was not that far away so I waited and went in for it. Again the female surgeon did her own ultrasound in her office and said it was fine and she wanted to compare it to the one at the hospital. She did not have a copy for me of the first one and the report for the second one at the hospital was not ready yet. I waited and heard.... nothing. I called her office, and she was "in Europe". I got scared and called and ordered my own 3rd ultrasound. I went to the hospital for it and THAT was the first time anyone told me that the first TWO had been BIRADS4's. This one was also. The rads doc was professional and polite but I have worked with them and I know when a rads doc is really peeved. I should not have been left uninformed as to the status of either of the first two reports; I should not have had to order my own third U/S; and I should never have been left without an offer of a biopsy.

    I'm sure most people don't run into this. But it is what people raised like I was can experience. I am not a person who jumps to conclusions or who assumes ALL doctors are as pitiful as that one, or as difficult as my oncologist was. Before I encountered these doctors, I was very respectful -- TOO respectful.

    One can lean too far and I know my experiences may have led to that for me. I don't dispute that. But reading thru the discussions about the absolute dedication "doctors and researchers have" in behalf of patients is hardly the truth either.

    My situation was presented by a conscientious practioner to the surgeon who had retired before the female surgeon was hired, and had a nice retirement income as Quality Control. It came to nothing. I researched her history and found that she was at that time on probation with the medical board for dispensing illegally to her significant other. A  medical board in another state had complaints about a death of one of her patients, and another patient pending. The surgeon in charge of quality control who reviewed my situation wrote a letter of support for her to that medical board, which I saw online myself.

    Not all or even most are like her or my onc, or the "retired" surgeon. But I was raised to respect them all. It certainly didn't pay for me.

    AlaskaAngel

  • voraciousreader
    voraciousreader Member Posts: 7,496
    edited January 2012

    AlaskaAngel... There will always be a few rotten apples. But you can't let the bitter taste of those apples linger. Move on, dear. Really.

  • AlaskaAngel
    AlaskaAngel Member Posts: 1,836
    edited January 2012

    I'm sorry, but we all aren't perfect, any more than the doctors are. And sometimes that is because some doctors aren't.

    I was very lucky. My tumor was early stage. I am 10 years out after being much more selective about my treatments and the services, with no recurrence.

    And I am just one. But it would make no sense at all to me to endorse the previous hugely adorational comments about doctors. I would just be contributing to other innocent victimizations.

    A.A.

  • voraciousreader
    voraciousreader Member Posts: 7,496
    edited January 2012

    So, sisters, there you have it. We must be militants and question the motivations of every clinician and researcher. Otherwise we will be promoting the victimization of our brethren. AND, those same sisters who choose chemotherapy, are creating "consumer demand" and victimize ALL the sisters, as well, because they stand in the way of progress. AlaskaAngelWorld is quite a paranoid place.

  • AlaskaAngel
    AlaskaAngel Member Posts: 1,836
    edited January 2012

    hillck,

    Are you being selective?

    #1 - "The rads doc was professional and polite but I have worked with them and I know when a rads doc is really peeved."

    I think I indicated my respect for the rads doc.

    #2 - I am not a person who jumps to conclusions or who assumes ALL doctors are as pitiful as that one, or as difficult as my oncologist was.

    #3 - I'm sure most people don't run into this.

    #4 - ... reading thru the discussions about the absolute dedication "doctors and researchers have" in behalf of patients is hardly the truth either.

    #5 - My situation was presented by a conscientious practioner

    #6 - Not all or even most are like her or my onc, or the "retired" surgeon.

    A.A.

  • AlaskaAngel
    AlaskaAngel Member Posts: 1,836
    edited January 2012

    VR:

    I will make you a deal.  Make sure practitioners don't have the discretion to hide information from patients in the first place, such as rads reports and available options. It is a lot less harmful than being paranoid about the patients having access to them.

    A.A.

  • voraciousreader
    voraciousreader Member Posts: 7,496
    edited January 2012

    Thank goodness that there might just be SOME people in the medical community that are above reproach. I feel so much better now.





  • digger
    digger Member Posts: 590
    edited January 2012

    Wow, anyone else feel like they're back in fungal world, where things are a little topsy-turvy, i.e. any theory is true unless proven without a doubt to be false?  Kind of turn the scientific method on its head?

    AA, this obsession on ovarian ablation has taken over your life, I'm sorry to say.  How do you have time for anything else? 

  • voraciousreader
    voraciousreader Member Posts: 7,496
    edited January 2012

    Oy... Now I feel worse... "Hide". I haven't a clue what you are referring to. We live in a very transparent world. And nowadays, my doctors don't even know how to hold a pen. All their notes are done electronically. Furthermore, because of transparancy and electronic data, I have access to as much data as I can possibly want to read. When the DH was diagnosed, gathering data about his disease was a Hurculean task. Nowadays, I marvel at how easy it is to do research. That's why I call myself VoraciousReader. Some of my friends also call me MagicFingers... Because if the information is out there, these magic fingers will find it. No one is hiding anything. Believe me! The hardest part now is figuring out what is important and what is irrelevant. And finally, everyone wants their data out there. So hiding? I don't think so. and if someone chooses to deliberately hide something? Forgettaboutit!

  • voraciousreader
    voraciousreader Member Posts: 7,496
    edited January 2012

    Digger... In AlaskaAngelWorld the Renaissance has not occurred yet. We are still in the Dark Ages.

  • Kaara
    Kaara Member Posts: 3,647
    edited January 2012

    If I recall, you ladies (you know who you are) invited AA several times to create her own thread and now you are on here trying to sabotage it.  Evebarry is no longer posting on BCO because you sabotaged her thread.  I don't understand any of it.  What are you trying to prove?  Every one of you are far too intelligent to lower yourselves to this level.

     Why don't we stop the dueling egos and get back to the real world of BCO which is a site that offers an opportunity for education, comfort and support!

  • voraciousreader
    voraciousreader Member Posts: 7,496
    edited January 2012

    Kaara- Because many women come here when they are the most vulnerable, they are not looking to be more confused as they head through this maze. They should not become suspicious of doctors. I am sorry that AA had a bad experience, but she thankfully is well now. While she believes in her heart what she believes is the truth, there needs to be a voice of reason to counter what she says, so other sisters who come here, do not leave here confused and frightened. Furthermore, make no mistake about it, she asked for a polite discussion but crossed the line when she disparaged the medical community and insulted the brave women who choose chemo. And just like Eve had the choice to not do chemo, everyone needs to be respected for their choices.

    She is belligerent in her refusal to recognize that many of us are pleased with our care. And that message needs to get out there. And finally I will close by quoting Daniel Patrick Moynihan, "Everyone is entitled to their own opinion, but not to his own facts."





  • AlaskaAngel
    AlaskaAngel Member Posts: 1,836
    edited January 2012

    Kaara

    We are each passionate about our own situations and beliefs. Thanks for helping us to realize that our sincere beliefs and different feelings about treatment are opportunities for benefitting from each others' experiences.

    http://community.breastcancer.org/forum/121/topic/772883

    A.A.

  • orange1
    orange1 Member Posts: 930
    edited January 2012

    AA - do I understand you correctly that you say it is proven that OA +H has equal efficacy to TCH or AC TH?  If so, what is the proof?

    Thanks 

  • AlaskaAngel
    AlaskaAngel Member Posts: 1,836
    edited January 2012

    Orange1,

    No, it is not proven. 

    Tne neoadjuvant use of H (or alternately, H and lapatinib) indicates that H alone (or alternately, H and lapatinib) is active. So, for HER2 positive HR+, accomplishing OA + H may be equivalent to TCH or AC+TH, given that with OA + H the immune system is intact, whereas with TCH or AC+TH it is not. Intact immunity is a genuine factor, not imaginary, when comparing regimens objectively.

    A.A.

  • voraciousreader
    voraciousreader Member Posts: 7,496
    edited January 2012

    Orange1...You ask a great question...However, do you see my point? Sisters who are new to the breast cancer maze will find this thread and ask themselves, "Hmmmm....Why isn't my doctor offering me O/S and Herceptin."  Mind you, AA is advocating a clinical trial to discover whether or not that is a viable option for BOTH pre and POST menopausal women.  Haven't we already been through this discussion on several threads?  However, for a "newbie" THIS TYPE OF QUESTIONING WITH ALASKA ANGEL'S ANSWERS ....AND THEN HER DISPARAGING OF THE FOLKS WHO WORK IN THE TRENCHES, creates confusion.  Furthermore, as pointed out to her over and over again, by me and many others, finding early stage patients  WITH VERY AGGRESSIVE TUMORS, willing to take the risk of participating in a clinical trial, is difficult to find especially when there are EXCELLENT available treatments already.  And, according to retrospective studies, there seems to be a small co-hort of women with aggressive tumors that are found extremely early...making it difficult to find a sample population for a study.  And despite the latest SPECTACULAR news coming out of The Lancet concerning HER2+ tumors and neoadjuvant treatment, which makes it appear that researchers ARE making HUGE discoveries in their fight against breast cancer AND that it should be welcoming news to EVERYONE..... IT IS! Except of course, to AA......

    And since this is a thread on the Alternative site...I will say it again, and again AND once more to make it loud and clearER,  I am doing alternative treatment to chemotherapy BECAUSE my MO, bless him, RECOMMENDED IT TO ME.  So I am NOT adverse to ALTERNATIVE treatment, when appropriate.

  • Beesie
    Beesie Member Posts: 12,240
    edited January 2012

    A quick detour back to the question raised earlier about why it is that the risk to get BC increases as we age, despite the fact that we have less and less estrogen in our systems as we get older.

    First of all, here is the latest data (from the U.S.) on breast cancer risk by age:

    • from age 30 through age 39 . . . . . . 0.43 percent (often expressed as "1 in 233")
    • from age 40 through age 49 . . . . . . 1.45 percent (often expressed as "1 in 69")
    • from age 50 through age 59 . . . . . . 2.38 percent (often expressed as "1 in 42")
    • from age 60 through age 69 . . . . . . 3.45 percent (often expressed as "1 in 29") 

    I was looking this up recently for someone else who asked so I can fill in the rest of the chart:

    • from age 20 through age 29 . . . . . . 0.05 percent (often expressed as "1 in 2000")
    • from age 70 through age 89 . . . . . . 4.44 percent (often expressed as "1 in 23") 
    • TOTAL LIFETIME RISK:  12.2 percent (often expressed as "1 in 8") 

    So why does our BC risk increase with age?  For the same reason that our risk to get most cancers and many other diseases increases with age... as we get older, our bodies start to break down while at the same our cells lose the ability to repair themselves. 

    Cancer arises from one single cell. The transformation from a normal cell into a tumour cell is a multistage process, typically a progression from a pre-cancerous lesion to malignant tumours. These changes are the result of the interaction between a person's genetic factors and three categories of external agents, including:

    • physical carcinogens, such as ultraviolet and ionizing radiation;
    • chemical carcinogens, such as asbestos, components of tobacco smoke, aflatoxin (a food contaminant) and arsenic (a drinking water contaminant); and
    • biological carcinogens, such as infections from certain viruses, bacteria or parasites.
    Ageing is another fundamental factor for the development of cancer. The incidence of cancer rises dramatically with age, most likely due to a build up of risks for specific cancers that increase with age. The overall risk accumulation is combined with the tendency for cellular repair mechanisms to be less effective as a person grows older.   http://www.who.int/mediacentre/factsheets/fs297/en/

    .

    The other explanation I read that really helped me understand why cancer develops as we age related to the BRCA mutations.  Basically it explained that the BRCA genes are tumor suppressor genes - they control cell growth & death and thereby serve to prevent the development of cancer.  But as we go through life, cells become damaged and fail.  It could be aging or it might be damage caused by some environmental factor that causes a cell to stop working properly.  We all start with 2 copies of each of the BRCA genes, one inherited from our father and one inherited from our mother.  Both copies of these genes need to fail in order for cancer to develop.  Those born with a BRCA mutation start off at birth with one copy of the gene already not working properly or at all.  If at any point the other gene is damaged, cancer can develop.  But the rest of us start with two healthy copies of each gene.  If one is damaged, the other still protects us. This is why those with BRCA mutations are more likely to develop BC (and other cancers) and why they are more likely to develop these cancers at an earlier age.  If both a BRCA+ woman and a BRCA- women lose one copy of the gene at age 39, the BRCA woman now might develop BC whereas the BRCA- woman will still be protected until such time as the second copy of the gene also fails - and that might never happen or it might not happen for many years to come. That's why the risk to develop BC becomes greater as we get older. 

    The other thing to keep in mind is that even if a breast cancer is ER+, it just means that estrogen to some extent fuels that cancer.  It doesn't necessarily mean that estrogen caused the cancer or even had much of a role in the development and growth of the cancer.   

    Now, back to the discussion already in progress ...... 

  • Kaara
    Kaara Member Posts: 3,647
    edited January 2012

    Beesie:  Now there was some really educational information that I can get my arms around.  If cancer goes up as our bodies age, because the cells lack the ability to repair themselves, then taking the kind of supplements and antioxidants that assist in that endeavor would certainly make one more resistant to getting bc.

    Since being dx with bc at 71 years of age, I have been on a strict anti cancer diet and have been taking supplements and high levels of antioxidants, all designed to boost my immune system and repair damaged cells.  As a result, my RO called yesterday and told me that the site where my tumor was located has healed so well it's as though it never existed!  There was not enough at the "tumor bed" to even do the planning that she needed to do for the PBI that I was looking for.

     That says a lot to me about the role of diet, supplements, and antioxidants in keeping the body in optimal condition.

    Science...no....common sense....yes. 

  • angelsister
    angelsister Member Posts: 474
    edited January 2012

    Yo! I knew you'd come thru beesie! Now this kind of education and information is not readily available or easily accessible elsewhere. Brilliant! Just a thought about how the discussion is going...this is really informative stuff and you know just talking about difficult situations and talking about the 'what ifs' no matter when can be therapeutic. Noone is perfect but we can try to be kind?

  • AlaskaAngel
    AlaskaAngel Member Posts: 1,836
    edited January 2012

    As a community, bc patients are a subset or microcosm of the human population just like the doctors or researchers are. There is not total agreement among them, either -- even among those who have established, solid reputations. Questioning medical or scientific dogma is how science moves forward -- often because of a common sense observation, or the proposal of consideration of a new possibility. (Otherwise, we would still be buying into doing the radical mastectomy simply because at one time those with authority were using it as standard therapy).

    Here is an interesting current example:

    http://www.guardian.co.uk/science/2012/jan/23/breast-cancer-screening-not-justified?INTCMP=SRCH

    The Cochrane group has a major reputation.

  • voraciousreader
    voraciousreader Member Posts: 7,496
    edited January 2012

    Kaara...That's great news regarding your what your RO said to you about your healing.  I'm glad you feel that perhaps your anti-cancer diet has promoted your healing.  It would be nice if there was a clinical trial that could be certain of the benefits.  However, I just want you to know, I had MAJOR surgery more than a decade ago to repair a hole on my lung. The doctor had to open my chest to repair the hole.  Two years ago, at age 53, when I was diagnosed with BC, my MO was examining me and said to me that he could not tell from my X-Ray that I had had major lung surgery, nor could he find my scar.  I've never taken ANY supplements or vitamins in my adult life and healed wonderfully as well.

    I'm going to go a little off topic here and try to present to you and the sisters the difficulty in trying to understand the benefits we infer from taking supplements and vitamins by using this terrific study I found two weeks ago regarding Vitamin D and heart health.  The original study from Johns Hopkins came my way via Theheart.org.  I found the study VERY interesting and then found the following article which I think exemplifies how little we ACTUALLY know about supplements and vitamins.

    "Response to CRP and vitamin D association finding

    Posted on January 11, 2012 by Dr John Cannell

    In a paper critical of higher levels of vitamin D for allegedly increasing a marker of inflammation, c-reactive protein (CRP), Drs. Muhammad Amer and Rehan Qayyum of the Johns Hopkins School of Medicine, began their paper by saying:

    "The cardiovascular protection offered by vitamin D and its analogues is probably mediated by modulation of inflammatory cytokines."

    Amer M, Qayyum R. Relation Between Serum 25-Hydroxyvitamin D and C-Reactive Protein in Asymptomatic Adults (From the Continuous National Health and Nutrition Examination Survey 2001 to 2006). Am J Cardiol. 2011 Oct 12.

    25(OH)D levels of 20 ng/ml were associated with a CRP of 1.7, while 25(OH)D levels of 50 ng/ml were associated with a CRP of 1.9,

    If you will notice, both physicians know that vitamin D offers "cardiovascular protection." However, they are concerned 25(OH)D levels higher than 20 ng/ml will increase inflammation as measured by CRP and thus worsen cardiovascular protection. CRP is a protein in the blood which tends to rise in response to inflammation or injury. Its physiologic role is to take part in the "complement system."

    The authors arrived at this conclusion by adjusting their data for up to 9 variables and finding that a 25(OH)D of 20 ng/ml is associated with a CRP (range 0-5) of approximately 1.7 while a 25(OH)D of 50 ng/ml is associated with a CRP of 1.9. Their raw findings contradict their adjusted data in that the raw data showed what we have known for some time and that is that in the lower ranges of 25(OH)D, vitamin D reduces CRP. As with most biomarkers of vitamin D, the big improvement is in people who get their 25(OH)D up  from 5 ng/ml up to 20 ng/ml. We know that in most cases, the biggest bang for the buck is in treating severe deficiency in people with such low levels.

    So if you have natural levels of vitamin D, say a 25(OH)D of 50 ng/ml, and you want to decrease your CRP by 0.2, then stop your vitamin D and stay out of the sun, get your levels to 20 ng/ml, and see if all the corrections and adjustments the doctors performed were correct. I certainly am not going to do such a silly thing.

    Dozens of studies now exist showing supplemental vitamin D3 reduces mortality rates, in part due to its cardiovascular protection. The majority of these studies show that improvement in mortality continues through 30 ng/ml and even up to 40 ng/ml. Not enough people have levels of 50 ng/ml for scientists to see if such levels offer further protection. However, cardiovascular disease is rare in native peoples around the equator where vitamin D levels of 50 ng/ml are not uncommon.

    The takeaway message from this paper is that scientists will need to recalculate lots of different "normals," using vitamin D sufficient subjects. It's not just that normal CRP may be a bit higher in vitamin D sufficient people, their red blood count and the protein albumin may be a bit lower, for example. The point is that pathologists and epidemiologists will need to redo much of their work. We don't know the normal range of CRP in 65-year-old men; we know the range of CRP in 65-year-old vitamin D deficient men. Likewise, we don't know the incidence of heart disease in 65-year-old men; we know the incidence of heart disease in vitamin D deficient 65 year-old men. We have lots of work to do.

    About Dr John Cannell

    Dr. John Cannell is founder of the Vitamin D Council. He has written many peer-reviewed papers on vitamin D and speaks frequently across the United States on the subject. Dr. Cannell holds an M.D. and has served the medical field as a general practitioner, itinerant emergency physician, and psychiatrist. "    

    Anyone see how complicated STUDYING vitamins is?Kiss          

     Now, if you are still following me on this journey....I'm going to make things slightly more complicated by explain to you a little bit about rare genetic metabolic diseases....

    The DH's genetic metabolic muscular dystrophy causes a defect in fatty acid oxidation.  That means, his body doesn't produce enough of a particular enzyme to make it's way into the mitochondria to make energy.  Many of you might recall from learning in school that the mitochondria is called the "powerhouse" of the cell because that is where energy is made and released from.  People who have all kinds of genetic metabolic diseases have defects that affect the cell's functioning.  Now here's where it gets interesting and complicated for researchers to understand.  You would think that two siblings who BOTH have the same genetic metabolic mutation would both have the same amount of enzymes and would be affected the same way.  No and No.  What is facinating and incomprehensible to researchers today is that one sibling can have more of the enzymes and yet be more symptomatic than the other sibling who has less enzymes.  And, there are siblings who have the genetic mutation and while deficient in enzymes  are asymptomatic!  Have I confused anyone reading this yet?

    I always am amused when people tell me they are deficient in this or that and to "correct" the deficiency, they take this or that.  But from the example I just gave you and the study about Vitamin D, it really isn't clear how people might benefit from taking a supplement or vitamin.  I would love to explain how my husband's endocrinologists and genetic physicians find ways to treat him...but alas, this is a breast cancer website and I don't think it's fair to take all of us on another journey...because I think I would confuse all of you and I simply don't want to do that.

    I hope however, you have all learned from these examples, though, that the human body is as magnificent and elegant as the universe.  And both choose to unravel their mysteries to us very, very slowly.

  • AlaskaAngel
    AlaskaAngel Member Posts: 1,836
    edited January 2012

    VR: The post was interesting and informative.

    You find it amusing "when people tell me they are deficient in this or that and to "correct" the deficiency, they take this or that." I sometimes find it puzzling myself. But this is a forum specifically for people who do that based on their own decision-making process.

    I sometimes find it puzzling when I see people who have had tumors removed surgically and who have done chemotherapy make the assumption that it is "working" or "worked" to get rid of their cancer.

    A.A.

  • AlaskaAngel
    AlaskaAngel Member Posts: 1,836
    edited January 2012

    I appreciate both the factual and the theoretical discussions that have been offered here by so  many in answer to my original question. I appreciated the calculation presented about the size of the group that might stand to benefit, and wish there was better info based on studies to answer the question as to how reliable age (or even hormonal measurement) is in deciding who actually is postmenopausal.

    My original question was one of puzzlement as to why a far more immune-protective, briefer, less expensive, and less difficult therapy (OA + tamoxifen) that had been established by world studies to be genuinely equally effective as a prior chemotherapy regimen (one that is still being used although less commonly), would not have been tested in combination with a monocolonal antibody, to see whether it is equal to or even more effective than the current standard therapy + monoclonal antibody/antibodies.

    I think it is a common sense question to ask.

    If there is an objection to asking that question in itself in a forum that is about alternative therapies, personalizing it does not add weight to either side of the discussion. Using personal examples to explain can be helpful.

    As pointed out by me in a list previously, there are those for whom chemotherapy would not be an option. If there is an assumption presented that OA + tamoxifen is "inferior to all currently used chemotherapy" when it is not, and also no proof at present that it would not be when combined with newer therapies than chemotherapies, I don't think it is harmful to raise that question. Some may prefer to consider substituting something such as OA/tamoxifen (that is known to be equal to CMF or CAF) plus a monoclonal antibody, for example. Another consideration for the group of early stage bc is that it may not be as appropriate for some members of that group to jump to do standard therapy if there is a possibility that less invasive treatment is on the horizon. As adults, they would be the ones that would be best qualified to decide whether they are interested in doing that or not.

    Here is my original question:

    Can someone explain what the rationale is that is being used to hold up progress?

    TEN years ago when I was diagnosed, it was possible to do comparison studies in other countries that showed the effectiveness of such treatment as ovarian ablation plus "X" drug, versus standard chemotherapy for early stage bc:


    http://jncimonographs.oxfordjournals.org/content/2001/30/67.full

    and


    http://jncimonographs.oxfordjournals.org/content/2001/30/67/T2.expansion.html

    How long will it take for us to get a comparison of either ovarian ablation and trastuzumab alone (or possibly trastuzumab plus lapatinib) for premenopausal early stage HER2 positive bc patients, versus standard chemotherapy, in this country?

  • apple
    apple Member Posts: 7,799
    edited January 2012

    the broader the perspective one has at one's disposal to 'make decisions' is important.  I myself do not see science as antithetical to common sense.  gravity always works and that is a scientific and 'common sense' observation.

    I guess I am saying it is best not be 'against'.

  • voraciousreader
    voraciousreader Member Posts: 7,496
    edited January 2012
    Apple...One of the top books now is Thinking Fast and Thinking Slow written by a Nobel Laurete.  The premise behind the book is that usually when our gut is telling us to do something....it's usually WRONG!Surprised  Check out the book!  One of my walking companions is reading it and is raving about it! 
  • apple
    apple Member Posts: 7,799
    edited January 2012

    I've heard of it!!!  will do.

     (we are crossthread topicking or whatever that is called)

  • AlaskaAngel
    AlaskaAngel Member Posts: 1,836
    edited January 2012

    I don't think of science as being antithetical to common sense, either -- although sometimes science is a bit blind. In terms of cancer, whether it is group-think or what I don't know, but to me it is a major lack of scientific discipline (and a lack of common sense)  to have failed for the most part over time, to understand the need for much, much more scientific analysis involving endocrinology and endocrine specialists in coming up with better answers for cancer.

  • digger
    digger Member Posts: 590
    edited January 2012

    Interesting, just as science can be blind, group-think in the alternative arena can be blind as well.  

    I always think it's funny when one is accused as not being able to think "outside of the box" by someone who can't think outside of her own box, in this case, a self-imposed ovarian ablation box. It's like the anti-elitists who rail against those out-of-touch elitists in Washington, but once they win and come into office in Washington, they don't realize that they themselves now qualify as their own definition of "elitists!"

    Group-think and obsession in any arena can be very harmful.

  • voraciousreader
    voraciousreader Member Posts: 7,496
    edited January 2012

    Digger! Lol! Funny and sad and also true!!!

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