Cost of Cancer

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  • Triciaski
    Triciaski Member Posts: 145
    edited May 2009

    Wow, that's rough. The only thing I can say about the insurance is that $100/month for private medical insurance is a very low rate, so I'm not surprised it isn't providing full coverage. I would think that AARP would give the information up front, though, about what is and isn't covered.

    I don't have any good advice except that I know hospitals sometimes write off charges if you go to their business office and explain your situation. You might also check for programs through your state that might be of some help. I know that the less populated western states (I live in Nevada) don't have as many programs as California and some of the eastern states, but it's worth at least looking into. The state's website might be a place to start.

    I'm so sorry to hear you lost your job.

    Tricia

  • lexislove
    lexislove Member Posts: 2,645
    edited May 2009

    *YAWN*

    I'm glad you have never felt better in your life. and...I'm even more ecstatic that you and your "lover" enjoy your breasts sooooooo much.

    Just to clarify with you, I have one natural breast, the other is getting ready for an implant. BUT....now...I'm strongly thinking of having the healthy breast removed just to piss you off.

    BTW...I'm in Canada, the country where the government pays for our healthcare. And yes...that means I pay for it! But that is ok..because frankly if I were to get some other serious illness, I don't want to have to sell my home,business,car, borrow money from friends/family and cash in my savings and daughters college fund to get well.....I have never had to wait for treatment or been denied anything. Sure, there are horror stories about any countries health care, but overall I think we are doing pretty good...

  • idaho
    idaho Member Posts: 1,187
    edited May 2009

    "without screening and early detection a person life is at stake", HELLO! everyone's "life is at stake!"  NOBODY is going to live forever! Even though you probably don;t want to believe it Leia I agree with you!  I feel awful looking for help from the government right now, but I just don't know what else to do!  I agree with you also about the treatments really not extending life for any substantial amount of time.  I have put my stats in many places and all I can see is that surgery and radiation extended my life 6 months!!??? Ok, well I just spent 6 months doing surgery, rads, worrying myself sick and not feeling good.  So I guess I "wasted" the 6 months I just gained!!??? Sorry I am rambling, I just feel that if I had never had that mammo and didn't know I had cancer I probably would have lived another 10-15 years without knowing I have cancer and all this stress and cost and died quick!  I felt perfectly fine until this all started, now all I can look forward to is feeling like crap the rest of my life!  AND I get to spend ALL my money on treatments, tests, pills, and shots.  I am in the system now and don't know how to get out!!!! Just my thoughts on the matter....Tami

  • pip57
    pip57 Member Posts: 12,401
    edited May 2009

    I guess for early stage cancers you can shrug off detection and tx as being useless.  As a stage III girl, I owe my life to both.  Perspective is everything!

  • mzmiller99
    mzmiller99 Member Posts: 894
    edited May 2009

    My best friend's cancer was discovered as a stage 4.  And it took her 3 miserable years to die. Nothing quick and easy about that.

    I'm very thankful for early detection, even if all I have is run-of-the-mill old lady cancer!  No one should go through what my dear friend went through. 

  • Brenda_R
    Brenda_R Member Posts: 509
    edited May 2009

    I'm greatful for treatment. Without tx, with stage 3 her2 positive cancer, KI67 @ 70%, I would be dead by now.  I'm alive and doing fairly well this spring. I think I can say that treatment and especially herceptin has extended my life.

  • Leia
    Leia Member Posts: 265
    edited May 2009

    To all of you women, on this thread, with Stage 3 or 4 breast cancers; Just looking, above on this page, Brenda_R, prettyinpink100, lexislove.

    You do need, some medical intervention.  I guess, since the nutrition option, just eating better (FOCC) isn't an option. For you. 

    And you can look it up, just type in "Budwig protocol" in Google and the truth is that Dr. Budwig's FOCC Protocol SAVED people, with stage 4 cancer. Whatever cancer. By just eating better. 

    Yet, that makes $$$ for noone. What does make the $$$ is all of these 'treatments." And that is why the USofA spends more on medical care, and we're all sicker. 

    But what Dr. Budwig did NOT do, is have any "studies." And the current, medicine "standard of care" is ALL about, "studies." 

    Even when these "studies" reveal that X treatment "reduces breast cancer risk by 50%!!!" That is the headline. When the underlying study says that "X" treatment reduces breast cancer from 6% to 4%.

    That is just ... meaningless.  

    And Idaho, Tami, I HEAR you.  It is very hard to get away, from the Medical Industrial Complex. They sucker you, in. 

    That 2007 exisional biopsy that I had, on the non-cancer breast, was after a NEGATIVE MRI on that breast. That exisional biopsy, was negative. Duh. Well, except for the $25,000 my insurance company paid to the SCCA. And MY $2,500.

    Yet THAT was the "Standard of Care."  So, they "scared" me, into it. Like they are scaring all of the women, on this board. 

    And lexislove, don't get your other breast, cut off.

    Although, I wonder why you are berating me, and my lover, for enjoying my breasts.

    Life is short. Sex is fun!  

    I just want to enjoy life. And I am. Eating the FOCC, planting my new vegetable garden. And enjoying sex, with my lover.

    Tami, you do NOT have to live life, like shit. You WERE perfectly fine, before all of this. And you have a lesser diagnosis than I had. 

    This is NOT going, to kill you. I literally walked out, on my proposed radiation "Treatment"

    I just said, NO. Bunch of crap. 

    I don't believe you doctors, with your "standards of care." It's a bunch of bullshit.  

    And to just repeat, I've never felt better, than I do, today. Had a great Mother's Day, went to see Star Trek, with my children. My sister came over, we planted some veggies.  Which I'm going to eat more of, to prevent these cancers, from coming back. In addition, to the FOCC. 

    THIS is the answer. Not more drugs, chemo. That's the anti-answer.

    Life is about .... enjoying life.  

  • konakat
    konakat Member Posts: 6,085
    edited May 2009

    Lexilove -- that was great -- cut of your other breast to piss her off! 

    Gee, if I wasn't getting my chemo and at the rate my mets was spreading I probably wouldn't have much longer.  Thanks to my chemo the cancer is shrinking/disappearing. 

    It's great to go on a healthy diet, a lot of damage is done from a lifetime of bad eating.  I do not doubt at all that a healthy diet helps prevent some cancers.  Or helps your immune system fight.  I don't think anyone would disagree that a healthy diet is a good thing.  Perhaps Dr Bugwig doesn't have any studies because he doesn't have any proof that his theories work.  Does he keep track of people who follow his advice and get sicker or die?  Does he publish that, how many Stage 4 people died under his care, or only those who get better?

    BTW -- you don't have to pay 50% taxes to have the great system in Canada.  Health care is a right in Canada, money (or lack of it) does not prescribe your treatment.

    And Leia, I'm happy your biopsy was benign.  I wonder if you'd be singing another tune if it wasn't.

    And Leia, you're a very cruel woman.  I'm thrilled you have your breasts, but your statement "...At least, I still have my breasts. And I enjoy them, and so does my lover. But I guess, you don't" is a bit much.  I certainly hope you never have to go through what some of the women have here.  I do pity you, not myself, not the women here.  I pity you.

  • lexislove
    lexislove Member Posts: 2,645
    edited May 2009
  • crazy4carrots
    crazy4carrots Member Posts: 5,324
    edited May 2009

    FYI:  An organization that has been formed to fight healthcare reform in the U.S. has produced tv ads featuring the former President of the Canadian Medical Assoc.  The ads are running on Fox News and CNN.  Dr. Day is an orthopaedic surgeon and operates a private clinic in BC -- and is being investigated by the BC legislature for overbilling.  He is a major proponent of public/private healthcare and is, obviously, biased.  Guess he feels he just doesn't make enough money in the public system.....

    As has been said before on this thread, listen to those of us who are patients!

  • KEW
    KEW Member Posts: 745
    edited May 2009

    Science is based on the ability to replicate one's work.  The scientific method allows scientists around the world to have a common trust and method of practice that supports ethical research and the reporting of it in PEER-reviewed journals.  One's work should be repeatable by anyone else and the results should be verifiable. One's work should be transparent.  I have been unable to find anything like this that relates to Dr. Budwig's work.  We are all entitled to choose our treatment, I chose not to do chemo based on my Oncotype score and the recommendation of two oncologists, even though a third felt I should.  I would never berate a woman for choosing a different route, I'm not that insecure in my choices that I have to put others down for theirs.  I am deeply disappointed that this thread has been drawn away from the real concern of the cost of health care, to someone writing so coldly and cruelly to other sisters on the thread.  Sex is a beautiful, fun, and intimate expression of love between two people--breasts or not.  I will be planting my 20th summer garden and looking forward to my future.  Gardening is not novel or a recent discovery.  I'm grateful for the science we have, and excited about what the future will bring. Science is dynamic, except for the laws of physics, things are constantly changing with new research, this does not represent a flaw with science, it represents its strength, however for those of us diagnosed with bc, or other diseases, it can be unsettling that things change, doctors try new methods, and treatment regimes advance. It is wrong to assume that at any given moment in time doctors will have all the answers. Nutrition is hugely important for good health, that goes without saying, but so is kindness and compassion, if you don't have it for others how can you have it for yourself to be healthy and heal if needed?

    I look forward to a better health care system in the US as I believe a rising tide floats all boats, or we are only as strong as the weakest amongst us.  I believe in a nation that cares for all and frankly our taxes or not that much lower than Canada or France, and we still have to worry about losing everything if a serious illness comes along, that seems un-American to me. 

    I wish you all the best, I hope you all find comfort in your choices, and don't allow the vitriol displayed here to bring you down. Everyone is doing the best they can. 

    Karen

  • Katalin
    Katalin Member Posts: 230
    edited May 2009

    Beautifully put, Karen.  Thank-you.  As a Canadian, let me let you all in on something. My income tax is around 35%.  On top:  sales tax & goods & services taxes on things other than food, are around 14%. I don't make a lot of money.  Maybe 40K in a good year, working in theatre, lately because I missed time due to this lovely thing we all share...I don't begrudge a frickin' penny I spend on taxes, because I know that I've had the best possible care, never worried ONCE about who would be treating me, I always had the best of the best, with a great GP whose first reaction on hearing my diagnosis was to give me a big warm hug...after that:  any test, any specialist, no holds barred, fast fast treatment.  My mother, my aunt, all had the same type of treatment.  All of us are working-class.  It never even occurred to us to think even ONCE about cost of treatment or whether our  insurance would cover us.  Now where we fall down is with unemployment insurance, which only covered me for 16 weeks.  Not enough. Should have been one year, as it was in the seventies. But my work voluntarily stepped up, even though I was on contract, and they were under zero legal obligation, to cover me for an additional 16 weeks.  With the help and love of family, I could take time to recuperate.  

    And I'm deeply sorry, but I read some of Dr. Budwig's protocol, and some of it is not entirely scientifically sound, as far as I'm concerned. On top of it, even she says that her protocol does not work for everyone.  And by the way!  No yoga!  Not too much exercise!  Good lord.  Bless everyone who takes that path, and bring on the big guns...and start firing at me for my opinion!  I'm careful about my diet:  but quark, which she recommends, is not exactly the same thing as cottage cheese, and the quality of dairy foods in Germany is entirely different from the normal stuff you pick up in the grocery in the US, which is different from the protocols for feeding and medicating cattle in Canada and other parts of the world.  So if you're medicating with dairy, be sure it's organic. 

  • Leia
    Leia Member Posts: 265
    edited May 2009

    Konakat wrote:

    "I certainly hope you never have to go through what some of the women have here.  I do pity you, not myself, not the women here.  I pity you." 

    Konakat, I have gone through more than you can ever imagine. 

    My first Cancer diagnosis was Leiomyosarcoma, Friday, December 7, 2004. Never heard of it? Well, you're not alone. I get this call, from my surgeon, on that date saying I had this deadly, malignant cancer. And the next Tuesday, I was in the operating room.  

    And then I had CT scans, and Liver MRIs and TransVaginal Ultrasounds and Upper GI series. And the tests went on and on. And on.

    Fortunately, for me, they were all negative.

    I was LUCKY.

    I know a woman, right this minute, with uterine Leiomyosarcoma. Which is where this cancer mostly presents. Mine was external. Easily, cut out. But this woman, is dying. Her Leio was discovered at Stage 4, spread everywhere.  She'll be dead, within the year. 

    And for my part, 2.5 years later, May, 2006, I'm diagnosed with this 2cm ER+PR+ HER- breast cancer. And in the midst of that breast cancer diagnosis, I had another transvaginal Ultrasound, based on some finding from my annual Leio Chest/Abdomen/Pelvis CT and they thought I had cervical cancer. So, another biopsy, for that. 

    Which was all, negative.

    And then, 2007, the bullshit with the negative right breast Inflammatory Breast Cancer "scare" and then the left breast negative results, all around. Based on some Atypical Ductal Hyperplasia, in the left breast.

    Nothing.

    And then, this 2009 stuff, which went on and on, until the negative biopsy. Yet, at the end, if I had not said, no, I would have had yet another negative, MRI-guided biopsy. On top of the negative Ultrasound biopsy. 

    I have gone through WAY more than most of the women, here.  

    Which is why I am now embracing Dr. Buddwig's protocol .Because I am tired of all of these useless medical "treatments."

    And Katalin wrote that Buddwig's policy is not "scientifically sound." That's true. It's not. But then, are any of these other, "standards of care?"

    The "standard of care" for breast cancer used to be double mastectomy.  Now, it's lumpectomy plus radiation. 

    But then, even the radiation standard, is changing, is it 7 days or 7 weeks?

    Everything is always, in flux.  

    Kew wrote, "don't allow the vitriol displayed here to bring you down." 

    I'm not promoting, "vitriol." 

    I'm just saying what I have done.

    I love my breasts, and I still have them. I didn't just cut them off, for a 2cm IDC. And my lover loves them, too. And I don't have cancer, anymore. It was cut out, via a Lumpectomy. 

    And I did not do, the radiation. Because it made no sense, to me. Why irradiate the entire breast, when the cancer was just in one place. And it was cut out.

    And to conclude, I believe in Dr. Budwig's  protocol. 

    Because I just feel ... FANTASTIC!

    You can all mock me all you want, but I feel so great. Without all of that crap food, I just feel so good.

    I don't need some "study" to tell me, that. But I guess, KEW does. 

    But to get back to the "Cost of Cancer?"

    I won't speak, for anyone else, but there is NO WAY that the govt can pay, for all of the treatments that I've had. Going forward, with Obama's plan. We're talking $Hundreds of thousands of $dollars. For all of these useless treatments that I've had to undergo.

    I would have just been, denied treatment.

    As you will be denied, in the future.  

    This is what is coming, for the USofA.

    No more Double Mastectomies, with Reconstruction,  for 2MM DCIS. 

    Ludicrous, in any event.  

    To you Canadian women, Canada has what, 30Million People? The USofA has 300,000,000 Million people.

    There is NO comparison. At ALL What works in Canada will NEVER work, in the US.  

  • helena67
    helena67 Member Posts: 357
    edited May 2009

    I think this whole thread is starting to get a bit strange with all these discussions about 'lovers' and 'cut-off breasts'. Is this necessary? I basically agree with the concept that health care should not be for profit. And that is how it is in the US. People that make money off other people's misery. I do think health care providers, including doctors, should have a good income. But all these insurance companies make billions. In any case, I am done reading this thing. Maybe we should just agree that everyone should do their own thing.

    Undecided

  • Katalin
    Katalin Member Posts: 230
    edited May 2009

    Helena67, no kidding, the talk of cutting off breasts and all that is unsavoury.  Let me say this, re:  Canadian population...we have massive land mass, and much higher cost per capita just to maintain our massive infrastructure per capita....and yes, 30 million vs. 300 million in USA...We contribute per capita...ie. per each.  Some get sick, some don't....you think in USA you don't have the resources to support each other?  WTF?  We do, with less resources than the states.  Tommy Douglas had a dream here in Canada, of health care for all...I certainly don't want to state this too strongly, but if we don't look after each other in this area, what are we here for?  What does our life mean?  To put a 10% extra dollars in our pockets, for what?  A rainy day?  So that when we get ill maybe it's your sister who bankrupts herself, or it's instead *you* who bankrupts *yourself*....we have to spend our RRSPs to stay alive, or for you, 401Ks, or sell our homes out from under our children and families just to stay alive.  If I spend an extra 10% to support my sister or YOUR sister every pay cheque, I say, bring it on....let me pay.  Maybe I'll need it now, maybe you'll need it next, my sister, my mother, my child, my friend.  It's do-able. You just need to have a paradigm shift, and figure out how.   Imagine it and do it.  How is it that we think that health care shoud be private and education should be the responsibility of the state.  Or the roads, or whatever?  That's okay?  But *health* is *private*????  A bit kooky,in my small opinion!!

  • ktym
    ktym Member Posts: 2,637
    edited May 2009

    The thread has gotten a bit surreal.  So, on the subject of cost and controversy regarding it in the US.  Did anyone catch this today?

    http://www.cnn.com/2009/HEALTH/05/12/us.genes.lawsuit/index.html?iref=newssearch

    Interesting controversy regarding patents on genes and the ACLU suing regarding it.  Anyone who has had BRCA testing has had it done by Myriad one of those being sued.  What they don't get into here is the additional controversy many have raised regarding researchers or Universities who make discoveries using NIH (taxpayer) funds and then apply for patents.  

    It does get messy when health care is a "business". 

  • Teild
    Teild Member Posts: 58
    edited May 2009

    Which is why I am now embracing Dr. Buddwig's protocol .Because I am tired of all of these useless medical "treatments."

    That's a good, logical reason for embracing an unproven protocol . . sarcasm intended.  I really tried to see the logic in your conclusions, but I just failed.

  • konakat
    konakat Member Posts: 6,085
    edited May 2009

    The US would have no problem supporting socialized healthcare -- as kaitlin said, it's based on a per capita formula, a population, whatever it's size, will support itself. Instead of paying for health insurance out of your paycheck, you have a bit more taxes.  Big deal.  It sure gives a peace of mind knowing that you will always get the tests and treatment that you need.  Isn't that worth a bit more out of your pocket every month?  I think so.

    And getting tests is good medicine -- better to catch something and treat it earlier than later.  Both healthwise, and cost-wise too.  Even better to find everything benign.

  • idaho
    idaho Member Posts: 1,187
    edited May 2009

    Back to the subject that started this....I am glad I live in Idaho and my 5 hour hospital stay ONLY cost $20,000, I just read that a lady that lives in Texas had the same thing and it cost her $60,000.  Exactly my point... How can there be such a difference.  And how come my insurance (AARP) won't pay for anything!??? I am so frustrated!!! Tami

  • Leia
    Leia Member Posts: 265
    edited May 2009

     Katalin wrote:

    "Helena67, no kidding, the talk of cutting off breasts and all that is unsavoury." 

    Do you read, this board? On the other threads. Where women are getting double mastectomies, for 2MM DCIS. 

    Is that,  "unsavoury?"

    For my part, I had IDC. 2cm. This thread. And I chose a lumpectomy, with clear margins and no other treatment.  

    But again, the point of this thread, is the "Cost of Cancer."

    And for my part, having lived it, I'll just repeat, IF this universal health care, happens, no more double mastectomies, for 2MM DCIS.

    There is literally, not enough doctors and machines. 

    Leia wrote:

    Which is why I am now embracing Dr. Buddwig's protocol. Because I am tired of all of these useless medical "treatments."

    And  Telid replied:

    "That's a good, logical reason for embracing an unproven protocol .. sarcasm intended. I really tried to the see the logic of you conclusions, but I just failed."

    So, Telid, where is the success in the "Race for the Cure." How many $Billions have been spent, on a cancer cure, and there's none. No "Cancer Cure."

    If there were a "cure for cancer," what would happen to all of the "treatments."  

    Budwig received no funds, for her "cure." Because there was no $$$$ in it.

    Eating right? Flaxseed oil and cottage cheese? Vegetables?

    I keep repeating, this, cancer cure, aside (and that's a BIG one) I just feel better. And not a tiny bit, but Quantum amounts. To the point, where I can NOT go back. Even though I love, junk food.

    Telid, I guess you want a "proven" protocol.  Well, these corporate assholes, you all hate, and  I do too, just want to cut your breasts off, and irradiate you and make HUGE profits.  And then, scare you even more, with making you demand Chemo. 

    Well, those are the current "standards of care." These are your "proven protocols."

    And they make HUGE profits, off of that. These Herceptin treatments are $50,000/year.  

    And apparently, you're all willing to go along with it.

    Well. I am not. Willing to go along, with it.  

    I chose the Budwig Protocol. 

    Because I just want to enjoy whatever life I have left. With NO Doctors, involved.  

    But just a statement of fact. with Obama Universal Health Care, NO ONE is getting $50,000/year Herceptin treatments.

    Can you people just not see that this entire scenario is unsustainable?

    WHERE is the $$$ coming from? There is only so much $$$ we can borrow, from China! Until the entire house of cards, comes crashing down.  

  • Katalin
    Katalin Member Posts: 230
    edited May 2009

    Leia, you've got very strong feelings about this.  We all do.  But I feel you took my comment on" all this talk about cutting off breasts is unsavoury" entirely out of context.  It was in reference to someone else's strong talk.  Anyway, we all make our own decisions on our treatment.  As a dear friend of mine says:  we do the best with what we don't have, and by that I mean, the best we can with the information we have at hand.  I decided on double mastectomy, with no regrets.  I also chose to eat very like Budwig's protocol, minus the cottage cheese, because I consider that much dairy to be suspect.  It seems to me that protocol was developed at a time when dairy was not being messed with to the extent it is now, with growth hormones and antibiotics, and some antibiotics even being given under some conditions to cows producing organic milk.  So when you call us "you people" you may be assuming a lot about us that may not be valid.  I'd also like to say that western medicine is a relatively new field.  I don't agree with everything that goes on, and I certainly believe that big pharma is out to make some big $$$ on us.  But it is a process, and I think we're making progress from both ends: both allopathic and complementary medicine/ nutritional approaches.  But in the meantime, we all have the opportunity to make our own choices based on our opinions of the facts, and our feelings on the issue.

  • konakat
    konakat Member Posts: 6,085
    edited May 2009

    I don't know where this no herceptin treatments on Universal Healthcare is coming from. It's simply not true!!!  In Canada you get the same standards of care as you do in the US -- you do get Herceptin, all the other treatments.  In Canada the pharmas and hospitals are not padding the costs to make a profit. That's the difference between Canada and the US.

    It costs less in Canada, the gov't has negotiated much lower prices with the pharmas for the drugs.  The hospitals aren't private companies out to make the owners/stakeholders rich.  There's aren't insurance companies making millions of dollars off your treatments.  That's how it works.  Universal Healthcare works because there aren't all the companies making a profit off of your illness.  It is non-profit, sustainable care.

  • Teild
    Teild Member Posts: 58
    edited May 2009

    Ultimately there will probably be tiered levels of health care in the US.  Everybody will be able to obtain basic and minimal health care under a government run or mandated program - with no exclusions for preexisting conditions , but those with private insurance or their own resources will have more choice of their medical providors and more access to treatments that the government might deem as unnecessary or unreasonable.  Highly unlikely proven drugs for cancer will be excluded under even the government subsidized part of what is coming.  This person saying otherwise is clearly is speaking out of anger and not out of logic or knowledge.

  • Teild
    Teild Member Posts: 58
    edited May 2009
    IF this universal health care, happens, no more double mastectomies, for 2MM DCIS.

    There is literally, not enough doctors and machines. 

    How many women have double mastectomies for minimal DCIS?  And what happens to all of the doctors and machines we already have.

    So, Telid, where is the success in the "Race for the Cure." How many $Billions have been spent, on a cancer cure, and there's none. No "Cancer Cure."

    But there is.  People are cured of cancer all the time so long as it is gotten to early enough.  If not, no protocol based on healthy eating is going to cure anybody.

    If there were a "cure for cancer," what would happen to all of the "treatments."  

    I guess doctors and pharma would have to concentrate on other things, like heart disease and auto-imune diseases.  Maybe even anti-aging drugs.

    Budwig received no funds, for her "cure." Because there was no $$$$ in it.

    There were no dollars in it only because she didn't have a cure.

    Eating right? Flaxseed oil and cottage cheese? Vegetables?

    Sounds good for regularity.  Probably very worthwhile.  And vegetables may help prevent cancers. . sometimes.

    I keep repeating, this, cancer cure, aside (and that's a BIG one) I just feel better. And not a tiny bit, but Quantum amounts. To the point, where I can NOT go back. Even though I love, junk food.

    Much healthier to not eat junk food. 

    Telid, I guess you want a "proven" protocol.  Well, these corporate assholes, you all hate, and  I do too, just want to cut your breasts off, and irradiate you and make HUGE profits.  And then, scare you even more, with making you demand Chemo. 

    Like the rest of society I suppose.  Still, I would hope that the industry really wants to cure cancer if it can.  Imagine the money to be made by any drug company who discovers a cure to any particular cancer . . especially breast cancer.   

    And apparently, you're all willing to go along with it.

    Speaking only for myself of course, I want to live to see my children grow up . . if at all possible.  Maybe I am unusual. 

    I chose the Budwig Protocol. 

    I'm all for healthy eating so long as a scammer isn't asking to profit so I can eat healthily 

    Because I just want to enjoy whatever life I have left. With NO Doctors, involved.  

    Best way to do that is to stay healthy.   Sometimes easier said than done of course.

    But just a statement of fact. with Obama Universal Health Care, NO ONE is getting $50,000/year Herceptin treatments.

    I agree.  The price of medications will have to probably be regulated to some extent . . without damaging the incentive of companies to continue researching newer medications. 

    Can you people just not see that this entire scenario is unsustainable?

    You mean like a Ponzi scheme?

    WHERE is the $$$ coming from? There is only so much $$$ we can borrow, from China! Until the entire house of cards, comes crashing down.  

    We already may be past the point of no return.  But it has lots to do with bailouts, wall-street and wars.

  • konakat
    konakat Member Posts: 6,085
    edited May 2009

    Hi Telid,

    I loved your responses. 

    Yes, there probably would be a 2 tiered system.  There is some push for that in Canada -- there are already some clinics where you can go a pay for a test if you don't want to wait a couple of weeks for one by the regular route. 

    No system is perfect, but I do think the Canadian one is better.  There's a lot of misconceptions in Canada and the US about each other's systems.  I tell Canadians that it's not so bad in the US, IF you have insurance.  There is medicare but there are people who fall through the cracks, lose their insurance, etc.  If you have insurance here it is great.  I do think they over-test though -- I was dizzy and falling. I had an MRI for spinal column pressure and a trip to a neurologist in one week.  Ended up it was just the chemo and low BP. Cut my bp meds in half -- maybe that should have been considered first instead of all the expensive tests.

    Also, a friend who's in the healthcare field here told me that the drs intentionally give more expensive treatments.  For a long time I was getting an IV of benedryl before my chemo.  But it was burning up my arm so now I just get a couple of claritin pills instead.  Now, why don't they do the simple pills right from the start, you're in the clinic for less time and it is easier?  Because the hospital can bill at a higher rate if they do a drip instead of a pill.  This is all part of the problem in the US.  It's all these little things that are contributing to needless expense.  Annoys the heck out of me!! 

  • crazy4carrots
    crazy4carrots Member Posts: 5,324
    edited May 2009

    Correct me if I'm wrong, but could there be a few reasons for all the tests and over-medication, such as:

    1. the docs' fear of litigation if they don't do EVERYTHING possible to uncover a problem. 

    2. tv and magazine advertising by the pharma and medical supply companies, so that patients are more inclined to demand expensive medications, even if they're not needed/recommended.

    3.  Profit motive, of course, for the for-profit medical establishments.

    Konacat is absolutely right; universal health care, if properly managed, WILL NOT result in rationed care.  The U.S. has the perfect opportunity to examine the best and the worst parts of universal health care in every other first world country, and the only thing preventing it from happening (IMO) will be the intense lobbying of the pharmas and insurance companies, as well as concentrated advertising by organizations who are against it, and the caving in of your senators and reps who put their own needs (getting re-elected maybe?) ahead of their fellow Americans.

  • konakat
    konakat Member Posts: 6,085
    edited May 2009

    Agreed Linda.  Well said.

    And it is a much more litigious society here in the US than in Canada.  Don't know why, but it just is. And since healthcare is regulated by the gov't in Canada I suspect it would be harder to make a case in Canada for under-testing -- if the doctors do as much as prescribed by protocols.  If they don't do all the tests they can, then there is a case against them. 

    I must admit I find the drug ads a bit humorous -- all the side effects that they have to mention -- you'd think it would scare more people off than not. 

    Anyway Linda, I think you hit the nail on the head.

  • crazy4carrots
    crazy4carrots Member Posts: 5,324
    edited May 2009

    My dh always adds, at the end of each commercial listing side effects "....and death".  (As you know, we get several U.S. networks north of the border).

    The ads are even funnier here!  About the only Rx drug commercials we see are for Viagra and Cialis.  Laws prevent mentioning in the ad what they're used for, so they end up being "nudge nudge, wink wink" ads!

  • Leia
    Leia Member Posts: 265
    edited May 2009

    Telid, glad you responded. But I can't even begin, to refute you, point, by point. 

    You've obviously "bought in" to the Medical Industrial Complex. But just a few comments.

    People are not "cured of cancer, all of the time." They are 'treated' for cancer. With all of these bullshit 'treatments." And for my part, the only 'treatment' that I will accept, is surgery. Surgery is a treatment that eliminates cancer.

    For early stage cancers, such as I had? These other 'treatments," this radiation and chemotherapy are useless.  Women do it, because they are frightened into it, by their doctors. Who don't want to get sued. 

    The only treatment, going forward, is to prepare your body to NOT get cancer, anymore. ANY cancer.  

    That was my dilemma. When, in January, 2009, I had that X-Cancer breast MRI, Birad 5, for cancer. Which after the biopsy, turned into Birad 0.

    But not after I had to pay $1,500, out of pocket. And the insurance company, $15,000.

    What is your point again, Telid?  

    Leia said:

    I chose the Budwig Protocol.  

    Then, you said.

    "I'm all for healthy eating so long as a scammer isn't asking to profit so I can eat healthily." 

    What "scammer?" 

    There's no "scammers."

    Actually, the trusted provider of the Flaxseed Oil, the Barlean's Company, they offer their flaxseed oil, to cancer patients, at 1/2 off the retail prices.

    What are you talking about, Telind? 

    Leia wrote: Budwig received no funds, for her "cure." Because there was no $$$$ in it.

    Telid wrote: There were no dollars in it only because she didn't have a cure. 

    Yes, she does.  It's called, the FOCC. But that doesn't make any $$$ for anyone. So noone pursues it. 

    It just makes scientific sense. Did you read the books, Telid? Where are "YOUR 'studies" that the Flaxseed oil/cottage cheese does NOT work?

    Although, I might seem, extremist, yet I'm not any different than any of you women, on this board. I've had  Breast cancer. And in my situation, with the additional Leiomyosarcoma cancer.

    I'm sick of all of these cancer "treatments." They don't work. Other than surgery, which I totally believe in. 

    We just have to eat right, and enable our bodies to  fight these cancers. For ALL of our body parts. 

    Everyone on this board is focusing on their breasts, like that is the ONLY place they will ever get cancer. Which is just .... ludicrous.  

    To conclude this message, today was  the happiest day, of my life.

    Nothing of import, happened. Yet, I took a great walk. Which I do every day, 60 minutes/day. But today, I just stopped, under this halo of lilacs. And it all smelled, so good. And I knew my two kids were safe and thriving. And it was great

    Because that is what life is .... one day at a time. And not all of this over-treating, for nothing breast cancers.  Which is what has happened, to me. And which I'm just not going to do, anymore. 

    The FOCC has renewed, my life

    Telid, everyone, can decide, for themselves.

    That's the beauty of the USofA. With Obama, if that can even last. 

    Obama just wants to inflict his "view," on everyone.

    I'm very afraid, with this newbie. He doesn't know WHAT he is doing.  And that is ... frightening.

  • KEW
    KEW Member Posts: 745
    edited May 2009

    I'm just curious what is the mechanism that makes Flaxseed oil/cottage so amazingly effective? Not to be inflammatory, I would like to know.  Where is the evidence-based science that supports it?

    Are you implying that a women who has chemo (remember I did not) cannot take a walk and enjoy flowers?  I have a friend who RAN a marathon during her chemo treatment, I think she enjoyed herself, she has run many since.  Chemo works for people who need it, and it works very well for women who are ER/PR-, there is some evidence that it may not be as effective for SOME ER/PR+ women, that is where Oncotype DX and TailorX come in. Also, some people believe strongly enough in chemo that in itself may lead to a positive outcome. Yes, some people who may not benefit from chemo may ask for it, yes it may be because they are scared--haven't we all be scared by this experience?  It is her choice, and you have no business to do anything other than nicely offer up what you are doing, and support her in her decision. We also have the ability to get up and walk out of any doctors office we want.  My second opinion said I should have done chemo, he admitted to being chemo-biased, not someone I wanted to work with, so  I left, and I keep working with someone who I don't always agree with, but he listens and we make decisions together.

    About $$$ when I looked up the "Budwig Protocol" all the websites I found required the use of a credit card to get more information.  Dr. Budwig may not be making money, but someone is.

    Also, just so you get full benefit, most registered (trained) and licensed (trained) dietitians (RD and LD) say use Flaxseed and grind it yourself everyday to get the greatest benefit, oil (of any kind) even when refrigerated, loses it potency.

    You have turned so many people off of this thread- which had great potential to intellectually explore the cost of cancer. I wonder if you realize how angry, bitter, and aggressively threatening you sound?  Everyone is entitled to their opinion, but cussing, putting other people down, throwing your sex life into peoples faces,putting down other people's treatment choices, and attacking the president are all ineffective means of communication.  I'm glad you feel so well.  Nobody here would have responded to you the way they have if you hadn't come out punching.  I read on multiple threads women who have different opinions, they are all expressed with kindness, patience, and compassion--you have displayed none of this towards anyone on this thread.  You are shrill and your arguments are distasteful--and they lack evidence--no matter how effective the Budwig protocol may be, nobody is listening because they can't get past your delivery.

    Obama a highly educated, insightful man, who taught constitutional law doesn't know what he's doing, but some woman with a PhD. in physics  knows enough about the human body and nutritional science to prevent and cure cancer? Seems a specious argument.

    By the way 1/2 of the scientists I work with are physicists so I know them well--I work with more than 40 scientists across 5 universities--no, we are not in medicine--we study ecosystem health, which does impact human health, but that isn't what we study.  You may not like science, or the scientific method, but that method and peer-reviewed publications are what ensures that decision makers, industry, and the general public, have the best available science to work with.  They may not use it, but that is a different discussion.  The best science will change as it should, as more research is conducted.  Is it perfect? Not always, I always say follow the money, see where funding came from.  The National Science Foundation and the National Institute for Health are great funding sources, they are non-biased.  If, just an example, the cotton candy industry  funds studies that say their product is nutritionally sound,...I might research the methods used in that study, look closely at the statistics, and try and find similar studies funded by other sources, to see if the outcomes were similar. Funding sources, the scientific community, and scientists themselves need to be unbiased to ensure the most reliable results.

    I'm sorry if this has been a harsh email.  I'm done with this thread, as it has become a surreal nightmare, and not a safe and welcoming place where people can discuss the real and important issue of the cost of cancer.

    Best,

    Karen

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