Susan Love Defending New Guidelines
Comments
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Colette said ~ If she had any kind of cancer...even DCIS...she should be able to remove them since it is easier (and cheaper) to pay for a bilateral, which verses the price of the chemo and radiation from the development of IDC.
Overtreatment is overtreatment. Just because something is permissable, doesn't make it medically necessary, efficient or effective. I have said NOTHING about what she SHOULD or SHOULD NOT have been able to do based on her BRCA status.
I was merely replying to her (by her own admission) sarcastic comment that she was happy to be "overtreated" by responding to DCIS with a bilateral Mx. It was an attempt to discredit the courageous stance of Dr. Love to question the number of medically unnecessary major surgeries in response to cancers that may have never grown large enough to sicken or kill their host.
Dr. Love has not questioned bilateral Mx's for women who were BRCA+ (as KittyCat is) or with a strong family history. KittyCat's sarcasm about her own situation unfairly misrepresented Dr. Love's stance on this and I felt it warranted correction.
Nothing I said has to do with what insurance should and should not cover.
Yet again, you have taken a fairly innocuous conversation about one topic and manipulated it into another argument about the evils of government and insurance companies.
As I said to you in another thread, you will be arguing those aspects alone (or with others who wish to engage you). I won't engage you on those topics.
Take Care! Alaina
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Great article AnneW! Thanks for the link!
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AnneW...Guidelines that have been based with the knowledge that between 3% and 9% of BC victims will die because of the changes. THAT fact comes from the very people who made the changes. Our government is supporting the USPSTF changes through who ever supports the Health care bill which gives more power to the USPSTF.
The above comments do not involve any emotion and are facts. You can't change them, nor the fact that these changes will kill women. You had breast cancer some time ago. I am currently undergoing treatment, and I am living what happens when you do not detect breast cancer early and are not listened to. These are facts and it also is a fact that if this health care bill goes through, that there will be MORE women going through what I am right now. It ALSO is a fact that breast cancer rates are increasing in women under 50.
You are trying to make it out as if it is not political, but yet, that is exactly what it is. Is your trying to state that it is not political an emotional response to people against the health care bill that the Democrats support?
You may not remember what it is like going through treatment, but I am right in the middle of it, and I have had every treatment that they give women.
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Alaina,
"Overtreatment" is an emotional response to medicine.
As far as politics and insurance companies go..the health care bill gives the reality that our government is intending on being part of the insurance companies and are having a major conflict of interest in this bill. The government will be playing on both sides of the fence with this by dictating law that the insurances follow and also policing what it wants to be part of.
These "Changes" that the USPSTF has made can not be separated apart from the health care bill because the health care bill is what gives these "Changes" power. I am sorry if you can not understand the cause and affect here.
Happy, Thanksgiving everyone!
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Colette, don't EVEN assume I don't know what bc treatment is all about. I may not have had YOUR treatment, but do NOT belittle my experience. I've been through the agony of diagnosis twice. I've lost friends and family to this disease. I've seen the ravages AND success of cancer therapy.
I'm sorry you and everyone else here has had bc. It's horrible, unfair, and frustrating.
Maybe this task force will just end up as a blip, and we'll keep the status quo of breast cancer screening. To me, the argument is less about what age we institute routine screening, and more about putting forth dollars and effort to finding better tools. In the meantime, we can only use what we have. The triad of mammos, self-exam, and clinical exam works better together than one part standing alone. And even then, with all three legs of the triad standing as they should, women will die from this miserable disease.
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I was diagnosed at 42, and many of the members in my support group were in my age group and younger, I believed that all women should have a base line mammogram at 25 and later for compare changes, I did this for my daughter, all this has to do with money.
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I prefer to be "over treated" than "untreated" I have seen to many die because of the latter, none from the first.
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dreaming - I AGREE!
But with the BIG GOV run health care - there is no doubt - the words "OVER TREATED" will cease to exist.
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November 26, 2009 - Kansas City.com
Breast cancer strikes many women under 50
When I heard the government task force recommendations for mammograms, I was didn't believe it. I feel that I would have been dead before age 50 had I followed those recommendations.
In my 40s, a self-exam revealed a lump. A mammogram agreed, and surgery confirmed breast cancer. This occurred a number of years before age 50.
Following recuperation, I became a Reach to Recovery volunteer. Over a period of 33 years volunteering, I had the opportunity to meet many other women who would have had little or no chance to survive had the government recommendations been followed. A large number of women were under age 50.
As a 37-year cancer survivor, my personal recommendations would be: monthly self-exams, mammograms starting at age 40 (earlier with breast cancer family history) and regular checkups. And get rid of Dr. Susan Love's books and literature pertaining to breast cancer.
Beverly Rizzo
Turney, Mo. -
Mammography and the Corporate Breast
The USPSTF would seem as unlikely a target for attack as Santa's elves. For a quarter-century, this squeaky-clean, underappreciated group of doctors and nurses who are specialists in preventive medicine has toiled away in obscurity in the selfless service of public health.
Appointed by the Agency for Healthcare Research and Quality, the task force panel is independent and does not take costs into consideration and it evaluates only the risks and benefits of preventive medicine strategies. The task force must be reeling over the vicious reaction to its latest recommendations regarding screening mammography.
The guidelines are based on an exhaustive analysis of recent studies from Sweden, the United Kingdom, and the U.S. Breast Cancer Surveillance Consortium involving a total of more than 830,000 women, and a specially commissioned study funded by the National Cancer Institute in which six separate teams studied the risks and benefits of 20 screening strategies through mathematically modeling.
The panel recommended against routine screening mammograms for women 40-to-49 years old, and screening every two years for women 50 to 74. These not-exactly-radical recommendations are almost identical to the World Health Organization guidelines, which recommend screening every one-to-two years between ages 50 and 69.
Because mammography is less effective at distinguishing cancers from normal breast tissue in premenopausal women, mammograms miss cancers in some younger women and raise a false alarm in others. This can cause real harm; one woman may ignore a cancerous lump because her mammogram was normal; another may undergo an unnecessary surgical procedure because her mammogram was suspicious.http://www.thehastingscenter.org/Bioethicsforum/Post.aspx?id=4194
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Great article GPawelski! Thanks for sharing!
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I'm not sure I should jump in here, but the two concerns are not mutually exclusive.
As a 42 year old-no lump-stage two-node positive who hit the jackpot on a first screening mammo, I strongly oppose the guidelines.
No question my life was saved.
So why do I worry about over treatment?
We know some invasive cancers and maybe more DCIS cases would never be fatal, and it is a shame there is no way yet to figure out the difference. There are women who go though unneeded surgery and maybe even chemo, and that breaks my heart.
I hope we figure out how to tell the difference.
On top of that I have friends who have had multiple B9 biopsies. One who is small breasted and single now has a mis-shapen breast, and is refusing to do anymore, even though her mom has BC.
While it is easy to criticize her choice, it is also easy to have sympathy. Imagine being single and dating and every year losing a chunk of your breast. Sure I would trade places with her in a flash, but still.
Last night I was out at a party and met a 43 year old woman who just canceled her first mammo. I think it's the wrong choice, but if she wants to take that gamble, it's her body and life.
Let's face it chances are higher she will be my friend than me.
WE NEED BETTER DIAGNOSTIC TOOLS AND BETTER ACCESS TO THE TOOLS WE ALREADY HAVE!!!
The sooner we can cut down on biopsies, the sooner women will have no reason to fear screening.
I was glad to learn about a new tool that can look at how dense a lump is, and predict whether it will be likely to be cancer.
I had an MRI show a second tumor, and was lucky enough to have a PEM that showed it was a false positive. I am not sure there are more than a handful of radiologists that even do PEM in the whole USA.
Dr. Love's concerns are rational, though I disagree with her, they should not be dismissed. They are a piece of the puzzle we should not ignore.
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Well I would rather be screened and rule out a false positive then to be told to do nothing. Yes, there is stress and anxiety during these screening procedures - but - it wont' kill you where breast cancer left undetected CAN KILL. This is an individual patient choice to get a mammogram or not - if you don't want one then don't get it. However, we do not need a task force to run interference between a patient and their doctor, when this is an individual personal patient by patient decision.
Ditto cookiegal - more funding for better diagnostic tools and methods to distinguish which cancers require needed treatments - and to what extent. Considering the MAJORITY of women diagnosed have NO family history - Susan Love is ignoring who makes up her so called army of women.
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All excellent points Madalyn! Well-stated!
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I just watched the news which stated that the radiation from mammograms increase the chances of developing breast cancer. They are finally admitting it!!!! I think that is a big reason that the task force is recommending the change.
My packet of films is at least 1/2 inch thick! There is no way all of that radiation passing thru a smashed breast is good for you.
I agree with Madalyn. Where there is smoke there is fire.
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National Institutes of Health
WHAT WE KNOW ABOUT RADIATION
"Much of our data On the effects of high doses of radiation
comes from survivors of the 1945 atomic bombs dropped on
Hiroshima and Nagasaki and from other people who received high
doses of radiation, usually for treatment. The National Cancer
Institute (NCI), part of the National Institutes of Health (NIH),
in collaboration with the Radiation Effects Research Foundation,
an international group supported jointly by the U.S. Department
of Energy and the Japanese Ministry of Health and Welfare,
continues to study the long-term effects of radiation on the
survivors of the bombs." "Half of all people with cancer are treated with radiation,
and the number of those who have been cured continues to rise.
There are now tens of thousands of individuals treated and cured
from various cancers as a result of radiotherapy. In addition,
there are many patients who have had their disease temporarily
halted by radiotherapy. Radioisotopes are also being used to
decrease or eliminate the pain associated with cancer- - such as
that of the prostate or breast-- which has spread to the bone."
More at: http://www.gwu.edu/~nsarchiv/radiation/dir/mstreet/backgnd/exper/known.txt
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The purpose of my post above is to cite what I heard amidst all of the debate on mammograms and increased risk of breast cancer. I now understand that no clear answer is available. Furthermore the statistics on risk from mammogram appear to be based on mathematical projection from Hiroshima radiation exposure. Perhaps others might lend a hand if different with citations.
Secondly on reading the full NIH article, I thought it noteworthy that radiation therapy has cured and saved lives. This is O/T, but important in breast cancer.
Tender
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Yes, radiotherapy has been used for many decades to treat cancer and the pain resulting from mets And onco-radiologists and radiotherapy machines have become increasingly more precise at pinpointing the area(s) to be irradiated, to ensure that healthy tissue is not damaged.
But there are several instances of patients with Hodgkins Disease who were successfully brought into long-term remission after undergoing radiotherapy who -- some 20 or so years later -- are now diagnosed with BC.
I had my first mammo at age 37. I was dx'd with BC at age 59. My mother had many, many X-rays over a period of several years in an effort to diagnose a severe gastrointestinal problem. She was dx'd with BC at age 57. Who knows if radiation caused our cancers? Maybe it was a gene "thing" but then again, maybe radiation just helped it along.....
IMO, there is no doubt that excessive radiation causes cell damage. How much is too much? Can't be too careful.....
Linda
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Radiation has helped to clean up my cancer....no doubt about it.
However, it has also left me in constant pain and some disability.
I did it because it was part of the package deal that served to try to kill the cancer wrapped around my chest wall.
6 Fields max dose with 2 sets of boosts.
Part of the risk is that I may be partially paralyzed in my advanced years...if I were to see them.
Radiation: I don't know that I would recommend it to someone who didn't need it.
Not suggesting that mammograms are on this level...but, we do know that rads are cumulative and that they are POWERFUL cell damagers.
As for treating cancers that "don't need to be treated"...not so much. I KNOW what the aftereffects are of cancer treatment...and I wouldn't wish them on anyone.
Just sayin'.
tl
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Tender, here's a link to a news story about the study Baywatcher referenced. It was a meta-analysis of other studies that looked specifically at mammograms; it was not an extrapolation from other sources/levels of radiation exposure.
http://www.reuters.com/article/healthNews/idUSTRE5B042220091201
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To All - as posted before I disagree with the guidelines - my opposition to Dr. Susan Love is the harm she does with her terminology. When I was first diagnosed in 2000 - she described treatment as mutilation, poisoning and burning. I was not mutilated by my breast surgeon or poisoned by my oncologist. These dedicated professionals, who have given their professional lives to deal with us in our darkest hours, used their expertise to save my life. I have always worried about newly diagnosed women hearing such inflammatory language. Right now, here in 2009, mammography and BSE are the most effective, mass screening tools we have. They are not perfect as our treatment options are not perfect. We need better, but we are making progress. Digital mammography, MRIs . .. . The guidelines do not say that screening does not save lives between 40 and 49 - it says they don't save enough lives. Since BC is unfortunately a very common cancer - how many lives is enough? My mother died in 1972 at the age of 49 from BC - she didn't have any options, mammography was not being used commonly, use of chemo was not common. I was diagnosed at 42 by mammography and am 9 years out. We have made progress - we must not go backwards. We must continue to utilize the tools we do have and work to improve those tools for our daughters.
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Just a note, as a nurse, mutilate, poison, etc, is a group of descriptions often used by many of us and is not meant, by the folks I know, to be a put down or to make folks angry. If you think about it, that's exactly what Does happen to us. We have amputated boobs and chemo is poison and rads are rads. IMHO
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I second what iodine says: I think mutilation describes what happened to me. I didn't have chemo or radiation, but everyone I know who has would would agree with Dr. Love's description. I like Dr. Love because she doesn't sugar coat things.
By the way, I also don't feel like my doctors used their expertise to save my life and I certainly never felt like my bc would kill me. My doctors treat me, but at every turn I have had to research my options and make decisions for myself. Their judgement can be/has been wrong - what I want them to do is to explain their logic to me and to listen to my logic. Then I make a decision. -
lisa-e...I do agree with you that the Dr. needs to sit down and talk with you about the treatment. I can say that the only one who I felt actually LISTENED to me 110% was my Oncologist. Of course, I think that is also part of his job because he deals with life/death every day directly..and knows what quality of life is and why it is important.
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For those of you who were mutilated - I seriously suggest you change Dr's.
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Then we need better and SAFER diagnostic screening techniques. Maybe this strong reaction will move this reasearch along and we will not be ignored.
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Laura, my treatment for bc has been surgical and hormonal. The fact that I feel like the treatment is mutilating has nothing to do with my doctors (particularly my surgeon), but the vary nature of the the surgery. A mastectomy, the amputation of breasts, no matter how skillfully performed, is mutilation, imo.
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The removal of a Diabetic's leg is performed in an effort to save their life. I doubt few would consider it mutilation. What's the alternative? Until there is one, I'm sure they welcome the mutilation. I had multiple surgeries, and never considered it mutilation. It was surgical procedures that saved my life. Have you ever seen photos of bc when women chose to NOT be mutilated? Simply horrifying. As for chemo and rads being poison...it is NOT mandatory to receive either form of treatment. No one is forced to receive the "poison". For those who think of it as poison, they do have the option to simply go untreated. Other than natural alternatives, nothing else is available. So until that time...I choose to be thankful for what was available for me at my time of dx.
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For what it's worth....my BS says it was the ultrasound that really found my cancer, because the mammo's were inconclusive.
Can't we all just get along?
I wish we could all respect each others right to disagree.
It's true Dr. Love says cut,poison,burn. Not the most comforting language I'll admit, but for some women it rings true.
While I don't agree with every thing she says, the ideas are important.
For almost every treatment there is a downside. That doesn't make them not worthwhile. It's kind of a yin-yang thing to me.
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RIGHT ON!
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