The Truth about Cancer

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  • chef127
    chef127 Member Posts: 891
    edited November 2014

    abigail, why don't apply for obama care? My friend who had no ins and no income applied and was put on medicaid. ALL of her medical is covered including dental, vision, and all diagnostics etc. Better than medicare.

    Maureen xox

  • abigail48
    abigail48 Member Posts: 1,699
    edited November 2014

    I don't need medicaid & am not eligible for it. I have plenty of income, that's the reason I need insurance. if I was to fall ill the they would try to take everything which I feel belongs to my heirs. & I don't need dental or visual, I don't do doctors. but I[m nearly 78 & things happen especially to the old. I need it for back-up before catastrophy if any

  • Momine
    Momine Member Posts: 7,859
    edited November 2014

    Abigail, you are eligible for medicare. Everyone your age is eligible, but you do probably have to sign up for social security.

    How do you make money?

  • exbrnxgrl
    exbrnxgrl Member Posts: 12,424
    edited November 2014


    AARP is a reliable source for information. Scroll to the section that deals with those who are over 65, but not eligible based on their or their spouses work history.

    http://www.aarp.org/health/medicare-insurance/info...


  • abigail48
    abigail48 Member Posts: 1,699
    edited November 2014

    will keep this in mind, bronx, I've belonged to aarp for many years now, I think I must have explored this at some point but not sure

  • exbrnxgrl
    exbrnxgrl Member Posts: 12,424
    edited November 2014

    It seems like a way to obtain Medicare, regardless of your work history.

  • abigail48
    abigail48 Member Posts: 1,699
    edited November 2014

    yesn I've seen this site before & I am eligible if I pay for part a & part b WHIXH I'VE WANTED TO DO FOR A LONG TIME NOW IF ICOULD GET THE COVERAGE

  • exbrnxgrl
    exbrnxgrl Member Posts: 12,424
    edited November 2014


    Why can't you?

  • abigail48
    abigail48 Member Posts: 1,699
    edited November 2014

    I havn't the faintest idea. all I need is a monthly bill. many offices have my ss# and my mailing address. I don't want coverage c, as you all know I don't take pharmaceudicals, but I do want coverage F. with those 3 I can get perhaps get a special ins which covers everything. it needs a doctor, but I'm on that too. If he would comply with my excentricities, no needles etc, I'd be home free. not that I wouldn't still need the 40 or so dollars a week + for supplies. the dressings cost that plus the castor oil packs, rosemary oil, witch hazel for cleaning, essential oils, & on & on. I've never calculated the whole deal. plus the time. I no longer have the time to juice every day for instance, or the energy to take that much compost to the studio compost pile.

  • caralex
    caralex Member Posts: 35
    edited November 2014

    I never fail to be amazed, leggo, at how barbaric the treatment for breast cancer STILL is - cut, burn and poison. Yet with the zap of a lazer, prostate cancer can be cured. I fail to see how cutting, burning and poisoning an ill body back to health is supposed to work. What's the logic behind it?

  • wrenn
    wrenn Member Posts: 2,707
    edited November 2014

    I think one of the most healing things you can do for yourself is to find peace. Accept the treatment or no treatment you intend to do and then let it go. Accept that your body will do what it has to but stay out of it's way. Don't create more stress hormones to tax your system.

    Caralex I think you will find peace by reading what like minded people are doing and avoid reading about current conventional treatments. This is scary shit. We need to hug ourselves and breathe deeply. Take care.

  • juneping
    juneping Member Posts: 1,594
    edited November 2014

    caralex - care to share more about laser surgery on prostate cancer?? i am intrigued.

  • caralex
    caralex Member Posts: 35
    edited November 2014

    Juneping, I'm referring to the HIFU treatment. Take a look here: http://www.hifu.ca/

    or here: http://www.prostatecancer.ca/Prostate-Cancer/Treatment/High-Intensity-Focused-Ultrasound-%28HIFU%29#.VF_eg8nYcnQ

    In fact, just google 'HIFU' and see what comes up. Hope this is of some use to you!

  • juneping
    juneping Member Posts: 1,594
    edited November 2014

    thanks cara!!!

  • holly961
    holly961 Member Posts: 3
    edited November 2014

    Nineteen years ago I had a Lumpectomy.  Recently I had a reoccurrence and had to have a mastectomy and I, too, was totally amazed that all choices are the same as they were 19 years ago.  Same process for a lumpectomy and same with the mastectomy.  Wouldn't you think something better would have come along by now?  I read an article a long time ago entitled "The Cancer Industry".  It is a 72 billion dollar yearly industry so I don't think they are in any hurry to cure us as fast and they can.  Sorry, if they did find a cure hospitals will lose 75% of their business. It makes one wonder.

  • new_direction
    new_direction Member Posts: 449
    edited November 2014

    I think the problem is that most people only start to wonder when they end up here and have to rely on the treatment available.
    I'm no different. I thought this system had no faults, was doing only good, only had one interest. That is clearly not the case.
    But it was not clear to me before. I would have been one of those people saying "you are paranoid, get real. Of COURSE they are doing everything they can - that's their job".

  • leggo
    leggo Member Posts: 3,293
    edited November 2014

    Holly, I hear ya! I was originally diagnosed in 1996. I had one of the same chemo agents as my dad had in 1971 for lung cancer. That kind of progress is unacceptable to me.

    Just wanted to add my perspective to your post New. I was the same, always thought it would be ok and had great faith really, that it would be ok. It really didn't become CRYSTAL clear to me until I was told there were " no other drugs available....you've failed them all".  We can do this, that, blah, blah to keep you comfortable. That's when I got mad and went looking for something better. I didn't fail treatment, it failed me, and the fact that it was even phrased that way pissed me off. Don't put the blame on me for your shitty drugs not working. Been plenty of time and had plenty of money to come up with something better. You can't find it, I will.

  • Janetanned
    Janetanned Member Posts: 532
    edited November 2014


    I watched my mom go through treatment for breast cancer in 1975.  She eventually passed away in 1981 at 57 yrs old.  I can assure you that I did not receive the same treatment as she did.  We both went through surgery, chemo, and radiation.  The options for surgery for her were limited to a radical mastectomy with no reconstruction. Her surgery left he disfigured. I had SNBs on both sides to determine how aggressive my surgery would be.  Even with positive nodes, I did not have a radical mastectomy.  I also was given the option of reconstruction (DIEP), which was not available for my mom.  We both had chemo.  She was deathly sick and obviously in great distress during chemo.  I worked full time throughout and was never sick.  Neither of my chemo drugs was available in 1981.  We both had radiation.  My mom received terrible burns, my skin survived with just a bit of irritation. My mom's treatment stopped at radiation, I can continue to fight this disease with AIs.  I don't know about anyone else, but I can say that, for me, treatment has come a long way since the 80's.

  • leggo
    leggo Member Posts: 3,293
    edited November 2014

    Cyclophosphomide was that agent, btw. I know one might argue that they knew how to better use it by 1996 than they did in the 70's and so on. Doesn't change my opinion though. I don't know if it's still being used today, but I would suspect it probably is. It's so hard to come to a concensus on all this stuff. Everyone's experiences are so different.

  • new_direction
    new_direction Member Posts: 449
    edited November 2014

    I also don't buy into the crap about treatment getting better. When almost everyone go through chemo and they have screened their way to lots of women who don't need chemo all of them - because the disease is chronic in some cases, because the disease disappears by it self in some cases, then it just makes it look better. The Progress in treatment will be when everyone, no matter stage and characteristics, have a chance of a cure.

    The problem is that there are arguments on both side and as long as you are not open to the other idea you will just stick to the arguments on your side.

    Why aren't Money spent for Experts to choose e.g. the 10 most promosing treatment strategies and the 10 areas of breast cancer we need more information about - and then scientists could be occupied with intense investigation of these areas. There are many new studies where it feels like ressources could have been used MUCH better. Is it just me who lack knowledge or is it true - it seems like there is little coordination, no control, no longterm plan with research and whats going on.

  • new_direction
    new_direction Member Posts: 449
    edited November 2014

    janetanned - i know there have been many new steps added to treatment so that it has been optimized over the years. But isn't the problem that this treatment has proved not-good-enough and instead of researching more promosing treatments there have been so many studies conducted about this old stuff, "should we use SNB before/after/in what stage" "should margins be 1 mm, 2 mm, 2,5 mm" "should chemo be before/after" - who cares, this is just not good enough, we need information about something different.

  • Momine
    Momine Member Posts: 7,859
    edited November 2014

    I recommend The Emperor of All Maladies, by Siddharta Mukherjee. It is an interesting and well written book.

    Yesterday I was rereading one of the chapters, where he describes the invention of Gleevec, an oral, non-toxic medication that can keep a rare form of leukemia in permanent remission for the vast majority of patients. This particular leukemia used to be fatal in most cases, killing half of the patients within 2 years of DX.

    The development of the drug cost some horrendous amount of money and for a cancer that something like 2500 people are DXed with annually in the US. Thing is that what used to be a very rare cancer is now a very common cancer, because people are living full life spans with this leukemia. The treatment is for always, similar to HIV or diabetes meds, so what seemed like a huge gamble for the drug company has actually paid off in spades.

    Point being that even with the profit structure as it currently stands, there is plenty of incentive for coming up with better drugs and treatments.

    However, with most of the common cancers, it is like looking for a needle in hay stack to identify the genetic vulnerabilities that might be targets for more effective and less toxic drugs than the standard chemos (the book explains why/how in detail). Herceptin, however, is the result of one such target that has been identified and exploited.

    In the case of breast cancer, Mukherjee outlines that the advances in treatment greatly depend on what type of breast cancer you have. If you have a 3+ cancer and a small tumor, both your treatment and your prognosis will be vastly different than it would have been even 50 years ago. If you have a 3- cancer, then the advancement is far more modest and prognosis has not really improved much.

  • juneping
    juneping Member Posts: 1,594
    edited November 2014

    I think the problem is most of the tx has been about how to improve chemo instead of about cure cancer.

    It's about keeping us alive and not about the cure. It's about XYZ side effects instead of the cure.

    With chemo this toxic and harmful to our bodies, it shouldn't be that controversial how effective it is. Why would I go thru all that to have a single digit successful five yr survival rate.??!!

  • abigail48
    abigail48 Member Posts: 1,699
    edited November 2014

    I suspect most such cancers will let you live at least 5 years if you do nothing except better diet exercise like that

  • leggo
    leggo Member Posts: 3,293
    edited November 2014

    That five year thing is a real sore point with me as well. A WHOLE five years. Might sound good when your 60 or 70. When you're 30, it's an insult to your senses.

    Momine, I always appreciate your info, but I'm not sure what you mean by "Herceptin, however, is the result of one such target that has been identified and exploited". Do you think it's a good thing or bad thing? I ask, because with the story behind this drug, it was pitched as the new miracle for us HER 2's. For all that I was told about it, I was devastated when I got two years of stability (which is oncology code for it grew a little, but not enough to worry about) and a ruined heart. I feel duped when it comes to Herceptin. Had I known then what I know now....

  • Momine
    Momine Member Posts: 7,859
    edited November 2014

    Leggo, herceptin is a good thing, IMO. It is NOT a cure and it does not work for everyone. There is also the heart toxicity, as you mention. However, when it does work it can make a huge difference to a patient. The process that brought herceptin to the market on an accelerated schedule was largely the result of patient activism.

    I am really sorry that herceptin did not work well for you. My main point is that herceptin works in a similar way to gleevec, the medicine for the rare leukemia that I mentioned. The drug targets specific protein pathways of the cancer. The reason herceptin is heart toxic is because the HER2 is present in cancer cells AND, unfortunately, in heart cells. In spite of such problems, many researchers believe that this kind of mechanism is the way forward in cancer treatment.

    I agree, by the way, that the 5-yr thing is stupid and that we need much better stats on this disease.

    June, I would love to see a cure too. At the same time, though, if I could take a pill every day, a pill that did not cause me any serious trouble, and that pill would keep my cancer in remission for the rest of my natural lifespan, then I would take it. My cousin has lived with HIV for 30 years. Yes, it is a bitch, and it has put some limitations on her life, but as long as she takes her anti-virals, she rolls on without any terrible problems. I would be OK with an "anti-BC" drug for me to take while they fiddle with the cure. Also, I agree that refining chemo regimes is not any giant leap forward. But I am still very happy that because of these refinements I was able to walk my dogs every morning, travel, work and play through 6 months of chemo.

    Because the cancer I had was locally advanced, both my 5- and 10-yr prognosis improved by more than a single digit from the chemo. In cases where the benefit is much smaller, I do think the validity of chemo is anywhere from questionable to highly questionable. Thankfully though, doctors increasingly think so as well and are getting better at evaluating the cost-benefit ratio for any given patient.

  • abigail48
    abigail48 Member Posts: 1,699
    edited November 2014

    ant-virals for "aids" bah humbug. worse than that. hiv or the 30+ troubles which are called aids, often as so many troubles age out. doesn't seem like this one does, however that's still to be seen. probably not, as the trouble is thousands of years old with little to help. how is your cousin's liver, momine. after all those years of such toxic drugs?

  • exbrnxgrl
    exbrnxgrl Member Posts: 12,424
    edited November 2014

    momine,

    Thank you for your thoughtful take on bc, tx and cure (or lack of). The Emperor of All Maladies is a great read, especially, for those like myself, who had little knowledge of the history of cancer and it's tx through out the ages. My grandmother passed away from bc in the mid -1960's. The tx she received and what was known about her bc were far, far different than my tx. What leaps immediately to mind is radical mx, a given then, virtually never done (at least in the US) now. My grandmother also had little to no involvement in her own care and tx, nor was she encouraged to. Many patients, today, are not only actively involved in their own tx and decision making but are encouraged to do so by their doctors. You may have to take the bull by the horns on this one, but those doctors do exist.

    Lastly, we all want a cure but no need to tell you all how complex bc is. Like momine, I will gladly swallow a pill, or a few pills, until that happens. Oh, wait a minute...I already do. Grandma Esther didn't have aromatase inhibitors either.

    Caryn

    PS: it's also clear that we are colored by our own experiences. Mine has been a good one, even at stage IV. Is it my medical care? My particular bc? My diet or my attitude? All of these things? Darned if I know!

  • leggo
    leggo Member Posts: 3,293
    edited November 2014

    Thanks for clarifying for me Momine. I won't comment on AIDS, because frankly I'm not informed...but I will say that if cancer patients were half as aggressive and out-spoken as AIDS patients, we'd be a lot further ahead. We just shut up and take it and that bugs me. We need activists, marches. Not necessarily more research dollars. Those billions have already been squandered and I hope they're ashamed of themselves with their early detection and awareness bullshit. Now they just look like fools, IMO.

    And can I just add, these stipulations for getting into a clinical trial are ludicrous. I don't know how many of you saw a recent post that was in the Stage IV forum about ELI LILLY recruits. It has since been removed. It was hilarious.....about 50 lines long about what you could and couldn't do, had, will have. I guarantee there's not a dying cancer patient out there not willing to be a guinea pig, but no, they have to make it virtually impossible. Heaven forbid they don't get a favorable outcome. Seriously, how can they expect people not to get angry. You have AIDS, you got the drugs, Ebola, you got the drugs. WTH is it with all the ridiculous stipulations with cancer. And no, I won't buy " it's a far more complicated disease". I don't give a rat's behind. They've had a million times more research dollars than any other disease.

    ETA: to me, poison does not equate to acceptable treatment. Call me picky.

  • abigail48
    abigail48 Member Posts: 1,699
    edited November 2014

    lots of interesting quotes from mukherjee's book on goodreads

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