Thinking of surgery + B17 + CoQ10, but no chemo/radiation

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Thinking of surgery + B17 + CoQ10, but no chemo/radiation
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  • CrunchyPoodleMama
    CrunchyPoodleMama Member Posts: 1,220
    edited November 2009

    Hi there... I still haven't been diagnosed beyond BI-RADS 5 (tons of clustered microcalcifications around a 5cm mass... yikes), but I've already started self-treating with things like:

    4000 IU vitamin D (and sunshine when possible)
    400 mg CoQ10 (reversed breast cancer in at least one study)
    amygdalin (from eating raw apricot kernels)

    I have an appointment with a cancer surgeon tomorrow (third doctor I've seen... other two were bull-headed about forcing me to do a biopsy before they'll remove this mass).

    Until tonight, I've been 100% resolved to refuse chemo and radiation, and just have it removed surgically and continue to treat with nutrition/lifestyle changes (I've radically overhauled my diet and have switched from "I'm thinkin' Arby's" to "raw organic veggies all the way").

    But now, all of a sudden, I'm scared.

    If I could have a 5cm mass appear so quickly (6 months ago it wasn't palpable at ALL), doesn't this mean it's invasive and has probably metastasized and will probably kill me if I don't have chemo etc.??

    I know no one here can diagnose me, obviously (heh heh, wouldn't that make life easier??)... I guess I'm just scared out of my mind and am shooting in the dark for any words of wisdom or encouragement or even a strong dose of reality.

    I'm so glad to have found you all...  thank you in advance for reading my muddled thoughts! :)

    Julia

  • cp418
    cp418 Member Posts: 7,079
    edited November 2009

    It sounds like your pathology report is still pending these surgical procedures.  When you get this additional information it may help you think clearer with all the facts.  The diet changes and supplements are reasonable but maybe you have to consider more ammunition  - - again pending getting all the facts and determining the aggressiveness of your cancer.  Waiting is the hardest part IMO..... best wishes, Joann

  • CrunchyPoodleMama
    CrunchyPoodleMama Member Posts: 1,220
    edited November 2009

    Thank you for replying so quickly! By "more ammunition," do you mean as in chemo/radiation, or more aggressive alternative/homeopathic treatment? (I am guessing the former but just want to be sure!)

    You're right, I need to be armed with pathology info (and I guess my doctor's recommendation may play a small part, heh heh) before I can do anything else... you're right, waiting is HORRIBLE!!! Thank you again for being a voice of reason during my nightly freakout! Smile

  • Hattie
    Hattie Member Posts: 414
    edited November 2009

    I had a large mass appear rather quickly too--scary.  I got more info from the pathology and from doctors, and did chemo, surgery, and radiation.  When I made the decision that this is what I had to do, It got a little easier.  A plan really helps.  If you decide to do chemo and rads, then know that you can do it. You need to get more info and then make the decision that is best for you, that you can live with.  I am four years out, and well.  

    This is a great place for muddled thoughts.  Checking in with others can help you clarify your own decisions.  

    Take care,

    --Hattie 

  • deni63
    deni63 Member Posts: 601
    edited November 2009

    Julia - I so understand your feelings and clearly remember how terrified I was when I learned of my diagnosis. I struggled so much with what I should do about treatment. I think that was the worst part of that whole process. Once I looked at all of the information I could gather and could make a decision on how to move forward, I felt so relieved and could breathe again.

    I think it is important to know what you are dealing with. I wanted to do the diagnostics available so that I could more effectively make a decision on treatments. Just my two cents...

  • unklezwifeonty
    unklezwifeonty Member Posts: 1,710
    edited November 2009

    Dear Julie,



    This is a hard time indeed. I still remember how anxious I felt during my diagnosis. A couple of things:



    1. The surgeons are, it sounds like, recommending the right thing. They need to biopsy it first and then determine the treatment plan and then operate or chemo first.



    2. Read up and educate yourself in the next few weeks. Wait for full results before you draw lines thru' chemo and radiation. They are nowhere as bad as they used to be a few years back.



    3. See a reputed oncologist at a teaching hospital. The oncologist helps you draw up the overall treatment plan. Select one who isn't related to the surgeons you are seeing.



  • LJ13-2
    LJ13-2 Member Posts: 235
    edited November 2009

    Julia, in another post you said that in May 09 you had a 1" mass and then got "thermography" of the breast.

    As I count, that is 6 months ago and you have done little recommended by your doctors and a lot that will obfuscate a proper diagnosis. 

    When doctors insist on a biopsy, it is so they can actually determine if a mass is cancer, not because they are bull-headed. I'm seeing a pot and a kettle here ....

    If this mass is 5 cm now, you are likely at Stage 3 or later and this possible tumor has had at least 6 months to find new organs to grow on. 

    The decision of what to do is yours, but if you come here looking for validation of the poor choices you seem to have made out of fear so far, perhaps some people will provide it. Not everyone will.

    If you want to live, start listening to the doctors. Start opening your mind to the reality of what is occurring. Have a biopsy done to find out what this mass is. If it is cancer, and it is 5 cm, you will likely need chemo to address the likelihood that the mass has had the chance to spread in your body.

    I offer this advice not because I like telling people what to do, but because I don't like to see people die of breast cancer. Stop acting out of fear. Act like you want to live.

    PS - B17 is not a vitamin and amygdalin is not going to do anything about breast cancer, if you have it. It has been tested extensively and has shown no ability to kill tumor cells in controlled studies.

  • Yazmin
    Yazmin Member Posts: 840
    edited November 2009

    Julia:

    I totally understand why you are feeling superscared. Nevertheless, I think it is time for you to face this situation. I know it is impossible to perform surgery on a tumor without a biopsy: I also tried to do it that way, but was told it cannot be done; my surgeon said: "...We need to know how to approach this tumor before removing it..."

    You need to see your doctor as soon as possible, then you can make treatment decisions. Perhaps, yours is one of the tumors that chemotherapy can help. Perhaps you'll go another route, after doing your own research. But for now, you need to set up an appointment and start a dialogue with your doctor.

  • CrunchyPoodleMama
    CrunchyPoodleMama Member Posts: 1,220
    edited November 2009

    Thank you, everyone... I went to see a new specialist today who actually explained WHY a needle biopsy first is important.

    The first two didn't give me actual answers... they got frustrated with my questions and said things like, "What you're describing is the way things were done 30 years ago"... okay, but why is the new way better? (Is that so weird to ask a doctor??)

    Anyway, apparently I've finally found a doctor who is interested in actually answering questions, instead of rolling their eyes and giving me non-answers as if I'm 2 years old.

    I scheduled a needle biopsy for a week from today. I guess the surgery will come afterward, but I still have no intention to go through chemo. I don't want my immune system, liver, and reproductive organs destroyed when I have (I hope) a baby still in my future.

    BTW, this doctor said the mass is only 3 to 4 cm. I had thought it seemed smaller, but was sure it was my imagination/placebo effect... couldn't possibly be the CoQ10 etc., hm? But, the doctor said it, so there ya go!

    PS - B17 is not a vitamin and amygdalin is not going to do anything about breast cancer, if you have it. It has been tested extensively and has shown no ability to kill tumor cells in controlled studies.

    Yes, I know what quackwatch says. Smile It actually shrank tumors in animal studies at Sloan-Ketterling but the research was abrubtly halted on orders of the FDA and the ACS. But, I 100% respect your right to believe what Big Pharma and the FDA preach. Wink

    One thing that was dismaying about all three cancer specialists I've seen is that not ONE of them believes nutrition and lifestyle have any bearing whatsoever on cancer. When I asked, they gave answers like, "Well, you want to try to eat healthfully" or "You don't want to go on a diet, just keep your calories under 2,000 per day." Tongue out Seriously?? Even the "big business" cancer organizations acknowledge that food and lifestyle choices can have some bearing on cancer risk... why can't medical schools teach that??

    My friend who went through the standard cancer treatment two years ago said that they had her meet with a nutritionist. I was so glad to hear that and asked what they went over with her.

    She said it was stuff like how to deal with the side effects of chemo... such as to eat freaking JELLO to help with nausea!! Yell I might have more respect for the medical establishment if they didn't have this God complex that all the world's diseases can be solved with more chemicals, while refusing to consider that the answers just might lie in NATURAL FOODs. Ugh, it's frustrating.

  • unklezwifeonty
    unklezwifeonty Member Posts: 1,710
    edited November 2009

    Dear Julia,

    Asking the doctors is a GREAT thing but you also need to educate yourself. In this day and age, there is not much that is not available online. You should not have to wait six months for a doctor who could answer a question when the answer is available here, or nccn.org or even through google.

    If as another poster has said you knew of your lump back in May '09 and have not gotten it completely diagnosed, I am afraid you could be letting the disease spread thru' your system. I strongly recommend you proceed with utmost urgency and get this diagnosed fully. If it turns out to be malignant, start treatment immediately. Complimentary medicine works but no one really knows exactly how much. Some of it depends on your faith, in your case is obviously strong! There are enough doctors who practice holistic medicine now so you don't have to listen to doctors who have had the "pharma koolaid". Traditional medicine improves your odds by certain known percentage points. I suggest you not discard any possible treatment option at this time until the full picture of your condition is known.

  • sakura73
    sakura73 Member Posts: 467
    edited November 2009

    Julia, there are things you can do to preserve your fertility before chemo, including egg harvesting and ovarian tissue freezing. You can also take a drug called Zoladex which shuts your ovaries down during chemo and has been shown to reduce the risk of permanent infertility. So don't let those concerns make you automatically refuse chemo.

    Natural foods etc can indeed do a lot to heal our bodies and balance our hormones, etc, but if you have a large and fast growing mass which turns out to be cancerous then you may be well advised to consider chemo. I took lots of supplements during my 6 months of chemo and was not ill at all. It is too simplistic to think of chemo etc as poison. Vitamin D is poisonous too in excessive doses, but useful and necessary in appropriate amounts. So too, sometimes, with chemo.

  • CrunchyPoodleMama
    CrunchyPoodleMama Member Posts: 1,220
    edited November 2009

    Thanks for your replies. I've been trying to sleep for the last two hours but can't stop crying after reading the post pointing out I found this in May so it's probably spread everywhere.

    I need to see if there is a subforum here for "Choosing to die with dignity"... because at this point, that's what I've decided to do. I don't have the $15,000 to do egg freezing/IVF, especially since my medical insurance basically ends as of December 31 and I'll have to pay 15% to 40% of any cancer surgery/treatment. I'd rather die than not be a mother. In fact after my last miscarriage I prayed to die... so maybe this is an answer to prayer.

  • makingway
    makingway Member Posts: 799
    edited November 2009
    SuperScared-Don't let anyone rush you before you do your research. Doctors and the 'medical community' aren't the 'Be All, End All'. There are other methods you can take to be proactive for your health. Check the Natural Girls thread on this website. It's a wealth of information. Also breastcancerchoices.org. Private Message me if you'd like. You might try to google Bill Henderson. He wrote a book of cancer cures, and although some of it sounds kind of 'out there', there are some valid suggestions. Also read Anticancer by Servan-Shreiber. With an MRI I was told my tumor was 5.9 cm. After surgery it was 4.0 cm...that's quite a difference. The only reason to do chemotherapy before surgery is if you are planning to do a lumpectomy. That is my opinion.
  • CrunchyPoodleMama
    CrunchyPoodleMama Member Posts: 1,220
    edited November 2009

    Thank you so much for replying... I'm still crying so hard my face is swollen and I can barely see the computer screen... the nurse today told me that cancer grows over many years so a few months rarely makes the difference between life or death, but now I'm thinking she was just giving me a comforting lie.

    Thanks for the book recommendations... I will check those out (and definitely Natural Girls -- I don't know why I didn't before)! And wow, so the MRI was wrong about the size? I didn't realize that was possible... thank you SO very much for your reply... just knowing someone was "listening" out there, while I've been feeling so alone and hopeless the last few hours, makes a huge difference. THANK YOU. Smile

  • chiquita
    chiquita Member Posts: 135
    edited November 2009

    I think you should wait until diagnosed and then see what can be done...do not start planing to die before you know if that is cancer or just a benign lump...I will pray for you.

  • Fairyfloss
    Fairyfloss Member Posts: 32
    edited November 2009

    please see my posts about diet.  i think if you are gonna go this way you HAVE to be on the right diet.  i would consult your chinese doctor about this and get some chinese herbs as well.  some have strong anti cancer properties.  correct diet from my research and which my chinese doctor agrees with is:

    No red meat, no dairy, no alcohol, no processed or fast food, no sugar (tiny bit of maple syrup/honey very occasionally okay), no caffeine (coffee or black tea), no soft drinks or cakes etc. no lollies etc.

     Correct foods to eat: vegetables of all types, raw, juiced as well, and steamed; focus on brocolli, kale, bok choy, leeks, oninon, garlic, green leafy vegetables first, then coloured vegies as well; then some fruit (dried or berries or what you like.  berries have anti oxs) less fruit than vegeis; must be a lot of GREEN vegies; drink wheatgrass juice as a boost of green as well, eat nuts (ALMONDS are v. good and brazil nuts), SEEDS - of all kinds; beans, lentils, chickpeas, corn, WHOLEGRAINS (brown rice, basmati etc).  make sure you arent allergic to wheat - if you get bloating after a meal you may be.  if so , switch to corn/rice.

    drink: vegetable juice, wheatgrass, green tea, herbal teas, WATER (no flouride and dont shower in flouride either), and some fruit juice ok, but minimize.

    and thats pretty much it.

    anti cancer foods: apricot seeds, apple seeds, bitter almonds, cats claw herb (boosts immune system), green vegies, certain chinese mushrooms, SEAWEED.  you should eat sushi or seaweed quite often as iodine deficiency is linked to breast cancer; i wud drink soy milk to (non gmo) as if you have hormone positive cancer its said to sit on the oestrogen receptors and occupy them, similar to tamoxifen. 

    if you're going it alone, i would seek help of a chinese doctor so you have some extra assistance.  and guidance on diet.  also dont eat hormone filled chickens (bad for you if breast cancer).  i wud steer clear of chicken and only eat fish - if any meat.  eggs are okay tho.  i still eat eggs.  (and fish occasionally)

  • Fairyfloss
    Fairyfloss Member Posts: 32
    edited November 2009

    i read that post too, that you were crying about, and thought about reporting it.

    it really was not a very helpful or pleasant post at all.

     i wud say go with your gut instincts and dont let anyone push around or rush you into anything.  i perhaps wish id gone with my gut insticts more.

    they were telling you not to act out of fear, then making you scared, which i think is hypocritical and wrong.

    and you are right about big pharma.  i dont trust them.  cancer is a 72 plus BILLION dollar industry.  sorry but i have read too much disturbing stuff to trust drug companies anymore.  also, my cousin is a drug rep, selling drugs to doctors, and since she joined them shes started eating really healthy on this strict mostly vegetarian diet (almost as strict as mine) and become a health nut.  she also wont TOUCH any drugs.  and last time i spoke to her she was saying how disturbed she was that hardly ANY of the doctors she spoke to knew ANYTHING about nutrition.  they just swallowed all the marketing stuff about the drug she was selling without questioning anything or mentioning diet to her at all, in some cases when she knew they should have.  disturbing?

    ps, good books to read are: the china study, by dr colin campbell (a harvard etc study); your life in your hands by professor jane plant; dont drink your milk by dr oski? i think; and quite a few others out there on amazon.com you might want to investigate.  if you want i can give you any links to studies supporting various stuff or other books if you like.

     ps, keep asking them questions too, like the biopsy.  i asked questions and drove everyone nuts, but i dont like doing things until i know why.  for all you know, this approach could save your life.

    ps love and hugs and hope you feel better soon.

  • MsBliss
    MsBliss Member Posts: 536
    edited November 2009

    If you read the history of the laetril study that took place at Sloan Kettering from 1974 to 1977, you would see that it was abruptly halted because it was showing some promise as a nontoxic agent.  It was a very interesting event.  Even if it is ineffective, the doubt of how this was handled makes one wonder. 

  • MsBliss
    MsBliss Member Posts: 536
    edited November 2009

    Have you had a biopsy yet?  It is not clear from your post.  There are many of us who have chosen other paths for a breast cancer diagnosis.  You don't have to do chemo rads...you have to educate yourself and you have to learn the biology of the mass that you have.  Once you know what it is you are dealing with, you can plan a course of action and it doesn't have to include chemo--but it should include removal of the mass if it is malignant.

    Beyond B17, and COQ10, there are a host of supportive nontoxic therapies which have evidence that they are effective.  Avemar Ultra, coriolus, chaga, AHCC, Vitamin D, and the list goes on. Plus there are ways to minimize any downside to traditional therapies.   Let's see what you are dealing with first, then you need to plan a course.  

  • rreynolds1
    rreynolds1 Member Posts: 450
    edited November 2009

    SuperScared,

    I would totally delete that horrible responce from your memory banks.  Before your biopsy, no one can tell you the status of your health.  How rediculous for anyone to predict how fast your lump is growing.  It takes a lab to do that.  There are so many types of breast cancer that before it is removed, they still don't have all the information.  I see women on this site who have 8 cmm tumors that have not advanced to the lymph system.  Panic and fear are not what you need right now. 

    I agree that if you are planning to do alternative only treatment, you need to be well educated and put a healing team together.  I chose to do a combination.  My tumor had not spread to my lymph nodes but my oncotypedx test ranked it intermediate.  I chose not to have chemo, but I had the tumor removed and had radiation.  I have totally changed my lifestyle.  I eat no red meat, buy organic, excersize, cut out alcohol, take supplements, meditate, etc.  I feel terrific.  I have my first post surgery mammo on Nov. 30th and I know it will be fine. 

    Please pick up some guided meditation tapes.  They really helped to calm my nerves.  Try to stay in the present rather than worry about what may not happen. Whenever I was overtaken by fear, I would say "Thank you for my healing."  I would visualize my white blood cells surrounding my tumor and lovingly destroying the cancer cells.  I found that very comforting.

    I'm sorry someone felt the need to express her concern so insensitively.  I'm sure her motives were good but please dismiss her predictions.  Even a doctor would not stage your cancer at this point.

    Keep the faith.  Healings happen every day to those who believe it is possible.

    Roseann

  • CrunchyPoodleMama
    CrunchyPoodleMama Member Posts: 1,220
    edited November 2009

    To my wonderful new friends here, THANK YOU!!!! I can't tell you how much I appreciate your suggestions AND encouragement.

    Fairyfloss (love your user name! Laughing), thank you for all the GREAT diet change suggestions... what I've done so far (starting a few weeks ago) is very much in line with your suggestions... I'm in an organic farm co-op so I get a crate of wonderful seasonal organic produce every week, and I'm eating mostly that, raw as much as possible. I totally cut OUT all caffeine (I had tried so many times before and utterly failed... I was so addicted! yet, as soon as a doctor told me the "c" word, I instantly lost all desire for it... I went cold turkey and am so glad I did!!). I haven't drunk tap water in years, although we do need to get a shower filter or whole-house filter.

    MsBliss, my biopsy isn't until Tuesday (the 10th)... so no diagnosis beyond "you have breast cancer" (and supposedly that's based on how it "feels," not on the ultrasound - the mammogram did show regional microcalcifications though). They didn't see any indications that it's in any lymph nodes, but I guess we'll see what the biopsy says! Thank you for mentioning those other complementary possibilities... I hadn't even heard of some of those and am glad to have new (positive!) things to look up!

    rreynolds, that is so inspiring! Which guided meditation tape did you get? I bought a self-hypnosis one that is okay, but the guy's voice is a little annoying (LOL!). I'd love to get another one or two!

    BTW, here is what I'm doing so far:

    - Total diet revamp -- mainly raw or lightly steamed/sauteed organic veggies, heavy on cruciferous veggies (broccoli etc.)... NO sugar... NO caffeine... NO alcohol... hardly any meat/poultry but I haven't been 100% strict about that... no dairy except for the Budwig concoction

    -400 mg CoQ10 daily

    - almond kernels daily (15 daily so far; will build up to more - not sure how many yet)

    - 4000 IU vitamin D

    - Budwig's cottage cheese + flax mixture once or twice a day, with nuts, berries, etc. mixed in

    - milk thistle (to help detox my liver... I spent a year drinking entirely too much red wine!)

    - Essiac tea (as soon as it arrives)

    - 30 minutes not-crazily-intensive exercise daily

    - some sunshine daily (when there IS sunshine)

    - good sleep every night (umm, last night was clearly a failure!! Laughing)

    - praying a LOT!

    - hypnosis mp3 each night

    Got to run to a photo shoot but THANK YOU ALL so much for everything!! I can't tell you how much I appreciate it!!

  • deni63
    deni63 Member Posts: 601
    edited November 2009

    SuperScared - I take amygdalin too. I have been taking it intravenously with vitamin C since last May. The center where I take these treatments has many success stories. I also take amygdalin (laetrile) in pill form daily. There has been good research behind it and I believe that it can help to kill cancer cells.

    I agree with you about doctors not knowing enough about nutrition. My surgeon admitted that research has shown that breast and prostate cancers (both hormonally driven) have been linked to nutrition. When I told her I changed my diet and lifestyle, she looked at me like I had two heads. I didn't get it. She herself was finding in research that diet does play a role, yet refused to recommend any changes to the diet. VERY frustrating!

    I had surgery and no chemo or radiation. They didn't feel right for various reasons. But, I am glad that you are going for a biopsy so that you can find out what you are dealing with. Surgery gives you the best chance of preventing a recurrence. In terms of cancer a few months does NOT make a difference. The lump you have, if it is cancerous has been growing for years. But, you shouldn't delay any longer. Get yourself on the road to recovery! We are here to help.

    Some great books have been mentioned here for reading. In particular, I found The China Study and AntiCancer extremely helpful - plus so many others.

  • unklezwifeonty
    unklezwifeonty Member Posts: 1,710
    edited November 2009

    Dear SuperScared,

    I'm sorry I caused you grief.

    Please know that whatever your diagnosis and treatment choice, you are still loved.



    Love and hugs



  • thenewme
    thenewme Member Posts: 1,611
    edited November 2009

    Dear SuperScared,

    My tumor was 5cm.  Yes, I was super scared too, but without a proper and complete diagnosis, you don't have enough information to even start to make decisions!  My tumor was huge and invasive, but there was no lymph node involvement found (except for a suspicious IM node that lit up on a pet scan but disappeared after treatment!), and as of yet I have no mets identified.  So the fact that your tumor may be large doesn't necessarily mean you're doomed. 

    You said in your post, " One thing that was dismaying about all three cancer specialists I've seen is that not ONE of them believes nutrition and lifestyle have any bearing whatsoever on cancer."  I think you may have misunderstood.  I'll bet dollars to donuts that they said something along the lines of "....nutrition and lifestyle are important factors in overall health, but alone are not a CURE" for cancer.  

    Of course we all make our own treatment choices, but please do a lot of research so you can make informed choices.  Play devil's advocate and research the different treatment options, keeping an open mind.  Then make your choices based on facts rather than fear.  In my experience, my entire treatment team is very supportive of complementary medicine, and they're quick to recommend nutrition, healthy lifestyle choices, yoga, acupuncture, supplements, etc., but they also advise to use caution and common sense.  

    Best of luck during this super scary time!  Let us know how you're doing!

  • CrunchyPoodleMama
    CrunchyPoodleMama Member Posts: 1,220
    edited November 2009

    deni63, I'm glad to hear someone else is doing something similar too... you are very fortunate to have found a treatment center who will administer it intravenously! The two books you mentioned are fantastic... I read (most of) the China Study earlier this year, and I just received Anti-Cancer from Amazon (though I mistakenly ordered the audio CD edition)... can't wait to listen to that one!

    unklezwifeonty, please don't feel bad; it wasn't your post that upset me. I appreciated the good suggestions you had as well as the positive spirit in which you intended it. It was an earlier post that struck me as telling me I had doomed myself, cancer is probably growing all over my other organs, and complementary/nutritional medicine is complete quackery... something along those lines is what another post said without much positive or helpful advice.

    I do want to hear all sides, absolutely... but I think there is a way to say something without trying to crush someone's spirit and tell them they've been a fool and are probably now dying because of it... something I didn't get at all from your posts. Thank you again for your perspective! Smile

    thenewme, thanks for sharing your situation... so glad there wasn't lymph node involvement! I hope everything continues to go well for you!

    About this:

    You said in your post, " One thing that was dismaying about all three cancer specialists I've seen is that not ONE of them believes nutrition and lifestyle have any bearing whatsoever on cancer." I think you may have misunderstood. I'll bet dollars to donuts that they said something along the lines of "....nutrition and lifestyle are important factors in overall health, but alone are not a CURE" for cancer.

    Believe it or not, two of the doctors told me, when I asked them how important they thought nutrition and lifestyle factors for cancer recovery, "Well, it can't hurt, as long as you're doing the recommended treatment" (meaning chemo, radiation, etc.). It "can't hurt"?? How about, it's really really IMPORTANT in recovering from cancer to eat natural whole foods, stay away from processed/chemical-laden food products, etc.? They didn't even say that it's "important"... they had the attitude of "Well, if you think that's what you need to do, I guess it can't hurt, whatever."

    One of them flat-out said, "Well, make sure you keep your calories under 2,000 per day, and that's pretty much it"... that is insane... what if he had a patient who thought that meant it was okay to eat 2,000 calories' worth of Arby's and Hostess Cupcakes? (I would love to think no patients are that stupid, but I personally know some people like that... the kind of people who take a synthetic cholesterol pill and think that's their license to eat anything they want.)

    I haven't met with the designated nutritionist yet, but I asked my friend who was treated at the same center what kind of recommendations the nutritionist had... I asked, "Did she say things like garlic because it has such-and-such, and be sure to eat plenty of leafy greens, that kind of thing?"

    She said, "No, it was really more along the lines of dealing with side effects of the chemo... like have popsicles and ice cream on hand when you need them." Yell And that was the nutritionist!!

    Anyway, rant over... LOL... you can see I'm pretty passionate about this because there is so much that people SHOULD be told about how to prevent cancer (as well as things to consume and avoid while you're being treated for it), that doctors just don't give a bleep about telling patients. Just one example... all through my 20's, I LIVED on Lean Cuisine. I thought I was being so healthy! Little did I know, those things are three-fold poison:

    1. All the chemicals, preservatives, MSG, etc. to make them palatable. (I was so dumb... I remember telling people, "Frozen dinners have come such a long way... they taste so GOOD now!" Duh, if only I had looked into the scary ingredients list to see why.)
    2. Carcinogens leeching from the flimsy plastic into the food while it's being microwaved.
    3. Then there's the microwave process itself... there are studies now that show that heating food via microwave chemically alters it and at best, robs it of nutrients. I made the decision two weeks ago not to eat irradiated food any more... I bought a convection oven, which heats almost as fast but without radiation... but how many of us have lived for years, DECADES, on microwaved food, and no one ever told us there was anything potentially harmful about it?? I would bet you $100 right now that if I were to call up my cancer doctor or even the nutritionist and asked, "Are Lean Cuisines okay to eat?" they would say, "Sure, that's good and healthy, if you like the taste." Tongue out  
  • deni63
    deni63 Member Posts: 601
    edited November 2009

    Superscared - I have AntiCancer on CD too. It was great to listen to it while I was walking, etc. Great book with great info - you will love it.

    Where do you live? There may be a good Naturopathic center near you as well.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited November 2010

    Super,

    Please look into an "excisional biopsy," also called a "surgical biopsy."  That way you aren't refusing a biopsy, you are getting the cellular information by cutting around the mass rather than piercing it. You may have to go to a couple of doctors but you can tell them the truth, that you have a "phobia" about piercing or stereotactic needles..

    "Not knowing when the dawn is coming, I open every door." -- Emily Dickinson

  • Colette37
    Colette37 Member Posts: 387
    edited November 2009

    Superscared...

    I know EXACTLY what you are going through.  I looked into the B17 also...even got some apricot seeds to supplement with..I also have started taking D vitamins and lost 50 lbs with exersize and watching what I ate along with cutting out pop in my diet and started stearing clear of MSG and High Fructose Corn Syrup.

    I also realized that while I was doing these things, that I did need to look to traditional medicine to help hit hard what was in my body so that I would never have to go through this horror again.  My sister-in-law is a nurse and she saw a woman that they were treating with breast cancer.  She left for a short time to go and be treated in Mexico doing the alternative treatments.  A few months later she was back where my sister-in-law worked, but this time it was because her cancer progressed too far, and the hospital was not able to do anything else but keep her comfortable.  My sister-in-law was there when she died leaving her family and the small girls with their Dad.

    I am not telling you what to do...all I am saying is that I understand and I know the fear you have (your name even shows how scared you are)...but don't cross off everything just because you are afraid of LIVING through what they may do to you.  You say that you want a family.  I understand that.  I was nursing my 7 month old when I found the lump and I had to immediately wean (I nursed her bothers until they were 2 1/2)..but it was what I had to do to stay alive.

    My story...I wasn't afraid of chemo..which I did have...BUT I swore I would not do radiation.  Well, after 6 treatments of chemo, when I had my surgery I found that I still had a 10 cm Ductal Carcinoma In Situ left and it was .01 mm close to my chest wall.  With that information, I decided that I obviously needed radiation because it was 5 1/2 months from when I was diagnosed to when I had the surgery and everything that I did was not enough.  It is so bad that I need to take a xanax every time I go for rads..The dr. know this and understand.

    I have also been seeing a Natropath Dr. and she says that I need to do what I can to get rid of this cancer and then we will deal with everything later...she is giving me what she can to help deal with the side affects from treatments..but even she says that wait until AFTER my treatments to really deal with getting better.

    My heart goes out to you because the worst part of all of this (apart from having to deal with the reality of what is going on and the affects of what it will have on you and your family) is the waiting game.

    With all this being said, you ultimately are the boss of what will happen to you.  You need to make the choices that are right for YOU.  Get the information.  I am glad that you found a Dr. that will talk to you like a human and answer your questions and not be rude while doing it.  Based on the information that I got from the path report and the information that my husband and I find out is choosing what my actions are.

    If you explain to your Doctors what your fears are, they can give you information so you aren't so afraid and you can make the choices.  Dr. can work WITH you to protect your fertility.  If there is nothing that they can do to protect it, there are other ways you can have a child.  I have a friend who had lymphoma and they needed to radiate her abdomen.  The gave her an operation which moved all of her female organs to one side to protect from the radiation.  Since then she has had 3 healthy kids..so there ARE ways that are out there.

    PM me if you ever want to talk.  I know it is scary, and it is even worse since you sound like you are so young.

  • CrunchyPoodleMama
    CrunchyPoodleMama Member Posts: 1,220
    edited November 2009

    Thank you!!!

    deni63, I'm in metro Atlanta, and I'm sure there must be a good one around here.

    lucy88, that is good to know about tumor size... it sure didn't show up that big on mammo or u/s, so I have to guess that's not ALL wall-to-wall cancer. I actually did ask all three doctors if they would do an excisional biopsy, but all three of them refused and said they absolutely wouldn't do that without doing a core biopsy first. One of them actually told me only a "bad" doctor would do an excisional biopsy rather than core. Undecided

    Colette, thank you for your encouragement and for sharing your story! I'm confused, though... had the mass been larger than that before chemo? I thought the whole point of chemo before surgery was to shrink it? This is what scares me about chemo... my doctor (the one I trust and am going with for the surgery) said something to make me think there are so many types of chemo that it's basically trial and error. *sigh*

    Thanks to all of you, I'm feeling so much better today... thank you again SO very much!!!

  • CoolBreeze
    CoolBreeze Member Posts: 4,668
    edited November 2009

    Superscared,

    I stopped reading this thread where you were scared because you found your cancer in May and now think it's spread everywhere.  I want to tell you my story.

    In early April, I turned 51.  I was getting undressed and I looked at myself in the mirror and thought, "Hey, I'm holding up well for my age".  In May, I looked in the mirror and noticed a dimple in my right breast, and felt a lump.  I ignored it because I have a history of lumps.  In August it still had not gone away, so I got tested.

    It was cancer.  I had a mastectomy two weeks ago.  And, no spread to lymph nodes or any evidence of vascular invasion.  So, just because you haven't treated it yet, doesn't mean you have a death sentence.

    Untill the lump is removed, there is no accurate way of estimating how big it is.  Ultrasound said 2.4 cm.  MRI said the same.  In reality, the main tumor was 3.5 cm and I had 10 cm all together that never showed up anywhere else.

    I have a very aggressive form of cancer too - HER2+++, multifocal, grade 3 type.  I had numerous cancers in my breast and yet, no evidence of spread throught my body. So, if you do your medical care now, you may end up perfectly fine.

    Now, I have every intention of doing chemotherapy and getting herceptin and radiation if necessary.  These are things that have saved the lives of countless women.  It will be harder for you since I was done with childbearing and you are not, but if you want to live you have no choice but to do these things.  But, the fact is, until you have your tests, you won't know what you need to do.  Not everybody needs chemo, but the longer you wait, the more chance it has to grow and the more likely it is you will need it

    My best friends mother was like you.  She lived a natural lifestyle.  She ate organic, she didn't believe in modern medicine - she thought the chemicals were toxic.  When she got breast cancer, she treated it as you want to. She wrapped herself in heat wraps, she ate apricot seeds and took natural aids, including the enzymes you mention.

    She died a very horrible death.  In agony.  Her entire right side had rotted by the end, and it smelled bad.  Cancer was everywhere by then.  Her daughter had to watch it happen, knowing that if she had done chemo she would have lived. 

    Her cancer was milder than mine at the start, but it was invasive and invasive cancers grow if not stopped.

    She was a lovely woman.  She had long, beautiful silver hair down to her waist.  She was forward thinking - married a black man in the south in the 1960s.  That made her brave for the times. She was only in her 60s when she died, and had a lot to give, for her and her family and society. She never saw her grandchildren.

    I hope you will change your mind about modern medicine and use your supplements as they were meant to be used - as supplements to medicine.

    Good luck to you.

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