Budwig protocol?

135

Comments

  • candygurl
    candygurl Member Posts: 130
    edited June 2012

    Ang7, I have no time to explain my post to you. I know that Himayala is actively looking for another BS.:)

    She has a meeting scheduled with a third BS. In the meanwhile, she is keeping an open mind,  exploring her options and taking care of herself.  Let's not be too judgemental and rude. It's not helping. (DUH!) Again read my posts. I wanted her to see Leia's story, hoping she'd have someone with a similar DX and mentality to identify with. As we all know Leia had surgery and only uses the Budwig protocol.

  • candygurl
    candygurl Member Posts: 130
    edited June 2012

    Himalaya said,

    "Thank you i will search for LEIA, that seems more familiar to my situation." But, no SusieQ58's big fat ego was not having that. She had to keep nagging. And then the rest of you just joined in the chorus here and on another thread. 

  • Ang7
    Ang7 Member Posts: 1,261
    edited June 2012

    zuvart~

    I was not being rude.

    However, you seem to be with your comment about a "big fat ego."

    That is not helping.

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited June 2012

    Himalaya - I had a thought this morning - these people you are talking to here ie the BC.org community - have all had surgery (probably all) and we are here to respond to you - surgery didn't kill us. So our numbers certainly outweigh the 2 relatives you lost. I hope you find a doctor you can trust.

  • Leia
    Leia Member Posts: 265
    edited June 2012

    Leia, here. 

    I will just repeat what others have reported that I said; I believe in surgery if you have a diagnosed cancer. 

    Cut it out. And in both of my cancers (the other one, the 2cm Leiomyosarcoma) were cut out with huge margins.

    Where I stray from what a lot of people choose, is what do you do then. The common medical recommendation after a Lumpectomy, which is what I had is daily whole breast radiation for 4 weeks, and either Tamoxifen or Arimidex, for five years. 

    I have said this before, on this board, but to just repeat it; I only had surgery for my 2006 2cm IDC. My cancer did not return.

    But then, in January, 2009, I had a breast MRI and the result was BIRAD5, certain cancer.  On the same breast. So, I had the biopsy. 

    But before I even got the biopsy results back, my mind was made up. I was going on the Budwig. Even if I had cancer, again, enough. So, I went on the FOCC.  

    A week later, I got the biopsy results, BIRAD 0. No sign of Cancer. But then, the docs did not believe it and wanted me to have an MRI Biopsy. I was like, "What are you talking about?" I refused that MRI biopsy. 

    That was my last interaction with the Medical People. 

    I have been thriving on the FOCC ever since. And September, 2011 had a breast thermogram, totally blue, no sign of cancer activity at the cellular level. Which is where cancer starts. I am not getting another mammogram, again. Unless my thermogram indicates there might be cancer activity at the cellular level. 

    I believe that we can do everything, to heal ourselves. With the FOCC (the Omega3), with an 85 D3 level, with exercise, with a low stress life style.  

    This has been my experience.  

  • sweetbean
    sweetbean Member Posts: 1,931
    edited June 2012

    Leia, how much Vitamin D do you take?  85 is a great level!

  • Leia
    Leia Member Posts: 265
    edited June 2012

    For a person that has had two cancers, 85 is a great level,for me.

     I take 10,000 IUs/day. Although, in the US we are coming into summer, so I will cut back. And get D3 from the sun. I love the sun. And the beauty of the D3 from the sun, our bodies will automatically cut off, when we have reached our maximum level. 

    We do have to avoid sunburn, but just 20 minutes of sun exposure between 10AM and 2PM. That is all it takes. On a daily basis.

    But in the winter, we need supplements.  

    The key for me is self-monitoring. I buy this $45 test, to monitor my D3 level.  $90/year to keep me on track. 

  • sweetbean
    sweetbean Member Posts: 1,931
    edited June 2012

    When I was diagnosed, my D3 level was (brace yourself) 13.  Ugh!  I've been taking 10,000IU's a day and have it up to 47, as of my last blood test.  Sometime in the winter, it fell to around 35, which was distressing.  Where do you buy the test?

    Thanks!

  • Ang7
    Ang7 Member Posts: 1,261
    edited June 2012

    Hey sweetbean~

    My level was 17 at diagnosis.

    It went up to 55 after taking 10,000 for awhile and now per my oncologist I take 3,000 a day.

    I will be retested this summer.

  • candygurl
    candygurl Member Posts: 130
    edited June 2012

    I started taking 8000IU  in the winter and my serum level is now 70 ng/ml. Now that the weather is warming up, I sit in the sun every day at lunch time. Apparently, washing your body with soap the same day can wash away the vitamin D that is being formed there from the sunlight.

    As well, certain medications and caffeine can interfere with the body's ability to absorb vitamin d.  Both can also make the body acidic too. So besides testing your vitamin D level, you may want to get an alkaline test kit. Maintaining proper body cell and tissue pH is absolutely essential for overall health and creating an inhospitable environment for cancer cells to multiply.

  • candygurl
    candygurl Member Posts: 130
    edited June 2012

    Leia, I was reading the Budwig guide. It mentioned that apricot seeds could be added to the FOCC recipe. Have you been doing that or things like tapping, coffee enemas, colon hydrotherapy, apple cider vinegar kidney detox, glutathione infusions etc. that are mentioned in the guide and on www.budwigcenter.com. And do you have a ND? ?

    Also, my ND wanted me to wait until spring to do a 10-juice feast, I noticed that the guide said not to juice spinach. However, it didn't explain why.  After the juice feast, I will do FOCC on a daily basis and some other things. I'll probably do wheat grass enemas once every other week. :)

  • Leia
    Leia Member Posts: 265
    edited June 2012

    sweetbean, I order my D tests from zrtlab.com. Although, just going out to the site, the price is now $75/test. Although, if you access the zrtlab.com site from vitamindcouncil.org, the price is $65/test and $55/test if you order 4 tests. Inflation. 

    I have always ordered the 4 tests, since it is not only me but my two kids, 23, and 20.  

    This is just so cheap compared to most of what else is spent on medical treatments.  

  • Leia
    Leia Member Posts: 265
    edited June 2012

    zuvart, I have been doing ONLY the FOCC of Dr. Budwig's protocol. Nothing further. Although, I don't eat processed foods, or sugar, or anything like that. 

    But, if I did develop another cancer, I would go on the Protocol full time and whole hog. As opposed to the radiation, pills, chemo bent of our current Medical System. As I have said, I first went on the FOCC when faced with another BIRAD5 cancer diagnosis. Which turned into BIRAD0. No Cancer.  

    That was the writing on the wall, for me. I need to take care of myself. If it had been BIRAD5, the total Dr. Budwig, for me.

    At this point, I am glad I got that BIRAD5/BIRAD0 misdiagnosis. It changed my life. Because I just feel so much better, now.

    By now, I almost forget how horrible that I used to feel ... but then, I remember, and enjoy my FOCC.

  • NNBBFL
    NNBBFL Member Posts: 89
    edited June 2012
    I haven't checked in on this thread for awhile and see others asking about coffee enemas on the Budwig plan and mentioning the Budwig Center. To clarify, neither of those are the original Budwig protocol. The Budwig protocol also prohibits supplements. I started the Budwig protocol and diet with FOCC back in January when I had no insurance and could not even get an oncologist to see me. I also knew I was against regular chemotherapy and since I was diagnosed at Stage IV (with bone mets and open wound through the skin) I also did not want surgery. After 3 months on the diet (during which the pain at the tumor site went away) I went to an oncologist who recommended Arimidex. I did start the Arimidex but continued the Budwig protocol knowing that taking anything was a violation of that protocol. But since Arimidex's mode of action is just to keep the body from producing estrogen I felt it would have minimal interference to the Budwig plan. A month and a half later the wound started to heal and is now pretty much healed over. I have no pain and feel great. Of course now that I do both it will be hard to know which is the reason but I feel I am on the right route for me. The Budwig plan should show some results in 3-5 months so I would wonder why someone who admitedly had already tried several things would be on it 14 months and then attribute bad results to that plan. Budwig literature states that most failures are from not following the plan correctly. I understand that I too am compromising it to a degree but still believe that it is working for me. I guess I will know for sure at the next PetScan but for now I am just happy to be in the swimming pool again and feeling great. We all have to find our own path and I think feeling good about which way you choose is also very important.
  • candygurl
    candygurl Member Posts: 130
    edited June 2012

    NNBBFL,  from what I recently read on an old Budwig thread, Chilli's unfortunate situation may have had something to do with eating too much grapefruit. Apparently, grapefruit is a no no.

    Anyways, I'm glad that you're having success on the protocol and enjoying life. And please let us know the results of your PetScan.

  • LuvinMyLife
    LuvinMyLife Member Posts: 65
    edited July 2013

    No one here for a while. Well I haven't posted in a bit. DX in Feb. 13 - I had surgery back in March. Right Mastectomy with node disect.  Triple Negative. Grade 3 - Yeah from the time I felt the lump until it was all done it was like one bad thing after another.

    Before I was diagnosed I had a very low Vit D level. Get ready for it. It was at a 9. I was also diagnosed with Multiple Sclerosis back in 2008. So as you can see the last few years have been S***ty. I have a son that will be 3 in September. I have had every bit of my hope ripped from me slowly over the last 5-8 years.  I knew about Budwig before my surgery but I was so flippin terrified I went ahead and had surgery. The Triple neg and grade 3 freaked me out. I was so upset I had a nervous breakdown.

    Now here it is July 2013 - I will tell everyone with my head held high that i have not taken one bit of chemo or radiation.  The very first scan for me will be in one to two weeks. More than likely an MRI because the doc will want to look for MS lesions as well. Well whatever, kill two birds with one stone. See if you can detect any other cancer because they sure didn't give me a pet or bone scan before surgery.

    I started on the Budwig protocol 3 days ago. I am posting it here because I intend to give updates.  God bless each of you. It's a personal journey and each decision is weighed and above all do what you feel is right in your hearts.

    Much love and I'll report back every so often. Laughing

  • annab22100
    annab22100 Member Posts: 24
    edited August 2013

    This protocol is known to work with cancer. No one could ever claim or prove it was not efficient. Dr Budwig was a few times nominated to the Nobel Prize, but never got it. I think it is a good idea to try. The diet is not that hard and it is rather cheap.

  • Leia
    Leia Member Posts: 265
    edited August 2013

    LuvinMylife, good luck to you! I am looking forward to your updates on the Budwig.

    Here is my update; it is now seven years past my breast cancer surgery and 9 years past my Leio surgery and I am doing Very Well. No cancer recurrence. And I feel great. Still on the FOCC. It has been 4.5 years, by now, and I will be for the rest of my life. And in the past year started taking a Krill Oil Supplement. Just as added insurance. More Omega3s. Anti-inflamation. 

    As I said, long ago, our bodies want to live. Inflamation is what our bodies fight against. The constant toxic attack of our environment. But if we give our bodies the proper tools, they will fight for us.The FOCC, the D3. The anti-inflammatories.

    And my new line of attack; fresh juice. By now, I drink a quart of fresh juice/day. From my great Hurom juicer. I am not claiming this has any breast cancer curative properties, but it does have health properties. And it is just delicious. 

    All of our bodies have cancer cells; the healthy bodies destroy those errant cancer cells. The not so healthy bodies develop cancer. 

    In the years prior to my two cancer diagnoses, my soul mate, the love of my life, died, unexpectedly. Literally, two weeks later, I was laid off from my job of 10 years. And during all that time, I ate nothing but processed foods. Four years later, diagnosed with the Leio cancer. 2 years after that, the breast cancer. 

    Correlation is not causation, but that is certainly interesting. I think I gave myself cancer. Too much stress and I was giving my body nothing to fight it. 

    By now, I am striving to give my body the tools that it needs to prevent cancer. With the FOCC, the D3, the veggie juicing. 

    But the bottom line of it all, I just feel great! Isn't that what living life is all about?

  • annab22100
    annab22100 Member Posts: 24
    edited August 2013

    Leia, I am so sorry what you have to go through. I promise to search for more info about this protocol. I have a book of a Polish doctor who strongly recommends Dr Budwig's diet. I will find it and cite what could be important. I also have another book and there is a recipe about some kind of an ointment made of tulip and some other things  which works as chemo for breast cancer, the book was written by a famous pharmacist (also Polish , I come from Poland). Maybe I will start another thread. I will keep you informed. I am thinking of you, big hugs. Stay strong.

  • GlobalGirlyGirl
    GlobalGirlyGirl Member Posts: 269
    edited August 2013

    Leia - Thank you for sharing your story. I'm sorry for your loss. I am fully convinced that stress caused my cancer, and I, like you, gave my body nothing to fight it. My diet was really crappy - a ton of processed food. I was in a bad car accident in 2008 - rear ended at a stoplight by a minivan going 45 mph. I had to have nerves in my cervical spine ablated - burned (5 procedures). It took almost 3 years to settle after suing the insurance company which did not help financially. I, too, was laid off, but found a job within two weeks, thank God.

    Fast forward to May of this year.  4.2 cm IDC tumor and DCIS. I'm going alternative as well. Curcumin (8000 mg.), DIM, Vitamin D, and Omega 3s. I'm also eating much better than I have.

    I'm in "excellent health" according to my oncologist. I am not going to mess with that, despite the fact that he tried to sell chemo and rads like he gets a commission on it. He's a very nice man and has agreed to keep seeing me even though he was "saddened" by my decision. The tumor is gone, and I had no node involvement. I will give my body what it needs to kill off any of the rogue cells.

  • annab22100
    annab22100 Member Posts: 24
    edited August 2013

    The Budwig Protocol is just based on Omega 3 intake. So sorry GlobalGirly to hear to your story but you are giving much hope. Lots of love.

  • new_direction
    new_direction Member Posts: 449
    edited September 2013

    I have just begun to look into the Budwig protocol and have tried following the diet for the past 2 days. I don't know if it's just "placebo" effect but I actually feel more energized already. I read somewhere the target was around 6-8 tsp of flaxseed oil per day - is this true? What about the grinded flax seeds when hormone positve?

    Leia I noticed you wrote you only did the FOCC part of the budwig diet. That really sounds doable in the long run!
    Im very excited to try this and see what happens. Thanks for posting about your experiences...

  • Leia
    Leia Member Posts: 265
    edited September 2013

    new direction, as you have probably read I have been doing the FOCC since January, 2009. It is doable, in the long run. 4.5 years later, I am still doing it. And loving it. 

    Although, I am on the lower end of what you stated in your message. 4Tbs of cottage cheese to 2Tbs of Flax seed oil is my regimen. But if you have an active cancer, higher levels are better. Just retain the 4/2 level of CC to the oil. 

    Flaxseed has phytoestrogen. From everything that I read flaxseed is not harmful at all for breast cancer patients or anyone. That is just my opinion.  Although, one quote I found "flax contains lignans. Some studies seem to point to flax being able to help fight against breast cancer." 

    Although, at this point, I do not care about "studies." If you have read my posts, you know it changed my life. Literally. As it sounds like it is changing yours. By now, 4.5 years later I can not even remember how awful I was and how awful I felt. Although, I am sorry to say that my kids remember it. Now, 24 and 21, they are slowly getting used to the "new me." But I am winning them over. Because I just feel great. And I have no cancer recurrence after 7 years. With only surgery to cut out the cancer. Back in 2006.

    Please post again how it is going with you. 

    Leia

  • new_direction
    new_direction Member Posts: 449
    edited September 2013

    Leia thank you for your helpful and motivating post. I'm looking into so many things that it does become a little overwhelming... I just ordered 5 books I'm looking forward to reading.

    At the moment I'm doing the FOCC part of the Budwig and avoid sugar and flour. Would it be okay to divide the CC part into half CC and half yogurt? I saw a video where someone blended banana into the mixture but then another place read that it was not allowed to add anything into the blend. Would it be ok to add banana or something else?

    That being said the first few days were easy and I did well. That was followed by 3-4 days where I felt extremely tired, a bit nauseous and thirsty. Now things have begun to get better... I don't know if it's the diet or the fact that I had flu last week and am in bit of a vulnerable state. No matter what, it does FEEL good to be on this diet and although the taste was a little strange in the beginning I find myself looking forward to my FOCC meal!

  • Leia
    Leia Member Posts: 265
    edited September 2013

    New Direction, I believe that it is the protein in the CC and the flaxseed oil that combines with the blending that gives the FOCC its healing power. Yogurt just does not cut it. In my opinion.

    But you said you just ordered five books, so read them and you will make a decision. And as all of us do, do what is right for your own body. 

    You mentioned you felt worse and then you felt better. That makes sense. When your body is full of toxins you will feel worse getting rid of them. And then you will feel so much better having gotten rid of them. 

    And like you, I will always do the FOCC.  Because I just feel so much better. With it. As I have said, I started the FOCC to prevent a breast cancer recurrence; I continue it, because I just feel great on it. 

    It is a Twofer. And the feeling great part is the most important of all. 

  • new_direction
    new_direction Member Posts: 449
    edited September 2013

    I have tried the ketogenic diet as well. I'm searching for the most optimal diet for me... Who knows, maybe the FOCC turns out to be it, like it has been for you. Maybe a combination? What Ive recently thought about was a book which mentioned not mixing protein and carbs. On an upset stomach eat very simple. I thought, maybe eating very simple is good - not mixing a whole bunch of things, maybe just one or two ingredients?

    Just one of many unanswered questions.

    For many feeling-great-days to come.

  • Leia
    Leia Member Posts: 265
    edited September 2013

    Back in 1971, when I was 17, I went on Dr. Atkins ketogenic diet. If by your statment of ketogenic that means high fat/zero carbs. Which is the Atkin's diet. He said you had to achieve ketosis. I did that and I lost 30 pounds in three months. Went from 160 to 130. It was amazing. I was 17, not much food choice, so I ate mostly eggs and Tuna and high fat mayo. And the weight literally dropped off. 

    In that same time frame, the FDA came out with their "Food Pyramid," with carbs at the bottom; eat more carbs! Which by now we know is totally backwards. Oh, and the eat margarine and not that horrible "butter." Which is now totally debunked, as well. 

    By today, I am on the FOCC. Similar high fat/high protein. And thriving. 

    We all just have to choose what is right for ourselves. 

  • bluepearl
    bluepearl Member Posts: 961
    edited September 2013

    The marg vs butter thing hasn't been debunked. Carbs come in two basic forms, complex as in fruits and vegetables and whole grains and simple, as in sugar, honey and those things that act on the blood stream like sugar, as in white bread, white rice, white potatoes. One can safely eat a high protein diet (low fat) in combination with complex carbs; eat strictly high fat protein and ketosis affects the kidneys in a very negative fashion. Margarine is now made without trans fats, butter is still a saturated fat and neither are good for you in large quantities. What gives you healing power is a balanced diet combined with exercise.,,and stay away from simple carbs. Two days a week fasting, either with a 500 caloric maximum OR a two day eating only protein (with a max of 50 g of carb if you want) results in significant improvement for weight loss and blood profiles as long as you aren't goprging on donuts the rest of the week....balance.

  • MsMo
    MsMo Member Posts: 1
    edited September 2013

    This is my first time here looking to see what others are doing. I had a mastectomy 3 weeks ago and a refusing chemo and radiation--I will look into the Budwig protocol. Thanks for the information.

  • new_direction
    new_direction Member Posts: 449
    edited September 2013

    a little update from me.

    I've stopped the diet until I get a clearer picture of what has happened.

    Almost simultaneously with the budwig diet I began having pain under my right rib/ above the liver. I didn't really connect the two until after a while so did the diet for 2 weeks until I decided to try and stop and see what happened.

    Have been off the diet now for 3 days and the pain has gone away. Oh... I've been so worried Frown. Still don't know the exact explanation to this but it seems more likely now that it has something to do with the diet.

    Has anyone experienced anything like this?

    I've never had gallstones but I actually thought it might be something like that although the pain was tolerable. And it was not like attacks but more like a little all the time, especially at night time. Felt like an open sore on the inside.

    I'm kind of relieved because I think I can rule out the worst explanation because of the onset and disappearance of symptoms with the diet. However it would be nice to find the exact explanation... Must say besides from the pain in that area I really felt good on the diet and i also miss my FOCC breakfast...

    Hopefully the pain will stay away the next days and then I might try out the diet for a few days to see if the pain returns again...

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