For Informed People Using Alternative Treatments
Comments
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Kareeis, Quick question regarding chronic leukemia. A friend of mine has very low white blood cells and has to get tested for leukemia every 6 months. Do you know much about the homeopathic remedy you are taking and do you know if it could possibly help my friend? I don't think she'd be able to afford an ND or if she'd be open to going to one, but I think she'd try a homeopathic remedy. Thank you, Shira
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Hi Kireeus Wow your naturopath sounds amazing! I am considering colon hydrotherapy myself. Overall, did you think it was helpful?
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sorry for stupid questions...what's coffee enemas? i googled it, and you put it in your behind?? can some of you shed some lights?
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Ponyo,
One thing that helped me give up alcohol was reading about the "feminization" of men who drink a lot of alchohol (man boobs). There's a few theories about why this happens, one is that alcohol is a powerful phytoestrogen because of the plants it's made from. Another is that alcohol impedes the liver's ability to get rid of estrogen. So, whenever I consider drinking a glass of wine, I think of it as a glass of estrogen, and that stops me cold. At restaurants with friends I order sparking mineral water. At first I feel deprived, but later in the evening when everybody else looks kind of saggy, and I still feel pretty good, I'm glad I avoided the alcohol.
Ponyo-regarding the citrus pectin, I mix one scoop with a very small amount of water, stir that up, then add more water. Kind of like making gravy. Sometimes I get a couple lumps, but I smash them out then lick the spoon to make sure I'm getting it all. I first started taking it when I asked Dr Darvish about getting something to be radio-protective when I decided to get the pet/ct scan. But I was really impressed when I read the research about it and breast cancer, and I've been testing positive for it ever since.
I admire your ability to meditate. I'm hoping to start. At my naturopath's clinic, there is one person who specializes in helping people do "emotional releases". I haven't gotten to this phase of treatment yet. But I met and talked with her when she was the substitute technician for my Ondemed treatment. I was telling her about how my white blood cells had gone up after taking a homeopathic remedy that basically has nothing in it - the original drops of something are diluted down 300 to 700 times by nothing. She said that it was energy medicine, and that our minds have the ability to be even more powerful. She started having me think of my white blood cells as employees of mine, directing them what to do, praising them. She told me to think of how I would motivate my real (human) employees to work, and treat the white blood cells the same way. So now, when I make my green juice in the morning, I tell my white blood cells that it's pay day! And sometimes I think of my body being like spinach when you wash it. I breath in the clean water, and when I breath out, all the silt and dirt fall into the earth.
Shiraz - I spent twelve years, and have seen many naturopaths before my current one without being able to raise my white blood cells much. I sympathize with your friend. I have no idea if the homeopathic remedy I took will work for her. My naturopath thinks it's the combination of the poly MVA and the Medullosseinum. But I also think it's transdermal magnesium. Before I started seeing this naturopath I did manage to once get my WBC up to 2.3 (normally 1.3 to 1.8) when I worked on absorbing transdermal magnesium In a big way 4 or 5 epsom salt bathes a day, plus massages with magnesium oil, but I couldn't keep that up long term. But I still do some, so now, in addition to everything else, i'm also taking one 20 minute daily epsom salt baths and having my husband give me a daily massage with magnesium oil, just before bed - we bought a gallon size jug of Ancient Minerals Magnesium oil. I feel like for me problems with magnesium absorption have been part of my white blood cell problem. I have celiac, which impedes absorption of minerals. And I also have chronic lyme disease which depletes magnesium. My naturopath thinks i've had the lyme disease for thirty years, and that it "opened the door" for the leukemia to happen after I was exposed to a big dose of radiation at work. I imagine the leukemia then "opened the door" for the breast cancer. Now I'm trying to usher them all out and close the door. A kind of cheap thing to try for your friend would be try out doing two or three epsom salt baths a day(epsom salt is cheapest from Costco), try out the Medullosseinum, and get a bottle of Poly MVA and try it orally. And see what happens. Also, if she hasn't already, she should try giving up gluten and dairy. She too may have absorption problems. And she might want to try 5-L-MTHF. But working with someone would be best. Her insurance may pay for a naturopath, she might want to check. It took me a long time to find a naturopath who could substantially help me, but everyone i saw along the way was able to contribute to some degree. And at least they can order the test to see if she needs 5-MTHF, and figure out if maybe she's got allergies that are getting in the way. Also, there's a pretty cheap juicer at Costco that she might want to get, the jack lalaine one (about $100) was my first one - the plastic got kind of dis-colored afer a year , so I replaced it with a stainlesss steel one, She might want to try to juice greens every morning, spinach, celery, cucumbers, ginger, and half a green apple. No fruit, no sugar, and no alcohol. Good luck to your friend!
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GlobalGirly- I went into colon hydrotherapy reluctantly, and nearly didn't go at all. I think I wouldn't have done it at all if I hadn't begun to gain such trust in my doctor. I really didn't want anybody to touch my private areas. But I'm so glad I did it now. It only hurt my pride to have the speculum inserted. And then the "fill" happens. On the first session, each "fill" lasted only 10 or 15 seconds before I felt pressure and the technician would then release the water. There's two separate tubes, one for water going in, another for dirty water coming out. There's a window, so I could see what came out. It was these hard, black rock like chunks. Before anything big came out, I would feel a kind of shuddering in my body. The technician said that this was because when things break loose, my colon was partially re-absorbing them, and the shuddering was my body's reaction to the toxins. When stuff comes out, she calls the "releases". She told me that some people get cramps, but I haven't experienced that. As I continued the sessions, then "fill" part lasted longer and longer. I think I had one fill that lasted 20 minutes. And I've had some "releases" that consisted of a lot of black stuff, and I felt incredible amount of shuddering as my body let it go. They told me that a lot of people with cancer also have parasites. And sure enough, the day after my sixth colonic, I felt an urgent need, and afterwards, when I looked in the toilet, there were two long (3 inch?) white things attached to black fecal matter, one with a fuzzy head. I was revolted and flushed as quick as possible. I now wish I'd taken a picture so they could have identified them for me. My doctor told me there are probably more of them and to get back in for another colonic as soon as possible, but I have this port surgery scheduled and the colonic therapist's schedule is very crowded... So I'm having to live with the thought of parasites inside me. But I've made myself feel a little better about this by remembering that bacteria and viruses are also living things inside of me, the only difference is that parasites are just bigger. I've never had a colonoscopy. When you do a cleansing prior to a colonoscopy, you're basically cleaning out all the stuff that a colonic clears out. I think that's why the preparation is so uncomfortable for some people, having all those toxins release at once can be overwhelming. The reason I've never gotten one is that my mother told me that her preparation for colonoscopy was the worst two days in her life. She went on to die of cancer three years later, they think it started in her lungs. But I now think I understand why it was so horrible for her. So, I think for somebody like me, getting a series of colonics is a gentler way to get rid of the toxic stuff that's built up.
After each colonic the therapist gives me a handful of tablets to swallow, probiotics and electrolytes, both of which get washed away by the colonic procedure. At home I swallow down fermented coconut water daily to replace the good bacteria and I juice to replace the electrolytes.
Juneping-I haven't done the coffee enema yet. I too only know what I've read on the Internet. My doctor told me to go to sawilsons.com and order their equipment and their special type of coffee(apparently not very roasted and smells like peanuts instead of coffee). There were some instructions on the site, but i'm hoping the equipment comes with more details. i was able to talk a little bit on the phone with them when i ordered. But it still feels very odd to talk aloud about this sort of thing. I'm pretty certain that the idea is indeed that I have to put it in my behind. Supposedly, i will boil up the the coffee and water, let it cool, pour it in the bag, lay on comfortable bathroom floor (lots of towels and i'm lucky to have a heated floor - but a heating pad would probably help comfort too), insert tube, let coffee go in, hold it for 12 minutes, then go to toilet and let coffee come out. The colonic therapist has helped me become more comfortable with this notion. She says that she sees people all the time who want to pretend that they don't have a behind, and she says that she wants to tell them, "look, you brush your teeth twice a day, but there is another very unclean part of you that you completely ignore!"
My naturopath tells me that the coffee will stimulate my liver to release bile that is full of toxins. She says that this will unburden my liver and allow it to do a better job filtering bad stuff out of my body. Estrogen came to my mind. And I guess it unburdens the gallbladder as well. But, I don't know much about the gallbladder yet.
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Kireeus - Thank you so much for that information. I want to go ahead with it. Sounds like the perfect detox!
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kireeus,
thanks for your detailed post.....
my friend recommends me detox regimen as well. two regimens came from two doctors but i am switching to a less intense and more effective regime. they're the same stuff but with different dosage. now after i change to a lower dosage and before each meal, i am gassy after noon (started on saturday)....very embarrassing to be honest.
i am very impressed with your alternative plan / regimen.
i like reading everyone's regimen.
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Wow. This current discussion is way over my head! I don't know what half of this stuff is. hahahaha
On a different note I just wanted to say as a second time BC survivor the more I am reading about mammograms the more bothered I am becoming that I was subjected to so many from ages 28 to 41. I just got done with the book "Breast Cancer: 50 Essential Things You Can Do" and am now reading "What Your Doctor May Not Tell You About Breast Cancer" and both books mention how harmful the continued radiation is -- especially for younger women! Ugh! Not to mention that neither time did a mammogram even help- I found my cancer both times on my own even with recent mammograms done. On a positive note, both books are making me feel even better about my decision to skip chemotherapy both times.
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hipz -
Fascinating. Mind telling us more why no chemo? Which book is better or easier? I want to order it...but can't do both for now. My second opinion is in feb 4 so I want to educate myself.
Thanks...
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Kireeus, that is an amazing regimen you are on. I have to say, I'm not sure I would have the self-discipline to do all those things, even with so much at stake. I am thinking of convincing my husband of the need to do daily magnesium oil massages, though
hpjz, I'm with you on the mammograms. They have given me no helpful information in my life (dense breasts, found lump myself), yet I can't get an ultrasound without having a mammogram first according to my doctors and insurance! Really irritating. I think I will qualify for a yearly MRI, which I plan on availing myself of.
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Kireeus - thanks for your very detailed posts! I also was tested and have the MTHR gene defect regarding folate metabolism -- my nutritionist has me on a similar supplement as 5-L-MTHF. I wanted to thank you for the information for MCP - modified citris pectin - you helped jog my memory regarding this supplement and all it's good qualities.
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I got both books from the library so you may want to check yours if you use it. I am only 50 pages into the second book so can't fairly judge yet but will keep you updated. The 50 Essential things book was good but I think the other one is going to be a little more informative about how to live/ eat to control hormones which I am interested in. Both books stated there is no medical evidence that chemo is effective in breast cancer. Neither are fans of Tamoxifen either, which I am on so I need to check into this more.
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Fallleaves - I think fear is a powerful motivator. Just last year at this time, when BC was something that I thought only happened to other people, I couldn't summon up the self discipline to cut back on drinking a nightly glass of wine, or to cut back on carbs so I that I could fit into my favorite jeans. And then the bad news started rolling in, and I felt very scared. And somehow, the strength to be self-disciplined about diet and alcohol just arose within me. I think it must be a survival instinct that kicked in from all the fear. And I do really believe that the diet and health regime will help me to reduce the CTCs in my blood. I can sense that it's right for me. If I wasn't so confident in that belief, I probably wouldn't be able to stick with it. Plus, I think the hardest part of making diet changes happens in the first two weeks, after that it gets easier and easier.
In the same way, I think that maybe it's fear that motivates other people to submit to radiation therapy and chemo, because for them, they really believe that will help them survive. Which for all I know, is perfectly true for them, and I think it's a brave choice. But I don't have that belief for my particular complicated health situation, so I wouldn't have the strength to force myself to follow that course. My fear gives me strength to go in another direction. Writing this makes me think that maybe that horrible fear that struck me in waves at the beginning of this chapter of my life wasn't all bad after all. It bought strength with it.
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Kireeus, thanks so much for sharing your journey with us. It can be a lonely road for many of us and I'm so glad that we have finally found a safe place to share, discuss regimens and research, and for everyone to find some support, regardless of their individual choices.
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ITA with lightandwind. Thank you Kireeus. It is definitely a lonely road for me. Once I told the oncologist (former) I wasn't doing radiation or chemo, I stopped getting calls from my nurse navigator. Pissed me off and made me sad at the same time.
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Lightandwind, thank you for creating this place. It does help me to feel less alone. Which really helps.
GlobalGirly, I know exactly what you mean. I wanted oncologists and oncology clinics to be about figuring out why I have cancer, and how to get me healthy. But in my experience, they're limited to deciding what chemo will work best,, and then administering it. I've begun to think of oncologists as chemo therapists. In my experience, they don't have any interest in me unless I'm willing to do chemo. But they hold the keys to the technology, the scans and the more expensive blood tests. So I still make appointments with the onc, but I feel kind of guilty about it. I suspect that they make quite a bit of money from chemo, and oddly enough I feel kind of guilty about being a low profit patient. I wonder if they feel that people like me, are a waste of their time.
When my white blood cells went up, I thought the onc and the surgeon would be interested in knowing how it had been achieved. But they had no interest. When I told this to my naturopath, she said that western medicine is about treating emergencies, not about getting to the root of why you're having the problems. So, I suppose that's why they don't know what to do with me if I don't want the chemo. Chemo is kind of the emergency treatment for cancer. And I think that only we ourselves can decide whether to get the emergency treatment, or work on figuring out and treating the root cause or some combo of both.
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kireeus,
You took the words right out of my mouth only more elequently. Thanks for saying my thoughts out loud. Will they be interested in my health if I decline chemo...I always wonder. Sigh...I also feel guilty as well. But will know more after meeting the second onco.
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Hi Pioneer07, where did you come from? I see you just signed up today. Do you have bc? what brings you to these boards? where did you learn of this "survival protein?
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may be she's talking about this link
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Great article Juneping....Thanks for posting.
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I 100% agree about fear being a motivator and that is why so many people just go with the status quo. It makes me so sad for them. I refuse to let fear dictate my heath decisions. My oncologist was very open with me about the amount of thousands of dollars a round of chemo costs the last time I had BC (I asked) and it made my eyes pop out. My health insurance company probably loves me since I haven't had them foot that bill either time!
I saw my oncologist for 10 years the first time around and used my appointments to send him a barrage of questions about the latest news or treatments in BC because I figured I should keep him on his toes! The more I read, the more upset I am becoming that billions of dollars are raised for this disease and yet there is no real progress since my mother had it 40 years ago (except of course surgery wise). It really makes me wonder where all the money is going. (sorry I get into these conspiracy theory moods sometimes!)
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juneping - thanks for calling me eloquent instead of long-winded!
I think talking about this is helping me to kind of be at peace with the idea of being a disappointment to oncologists. Partly because I've begun to accept that all they really have to offer is chemo, and their experience is all limited to treating people with chemo. And, who knows, maybe having to deal with somebody like me who comes in begging for them to just order up a scan or a lab kind of breaks up the monotony of just prescribing chemo and dealing with side effects.
Lacking an oncologist to kind of direct the operation, I rely a lot on my naturopath, but i have devised my overall strategy for myself. After all, no doctor in the US, not even a naturopath, is allowed to tell you not to get chemo. And I don't really disagree with that policy, because I do think it has to be your own decision.
In a nutshell, my overal strategy is: I will monitor for local recurrences with ultrasounds and thermography, probably every three months.
For distant metastasis I will monitor CTCs in my blood every 3 months. The results my first RGCC (Greek test) showed that the CTCs in my blood (8.2/7.5 ml blood) were completely different from the cancer in my tumor. They were triple negative, whereas my tumor was triple positive. The chemo that MO wanted to give me wouldn't have killed them. But I'm hoping that building up my immune system will.
And in the months between monitoring, I will devote myself to getting healthy doing everything the naturopath prescribes.
I recently found out about two websites where women who were treated with chemo and declared cancer free then found out about the Greek test and discovered that they still had CTCs in their blood. I found the websites kind of inspirational because the women worked on their health, and in follow up tests, they bought down their CTC counts.
In case you're interested, the websites are:
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light&wind, you're welcome. i just typed the survival protein and few links showed up...i picked the most popular one.
hipz - i bought the what doctors might not tell you about BC...fascinating. i couldn't put it down. but it's getting late now. need to wind down for bed time. i think my guardian angel has been sending me strong signals ever since...now i have more faith in my intuition. thank God.
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researchers have known about DACH1 for years. it is a tumor supressor, that can be present in estrogen positive and low grade BC. lots of research out there on it.
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Yay Juneping! So glad you got the book and are feeling more confident in your treatment decisions.
Kireeus - I am 100% with you on oncologists - they have no real "new" ideas and to be honest if they did they would be shunned if they used them (my oncologist told me point blank even if my alternative treatments or refusal to do chemo works Dr.s will still just recommend chemo to the next patient - it is just what is done). I wish you the best of luck with your treatment! You are not alone
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question...while reading the book.
If tamoxifen can only put cancer cells to sleep, what happen after we stop taking it? I asked dr Wong and hopefully he'll get back to me. What did your doc say? C is a nightmare
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juneping - I read that 10 years on Tamoxifen is recommended now. http://www.medicalnewstoday.com/articles/261363.php I'm curious as to what your oncologist says. I hope you can share what he tells you.
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I will for my second opinion appt in feb.
At the meantime I hope dr Wong gets back to me as well.
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Dr Wong teas tastes awful! Lol
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I don't mind Dr. Wong's herbs/teas! I actually drink them room temp out of the bag!
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