Radical Remission Book Club by Kelly A. Turner, Ph.D.

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  • AmyQ
    AmyQ Member Posts: 2,182
    edited June 2016

    Hi Carol,

    Thank you for starting this thread and I agree with your philosophy, modify your diet but still enjoy some unhealthy from time to time. If I was as strict as some are, I don't view that as a good quality of life.

    Amy

  • DistrictGirl
    DistrictGirl Member Posts: 50
    edited June 2016

    I was just recently diagnosed (I start chemo on June 27) - this was the very first book I read!! I LOVED it - think it should be required reading :)

    I was very anti-chemo at first, but since I'm HER-2+++, every single doctor was very firm about me doing chemo - even the naturopath doctor! So I've come to terms with the fact that it's the best option for me, but am definitely taking all of these principles to heart so I can treat this well!

    Luckily I've already drastically changed my diet - I began getting very intense GI troubles beginning in March and have been on a very clean diet and a lot of helpful vitamins and supplements since then. Non-coincidentally, the docs think my tumor started acting up and growing around that timeframe, so I think my IBS was really just my body's way of talking to me and letting me know something was wrong. I never would have noticed this small-ish tumor if I hadn't been listening to my intuition!

    My hospital has a Center for Integrative Medicine, where I just started working with a Naturopath Doctor in addition to my chemo. If you have access to a resource like this, I highly recommended meeting with them for some expert advice on tapping into the suggestions in the book. Everything gets run by my MO, but she seems to be open to almost everything. The ND also runs every supplement through this system that checks it against your chemos and other meds to make sure there are no interactions. Great resource to have. We're currently doing supplements (approved ones), meditation, acupuncture, and exercise. I'm considering doing mistletoe injections and vitamin C infusions.

    I'm also making sure I smile and laugh a LOT every day, and have started a daily gratitude practice :)

    I love reading what you all think of the book and how you're incorporating these principles into your self-care. Thank you for sharing!

  • Longtermsurvivor
    Longtermsurvivor Member Posts: 1,438
    edited June 2016

    Hi DistrictGirl,

    It's good to meet you.

    If you do decide to try mistletoe, be sure to look me up. I've done quite well with it for 20 years!

    Here's a mistletoe resource you may not have found yet:

    http://www.believebig.org

    best healing wishes, Stephanie

  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2016

    Welcome District Girl! I am going to speak with my MO at the end of the month on all the questions I have about supplements and if she would recommend a Naturopath Dr to help with some of this. There is way too much controversy regarding supplements that I know nothing about certainly want to learn more.

    The two drugs that are helping me are also kicking my butt right now. Ibrance/Let I am very arthritic and really have to push myself to get the proper exercise. I have been away visiting grandkids and family that I have let a few things slide. Ready to get back on track again.

    Carol

  • DistrictGirl
    DistrictGirl Member Posts: 50
    edited June 2016

    Thanks Longtermsurvivor and LovesMaltese!

    Longtermsurvivor - I'll be sure to reach out!

    LovesMaltese - I was really amazed by my naturopath doctor. I met with her again today to finalize the gameplan for when I start chemo in a few weeks. It is so complicated - I could never figure out this on my own without a degree! She had to check the components and potential interactions with each and every supplement against the cocktail of chemos and targeted therapies I'll be having. I was really surprised to hear her say that I need to stop curcumin and a few other things when I start chemo, I never would have known that. She's also good about working with the MO - helps that they work in the same hospital system I'm sure. Maybe they can help with the arthritis too?? Good luck!!

  • HLB
    HLB Member Posts: 1,760
    edited June 2016

    Curcumin works really well for arthritis. It's too bad it is contraindicated with your treatment. I have no idea if I shouldn't be taking it but I am.

  • catsteme
    catsteme Member Posts: 48
    edited June 2016

    Thanks for starting this thread. I downloaded the book today on my Kindle and then coincidentally came across this thread. So far I've only read the first chapter on nutrition and am not sure I have the will-power to take it all on board. Though, if it gives me more time with my family I'll give it a damn good shot.

    I also believe that stress and a weakened immune system have a lot to answer for. My primary and secondary diagnoses both came during periods when I was under considerable stress and recovering from a seasonal virus.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2016

    Cath- Welcome to the discussion group!

  • Longtermsurvivor
    Longtermsurvivor Member Posts: 1,438
    edited June 2016

    Very long post, sorry!

    I admit to having mixed feelings about this book.

    I love that author Kelly A. Turner researched folks who've experienced Radical Remission from cancer and brought her findings to readers in an approachable, readable book. It's not a difficult read - she manages to skim right over difficult statistics, vocabulary and content that might muddle our minds.

    I am someone who's achieved radical remission by her standards (The American Cancer Society (ACS) states that the five-year survival rate after diagnosis for stage 4 breast cancer patients is 22 percent. This percentage is considerably lower than at earlier stages. At stage 3, the five-year relative survival rate is 72 percent. At stage 2, it's over 90 percent. Feb 19, 2014).

    20 years ago chemotherapy failed me and I took up anthropsophic medicine and Iscador while continuing to incorporate conventional and unconventional medical treatment options. No one expected me to see my next birthday.

    image

    40th Birthday 1996

    Because I have a rare and serious genetic condition, I've been blending alternative and medical treatments since my teens...stepping well off the well trodden tried and true path. For many years, I've been more focused on quality of life than quantity. Gradually, without intending to, I've outlived one prognosis after the next.

    But, because of my experience, I'm reluctant to be called an inspiration and I don't often share my survival secrets. What I've found is that other patients must walk their own paths - some will adhere and some veer wildly from the medically tried and true. And while some profess to wanting to follow my lead, it soon becomes apparent that what's worked for me, is unlikely to work for others.

    I prefer to listen deeply for what is being called forth from whoever I'm listening to and then responding based on their needs. Maybe I can offer one slim clue to lead them further along their maze-like path.

    And I do believe that healing can be a transformative journey, a quest, that initiates us to new ways of being, living and dying. This is based on my own experience and what I've witnessed in many others.

    MBC is Not a "Journey" https://community.breastcancer.org/forum/8/topics/...

    I chose to reread the Radical Remission chapter on intuition first, because intuition often informs us of the right next step in our "cancer journey". Gut feelings, guidance, higher wisdom, intuition, call it what you like, has been my constant companion whether I'm deciding on treatment options, life course steps, who to trust. When I tune in, I learn. When I tune out, I get further and further from my own truth.

    The chapter was okay, a bit simplistic, until I got to the radical remitter Susan saying, "I believe very much that the diagnosis of cancer - or the energy that was stuck in my body that appeared to be a mass or a tumor and which my doctors called "cancer" - was caused by these patterns that I was describing to you that don't get released, that are continually overlaid, over and over and over, wherever they are. So, if it's kidney cancer, it's probably excessive fears; if it's lung cancer, it's grief of some sort that hasn't ben resolved. I think they can very much be tracked back to thought patterns that are not releasing and therefore they hold in the cell memory." (emphasis added)

    I think she's on safe ground when speaking of her own experience with pancreatic cancer, but veers into dangerous territory when making generalizations about other people's cancer causes and experiences. She's building walls where I believe bridges are needed. Since she's teaching and has clients, she's set herself up as a guide to the territory. (It doesn't really bother me that she hasn't returned to her doctors so has not definitely confirmed the disappearance of the cancer with Western medicine's scans. That might be a deal breaker for other readers though.)

    I think that telling someone else the cause of their cancer is very iffy - whether one is focusing on energy patterns, genetics or lifestyle choices. There is very little clear causation in cancer, though a whole lot of correlation!

    This book is problematic for me when Dr. Turner goes from describing what others have done to suggesting action steps that read more like recipes for success than things to try...because they improve quality of life in the short and/or long term.

    I've had to face the fact that most cancer patients aren't going to change their diets, lifestyles, coping mechanisms, belief in the medical-industrial system and medical materialism or the efficacy of CAM/Integrative/Holistic approaches to healing. Even members of support groups like bco will deny the value of support groups! I've also had to face the fact that dozens of my intimate friends have died, in spite of trying harder to live than I have. To claim a recipe for success, then one must explain the "failures" too and I just don't see my friends as failures! Or having lost their battles against cancer (UGH!).

    Odd and interesting facts of life. I needn't agree or disagree with others to build a bridge and keep communication open between us. Now, connection and loving kindness are what I most value.

    I'd rather be happy than right!

    It's hard enough to intuit what's right for me, I don't dare tell others what action steps to take. I guess that's why I'm a bumbler and she's an author though. (Laughing at myself).

    be well, my bco friends, Stephanie


  • 3-16-2011
    3-16-2011 Member Posts: 559
    edited June 2016

    Longtimesurvivor Another beautiful post. I have started this book and have my own ambivilance. I do see the work that went into this book as an act of grace and love for all of us. (Here comes the but) However, I do feel the shoulds at the end of the chapters. This brings out my unattractive, likely unhealthy, oppositional self.

    I think my true difficulty is my fear of hope. If I could let go of this fear and embrace hope the instructions at the end of the chapters would read as lovely recommendations I could keep or let go.

    I will continue reading as the beauty of this book is it is helping me to face my fear.

    Peace to all

    Mary

  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2016

    Steph and Mary, Thanks for your thoughts, I have so much to comment on and I will as soon as my weekend guests leave. Especially Steph where you said "connection and loving kindness are what I most value" and Mary my feelings are the same as yours. Fear of Hope-- looking forward to responding soon.

    Have a great weekend.

    Carol

  • singlemom1
    singlemom1 Member Posts: 434
    edited June 2016

    Hi all,I just saw that Dr. Turner is having her first weekend workshop on radical remission at the Omega institute in New York. It is sometime in October 2016. I am going to try and attend if I can.

  • Longtermsurvivor
    Longtermsurvivor Member Posts: 1,438
    edited June 2016

    Long again, no apology this time.

    I woke up from a nap thinking about radical remitters, exceptional patients, inspirations, authorities and survivors.

    It happens less often now, but I still get my knickers in a knot when someone with early stage cancer of any organ claims to be a survivor a very few months out of treatment (whether mainstream, holistic or alternative). No, what really knots me is when they become a cancer coach and go on to give survival lessons to all and sundry without even realizing what they don't know or can't do.

    Many years ago, I could have gone that route. I had advanced breast cancer and was doing well on alternative treatments after mastectomies. Yes, the cancer continued to grow, but it was slow and my quality-of-life good. My name and home phone number circulated widely.

    One cold, dark and rainy night, I received a call:

    Her: Hi, is this Stephanie, the survivor who beat cancer?

    Me: Er, this is Stephanie.

    Her: Good, I need your help. I need to know what you did.

    Me: Mmm, okay, what's your situation?

    Her: My mom's cancer is out-of-control and she won't try any alternatives. The doctors are killing her with chemotherapy and now they say she's going to die.

    Me: Well, has your mother ever been interested in alternatives?

    Her: No! That's her problem. She doesn't take care of herself, then expects the doctors to give her some drugs to make everything okay.

    Me: Em, if she hasn't shown any interest in self-care thus far, what makes you think she's interested in following a fairly rigorous regimen now?

    Her: I don't want my mother to die! (hint in voice that I'm trying to kill her mom too).

    Me: Oh, I see better now.

    Basically, I fielded dozens of these types of calls and queries. Even when the caller was the patient, not the carer, very few really wanted or were able to DO everything to heal their basic life/health/medical situations. Or, it was too late. Or there wasn't any clear answer or approach. Or, most likely, my way wasn't their way.

    There was so much emotion bundled in those innocent questions about what to do next/now.

    What I did next was to become a volunteer hospital chaplain where I learned to listen to others as they spoke about disability, disease and dying (their own or a loved one's). I learned to listen to what happened in their hearts and psyches on recognizing limitation and mortality. I learned to listen to help them discover their very own unique next steps to peace and well-being. When others look to me to be an authority, I listen first and reflect back to them.

    Yes, I still read dozens of medical journal articles, textbooks, popular press books on all types of healing and have followed the work of some mainstream and very offbeat practitioners. But I don't give authorities my power or grant them responsibility for my well-being. I've even learned to forgive my mainstream healers for being human and having very limited medical toolboxes. That way, I'm gratefully surprised when they do help me with medical problems. Medical care is often necessary, but not sufficient for my healing/wholeness.

    I can't help but notice how many metastatic patients are part of this topic/thread. We are all playing a very high stakes game for keeps. Most of us are women, conditioned to be good and do the right thing - we want there to be a course or recipe to follow to get the results we want.

    Mary is so right, we want the prescription for healing, but we're afraid to try it and get our hopes dashed again. This leads us to rebel - to thumb our noses at authorities, including Dr. Turner. What a conundrum!

    Yet, the longer I'm at this, the more I think - there's not a right way or a wrong way. Not a "my way or the highway". Just an endless free fall into the unknowable. Being able to withstand that gravity-free, pathless existence calls forth new powers. And most of us don't have the time or inclination to do it. Instead, we must reach for an authority who seems to have the answers...until we don't get the results we so desperately want and are dis-appointed and find ourselves in don't know mind again.

    It can become a vicious cycle.

    Okay, off to read a wonderful book now!

    Healing regards, Stephanie

  • eelder
    eelder Member Posts: 169
    edited June 2016

    I really enjoyed this book. I was diagnosed in late March 2016, but only read it this past week. What's interesting is I started doing most of the 9 things she mentions the day I was diagnosed. I wasn't told to do these things.... I intuitively felt I needed to change. The first book I read upon my diagnosis was a Traditional Chinese Medicine book for breast cancer. This helped lay the foundation for me - the need to change.... the need to manage stress.... the need to adjust diet and exercise and focus on supplements. The TCM book talked about how we need to change the landscape of our bodies if we expect to assist western medicine to turn this around. It made sense then and it continues to make sense now. So I did just that. My diet changed drastically.... I started walking 4-5 miles a day.... I started meditating (my Type A self never thought I could relax enough to do that!)... I started focus on stress management.... I left my teaching job of 17 years to focus on me. Will any/all of this help? I sure hope so. But I don't know. And then I read Radical Remission. While I haven't incorporated all 9 things, I have put in most of these changes. I choose to be hopeful. I choose to be optimistic. And if others experienced success by doing some of these things then I want to believe I could too. After reading some of your posts I feel I might want to find a naturopath doctor that could help me along side my oncologist. I love my oncologist, but I intuitively feel I need more. I don't think you can tackle this from just one angle.


  • Andi67
    Andi67 Member Posts: 423
    edited June 2016

    I finally bought this book yesterday. Halfway through Chapter One, and can't wait to continue. I already know I need to change my diet even more than I already have....I have always been a sugar addict, so that has been the hardest change. After the few pages I have read, I know I will be cutting out dairy. The only thing that surpises me is that exercise isn't one of the 9 things, although I know she mentions it in the introduction. I truly believe that it should be...it's something that I try to do one way or another, every day. When I was going through chemo, I felt so bad I didn't even make myself walk to the mailbox, and it took me at least two years to recover from that complete lack of motivation.... now I totally push myself.

    Anyway, so glad to have this thread and the encouragement to read the book, and love the input and additional suggestions from all of you!

    XO

    Andrea



  • eelder
    eelder Member Posts: 169
    edited June 2016

    Andi67, I too was surprised to not see exercise as one of the 9 things! My oncologist, breast surgeon, and several practitioners ALL said the single best thing one can do in my situation is to exercise daily.... even walking for 20-30 minutes! Walking helps control glucose levels, improves mood, helps with losing weight/keeping in shape.... we all know this - the list goes on. It also helps move the ibrance around in your system and lessens side effects. On the days I don't go walking I definitely feel more sluggish, sad, and anxious. I believe in my heart the changes outlined in this book (including exercise) can make a difference. That said, I am hoping ibrance does its job too!

  • Longtermsurvivor
    Longtermsurvivor Member Posts: 1,438
    edited June 2016

    I'm learning so much from everyone's comments and really appreciate your viewpoints and experiences. I agree about being surprised that exercise isn't one of the nine. Keith Block's Life over Cancer has a couple of excellent chapters on the topic, for those interested.

    Thank you for participating!


    This is an early resource on Spontaneous Remission that is available in full at no cost.

    Spontaneous Remission: An Annotated Bibliography

    By Caryle Hirschberg and Brendan O'Regan

    http://library.noetic.org/library/publication-bibl...

    I actually had the book in my hands and read much of the 700+ pages. It's a tome, but convincing.

    Healing regards, Stephanie

  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2016

    Steph- It is so important to be happy rather than right- I work on that every day- My daughter's (a few months ago) said to me that I was not happy anymore. I felt like I was in denial and believed they were wrong about how I felt, but they were 100% right. I realized I had built this angry block around me that was filled with pity. I was angry at myself, (after an 18 year remission) what did I miss that should have been detected before I had to have a rod inserted in my leg? I really was upset with the MO that I got from a trickling down of MO's that left within the 18 year remission. Follow up protocol should have done more. I had this need to blame someone--

    What I would like to do next is find a Naturopath MD that can help me with supplements, I am not great at researching on line, too many controversial opinions. Especially with ER/PR + My diet has been perfect up until this weekend where I enjoyed some wine and some chicken which I have not had since October. Funny thing, I loved the wine... the chicken didn't taste like oh wow I miss this. I am focusing on sprouted grains for bread and cereal- and follow mostly vegan during the week- Not vegan for me is the times I add in salmon or steamed clams- Never dairy- that was the easiest for me to give up.

    I was notified by email that there is a weekend course (not far from me) in October (taught by Kelly Turner) that I may attend. I bet the workshop would really help with each chapter. I have the book on audio as well, and will listen to the chapters that I need to do better with. I was so tired the other night that I fell asleep listening to it.

    Steph- also thanks for the link to Spontaneous Remission, I am going to venture there later today.

    I also want to welcome Andrea! I hope I didn't miss welcoming anyone- if I did it was unintentional.

    Carol

  • ClarkBlue
    ClarkBlue Member Posts: 170
    edited June 2016
    DISTRICTGIRL - you and I have similar stats and are both on Taxotere. Would you mind sharing the supplements that your MO cleared? I am currently only taking Omega 3s, Vitmain D3, Biotin, and Keratin. Am staying away from any antioxidants until chemo is over, and have switched to almost entirely plant-based/organic diet (still have organic half & half in coffee and will enjoy organic/hormone free eggs).

    I ordered the RR book today. I also read the Anti-Cancer book mentioned on other threads and LOVED IT. It gave me another avenue to pursue in addition to the MO/RO recommended therapies. Boosting my immune system and leaning down are my #1 priorities right now. Secondarily I want to reduce/avoid inflammation and build muscle/bones. I want to do this primarily through diet and exercise, but also realize that some supplements are necessary to combat things (Omega 3s and vitamin D3) that I cannot control through diet. I live in MI where we just don't get enough D3 over the course of the year. These "feel right" in addition to the chemo/radiation/hormone therapy that is recommended for me. I know I have to eliminate the estrogen, and boost my immune system to fight off the cancer on its own, all while feeding and caring for my body to give it the best chance to heal itself. I also understand that even with all of this, there is no guarantee that it won't return - but I will have no regrets.

    -Keely
  • eelder
    eelder Member Posts: 169
    edited June 2016

    What would you all say are the *key* things we need to be doing to boost our immune system? Based on everything I've read that obviously seems to be the best way we can help our bodies fight off the cancer naturally.

  • ARCats
    ARCats Member Posts: 137
    edited June 2016

    Carol, thank you for bringing up this board and everyone else on all your comments about health issues and Radical Remission. I was on Amazon and will go back today to order this book. I've always wanted to know about health and how to better my chances of never having a recurrence or anything like this again. I had to stop Tamoxifen and restart again because of the SE's I was getting, so eventually I want to stop it all together but I may just take it every other day or something like that. I'm not sure what I'm going to do.

    I would like to ask does anyone recommend a easy cooking book that I can start looking at? Also, I was looking at Raw Food Diet as a possible way of maybe adding that to my new way of eating. Anyway, any recommendations that you all make will help me start looking at what's out there in the world of healthy eating.

    Thanks,

  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2016

    Eeller- Great Question!! I like to do as much as I can naturally with the foods I eat. I know how important dark green veggies are so I eat a ton of them and I am spending much more time outside breathing in the fresh air. I have the QiGong CD's that I ordered and will be starting with that soon. I also have had one Riki session, and plan on working with someone to help me with meditation. I take the following supplements: Calcium, Vit D, magnesium, Vit C and turmeric. I also have my medical marijuana card and did a 1:1 CBD:THC- for a few weeks, but I have not continued with that, but may in the future. Studies show that higher THC interferes with estrogen so for BC higher CBD is better- I would love to do some Yoga, but I need to find the right class that I could attend.

    Carol

  • Longtermsurvivor
    Longtermsurvivor Member Posts: 1,438
    edited June 2016

    Hi ARCatz,

    Rebecca Katz has two great cookbooks for folks facing cancer - One Bite at a Time and The Cancer Fighting Kitchen.

    http://www.rebeccakatz.com

    For most folks the raw food diet is difficult to follow after a detox period of 1-4 months. The best time for it is in summer when our bodies are able to live with less fuel/food. Nuts, seeds and avocados are used for protein and fat, but can create gas. Over the long term, most folks focus on whole foods and combine raw with cooked foods in some ratio.

    For folks on chemo, with weight loss, taste changes, disease progression or recovering from surgery, the raw food diet wouldn't be supportive enough to regain bodily strength and integrity.

    The Anticancer book has more great diet ideas.

    I've been addressing my health needs with diet and nutrition for all my life. My mother was a dietician and I entered the natural foods world as a teen. Believe me, I've seen and tried every possible Health Food Diet from raw to macrobiotic to Weston A. Price.

    A diet focused on the rainbow foods, complex carbohydrates and adequate good fats and protein is what works best for me. Avoiding the toxic SAD (standard American diet) is a good way to go.

    Healing regards as you expand your nutritional world, Stephanie

    Eat food, not too much, mostly plants. ~ Michael Pollan

    Michael Pollan's "Eat Food" Diet

    Summary:

    Eat food, "Food" defined as:

    1. Don't eat anything your great grandmother wouldn't recognize as food

    2. Avoid food products containing ingredients that are:

    a. unfamiliar

    b. unpronounceable

    c. more than 5 in number

    d. or that include high-fructose corn syrup

    3. Shop the peripheries of the supermarket and stay out of the middle

    4. Get out of the supermarket whenever possible

    What to eat, mostly plants

    1. Eat mostly plants, especially leaves

    2. You are what what you eat eats too

    3. If you have space, buy a freezer

    4. Eat like an omnivore

    5. Eat well-grown food from healthy soil

    6. Eat wild foods when you can

    7. Be the kind of person who takes supplements

    8. Eat more like the French, Italians, Japanese, Indians, or Greeks

    9. Regard non-traditional foods with skepticism

    10. Don't look for a magic bullet in traditional diets

    11. Have a glass of wine with dinner

  • DistrictGirl
    DistrictGirl Member Posts: 50
    edited June 2016

    ARCats - My mother-in-law (who has multiple myeloma) sent me the Soupelina cook book, which she swears by. I have to say I really love it! I've only cooked a few recipes but they're all really delicious, and she does a good job of explaining how each ingredient supports your health and fights cancer. The author is a breast cancer survivor.

    ClarkBlue - Here's my supplement regimen so far (starting chemo in a week, may need to be adjusted). Huge disclaimer that this is my specific plan that my doctors deemed appropriate for me based on my treatment, age, test results, etc. Please ask your doctors before proceeding with any of this, everyone is different! :) I'm meeting with my wellness coach today to create a plan to phase some of this stuff in over the next week before chemo and to figure out when to take each of these every day (so i'm not taking 32342309480239 pills at once!)

    To support my heart while on Herceptin:

    • Fish Oil - Omega 3s (I use the lemon-flavored liquid Nordic Naturals) - at least 3000mg - WITH FOOD
    • CoQ10 - 100mg
    • Vitamin E - 800 IU/day
    To help prevent/treat GI side effects from chemo: (note, I have minor IBS so I do the top 3 things every day anyways)
    • DGL tablets (I LOVE the german chocolate flavored ones) - 2 before every meal and as needed for heartburn/indigestion/nausea
    • Swedish bitters - 1 tsp before every meal
    • Digestive enzymes - 1 tablet with each meal
    • L-glutamine powder (I use Metabolic Maintenance brand) - 3g, 2-3x/day
    • Probiotics (I have Klaire Therbiotic Complete Powder, this is super potent at 100 billion count, whereas I was taking 10B before. going to gradually work this in) - 1/2 tsp 2x/day
    My Naturopath Doctor recommended I mix the L-glutamine with the probiotics with water at least once a day to swish around in my mouth and then swallow so I get a good coating that will help prevent and/or heal mouth sores. Can also put the powders in smoothies
    Other cancer-fighting stuff...
    • Vitamin B (she was very specific about me getting this particular brand - Metabolic Maintenance phosphorylated B-complex) - 1 daily WITH FOOD (can upset tummy)
    • Vitamin D3 along with Vitamin K2 - 4000-10000 IU/day (will depend on my D3 lab results, currently taking 4000)
    • Melatonin - 20mg /day before bed
    • Magnesium - 200mg
    Note - while Curcumin and EGCG (green tea complex) can be great for cancer-fighting, she told me to stop taking them because of my particular chemo cocktail, apparently it wouldn't mix well. Something to keep in mind and explore.
    Miscellaneous...
    • I'm getting my melatonin and magnesium in a formula called Prothrivers Wellness Sleep. It also has Theanine, which my ND described as "Nature's Xanax" - has a calming effect.
    • I switched my allergy meds from Allegra to Claritin since it helps with Neulasta side effects
  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2016

    Arcats- I will give you a sample of what I eat on a very dedicated good day which is today!

    Breakfast: Toasted sprouted english muffin- avocado (in place of dairy or fat) topped with wilted spinach.

    Lunch- Lentil soup, steamed broccoli with olive oil and lemon, roasted green beans with coconut oil, fresh grapes and strawberries, and yesterday I roasted some beets and turnips and made a veggie puree by adding in vegetable broth and nice red pepper to the food processor. So when I am craving junk I eat some of that... and I have not thought about dinner yet, just know that I have a bottomless stomach today-

  • jensgotthis
    jensgotthis Member Posts: 937
    edited June 2016

    I love whole wheat toast with avocado on it! When I do that for breakfast I add a protein smoothie made with greens, berries and my Sun Warrior protein powder.

  • Longtermsurvivor
    Longtermsurvivor Member Posts: 1,438
    edited June 2016

    Best Avocado toast recipe - from Smitten Kitchen

    nolita-style avocado toast

    http://smittenkitchen.com/blog/2016/03/nolita-styl...

    One thing I think about often is food combining - very popular in the 1970s and 1980s, seems to have fallen to the wayside in more recent decades - but anyone with digestive and tummy troubles should consider this -

    Here's just one of many online resources:

    image

    Best healing regards, Stephanie

  • txmom
    txmom Member Posts: 306
    edited June 2016

    Hi I read the book when I was diagnosed last year and made a lot of life changes as well.  As far as diet, I lost 50 lbs eating a mostly vegan diet.  I do eat some salmon and organic eggs as the omega 3s are good for brain functioning.  I also use a whole milk probiotic for gut health.  When I'm down, I read the website blog stories on radical remission.  I don't really care what kind of cancer.  I think all the stories are inspiring.  It gets me out of my funk.  My daughter makes me a frozen banana "ice cream."  You get 2 bananas and freeze them, once frozen you put them in a blender, once blended add your whatever u want such as vegan chocolate chips, cocoa powder, agave syrup, strawberries, peanut butter and then refreeze.  It's really good for a sweet fix.  So glad this thread was started. XO

  • ARCats
    ARCats Member Posts: 137
    edited June 2016

    This is great! I've printed everything, and I plan on using the information.

    Thanks again,

  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2016

    Laughter- I need to laugh more- But How? I do not find watching stand up comedians very funny anymore. I wonder if something is wrong with me? I would love to really laugh so hard that it hurts. I can't remember the last time I did that. Doesn't it feel so good after?

    I need to download some "I Love Lucy" episodes- any more suggestions?

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