Multiple Myeloma an incurable disease, but I have spent the last 25 years in remission using a blend of conventional oncology and evidence-based nutrition, supplementation, and lifestyle therapies from peer-reviewed studies that your oncologist probably hasn't told you about.
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A “non-transplant eligible patient” is a patient who is too weak to take the standard-of-care, aggressive high-dose chemotherapy and withstand the collateral damage aka side effects that come from an autologous stem cell transplant.
The article linked and excerpted below features oncologists talking about appropriate drug-combinations for this kind of myeloma patient. In short, conventional oncology gives the non-eligible multiple myeloma patient less chemotherapy than the transplant-eligable patient.
Less chemotherapy and less toxicity can be a good thing for newly diagnosed multiple myeloma patients. Chemotherapy is toxic. The less aggressive therapy a patient undergoes, the less toxicity the patient has to endure. The question then becomes if less chemotherapy sacrifices length of life or overall survival.
My experience as a long-term multiple myeloma survivor is that evidence-based, non-toxic, myeloma therapies such as curcumin (see below), can enhance conventional chemotherapy while killing multiple myeloma at the same time.
I have lived in complete remission from my multiple myeloma since April of 1999 by living an evidence-based, non-toxic, anti-MM lifestyle through nutrition, supplementation, bone health, mind-body, detoxification and more.
Click now to join a free webinar about the Multiple Myeloma Cancer Coaching Program that I researched and designed based on my 22 plus years of living with multiple myeloma.
“For the month of November, MedPage Today, has invited hematologists from leading medical institutions to “de-construct” multiple myeloma diagnosis and treatment. In this first installment, we asked “What is an appropriate drug combination in a non-transplant eligible patient?”
“Conclusion: Curcumin exerts a cytotoxic effect additive to that of lenalidomide on H929 myeloma cells, and it also enhances the chemo-sensitizing effects of this agent.”
“I was first diagnosed with multiple myeloma in ’94. The world of mm treatment has changed radically since then.The link below is to the google search page for “curcumin, myeloma.” Whether it is an article authored by Pat Killingsworth or Margaret, curcumin is documented with both anti-myeloma action in addition to enhancing the action of Velcade, revlimid and thalidomide.”
“Based on a review of these studies, it is evident that better bioavailability of formulated curcumin (CU) products is mostly attributed to improved solubility, stability, and possibly low first-pass metabolism”
A search of the Pubmed database for the word curcumin yields 601 studies spaning health topics from multiple myeloma and colorectal cancer, to chemotherapies that synergizes with CU, to Alzheimer’s Disease, arthritis and more. Based on years of reading studies and personal accounts, I think it is safe to say that CU supplementation is safe and relatively inexpensive.
I have read about myeloma patients taking daily doses of CU from 400 milligrams to 8 grams (1000 milligrams = 1 gram). By almost any measure, CU is a safe, inexpensive wonder drug.
The only challenge is that CU is famously difficult to absorb in the body. In other words, a person has to mix curcumin with some sort of fat (coconut oil, chocolate, etc.) or take a brand of curcumin capsule that is already formulated to be more “bioavailable” in order to derive the full benefit of CU.
The study linked and exerpted below reviews different formulations of CU. The study itself lists the three most bioavailable formulation/brand of CU and I’ve added an excerpt from a further review from Consumerlab.com that lists four additional bioavailable brands of CU.
I consult the independent evaluation service Consumerlab.com frequently. For one low annual payment, I can read about and evaluate all of the nutritional supplement that I take.
“CU is a bright yellow chemical produced by some plants. It is the principal curcuminoid of turmeric (Curcuma longa), a member of the ginger family, Zingiberaceae. It is sold as an herbal supplement, cosmetics ingredient, food flavoring, and food coloring.“
“Curcumin is a widely studied natural compound which has shown tremendous in vitro therapeutic potential. Despite that, the clinical efficacy of the native CU is weak due to its low bioavailability and high metabolism in the gastrointestinal tract. During the last decade, researchers have come up with different formulations with a focus on improving the bioavailability of curcumin. As a result, a significant number of bioavailable curcumin-based formulations were introduced with the varying range of enhanced bioavailability.
The purpose of this review is to collate the published clinical studies of CU products with improved bioavailability over conventional (unformulated) CU. Based on the literature search, 11 curcumin formulations with available human bioavailability and pharmacokinetics data were included in this review. Further, the data on clinical study design, analytical method, pharmacokinetic parameters and other relevant details of each formulation were extracted.
Based on a review of these studies, it is evident that better bioavailability of formulated curcumin products is mostly attributed to improved solubility, stability, and possibly low first-pass metabolism. The review hopes to provide a quick reference guide for anyone looking information on these bioavailable curcumin formulations.
Based on the published reports,
exhibited over 100-fold higher bioavailability relative to reference unformulated CU. Suggested mechanisms accounting for improved bioavailability of the formulations and details on the bioanalysis methods are also discussed.”
According to Consumerlab.com:
“Novasol has the highest bioavailability (185 x compared to unforumulated CU), followed by Curcuwin (136 x), Longvida (100 x), Meriva (48 x), BCM-95 (27 x), Curcumin C3 Complex + Bioperene (20 x), and then Theracumin (16 x).”