Recently Diagnosed or Relapsed? Stop Looking For a Miracle Cure, and Use Evidence-Based Therapies To Enhance Your Treatment and Prolong Your Remission

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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Multiple Myeloma Therapy- Healing Lytic Lesions

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“In conclusion, 1-yr treatment with melatonin (mel) increased BMD (lytic lesions) at femoral neck in a dose-dependent manner, while high-dose melatonin increased vBMD in the spine.”

I’m a long-term survivor of a blood cancer called multiple myeloma. According to research, 90% of all MM patients will experience bone damage aka lytic lesions at some point in their lives.

Maintaining bone health is a life-long pursuit for all newly diagnosed MM patients. Newly diagnosed MM patients often ask if their bone damage can be healed.

Conventional oncology says no. Those MM patients who are diagnosed with lytic lesions will not heal their bone damage.

My experience says that I have healed my own extensive bone damage. But this healing didn’t happen overnight and it took a mult-therapy approach to my bone health.

The trick is to figure out how to build bone strength with inexpensive, non-toxic multiple myeloma therapies. Melatonin is an excellent example of an inexpensive bone health therapy.

Further, many multiple myeloma patients struggle with circadian rhythms and sleep. Active therapies or long-term side effects can bother us. Keeping our bones strong and healthy is almost the same as keeping our cancer in remiss

Which brings me to the focus of this post. I take melatonin. Studies show that melatonin is a cancer therapy that increases bone mineral density. Melatonin supplementation helps me enhance my immune system as well as heal my lytic lesions.

The article linked and excerpted below explains that melatonin works in “dose dependent manner” meaning that 1 mg helps a little but 3 mg. helps a lot.

Ed. Note- I wrote those first paragraphs more than five years ago. Since then I discovered that melatonin is good for my chemotherapy-induced cardiomyopathy. So I’m adding heart damage to the list of healing properties of mel.

Below that study is research talking about mel. and MM. The research equivocates on the benefit of melatonin and MM. Each MM patient must decide for him/herself.

The brand of melatonin linked above, Life Extension Melatonin 1 mg  has been tested and approved by ConsumerLab.com and is pennies per dose.

Evidence-based, non-toxic therapies to heal lytic lesions-

  • Frequent, moderate exercise,
  • Nutrition (green leafy veggies, etc.),
  • Nutritional supplementation (melatonin, magnesium, vitamin k, etc.)

and more, scroll down the page, post a question or comment and I will reply ASAP.

thank you,

David Emerson

  • MM Survivor
  • MM Cancer Coach
  • Director PeopleBeatingCancer

Recommended Reading:

Multiple Myeloma Therapy, Magnesium, Bone Mineral Density

Mel in Heart Failure: A Promising Therapeutic Strategy?

“Conclusions- As highlighted in this paper, HF is a complex clinical syndrome with two predominant etiological aspects, ischemic and non-ischemic HF. In view of the significant alterations of melatonin levels in HF patients, the exploration of the role of melatonin in HF is clinically relevant. So far, results obtained from recent preclinical and clinical studies are promising. Administration of melatonin reverses major pathological processes associated with HF including oxidative stress, apoptosis, necrosis, fibrosis and pathological remodeling (Figure 2). Though additional mechanistic studies are still required to delineate the underlying mechanisms of the effect of melatonin in HF, melatonin is an important, safe, and affordable molecule worthy to be used as preventive and adjunctive curative therapy in HF.”

Melatonin improves bone mineral density at the femoral neck in postmenopausal women with osteopenia: a randomized controlled trial.

“Mel is known for its regulation of circadian rhythm. Recently, studies have shown that melatonin may have a positive effect on the skeleton. By increasing age, the melatonin levels decrease, which may lead to a further imbalanced bone remodeling…

Compared to placebo, femoral neck BMD increased by 1.4% in response to mel (P < 0.05) in a dose-dependent manner (P < 0.01), as BMD increased by 0.5% in the 1 mg/day group (P = 0.55) and by 2.3% (P < 0.01) in the 3 mg/day group. In the melatonin group, trabecular thickness in tibia increased by 2.2% (P = 0.04), and volumetric bone mineral density (vBMD) in the spine, by 3.6% (P = 0.04) in the 3 mg/day…

In conclusion, 1-yr treatment with mel increased BMD at femoral neck in a dose-dependent manner, while high-dose melatonin increased vBMD in the spine.

Serum melatonin in multiple myeloma: natural brake or epiphenomenon?

Melatonin (MEL), the main hormone produced by the pineal gland, seems to exert antineoplastic activity both in vitro and in vivo. Moreover, several studies reported increased melatonin blood levels in cancer patients.

Plasma mel concentrations were determined in 46 patients with multiple myeloma and in 31 age matched healthy subjects (57.8 +/- 6.9 versus 55.2 +/- 8.9 years). Venous blood was drawn between 7.30 and 9.30 a.m. and mel was assayed using a commercially available radioimmunoassay.

The data were analysed by Student’s t test and results reported as mean values +/- standard deviation. The patients with multiple myeloma showed significantly higher mean mel serum levels than healthy subjects (21.6 +/- 13.5 versus 12.1 +/- 4.8 pg/ml; p < 0.001).

This behaviour could actually represent a phenomenon secondary to an altered endocrine-metabolic balance caused by an increased demand of the developing tumor.

On the other hand, the increased mel secretion might be considered as a compensatory mechanism due to its antimitotic action and therefore as an effort to secrete substances capable of regulating neoplastic growth.”

Leave a Comment:

Nisha says last week

Hi David – you mean increasing the IV time to 1 hour minimises side effects ?

    David Emerson says last week

    Hi Nisha-

    I have read and been told by patients that increasing the infusion time reduces side effects for some patients. I cannot say that all patients will experience a benefit or not. Please ask your oncologist as well.

    Good luck,

    David Emerson

naseem cassim says a couple of months ago

Thank you for your swift response. I will be seeing the specialist in a few weeks time
for blood test results. I am hoping that my lesion is not cancer.
I am happy that you were able to manage your your health issues so well. I wish you everything of the best. Naseem

naseem cassim says a couple of months ago

Hi: I am 81 and a catscan shows lytic lesion 17mm on the roof of acetebular.
I have been advised to take fosamax or zolendric acid infusion. I am terrified after reading all the side effects. The lesion is in a critical area, ball and joint roof. What would you advise? Thanks

    David Emerson says a couple of months ago

    Hi Naseem,

    I am sorry to learn of your lytic lesion. A bisphosphonate infusion such as fosamax or zometa will reduce your risk of bone fracture. You can reduce possible side effects by slowing the infusion rate of the bisphosphonate therapy (from 30 min. to 1 hour for example).

    The more important issue is your possible multiple myeloma diagnosis and getting rid of the lesion. You can undergo low dose chemo in hopes of slowing the damage done by your lesion or you can undergo local radiation in an effort to get rid of the lesion.

    Let me know if you have any questions.

    David Emerson

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