Cell Stop Optimal Health

Cancer Cell - Cell Stop


Nature has blessed us with a bounty of cancer therapeutic substances…herbs, mushrooms, fruit and vegetable extracts that can help fight the very mechanisms cancers use to grow. There were 97 clinical papers in the last year alone on Curcumin’s effects on cancer in humans studies, Green Tea had 55 clinical papers during the same time. Many of these papers discuss not only their success in disrupting and killing cancer cells, they also almost universally show they increase the success of chemotherapy and radiation in doing so.

At Optimal Health Knowledge, our 20 year study of the clinical research on such natural, plant based substances has led us to design a comprehensive 17 ingredient formula called Cell Stop, collecting the most powerful of these ingredients known to science.

Curcumin is nature’s most effective, broad spectrum cancer preventative and therapeutic. It turns on tumor suppressing genes. (1) Curcumin inhibits the growth factors cancers cells use to proliferate and suppresses the growth of cancer stem cells. (2) In human breast, esophageal, and colon cancer, curcumin increased the malignant cells’ sensitivity to chemotherapy drugs and to the effects of radiation treatments. (3) The Curcumin in Cell Stop is BCM-95, the clinically studied, trademarked form of Curcumin with 7 times the bioavailabilty of standard Curcumin, containing essential oils of the root like Ar-Tumerone.

Green Tea contains a polyphenol called EGCG, which has been shown to suppress tumor growth by blocking the growth of new blood vessels to supply the tumor. (4) Exciting studies show that EGCG suppresses the growth and invasion of human breast cancer cells. (5) Green Tea also increased apoptosis, or programmed cell death, in cancer cells. (6) Our Green Tea contains 45% EGCG.

Astragalus Root Extract is known worldwide for its ability to boost white blood cell production from our bone marrow. (7) It has also been shown to inhibit proliferation of breast cancer cells (8) Our Astragalus is a 10:1 extract.

Turkey Tail (Trametes versicolor) mushroom has over 15 clinical studies that show it reduces tumor growth. (9) In a phase I clinical study of women with breast cancer, it was shown to increase Natural Killer Cell activity, the immune cells that target cancer. (10) Our Turkey Tail mushroom extract is standardized to 10% polysaccharides.

Maitake mushroom has decades of studies showing that it boosts the activity of our white blood cells. (11) Clinical studies show systemic anti-tumor immune response. (12) Our Maitake mushroom extract is standardized to 10% polysaccharides.

Reishi mushroom has been shown to boost apoptosis, or the destruction of the cancer cell, through the Caspase pathway. (13) It was also shown to reduce tumor growth and rate in Inflammatory Breast Cancer in human trials. (14) Our Reishi mushroom extract is standardized to 10% polysaccharides.

Quercetin exerts broad spectrum anti-tumor activity through multiple pathways. (15) Quercetin has shown synergistic effects when combined with chemotherapeutic agents or radiotherapy, while at the same time protecting healthy cells from the damage of such treatments, in a variety of cancers. (16)

Broccoli Extract contains components like Sulforaphane and BITC, that induce cancer cell apoptosis. (17) Sulforaphane mediates a number of anticancer pathways, including the activation of apoptosis, induction of cell cycle arrest, and inhibition of NF?B. (18) 4 to 1 extract

Bitter Melon Extract has shown multiple actions against Pancreatic cancer cells. (19) It overcomes Cisplatin resistance in Ovarian Cancer cells by exerting anticancer effects through activation of AMPK and suppression of the mTOR. (20)

Mangosteen Fruit Rind Extract contains a minimum of 30% a-Mangostin, which has been shown to inhibit cell growth in many cancers. (21) a-Mangosteen was shown to inhibit growth and induce apoptosis of breast cancer cells. (22)

Boswellia Extract powerfully inhibits NF-kB and 5-LOX, initiators of inflammation, and increases apoptosis. (23) Boswellia increased the cytotoxicity of doxorubicin and cisplatin in Triple Negative Breast Cancer cells. (24) Our Boswellia extract is the clinically studied, patented 5-Loxin, which is 30% AKBA, the most active Boswellic acid.

Milk Thistle Extract, in addition to liver protection, has shown an ability to prevent UVB-induced skin cancers. (25) Milk Thistle component Silymarin effectively suppressed cell growth and arrested cell cycle progression in Ovarian Cancer. (26) We standardize to 80% Silymarin.

Beta Glucan 1,3/1,6 is a well known stimulator of white blood cell maturation and activity. (27) ?-(1,3/1,6)-d-glucan boosted dendritic cells (DCs) maturation, and cytotoxic T lymphocyte responses. (28)

Chamomile Extract contains Apigenin, which inhibits migration in many cancers. (29) Apigenin suppressed tumor growth, lowered proliferation and enhanced apoptosis in prostate cancer. (30)

Flaxseed Lignan Extract reduces growth and metastasis in breast cancer according to studies. (31)

Pterostilbene selectively kills breast cancer stem cells, often responsible for reoccurrence of the cancer. (32)

Se-Methylselenocysteine, the natural form of Selenium found in vegetables, inhibits growth of prostate cancer. (33)

Vegan/Non-Gmo/Gluten Free

Whether you are adding Cell Stop to your existing treatment of chemotherapy and radiation, or have already decided to fight cancer naturally, add Cell Stop and it’s 17 powerful plant compounds that work together to target and disrupt abnormal cell growth on a cellular level. 

For Sale now-Click here to order Cell Stop Optimal Health



    1. Clin Epigenetics. 2010 Dec 1;1(3-4):101-116
    2. Cancer Prev Res (Phila). 2013 May;6(5):387-400
    3. Transl Oncol. 2010 Apr;3(2):99-108
    4. Front Biosci. 2008 Jan 1;13:440-52
    5. Cancer Lett. 2007 Jan 8;245(1-2):232-41
    6. Ann N Y Acad Sci. 2007 Jan;1095:428-40
    7. Chin Med. 2015 Jul 3;10:17
    8. Naunyn Schmiedebergs Arch Pharmacol. 2015 Sep;388(9):965-72
    9. Integr Cancer Ther. 2015 May;14(3):201-11
    10. ISRN Oncol. 2012;2012:251632
    11. Int Immunopharmacol. 2009 Sep;9(10):1189-96
    12. Int J Cancer. 2013 Jul;133(1):108-19
    13. Asian Pac JCancer  2014;15(9):3981-6
    14. PLoS One. 2013;8(2):e57431. doi: 10.1371
    15. Oncol Lett. 2016 Jul;12(1):516-522
    16. Curr Med Chem. 2015;22(26):3025-39
    17. Int J Oncol. 2016 Jun;48(6):2521-33
    18. Antioxid Redox Signal. 2015 Jun 1;22(16):1382-424
    19. Carcinogenesis. 2013 Jul;34(7):1585-92
    20. Integr Cancer Ther. 2016 Sep;15(3):376-89
    21. Biomed Res Int. 2014;2014:546353
    22. Int J Oncol. 2016 May;48(5):2155-65
    23. J Ethnopharmacol.2016 Jun 21. pii: S0378-8741(16)30413-5
    24. Environ Toxicol Pharmacol. 2014 Jul;38(1):58-70
    25. Int J Oncol. 2005 Jan;26(1):169-76
    26. Eur J Pharmacol. 2014 Nov 15;743:79-88
    27. Int JCancer. 2016 Jun 1;138(11):2713-23
    28. Hum Immunol. 2015 Mar;76(2-3):146-54
    29. Oncol Lett. 2016 May;11(5):3075-3080. Epub 2016 Mar 16
    30. Oncotarget. 2015 Oct 13;6(31):31216-32
    31. Int J Cancer. 2005 Sep 20;116(5):793-8
    32. J Agric Food Chem. 2015 Mar 11;63(9):2432-41
    33. J Cancer Res Ther.2015 Oct-Dec;11(4):840-5

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