sunnuntai 26. helmikuuta 2017

GcMAF Goleic Therapy - 4 Verita Life Clinical Programmes

Macrophages are large immune cells found in
our bodies that are able 
to recognise, engulf and
digest cancer cells. 

Also responsible for stimulating other immune cells, 
macrophages can be activated by ‘MAF’
(macrophage activating factor), a naturally 
protein. The precursor of MAF inside the body is called
Gc protein.

How Tumours prevent Macrophages

Tumour cells produce nagalase, a special enzyme inhibiting the
Gc protein’s function leading to high nagalase levels resulting in lower
MAF levels. The body’s macrophages subsequently cannot be activated,
leading to the suppression of the immune system.
Complementary oncology utilises breakthrough GcMAF therapy to
counteract this effect and enhance the immune system.

GcMAF Goleic Therapy

GcMAF therapy regulates the human protein required to reactivate immune
cells and boost patients’ immune systems. Many published peer reviewed
studies have proven that GcMAF Goleic therapy is not only an immune
activator, but can be used as a natural cancer treatment. In addition
to rebuilding a diminished immune system, GcMAF Goleic inhibits
angiogenesis (stops blood supply to tumours), activates macrophages
and apoptosis (suicide of cancer cells); reverts cancer cells’ phenotype
(characteristics) to normal healthy cells; reduces the metastatic
potential of human cancer cells and increases energy production at
the mitochondrial level.

The treatments available at Verita Life >

GcMAF Goleic is one of 15 separate core cancer treatments that can be
combined into your personal protocol.

The exact combination and frequency of treatments is planned
according to your specific needs.

Chosen for proven effectiveness, every treatment has been shown, through
numerous medical studies and extensive experience, to attack and defeat
cancer cells.
Following your enquiry and review of your case by our medical team, you
will receive a Doctor consultation.
A full personalised protocol will follow and this will recommend the
treatments needed. 

Treatments are delivered in 4 Verita Life Clinical Programmes

Whatever phase of treatment, or Stage you are at, Verita Life can help treat your
Cancer and your cancer-related symptoms.
GcMAF Goleic and the other treatments are combined and delivered in 4 separate
Clinical Programmes, one of which is best for you, or your loved one.
1. If you are currently having Chemo or Radio therapy – maximise results
and minimise side effects. Verita Life Oncoboost™ protects your organs and
boosts your immune system.
2. If you are looking for Alternative treatments to defeat cancer
– Verita Life 360 ™
– Complete treatment protocols combining cancer-specific treatments if you don’t
 want to, or can’t, undergo conventional treatments.
3. If you have not started treatment yet – Prepare your Immune system and
organs to withstand chemo and radio therapy with uniquely combined treatment protocols.
 Verita BodyBoost™.
4. If you are in remission. Recover from cancer side effects with All Clear Aftercare™
– rebuild a weakened immune system and damaged organs.
Regain your health and prevent cancer returning.


1. We treat the cancer and support the immune system at the same time.
2. We ensure a diet and lifestyle change so that patients remove the conditions
that promoted or supported tumour growth.
3. We give patients a chance to heal or maintain the status quo, even when
conventional medicine has given up.
4. In almost all cases, we achieve a stronger immune system and improved
quality of life.

 (or Gc protein-derived macrophage activating factor)[1] is a protein
produced by modification of 
vitamin D-binding protein. Proponents of GcMAF claim
that it is an 
immunomodulatory protein that has antitumor properties and strengthens
immune system bymacrophage activation.[2][3] /Wikipedia

Gene Review

Gc  -  group specific component

Mus musculus

Synonyms: DBP, Gc-globulin, Group-specific component, VDB, Vitamin D-binding protein, ...

 Hoffmann, R. A w iki for the life sciences w here authorship matters. Nature Genetics (2008)

Disease relevance of Gc

When maintained on vitamin D-deficient diets for a brief period, the DBP-/-, but not DBP+/+, mice developed secondary hyperparathyroidism and the accompanying bone changes associated with vitamin D deficiency [1].
Osteopathy and resistance to vitamin D toxicity in mice null for vitamin D binding protein [1].
After an overload of vitamin D, DBP-/- mice were unexpectedly less
susceptible to hypercalcemia and its toxic effects [1].
Specific forms of renal Fanconi syndrome are associated with endocytic
pathway dysfunction with disruption of megalin-mediated uptake DBP/25- (OH)D3 complex, producing metabolic bone disease in affected individuals as a prominent clinical finding [2].
Prognostic utility of serum alpha-N-acetylgalactosaminidase and
immunosuppression resulted from deglycosylation of serum Gc protein in oral cancer patients [3].

Psychiatry related information on Gc
Mice homozygous for a DBP-null allele display less locomotor activity and free-run with a shorter period than otherwise isogenic wild-type animals [4].

High impact information on Gc
We show that 25-(OH) vitamin D3 in complex with its plasma carrier, the vitamin D-binding protein, is filtered through the glomerulus and reabsorbed in the proximal tubules by the endocytic receptor megalin [5].
BACKGROUND: The vitamin D(3)-binding protein (Gc protein)-derived
macrophage activating factor (GcMAF) activates tumoricidal macrophages against a variety of cancers indiscriminately [6].
Peak steady-state mRNA levels of the vitamin D-dependent calbindin-D9K gene were induced by 1,25(OH)2D more rapidly in the DBP-/- mice [1].
A line of mice deficient in vitamin D binding protein (DBP) was generated by targeted mutagenesis to establish a model for analysis of DBP's biological functions in vitamin D metabolism and action [1].
Thus, the role of DBP is to maintain stable serum stores of vitamin D
metabolites and modulate the rates of its bioavailability, activation, and endorgan responsiveness [1].

Chemical compound and disease context of Gc
Phthalate esters with short alkyl chains, such as di-ethyl (DEP), di-n-propyl (DPP), and di-butyl phthalate (DBP), have adjuvant effects on an FITCinduced contact hypersensitivity mouse model [7].

Biological context of Gc
The fourth gene, Gc, encoding vitamin D-binding protein or group-specific component, maps to the same chromosome as the other family members, but linkage has not been established [8].
This report describes the genetic and physical mapping of Gc in mouse and establishes that, although Gc is genetically linked to the other genes, its physical distance from them extends beyond the resolution range of yeast artificial chromosome cloning and pulsed-field gel electrophoresis [8].
Population gene frequencies for these proteins binding vitamin D were in the range of those reported for Gc, and individuals of known Gc phenotype were found to have the corresponding vitamin-D-binding phenotype [9].
Vitamin D-binding protein (DBP) has been reported to contribute to innate immunity [10].
Anti-megalin antibodies produced a similar reduction in DBP/25-(OH)D3
endocytosis [2].
Anatomical context of Gc
Initial studies revealed a marked defect in the ability of these DBP(-/-) mice to recruit cells to the peritoneum after localized thioglycolate injection [10].
To verify prior in vitro and cell-based observations supporting this role, we assessed the ability of a recently developed DBP-null mouse line to recruit neutrophils and macrophages to a site of chemical inflammation [10].
The interrupted DBP allele had been generated by homologous recombination in 129X1/SvJ embryonic stem cells and these cells were subsequently used to generate a line of DBP(-/-) (null) mice [10].
Analysis of intercellular signal transmission among nonadherent (B and T) cells revealed that lyso-PC-treated B cells modify Gc protein to yield a proactivating factor, which can be converted by T cells to the macrophage activating factor [11].
Identification of the serum factor required for in vitro activation of
macrophages. Role of vitamin D3-binding protein (group specific component, Gc) in lysophospholipid activation of mouse peritoneal macrophages [12].

Associations of Gc with chemical compounds
Three lines of evidence are reported:
(1) Polyacrylamide gel electrophoresis 
and autoradiography of serum labeled with (14-C)vitamin D3 revealed patterns of radioactive bands identical to those expected of the two Gc alleles [9].
Group-specific component (Gc) proteins bind vitamin D and 25-
hydroxyvitamin D [9].
This review describes these new pathways for uptake of 25-hydroxyvitamin- D3 and the gonadal sex-steroids (17beta-estradiol and testosterone) bound to vitamin D-binding protein and sex hormone-binding globulin respectively [13].
This rapid process of macrophage activation was found to require a serum factor, the vitamin D3 binding protein (the human protein is known as group-specific component; Gc) [11].
Vitamin D3-binding protein (Gc protein), a serum glycoprotein, is the
precursor for the macrophage activating factor [3].
Physical interactions of Gc
Recent studies have shown that vitamin D-binding protein (DBP)/25-(OH)D3 complex is one of the megalin/cubilin ligands [2].
The influence of age, sex and strain on the serum concentration of
transcortin (corticosteroid-binding globulin) and vitamin D-binding protein (DBP) in mice was investigated [14].

Other interactions of Gc
Linkage between vitamin D-binding protein and alpha-fetoprotein in the
mouse [8].
In a previous study, the s locus was included in the same linkage group as serum albumin (Alb) and vitamin-D binding protein (GC) which are mapped on chicken (Gallus gallus) chromosome 4 (GGA4) [15].
Incubation of Gc protein with a mixture of beta-galactosidase and sialidase efficiently generated the macrophage-activating factor [11].
The antibody was subtyped IgG2b kappa and had a kd of 3.0 x 10(-8) M for antigen Gc [16].
Transcortin and vitamin D-binding protein levels in mouse serum [14].
Analytical, diagnostic and therapeutic context of Gc
(2) Immunoelectrophoresis and autoradiography of labeled serum reacted against antiserum to human Gc revealed labeling by (14-C)vitamin D3 of Gcantibody precipitation ares [9].
Deglycosylated Gc protein cannot be converted to macrophage activating factor, leading to immunosuppression [3].
Competition assays with vitamin D3 and Gc in enzyme-linked immunosorbent assay indicate that the epitope of hDBP-1 on the Gc molecule may be related to the vitamin-D3-binding site [17].
CONCLUSION: The difference of isoelectric focusing mobility in Gc protein and GcMAF would be useful to develop a GcMAF detection method [18]. Gc protein from human serum was purified by affinity chromatography with 25-hydroxyvitamin D3-sepharose [19].

1. Osteopathy and resistance to vitamin D toxicity in mice null for vitamin D
binding protein. Safadi, F.F., Thornton, P., Magiera, H., Hollis, B.W., Gentile, M.,
Haddad, J.G., Liebhaber, S.A., Cooke, N.E. J. Clin. Invest. (1999)
2. Proximal tubule endocytic apparatus as the specific renal uptake
mechanism for vitamin D-binding protein/25-(OH)D3 complex (Review
Article). Negri, A.L. Nephrology (Carlton, Vic.) (2006)
3. Prognostic utility of serum alpha-N-acetylgalactosaminidase and
immunosuppression resulted from deglycosylation of serum Gc protein in
oral cancer patients. Yamamoto, N., Naraparaju, V.R., Urade, M. Cancer
Res. (1997)
4. The DBP gene is expressed according to a circadian rhythm in the
suprachiasmatic nucleus and influences circadian behavior. Lopez-Molina,
L., Conquet, F., Dubois-Dauphin, M., Schibler, U. EMBO J. (1997)
5. An endocytic pathway essential for renal uptake and activation of the
steroid 25-(OH) vitamin D3. Nykjaer, A., Dragun, D., Walther, D., Vorum, H.,
Jacobsen, C., Herz, J., Melsen, F., Christensen, E.I., Willnow, T.E. Cell (1999)
6. Effects of vitamin D(3)-binding protein-derived macrophage activating
factor (GcMAF) on angiogenesis. Kanda, S., Mochizuki, Y., Miyata, Y.,
Kanetake, H., Yamamoto, N. J. Natl. Cancer Inst. (2002)
7. Effects of phthalate esters on dendritic cell subsets and interleukin-4
production in fluorescein isothiocyanate-induced contact
hypersensitivity. Maruyama, T., Shiba, T., Iizuka, H., Matsuda, T., Kurohane,
K., Imai, Y. Microbiol. Immunol. (2007)
8. Linkage between vitamin D-binding protein and alpha-fetoprotein in the
mouse. Guan, X.J., Arhin, G., Leung, J., Tilghman, S.M. Mamm. Genome (1996)
9. Group-specific component (Gc) proteins bind vitamin D and 25-
hydroxyvitamin D. Daiger, S.P., Schanfield, M.S., Cavalli-Sforza, L.L. Proc. Natl.
Acad. Sci. U.S.A. (1975)
10. 129X1/SvJ mouse strain has a novel defect in inflammatory cell
recruitment. White, P., Liebhaber, S.A., Cooke, N.E. J. Immunol. (2002)
11. Vitamin D3 binding protein (group-specific component) is a precursor for
the macrophage-activating signal factor from lysophosphatidylcholinetreated
lymphocytes. Yamamoto, N., Homma, S. Proc. Natl. Acad. Sci.
U.S.A. (1991)
12. Identification of the serum factor required for in vitro activation of
macrophages. Role of vitamin D3-binding protein (group specific
macrophages. Role of vitamin D3-binding protein (group specific
component, Gc) in lysophospholipid activation of mouse peritoneal
macrophages. Yamamoto, N., Homma, S., Millman, I. J. Immunol. (1991)
13. The role of plasma-binding proteins in the cellular uptake of lipophilic
vitamins and steroids. Andreassen, T.K. Horm. Metab. Res. (2006)
14. Transcortin and vitamin D-binding protein levels in mouse serum. Faict, D.,
De Moor, P., Bouillon, R., Heyns, W., Heiniger, H.J., Corrow, D., Lesaffre, E. J.
Endocrinol. (1986)
15. Mapping of panda plumage color locus on the microsatellite linkage map of
the Japanese quail. Miwa, M., Inoue-Murayama, M., Kobayashi, N., Kayang,
B.B., Mizutani, M., Takahashi, H., Ito, S. BMC Genet. (2006)
16. Binding of a monoclonal antibody E12 to Gc globulin (vitamin D-binding
protein) is inhibited by actin. Osawa, M., Sabbatini, A.R., Erukhimov, J.,
Werner, P.A., Galbraith, R.M. Biochim. Biophys. Acta (1992)
17. A monoclonal antibody against human vitamin-D-binding protein for the
analysis of genetic variation in the group-specific component system
(Gc). Hoffmann, R., Braun, A., Cleve, H. Hum. Genet. (1990)
18. Gc protein-derived macrophage activating factor (GcMAF): isoelectric
focusing pattern and tumoricidal activity. Mohamad, S.B., Nagasawa, H.,
Sasaki, H., Uto, Y., Nakagawa, Y., Kawashima, K., Hori, H. Anticancer Res. (2003)
19. Association of the macrophage activating factor (MAF) precursor activity
with polymorphism in vitamin D-binding protein. Nagasawa, H., Sasaki, H.,
Uto, Y., Kubo, S., Hori, H. Anticancer Res. (2004)

GOLEIC the vitamin D binding protein destroying cancer at any stage

GOLEIC the vitamin D binding protein destroying cancer at any stage and many other diseases

GcMAF is an essential human protein our bodies make to destroy cancer.
 All 5 billion healthy humans make their own GcMAF. A  human makes 10,000 – 100,000 cancer cells a day, but your GcMAF, which has six attacks on cancer, destroys them every day.
If you have a severe shock, such as losing your house or catching pneumonia, that may give cancer the chance to send out an enzyme (nagalase) to prevent your body making its own GcMAF. If so, that stops the six attacks on cancer; without GcMAF, your immune system also collapses, and the cancer becomes chronic.
If external GcMAF is administered, five of the six attacks on cancer restart in minutes, and in three weeks the sixth, your immune system, is rebuilt to above normal strength. GcMAF is, of course, without side effects.

As a result of research carried out in our laboratory, peer reviewed and published in prestigious scientific journals, we were able to build a new molecule, Goleic, which we patented. It is 200 times more powerful in the laboratory, and perhaps 30% more powerful in the human body. Goleic is the one we use in our clinics.
Unlike GcMAF Goleic can be used in a nebuliser (the most powerful form of administration), and made into suppositories. It also isn’t blocked by medicines such as heparin.
Using the Protocols, a big part of which is diet, we usually eradicate stage 4 cancer in 6 months, providing the patient carries out the simple protocols, the SWISS Protocol in the clinic, and the Home Protocol at home. If you have had chemotherapy it will take considerably longer. If you have been “over chemoed” and your blood / immune system counts are low, we will have to get those back up first.

Cases we treat include:

  • Autism
  • Terminal stage 4 Cancer
  • Chronic Herpes
  • Chronic Acne
  • Chronic cirrhosis of the liver
  • Chronic kidney disease
  • Chronic depression
  • Colitis
  • Crohn’s
  • Fibromyalgia
  • Hepatitis
  • Herpes
  • ME/CFS
  • Osteoporosis
And various types of Immune dysfunction including allergies. Research shows GcMAF can halt deterioration in Parkinsons, multiple sclerosis (MS), dementia and ALS, and in its role of immune system regulator, can reverse diseases that attack the immune system like Lupus and Arthritis. And is effective with wound healing.
There is nothing you need to avoid while on GcMAF.
Worldwide there are six billion healthy people with GcMAF inside them, and you can take anything with our GcMAF that they can. So we are not aware of any contra indications for GcMAF itself.
But there are contra indications for your immune system, which you are trying to rebuild. Generally, do not take medications unless you have to.
So, for the sake of your immune system
You should continue with any supplements that help the immune system. Anti-histamine is fine.
However, try to avoid anything that suppresses your immune system (or you may nullify the good effects of GcMAF:)
LDN appears to stop the action of GcMAF.
Externally administered heparin (used to stop blood clots) can completely block GcMAF, but not Goleic.
Aspartame -the well known sweetener – can negatively interact with your intestinal microflora and reduce your immune defences
All kinds of Corticosteroids (Prednisolon, Prednisone, Betapred, Solu-Cortef, Solu-Medrol etc). So avoid Cortisone and steroids if possible.
Anti- inflammatory drugs should be avoided. (NSAIDs like Ibuprofen, Diklofenalk. Celebrex Aspirin etc should be taken in moderation.)
Cytotoxic medications or chemotherapy (Cyclophosphamide (Sendoxan) Etoposide (Vepesid) Metotrexat, Taxotere, Taxol, Navelbine etc etc) although there is some evidence GcMAF may reduce the side effects and the damage these poisons do.
Radiation Therapy.
Morphine (Morfine) analogs, (Morfin, Tramadole, kodeine, Fentanylplasters, Oxynorm, Oxycodon etc). Take buprenorphine instead.
Dr Yamamoto also warns against beta blockers (seloken, Selo-Zok etc)
Carrageenan (Chocomel) can block macrophage (gcMAF) activity. Also known as E407 or E407a.
Remember, in men, high cortisol will cause a man to lose his testosterone down the road because cortisol will block testosterone from working at the cell receptor sites. A man will lose his sex drive and be 15 kgs overweight. He will frequently have high cholesterol and high triglycerides. It’s a perfect setup for a heart attack.
Food for your immune system (and neurological system)
Dr Tomas Tallberg MD, head of the Helsinki Institute for Bioimmunotherapy, has published numerous research papers over the last 40 years which state that lipids are needed to rebuild your immune and central nervous system where the patient has cancer or autism.
He states you are unlikely to recover if you are on a fast food diet, vegan or vegetarian diets, or processed foods.
Your immune and neurological systems need to be fed with the right amino acids, trace metals and lipids if GcMAF is to rebuild them:
You need the original human caveman diet without red meat or fruits, ie white meat, fish vegetables, and the lipids provided by butter, cream, chicken liver, salmon, nuts coconut milk, offal. (Unfortunately the fastest place to get lipids from is canned (prion free) pigs brain ! Turn it in to a Pina Colada mix below.)
We soon expect to have specific powders containing the right amino acids and trace metals for the 6 cancer groups.
We treat usually terminal stage 4 cancer patients, including multiple myleoma and pancreatic cancer. We expect you to have, on average, a 50% reduction in tumour size (50% improvement in myleoma numbers) in three weeks.
When you go home you MUST do our home protocol. If you do, we then expect you to be cancer free in six months.
If you have stage 4 cancer, at home afterwards you need:
  1. A full 1ml of Goleic a day.
  2. At least 10,000iu of vitamin D a day,
  3. Eat white meat, fish and vegetables,
  4. No sugar or carbohydrates (so no cereals or bread) which feed cancer.
  5. If your weight drops below your ideal, 20 MAP protein tablets a day from Dr Reinwald Healthcare Germany.
Avoid the five main causes of cancer:
  1. Too much sugar
  2. Lack of vitamin D3
  3. Poor nutrition lacking in amino acids and trace metals, ,
  4. Lack of oxygen and exercise,
  5. Severe shock stress.
Stay away from: sugar, which feeds cancer, carbohydrates which turn into sugar; and grains beans and potatoes, which also contain cancer inducing lectins and poisons – wheat is the worst. Avoid soya milk which blocks the absorbance of trace metals.
Some sweeteners are damaging in other ways – asparthame lowers your immune system; even Splenda is a chlorocarbon like DDT – See
The best appears to be the natural plant sweetener Stevia, to which they add relatively harmless maltodextrin for supermarkets. Second best is saccharin.
Breast cancer
If you have a root canal, you are advised to have that tooth removed. (See article)
Avoid molybdenum, which makes breast cancer grow. The richest sources of molybdenum are legumes, including beans, peas, lentils and soybeans. Nuts, leafy vegetables and grains like oats, wheat and rice also contain ample amounts.
And ordinary milk contains estrogen, which is a growth factor for uterine cancer, and for breast cancer but less so.
In addition to rebuilding the immune system and activating macrophages, Goleic also has five direct actions on cancer cells, where its half life is three days. As a macrophage stimulator its half life is 5 days (the half life of macrophages is 6 days), so most importantly hugely increase the GcMAF dosage, and put into different parts of the body at least twice a week. IV is best.
If you can have surgery to reduce tumour mass, do so, but make sure you are on GcMAF/Goleic for at least three weeks before the surgery, so that your rebuilt immune system can prevent secondaries caused by cancer cells released by surgery settling elsewhere.
And then keep the GcMAF up for 8 weeks after scans show your tumours are gone, or nagalase first drops below 0.65.
To support the treatment with Goleic you need additionally to: Sunbathe whenever you can.
Exercise, Drink Water, Vitamin C, Detoxing, Nutrition, Alkaline PH, Vitamin B 17, Oleic acid, Green tea, Curcumin

See Also - katso myös: 
  1. Elevated enzyme found in most cancer patients, could GcMAF be the cure?
  2. How GcMAF Works - Pre-clinical trials & what we have learnt
  4. GcMAF immunotherapy: It's all about activating macrophages to do their work
  5. GcMAF macrophage activation therapy FAQ
  6. Goleic protein - vitamin supplement therapy
  7. GcMAF: The Latest Discovery in Natural Cancer Treatments
  8. GOLEIC the vitamin D binding protein destroying cancer at any stage and many other diseases


Ternimaito luontaistuotteena

Kuten mainitusta tutkimuksesta [5] käy ilmi, ternimaidolla on suotuisia vaikutuksia. Jotkut juovat sitä sellaisenaan tai pakasteesta sulatettuna. Lähinnä erikoiskaupoista saa pakastettua ternimaitoa, yleensä 1 litran pulloissa. Teollisuus on alkanut myös valmistaa pakastekuivattua ternimaitoa kapseleihin. Myynnissä on sekä kotimaisia että ulkomaisia kapseleita ja jauheita, joissa luvataan olevan suotuisia vaikutuksia. Näitä tuotteita markkinoivat tahot ilmoittavat niiden tehoavan moniin vaivoihin. Useat tutkijat sanovat, että ne ainakin parantavat vastustuskykyä ja vireyttä. Monet tunnetut urheilijat ovat mielestään saaneet apua näistä valmisteista ja kertovat olevansa vakuuttuneita ternimaidon tehosta. Näitä seikkoja ei kyetä tarkemmin tutkimaan, koska vertailuaineisto on hajanaista ja perustuu käyttäjän omiin subjektiivisiin havaintoihin ja tuntemuksiin. Tämän kaltainen jonkun tietyn aineen hyödylliseksi kokeminen on tavallista monien muidenkin luontaistuotteiden osalla.
Erääksi ternimaidon keulakuvaksi nousi edesmennyt Petteri Jussila.

Suomalaishiihtäjien ternimaidonkäyttö

Jari Piiraisen mukaan suomalaisessa hiihtovalmennuksessa oli kova ternimaitobuumi 1990-luvulla, etenkin vuosina 1993–1994. Hänen mukaansa Lillehammerin olympialaisissa oli Suomen hiihtomaajoukkueella mukanaan ehkä jopa sata litraa ternimaitoa. Nykyisin ternimaitoa ei hiihdossa juuri käytetä. [6]

Now Foods, Colostrum, 500 mg, 120 Capsules 


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Gelatin (capsule), magnesium stearate (vegetable source), silica and soy lecithin (<1%%).
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