4Life Transfer Factor Plus

The Ultimate in Immune System Support

This product represents 4Life®'s highest level of immune system support. 4Life Transfer Factor Plus Tri-Factor Formula combines the intelligence of Transfer Factor E-XF™, the intuition of NanoFactor™ extract, and the added support of our Cordyvant™ blend to provide the ultimate in immune system support for your body. The proprietary Cordyvant blend features known immune-supporting ingredients such as maitake and shiitake mushrooms, cordyceps, inositol hexaphosphate, beta glucans, beta sitosterol, and olive leaf extract.
 

Primary Benefits

• Boosting and balancing support, according to what your body needs. A more efficient and intelligent immune system to fight off invaders
• Added immune system nutrients for a broad source of immune system support
• Support that promotes the health of all your body's systems
• Support for optimal energy levels
• A proactive strategy to maintain your health

What makes this product unique?

• Transfer factors are tiny messenger molecules that transfer immunity information from one entity to another, such as between a breastfeeding mother and her newborn infant.
• NanoFactor™ extract is 4Life's patent-pending extract of immune system-enhancing nanofractions. It helps “fine-tune” immune system function so that immune cells know when to act, how to act, and when to rest.
• The extraction process for transfer factors from egg sources is protected by US patent 6,468,534; and the combining process for cow colostrum and chicken egg yolks is protected by U.S. patent 6,866,868.
• Independent laboratory tests reveal that 4Life Transfer Factor Plus Tri-Factor Formula can boost immune system effectiveness by raising Natural Killer cell function 437 percent.
• 4Life Transfer Factor products are featured in the 2003, 2004, 2005, 2006, 2007 and 2008 Physicians' Desk Reference For Nonprescription Drugs and Dietary Supplements, the standard supplement guide for physicians that can be found in physician offices, hospitals, and pharmacies throughout the United States.
• 4Life Transfer Factor® products have been recommended by the Russian Federation for use in hospitals and clinics. This historic announcement was a result of ten separate scientific trials and two experimental studies extolling the benefits of 4Life Transfer Factor products.
   

Complementary Products

RiteStart®
4Life Transfer Factor Tri-Factor Formula
4Life Transfer Factor RioVida® Tri-Factor Formula

Ingredients

Transfer Factor E-XF (a patented concentrate of transfer factors and other natural components from cow colostrum and egg yolk), NanoFactor extract (a proprietary concentrate of nano-filtered cow colostrum.), Cordyvant Proprietary Polysaccharide Complex (IP-6, Soya bean Extract, Cordyceps sinensis, Beta-Glucan (from baker's yeast), Beta-Glucan (from Oat), Agaricus blazeii Extract, Mannans (from Aloe Vera), Olive Leaf Extract, Maitake Mushroom, Shiitake mushroom), and Zinc.

WARNING: 90%* OF FILIPINOS ARE AFFLICTED WITH LIFESTYLE DISEASES! THIS MEANS 1 OUT OF 5 HAVE CANCER OR HEART DISEASE.
ARE YOU ONE OF THEM?

The immune system is the most powerful weapon we have against any disease. If this is true, then why do people lose the battle against cancer, diabetes, heart disease and other fatal diseases? Why do people still get sick?

Answer: It is the lack of information.

Transfer Factor is not a vitamin, mineral, herb, antioxidant nor a drug. Transfer Factor is the IQ of the immune system. Transfer Factor is pioneering in Transferceutical Technology. The other supplements belong to the Neutraceutical Technology.

Transfer Factor is an information molecule thateducates, enhances and balances the immune system. First, it educates or teaches the immune system cells to recognize diseases in the body and send these soldiers to attack and kill invaders such as bacterial, viral, parasitic, fungal, malignant, neurological and autoimmune diseases. Second, it enhances the immune system by boosting it beyond its original state up to 437% increase in killing rate or immune activation. With this outstanding ability, the immune system can now destroy 97% of cancer cells in a 48-hour laboratory test in vitro, (please see test below an illustration by JEUNESSE Inc., Institute of Longevity Medicine, California USA). Third, it balances the immune system when it is over reacting causing autoimmunity, such as diabetes, an auto immune disorder of the pancreas, wherein good cells fight other good cells due to immune misfire or immune system mistake. This erratic behavior is balanced by Transfer Factor through its ability to command suppressor cells to suppress inflammation thereby

 normalizing it.

Vitamins, minerals, herbs and antioxidants are the building blocks of the immune system while Transfer Factor is the immune intelligence of the immune system.

CLINICAL STUDIES ON TRANSFER FACTOR:

1. AN AMAZING RECOVERY OF A 43 YR OLD WOMAN FROM BREAST CANCER IN JUST 3 MONTHS WITH NO CHEMOTHERAPY:

17 May 2008, A 43 year old woman with Breast Cancer (Grade II) has her Pathological Diagnosis: Breast mass, Left, Excision Biopsy: Infiltrating Ductal Carcinoma, Tumor Size: 1.5 cm . Gross and Microscopic Description: The specimen submitted consists of an ovoid, grayish, doughy mass measuring 1.5 x 1.0 x 1.0 cm. Cut sections reveal a brown solid surface RSEB1. Sections of the breast mass reveal an infiltrating ductal mass carcinoma characterized by nests of atypical cells forming minimal tubular structures. This tumor cells feature enlarged vesicular nuclei with prominent nucleoli and scanty eosinophilic cytoplasm. Some nuclei appear hyperchromatic. The stroma shows fibrosis.

The doctors recommended removal of breast by surgery.

Dosage of Transfactor taken: Transfer Factor Tri-Factor Plus (3 caps 3 x a day), Transfer Factor Tri-Factor Formula (2 caps 3 x a day) and TF Riovida (30 ml 3 x a day).

Her ultra sound shows an amazing Cancer-Free result on 2 August 2008 in justless than 3 months only After Transfer Factor.

2. Local testimony on Atopic Dermatitis (a.k.a Skin Asthma or Atopic Eczema):

A 21-year old woman who suffered from severe atopic dermatitis, a chronic infammation of the skin, also called atopic eczema, was told by her array of doctors from various hospitals that there is really no cure for it.

She started taking Transfer Factor Tri-FactorFormula : 2 capsules 2 x a day before each meal. In just 20 days she recovered. Now she's taking TF as maintenance supplement. Truly it was life changing as she's back on pictorial as a commercial model.

3. IN 3 WEEKS, A HIGHLY CONTAGIOUS HEPATITIS B WAS REVERTED TO NON-INFECTIOUS STATE WHICH IS UNUSUAL.

a) CLINICAL DIAGNOSIS: CHRONIC HEPATITIS C : A.C. , 44 years old, married, female with a history of blood transfusion secondary to massive bleeding when she delivered her third baby in Saudi Arabia. Patient took advantage of health benefits of his son, so she underwent a comprehensive executive check-up.

REMARKABLE FINDINGS:

Physical examinations: hepatomegaly , tenderness on palpation at the right upper quadrant of abdomen;

Diagnostic Tests: Abdominal ultrasound- beginning cirrhotic liver.
Elevated liver enzymes: SGPT, SGOT Hepatitis C- Reactive

CLINICAL DIAGNOSIS: CHRONIC HEPATITIS C

PLAN OF MEDICAL MANAGEMENT:

June 1, 2009: Interferon ∞-2B, 3 MIU (Million international Unit)/vial
Subcutaneous injection for 48 weeks, 1 vial per week

Transfer Factor plus, 2 capsule 3x a day

June 30, 2009: After 4 weeks of the said treatment,
Repeat physical exam. Liver size is now normal
Liver enzymes: normal
Hepatitis C : WEAKLY REACTIVE

AT present…
Patient is on the 2nd month of treatment..I believe she will not finish the 48 weeks treatment.

b) CLINICAL DIAGNOSIS : HEPATITIS B, HIGHLY INFECTIOUS : R.G. 23years old, single, male, newly graduate eager to seek employment, eldest of 4 siblings. However on medical examinations, he was found out that he is HEPATITIS B surface Antigen positive. Hence, he is not recommended to be fit to work

HEPATITIS PROFILE WAS REQUESTED TO CONFIRM THE
INFECTIOUSNESS OF THE VIRUS.

Result: HbsAg- Reactive
Anti-HbsAg- Non Reactive
HBeAg –Reactive- (THIS POSITIVITY SHOWS THAT
HE IS HIGHLY INFECTIOUS)
Anti-HCV- non reactive
SGPT, SGOT- ELEVATED

Physical examination: icteresia both eyes, palpable liver edge


DIAGNOSIS: HEPATITIS B, HIGHLY INFECTIOUS

Plan of Management:

June 8, 2009
Interferon ∞-2B, 3 MIU (Million international Unit)/vial
Subcutaneous injection for 48 weeks 2 vials/ week

Instead of giving Lamivudine (Zeffix) 100mg OD, the patient was given
Transfer Factor plus, 2 capsule 3x a day

June 30, 2009: After 3 weeks of the said treatment,
Repeat physical exam. Liver edge is no longer palpable
Liver enzymes: slightly elevated HbeAG: NON- REACTIVE

IN 3 WEEKS, A HIGHLY CONTAGIOUS HEPATITIS B WAS REVERTED TO

NON-INFECTIOUS STATE WHICH IS UNUSUAL.

AT present… Patient is on the 5th week of treatment..I

believe he will not finish the 48 weeks treatment.

4. CASE 1 USING TRANSFER FACTOR ON LEPROSY WITH LEPRA REACTION:

A 15 year old male child from Malabon City, in type II lepra reaction, was diagnosed with lepromatous leprosy in 2003 at the age of 12 years old, with an average bacteriologic index (BI) of 4.6+, was given MDT on 1Jan03-31May03 and 17Jun05-30April06. Lepra reaction developed on his 2^nd month of MDT, corticosteroid was started following the WHO recommendation. His intake of steroid beyond 12 weeks was either prescribed or as self medication. He was also prescribed NSAIDs, Colchicines and Squalene. Between May 2004 BI 2.8+ and May05 BI 2.6 with slackened drop in average BI and chronic use of steroid, coupled with high WBC 32.38 and high alkaline phosphatase 270 (44-155) it was deemed necessary to reinstitute another course of MDT under close monitoring. In March 06, there was worsening of the symptoms manifested as high grade fever 39C, joint pains, body malaise, increased erythema, swelling of digits of both hands and elevation and tenderness of plaques. There was also muscle weakness as he was incapable of feeding himself and writing his assignment.

With a BI 1.4+, an impression of steroid toxicity and or dapsone syndrome with lepra reaction required hospitalization, discontinue all medications and initiate supportive therapy. Transfer Factor 600mg TID was started initially, on his 3^rd hospital day, joint pains disappeared together with body malaise and fever. Plaques and hand swelling gradually diminished and he was discharged after 5 days confinement. Home medications were Transfer Factor in supervised doses, Vitamin B complex, colchicines and petroleum jelly. Patient condition continued to improve after consuming 108,000 mg pure Transfer Factor and 54,000 mg plus cordyvant Transfer factors. AFS turned negative in 2007.

5. Case 2 USING TRANSFER FACTOR ON Lepromatous Leprosy:

A 21 year old male from Bulacan, was diagnosed with lepromatous leprosy in 2004. His condition started as numbness on the R elbow 15 years prior to consult (PTC) but did not sought treatment. He was 13 years old when he was given MDT-MB but took only 3 blister packs and stopped because of improvement. For about 3 years PTC, he was suffering from increasing number of patches in his body and appearance of nodules on the face and earlobes before finally coming to our institution, and, with his younger brother who has the same problem.

His average BI 4.5+, highest on R earlobe 6+ solid, on admission, persisted from 4Nov04-25Sept05 until the end of his regular MDT-MB treatment. At this time, he complained of myalgia, dizziness and easy fatigability. CBC revealed severe anemia Hgb 77. Drug resistance to MDT and/or Dapsone syndrome was considered and so Ofloxacin 400mg OD 5Sept05-3Feb06 (fig 2.1) was added to his regimen with clofazimine 200mg daily in tapering dose with Dapsone was removed from the regimen.

He developed lepra reaction during his 2^nd blister pack and was prescribed corticosteroid following the WHO recommendation, NSAIDs and colchicine plus supportive medications of aluminum MgSO4, Vit D, Calcium and B complex. (fig 2.2) His signs and symptoms were generalized erythematous plaques, nodules, vesicles, ulcers, crusting, joint pains, nerve tenderness and fever.

In Feb 2006, with a persistently high average BI 4.5+ (fig 2.1) despite the 5 months treatment of Modified MDT-MB, and worsening skin lesions, accompanied by chills and fever, joint pains and deteriorating liver function SGPT 68.5(0-38) and SGOT 222.9(10-40) it was recommended by Internal Medicine to totally discontinue present Modified MDT medications. Multiple drug resistance was considered with lepra reaction. Alternative drugs were given in Mar 06 namely Transfer Factor 300mg with cordyvants TID and Lymecycline 600mg OD for 4 months. Solid M. leprae bacillis on smears became granulated after 1 month dose and thereafter. (fig 2.3) Prednisone was tapered till 5mg every other day but self- medicated as necessary, when new ENL lesions and joint pains were noted occasionally. There was also irregular intake of Transfer Factor because of financial constraints. In Nov 07, noting the presence of one solid bacilli on smear, and an average BI 4+, he was given another 3 months course of Lymecycline 600mg OD together with more regular intake of full doses of Transfer Factor Plus cordyvant. AFS as of Feb 08 was average BI 1+. ( fig 2.4). The patient will be maintained on Transfer Factor 300mg TID plus cordyvant till AFS negative. As of this writing, he still suffers of few ENL lesions. (fig 2.5)

6. Case 3 using TRANSFER FACTOR with Borderline Leprosy in type II Lepra Reaction:

A 22 year old male from Bulacan was diagnosed with Borderline leprosy in type II lepra reaction in 1Mar06. He was given MDT-MB treatment from 4April06-8March07 and Prednisone 40mg following the WHO recommendation with Clofazimine, Colchicine, Extra virgin coconut oil (EVCO), and Ranitidine. He was never totally off prednisone when in Oct. 30, 2007, he was brought to JRRMMC, wheelchair borne, unable to walk because of severe pain and swelling of both feet with deep necrotic ulcers. (fig 3.1) There was also ulceration on his knee. There was associated nausea and L abdominal pain. His baseline AFS was average BI 3+ and Ave. BI 2+ at the end of MDT-MB treatment.

His diagnosis was Lucio Phenomenon, released from treatment (RFT). Transfer factor 300mg TID plus cordyvants was prescribed as well as gradual tapering of steroid. Debridement with sandwich dressing was done on 2 weekly follow-ups and he was able to walk and go up the stairs on his 3^rd week. His latest ave.BI is .5+ as of Feb08. He will continue to take transfer factor plus until he is AFS negative and aim at removing prednisone 5mg q2d as security blanket treatment.

7. Local testimony on Atopic Dermatitis (a.k.a Skin Asthma or Atopic Eczema):

A 21-year old woman who suffered from severe atopic dermatitis, a chronic infammation of the skin, also called atopic eczema, was told by her array of doctors from various hospitals that there is really no cure for it. However, her dad heard my interview on Transfer Factor over DialM Channel 4, and immediately went to see me last Oct 18, 2008. She started taking Transfer Factor Tri-FactorFormula : 2 capsules 2 x a day before each meal. In just 20 days she recovered. Now she's taking TF as maintenance supplement. Truly it was life changing as she's back on pictorial as a commercial model.

8. Do you know that Cardiovascular Disease is also due to Chronic Inflammation?

This is proven in 48 countries around the world where Transfer Factor is widely used. Transfer Factor can help balance the immune system by commanding the suppressor cells to activate and result in normalcy. This plaque formation inside the arterial walls start with bacterial infection attracting the macrophage (immune system cells in-charge of wiping away the debris left by infections) to accumulate and surround the bacteria, which sensitizes the HDL, High-Density Lipoprotein (good cholesterol), to transform into LDL, Low-Density Lipoprotein (bad cholesterol), resulting into plaque accumulation or atherosclerosis. At this point, high blood occurs which if untreated may lead to bigger cardiovascular problems or even bypass surgery. However, with Transfer Factor, this can be reversed. The immune system cells will now have the ability to recognize the invading bacteria and launches an attack to kill the culprit bacteria and effectively destroying it therefore dissolving the plaque formation and commands the suppressor cells to balance it by flattening it back to its original state. This is a practical way to avoid surgery and angioplasty.

9. HIV/ AIDS:

In its Methodoligical Letter (Moscow 2004), The Ministry of Health and Social Development of the Russian Federation published the following:

"Acquired Immunorehabilitation Syndrome (AIDS) is one of the most serious problems confronting medicine. For HIV patients immune modulation therapy (i.e. the restoration of normal immune function) is aimed altered immune mechanisms and at the pathogenic agent(s).

The results of studies conducted showed that TRANSFER FACTOR (TF) PLUS treatment significantly improved the immune status of HIV patients. The product also proved useful in other aspects of therapy as for example the level of circulating immune complexes (CIC) decreased to normal values in 50% of patients receiving TF PLUS."

10. LEUKEMIA:

In the United States about 27,000 adults and 2,000 children are diagnosed each year with leukemia, a cancer of the white blood cells (WBCs). While exposure to radiation, benzene, and some anticancer drugs have been shown to increase the risk of developing leukemia, and a few cases are associated with genetic disorders or rare viral infections, the cause of most leukemias is not known.

What is it?

Leukemia is a bone marrow disorder that arises when one abnormal white blood cell begins to continuously replicate itself. These cells do not function normally, they do not fight infection as they should, and they do not die at the same rate as other WBCs. As they accumulate, they inhibit the production of the other normal blood cells in the marrow, leading to anemia, bleeding, and recurrent infections. Over time, the leukemic cells spread through the bloodstream where they continue to divide, sometimes forming tumors and damaging organs such as the kidney and liver. Since the spleen is responsible for filtering the blood and destroying old cells, it may become enlarged and swollen with the abnormal cells, as can the liver and lymph nodes. If the cells reach the central nervous system and build up in the cerebrospinal fluid that supports the brain and spinal column, they can cause headaches and seizures.

The bone marrow, located in the soft center of the body's larger bones, produces precursors (immature versions) of red blood cells, platelets, and five different kinds of white blood cells. The most immature of these is called a blast. Most of these blood cells mature in the bone marrow before being released into the bloodstream. The WBCs created are grouped into two main categories: lymphocytes and myelocytes (also called granulocytes for the granules found inside the cell). Myelocytes (which include neutrophils, basophils, eosinophils, and monocytes) circulate in the blood, killing and digesting bacteria. Lymphocytes, which are found in both the blood stream and the lymphatic system, coordinate the immune response and produce antibodies. Leukemia arises from one of these white blood cells. It is categorized both by the type of WBC involved and by how quickly it progresses. Although expanded classifications of the disease exist, the main types of leukemia can be grouped as:

* Acute lymphocytic leukemia (ALL). This is a rapidly developing disease that is characterized by large numbers of immature lymphocytes. It is the most common type of leukemia found in children, although it affects both children and adults (usually adults age 65 and older).

* Chronic lymphocytic leukemia (CLL). This disease progresses more slowly and is characterized by a mixture of mature and immature lymphocytes. It tends to be found in those over the age of 55 or 60.

* Acute myeloid (myelocytic) leukemia (AML). Affecting people of all ages, this disease is characterized by production of large numbers of immature granulocyte myeloid cells (immature neutrophils -- the most common, monocytes, basophils, eosinophils, platelets or red blood cells) that replace other normal cells in the marrow.

* Chronic myelogenous (myelocytic or myeloid) leukemia (CML). Chronic myelogenous leukemia is rare in children. It is an acquired condition that begins in an immature stem cell in the bone marrow when pieces from two chromosomes (9 and 22) break off and switch places (translocation). This results in an altered, fused gene (bcr/abl) on chromosome 22 that produces a protein called tyrosine kinase that affects cell growth regulation. This leads to an overproduction of granulocytic white blood cells, many with the bcr/abl translocation, and the presence of both mature and immature cells in the bloodstream.

LOCAL TESTIMONY ON LEUKEMIA USING TRANSFER FACTOR:

A 12 year old girl, Angel, from the Philippines was diagnosed with Acute Lymphocytic Leukemia (ALL) last July 2007, and went through chemotherapy, was in the ICU for 2 months in August 2008 and now back to the hospital. Last Nov 4, 2008 she was declared about to expire in 24-hours or less, however, her mother heard about Transfer Factor over the NBN Channel 4 DialM show where I (yours truly) was interviewed by Manoling Morato. Immediately, the mother went to see me on that same day and asked about TF. She lost no time to give TF to her beloved daughter, who at that time had a WBC count of 450,000. In just two days it was down to 211,000 and in Nov 8, 2008 Angel is declared stable. Now Angel is becoming stronger and is excited to check out from the hospital so she can play again. This mother is keeping it from her doctor because of some reasons so Angel told her doctor she's taking a "secret" food that's why she is going to live and enjoy life.

Dosage: (1) Transfer Factor Tri-Factor Plus Formula (4 capsules every 6 hrs round the clock), (2) Transfer Factor Tri-Factor Formula (4 capsules every 6 hrs round the clock), (3) Transfer Factor Riovida Drink (30ml every 6 hours round the clock).

However, doctors came in and interrupted with new doses of chemotherapy on Nov. 7 and again gave her two doses of chemotherapy on Nov 13, 2008, one in the morning and another in the evening. She died right after the session.

Before her chemo was administered, Angel pleaded "Mommy, please tell doc I don't want chemo anymore I cant take it anymore. I want only Transfer Factor, it makes me feel good." But inspite of these pleadings, the doctor said "Hindi pwede, kailangan to (I don't agree coz this is important) ".

During the wake yesterday, the mother confessed, that if they only knew Transfer Factor earlier, Angel could still be alive today! We would not even allow chemotherapy. But the miracle is Angel died peacefully, no bleeding in the nose, ears, mouth unlike others who died bleeding. Because of Transfer Factor she did not feel the pain in her dying moments and she was smiling when she expired. This mother said "The 10 day extension of Angel's life beause of Transfer Factor was enough consolation and blessing we recieved".

"Are you going to give chemo to a poor little girl who is feeling better with white blood counts reducing rapidly?" Think again , doc.

Today the whole family is on Transfer Factor and all the mothers in the ward are usingTransfer factor for their children in this hospital. The good news is that there will be no more cancer growing in these families as they all saw the power of TF during the last few days of Angel.

Thank you Angel for touching me. You are truly an angel. Pray that your doctor will change his regimen from now on.

I personally want to invite you to view the website www.transferfactor.com/. This site contains remarkable stories of an immune system product that has really impacted my life. View some of the videos on the site and let me know what you think. I will check back with you soon!