Universal Oral Vaccine: The Immune Milk Saga Part 2

Townsend Letter for Doctors and Patients, August, 2001 by Anthony Di Fabio

Scope of Protection

As already stated, appropriate scientific studies carried out in the early '60s found promising success. They included rheumatoid arthritis, multiple sclerosis, rheumatic fever, and pollen allergies. Subsequent research has expanded this list considerably, including drying up some cancerous tumors.

According to Herbert Edwin Struss, PhD, one unpublished report showed "spectacular" survival rates for small children from a poverty area in Mexico who were treated against colon bacteria with this method by cooperating Mexican physicians.

As a general principle, this method of preparing disease-specific colostrum will transfer adaptive immunity safely against any allergen or antigen -- any substance which, when introduced into the body, creates antibodies (such as allergenic pollens, house dust, animal hairs, or microorganism proteins). For allergy prevention, one can use a mixture of hair (cats, dogs, cattle), making a bovine cistern-injectable vaccine. Other allergens, like pollens, can also be introduced into the cow's cistern resulting in colostrum that has the beneficial effects of developing resistance to the antigens that produce the allergies.

Experimental studies in the patents listed in the references attached include: "bacteria, viruses, proteins, animal tissue, plant tissue, spermatozoa, rickettsia, metazoan parasites, mycotic molds, fungi, pollens, dust and similar substances...exemplary antigens include: bacterial -- Salmonella pullorum, Salmonella typhi, Salmonella parathypi, Staphylococcus, aureus, a Streptoccous agalactiae, g Streptococcus agalactiae, Staphyloccus albus, Staphylococcus pyogenes, E. Coli, pneumococci, streptococci, and the like; viral -- influenza type A, fowl pox, turkey pox, herpes simplex and the like; protein -- egg albumin and the like; tissue -- blood and sperm."

In an experiment using immune milk conducted at Notre Dame University's Lobund Institute, Impro Products, Inc. substances reduced tooth decay in laboratory animals as much as 87%. (Although bacteria are usually blamed, the work of dentist Dr. Trevor Lyons clearly demonstrates a synergism between protozoans and bacteria, and the devastating effects of certain protozoans. [5])

Trial mammals protected according to various immune milk patents were mice, cows, goats, chickens and pigs.

The immune milk method is also good for chickenpox, cold sores, genital herpes, Cryptocides sporidium, and for anti-inflammatory conditions, as it is heavy with complement (C3B) and anticomplement, substances that assist in the destruction of invasive organisms.

Other Sources than Immune Milk

Although not as economical or as easy to obtain as bovine or goat colostrum, the same disease-specific antibody and complement can also be obtained from other sources than colostrum. For example: (1) donors with high (cell-mediated) immunity to known antigens (cloning); (2) from human placentas, and (3) the spleen from immunized pigs or ducks, or even from humans who have good (cell-mediated) immunity to the relevant antigens.

Because these substances -- called "transfer factors" -- are so cheap, widespread, and easy to use, various countries outside of the United States use it, including China, Czechoslovakia, Germany, Poland, and Hungary. In Japan, the only high-wage country where it is used, 40 Red Cross Centers provide transfer factor produced from pooled leukocytes (white blood cells) of normal healthy donors to 400 hospitals for use in a wide variety of conditions.

(Use of transfer factor does not cause hepatitis, but is effective against hepatitis, does not cause AIDS, and may be helpful in some of the diseases associated with AIDS.)

There are many particles that can transfer immunity. Subsequently confirmed by other scientists -- in reporting on membrane filtered (dialyzable) white blood cells (leukocytes) to obtain "transfer-factors" -- they found that transfer of immunity had taken place in the following conditions: [26-27]

1. Familial T-lymphocyte dysfunction with severe recurrent infection (white cell dysfunction)

2. Herpes infection (viral)

3. Cytomegalovirus infection (viral)

4. Candidiasis (yeast/fungus)

5. Parasitic infection (e.g., pneumocystis carinae, cryptosporidiosis, etc.)

6. Mycobacterium tuberculosis infection refractory to antibiotics

7. Behcet's syndrome (skin condition/arthritis)

8. Lupus erythematosus

9. Pemphigus vegetans (skin disease)

10. Wiskott-Aldrich Syndrome (immune deficiency disease with decreased blood platelets and skin rash)

11. Florence Nightingale Disease (aka Chronic Fatigue Immune Dysfunction Syndrome)

12. Bone metastases after surgical removal of breast cancer

13. Bone metastases after surgical removal of kidney cancer

14. Guillian Barre (disturbance of two or more nerves, after viral or mycoplasma infection)

15. Amyotrophic lateral sclerosis (Lou Gehrig's disease; one subset)

16. Retinitis Pigmentosa (inflamed retina: one subset, 50%; Dialyzable Leucocyte Extract-Transfer Factor -- filtered through a membrane -- does not reverse the disease but prevents additional visual loss)