AUTISM PREVENTION FATHER BABIES 24-34 PATERNAL AGE IS KEY IN NON-FAMILIAL AUTISMVaccines

"It is very possible that PATERNAL AGE is the major predictor of(non-familial) autism." Harry Fisch, M.D., author "The Male Biological Clock". Sperm DNA mutates and autism, schizophrenia bipolar etc. results. What is the connection with autoimmune disorders? Having Type 1 diabetes, SLE,etc. in the family, also if mother had older father. NW Cryobank will not accept a sperm donor past 35th BD to minimize genetic abnormalities.VACCINATIONS also cause autism.

Wednesday, July 09, 2008

As a more sensible, “user-friendly” vaccination schedule, Dr. Miller advises the following:

Is There a More Sensible Vaccination Schedule?

Dr. Donald Miller is a cardiac surgeon and Professor of Surgery at the University of Washington in Seattle and a member of Doctors for Disaster Preparedness. His more sensible vaccination schedule, which I published back in 2004, is worthy of being revisited at this time.

Many are both scared and confused as they try to make healthier choices for their children, and his guidelines may help you devise a more appropriate vaccination plan for your child - a schedule that takes the best interests of your child into consideration rather than what biased government planners cite as being best for society. His is a far better approach than the “one-size-fits-all” dogma foisted on Americans by the CDC panel.

And, as Dr. Blaylock describes so vividly in this article, there’s plenty of information and knowledge in neuroimmunology (the study of how the brain’s immune system works) that raises serious questions about the wisdom of injecting vaccines in children less than 2 years of age.

A Child’s Best Time Table

Your brain has its own specialized immune system, separate from that of the rest of your body. When you are vaccinated, specialized immune cells in your brain, the microglia, become activated. Multiple vaccinations spaced close together over-stimulate the microglia, causing them to release a variety of toxic elements — cytokines, chemokines, excitotoxins, proteases, complement, free radicals — that damage brain cells and their synaptic connections.

The damage caused by these toxic substances is what both Dr. Miller and Dr. Blaylock refer to as “bystander injury.”

In humans, the most rapid period of brain development begins in the third trimester and continues over the first two years. (By then, brain development is 80 percent complete.)

From a risk-benefit perspective, there is little doubt that the risk of neurological and autoimmune diseases from vaccinations at this stage far outweigh the benefits of avoiding the childhood infections that they (supposedly) prevent. (One exception is the hepatitis B vaccine, IF the mother tests positive for hepatitis B.)

As a more sensible, “user-friendly” vaccination schedule, Dr. Miller advises the following:


No vaccinations until your child is two years old.
No vaccines that contain thimerosal (mercury).
No live virus vaccines.
The following vaccines should be given one at a time (not as a combination vaccine), every six months, beginning at age 2:
Pertussis (acellular, not whole cell)
Diphtheria
Tetanus
Polio (the Salk vaccine, cultured in human cells)

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