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FROM WOMB TO WORLD
‘The journey that shapes our life’
September 24, 25 & 26, 2010
9.30 AM- 5.30 PM

A 3-day dynamic Audio-Visual workshop by
Anna Verwaal, RN, CLE, Doula
Hosted by the Nizhoni Institute of Midwifery and San Diego Birth Network
18 BRN and CEU

This profoundly transformational and highly informative course is designed for birth professionals, midwives, doulas, childbirth educators, prenatal yoga instructors, couples planning to conceive or currently pregnant and anyone seeking to understand, prevent and heal from birth imprints & trauma

Over the course of three days you will learn
What we experience in the womb becomes a blueprint for life
How prenatal & birth experiences affect pregnancy, labor and the act of giving birth
The importance of understanding and healing birth imprints and trauma, personally & professionally
The physiological/hormonal design for birth, bonding & breastfeeding
History of childbirth, how midwives were replaced by obstetricians and why?
Cultural beliefs about birth; How normal is what we have accepted as the norm?
Birth-center, home or hospital birth? What you need to know before deciding a model of care
Birth outcomes, statistics and various models of care from around the world
How to consciously conceive, be pregnant and give birth; what your baby really wants you to know
Cost: $400, early bird $350, day of $450, cost for one day $150, (couples 50% off second tuition)
Location: Center for Natural Birth, 4135 54th Place, San Diego, CA 92015
To sign up & for more detailed info please contact:
Stephanie at 310-985-9985 or email This e-mail address is being protected from spambots. You need JavaScript enabled to view it
Anna Verwaal, RN, CLE, born and educated in the Netherlands is a Maternal-Child Health Nurse, Conscious Conception & Birth Consultant, Labor- & Post Partum Doula, UCLA Certified Lactation Educator and Birth Photographer. Currently she gives workshops and lectures internationally about the cellular memory of the birth experience, the physiological & hormonal blueprint for birth & bonding as well as the deeply psychological, emotional and spiritual aspects of giving birth. Her experience is based on working for more than 25 years in various countries as a nurse and doula alongside perinatologists, obstetricians as well as (indigenous) midwives attending hospital, birth center, home, lotus and nature-births.

For more info on Anna please visit www.fromwombtoworld.com

Squalene: The Swine Flu Vaccine’s Dirty Little Secret Exposed

August 4, 2009 by Dr. Morcola

According to Kathleen Sebelius, Secretary of the U.S. Department of Health and Human Services, your children should be the first target for mass swine flu vaccinations when school starts this fall.[i]This is a ridiculous assumption for many reasons, not to mention extremely high risk. In Australia, where the winter season has begun, Federal Health Minister Nicola Roxon is reassuring parents the swine flu is no more dangerous than regular seasonal flu. "Most people, including children, will experience very mild symptoms and recover without any medical intervention," she said.[ii]Sydney-based immunization specialist Robert Booy predicts swine flu might be fatal to about twice as many children in the coming year as regular influenza. Booy estimates 10-12 children could die from the H1N1 virus, compared with the five or six regular flu deaths seen among children in an average year in Australia.[iii]

“Cure the Disease, Kill the Patient”Less than 100 children in the U.S. die each year from seasonal flu viruses.[iv] If we use Australia’s math, a very rough estimate would be another 100 children could potentially die of swine flu in the United States in the coming year. If children are the first target group in the U.S. per Sebelius, that means we’re about to inject around 75 million children with a fast tracked vaccine containing novel adjutants, including dangerous squalene, to prevent perhaps 100 deaths. I’m not overlooking the tragedy of the loss of even one child to an illness like the H1N1 flu virus. But there can be no argument that unnecessary mass injection of millions of children with a vaccine containing an adjuvant known to cause a host of debilitating autoimmune diseases is a reckless, dangerous plan. Why are Vaccinations Dangerous? The presumed intent of a vaccination is to help you build immunity to potentially harmful organisms that cause illness and disease. However, your body’s immune system is already designed to do this in response to organisms which invade your body naturally. Most disease-causing organisms enter your body through the mucous membranes of your nose, mouth, pulmonary system or your digestive tract – not through an injection. These mucous membranes have their own immune system, called the IgA immune system. It is a different system from the one activated when a vaccine is injected into your body. Your IgA immune system is your body’s first line of defense. Its job is to fight off invading organisms at their entry points, reducing or even eliminating the need for activation of your body’s immune system. When a virus is injected into your body in a vaccine, and especially when combined with an immune adjuvant like squalene, your IgA immune system is bypassed and your body’s immune system kicks into high gear in response to the vaccination. Injecting organisms into your body to provoke immunity is contrary to nature, and vaccination carries enormous potential to do serious damage to your health.And as if Vaccines Weren’t Dangerous Enough on Their Own …… imagine them turbocharged. The main ingredient in a vaccine is either killed viruses or live ones that have been attenuated (weakened and made less harmful).Flu vaccines can also contain a number of chemical toxins, including ethylene glycol (antifreeze), formaldehyde, phenol (carbolic acid) and even antibiotics like Neomycin and streptomycin. In addition to the viruses and other additives, many vaccines also contain immune adjutants like aluminum and squalene. The purpose of an immune adjuvant added to a vaccine is to enhance (turbo charge) your immune response to the vaccination. Adjutants cause your immune system to overreact to the introduction of the organism you’re being vaccinated against. Adjutants are supposed to get the job done faster (but certainly not more safely), which reduces the amount of vaccine required per dose, and the number of doses given per individual. Less vaccine required per person means more individual doses available for mass vaccination campaigns. Coincidentally, this is exactly the goal of government and the pharmaceutical companies who stand to make millions from their vaccines. Will There Be Immune Adjutants in Swine Flu Vaccines? The U.S. government has contracts with several drug companies to develop and produce swine flu vaccines. At least two of those companies, Novartis and GlaxoSmithKline, are using an adjuvant in their H1N1 vaccines. The adjuvant? Squalene.According to Meryl Nass, M.D., an authority on the anthrax vaccine, “A novel feature of the two H1N1 vaccines being developed by companies Novartis and GlaxoSmithKline is the addition of squalene-containing adjuvants to boost immunogenicity and dramatically reduce the amount of viral antigen needed. This translates to much faster production of desired vaccine quantities.”[v]Novartis’s proprietary squalene adjuvant for their H1N1 vaccine is MF59. Glaxo’s is ASO3. MF59 has yet to be approved by the FDA for use in any U.S. vaccine, despite its history of use in other countries. Per Dr. Nass, there are only three vaccines in existence using an approved squalene adjuvant. None of the three are approved for use in the U.S. What Squalene Does to Rats Oil-based vaccination adjuvants like squalene have been proved to generate concentrated, unremitting immune responses over long periods of time.[vi] A 2000 study published in the American Journal of Pathology demonstrated a single injection of the adjuvant squalene into rats triggered “chronic, immune-mediated joint-specific inflammation,” also known as rheumatoid arthritis.[vii] The researchers concluded the study raised questions about the role of adjuvants in chronic inflammatory diseases. What Squalene Does to HumansYour immune system recognizes squalene as an oil molecule native to your body. It is found throughout your nervous system and brain. In fact, you can consume squalene in olive oil and not only will your immune system recognize it, you will also reap the benefits of its antioxidant properties. The difference between “good” and “bad” squalene is the route by which it enters your body. Injection is an abnormal route of entry which incites your immune system to attack all the squalene in your body, not just the vaccine adjuvant. Your immune system will attempt to destroy the molecule wherever it finds it, including in places where it occurs naturally, and where it is vital to the health of your nervous system.[viii]Gulf War veterans with Gulf War Syndrome (GWS) received anthrax vaccines which contained squalene.[ix] MF59 (the Novartis squalene adjuvant) was an unapproved ingredient in experimental anthrax vaccines and has since been linked to the devastating autoimmune diseases suffered by countless Gulf War vets.[x]The Department of Defense made every attempt to deny that squalene was indeed an added contaminant in the anthrax vaccine administered to Persian Gulf war military personnel – deployed and non-deployed – as well as participants in the more recent Anthrax Vaccine Immunization Program (AVIP).However, the FDA discovered the presence of squalene in certain lots of AVIP product. A test was developed to detect anti-squalene antibodies in GWS patients, and a clear link was established between the contaminated product and all the GWS sufferers who had been injected with the vaccine containing squalene. A study conducted at Tulane Medical School and published in the February 2000 issue of Experimental Molecular Pathology included these stunning statistics:“ … the substantial majority (95%) of overtly ill deployed GWS patients had antibodies to squalene. All (100%) GWS patients immunized for service in Desert Shield/Desert Storm who did not deploy, but had the same signs and symptoms as those who did deploy, had antibodies to squalene. In contrast, none (0%) of the deployed Persian Gulf veterans not showing signs and symptoms of GWS have antibodies to squalene. Neither patients with idiopathic autoimmune disease nor healthy controls had detectable serum antibodies to squalene. The majority of symptomatic GWS patients had serum antibodies to squalene.”[xi]According to Dr. Viera Scheibner, Ph.D., a former principle research scientist for the government of Australia:“… this adjuvant [squalene] contributed to the cascade of reactions called "Gulf War Syndrome," documented in the soldiers involved in the Gulf War. The symptoms they developed included arthritis, fibromyalgia, lymphadenopathy, rashes, photosensitive rashes, malar rashes, chronic fatigue, chronic headaches, abnormal body hair loss, non-healing skin lesions, aphthous ulcers, dizziness, weakness, memory loss, seizures, mood changes, neuropsychiatric problems, anti-thyroid effects, anaemia, elevated ESR (erythrocyte sedimentation rate), systemic lupus erythematosus, multiple sclerosis, ALS (amyotrophic lateral sclerosis), Raynaud’s phenomenon, Sjorgren’s syndrome, chronic diarrhoea, night sweats and low-grade fevers.”[xii]Post Vaccination Follow-Up Might as Well Be Non-ExistentThere is virtually no science to support the safety of vaccine injections on your long-term health or the health of your children. Follow-up studies last on average about two weeks, and look only for glaring injuries and illnesses.Autoimmune disorders like those seen in Gulf War Syndrome frequently take years to diagnose due to the vagueness of early symptoms. Complaints like headaches, fatigue and chronic aches and pains are symptoms of many different illnesses and diseases.Don’t hold your breath waiting for vaccine purveyors and proponents to look seriously at the long-term health consequences of their vaccination campaigns.[i] USAToday.com, Swine flu shots may go to kids first, Sebelius says, June 16, 2009 http://www.usatoday.com/news/health/2009-06-16-swine-flu-vaccine_N.htm [ii] ABC.net.au, Health minister reassures parents over swine flu, July 2, 2009 http://www.abc.net.au/news/stories/2009/07/02/2614972.htm [iii] Google News, AFP, Australia urges calm after child flu death, July 2, 2009, http://www.google.com/hostednews/afp/article/ALeqM5hVoGSwV_jPgg6J6Aoz8wSQiGyosg [iv] Meryl Nass, M.D., July 4, 2009 http://anthraxvaccine.blogspot.com/2009/07/h1n1-update-australiahong-kongus.html [v] Meryl Nass, M.D., July 3, 2009 http://anthraxvaccine.blogspot.com/2009/07/h1n1-vaccines-with-novel-adjuvants.html [vi] Rense.com, Vaccines, Autism, and Gulf War Syndrome, August 15, 2005 http://www.rense.com/general67/vacc.htm [vii] The American Journal of Pathology, The Endogenous Adjuvant Squalene Can Induce a Chronic T-Cell-Mediated Arthritis in Rats, 2000 http://ajp.amjpathol.org/cgi/content/abstract/156/6/2057 [viii] Vaccination Liberation, Adjuvant Index Page http://www.vaclib.org/basic/adjuvants.htm [ix] Autoimmune Technologies, News Release: SQUALENE FOUND IN ANTHRAX VACCINE, http://www.autoimmune.com/SqualeneInVaccine.html [x] Autoimmune Technologies, Gulf War Syndrome: ANTI-SQUALENE ANTIBODIES LINK GULF WAR SYNDROME TO ANTHRAX VACCINE http://www.autoimmune.com/GWSGen.html [xi] ScienceDirect.com, Experimental and Molecular Pathology, Volume 68, Issue 1, February 2000, Pages 55-64 http://www.sciencedirect.com/[xii] Adverse Effects of Adjuvants in Vaccines, by Viera Scheibner, Ph.D., 2000 http://www.whale.to/vaccine/adjuvants.html

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Should My Family Get The Swine Flu Vaccine?

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