SaneVax Asks the FDA: Gardasil® What is Wrong With This Picture? Medical consumers worldwide applaud the recent FDA decision not to expand the use of Gardasil to women over the age of 26. Now they want to know when the FDA will admit the original approval may have been a mistake.
Läs: http://childhealthsafety.wordpress.com/2011/04/13/fda-halts-hpv-vaccine-roll-out-sanevax-news-release/
HPV vaccines were never designed to attack the cancer cells; they were designed to produce a greater immune response to ‘foreign invasion’ by human papillomavirus. The hope is that by eliminating the virus, cancer rates will be reduced. No one will know whether this will actually happen for at least 15 to 20 years. However, based on the post-vaccination reports, many Gardasil-vaccinated women have continued to develop cervical cancer and precancerous lesions.
The SaneVax Team wants to know: Why is Gardasil® approved by the FDA as a cervical cancer preventive when there is no clinical evidence that reducing some self-reversing lesions is indeed associated with reduction of cervical cancer rates?
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