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World Leaders of The Campaign
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http://www.cmdahome.org/index.cgi?CONTEXT=art&art=1563&BISKIT=2029710460 Christian Medical and Dental Association
Personal Safety and Public Health Since
the pioneering work of Edward Jenner and others in developing a vaccination for
smallpox over 200 years ago, immunization has been of great benefit to
individuals as well as the public. Immunization practices have prevented
outbreaks of communicable diseases and resultant deaths or disability and
continue to prevent an ever-increasing variety of illnesses.
The use of medical
information and technology obtained through immoral means raises concerns about
moral complicity with evil*. Some currently available vaccines were developed
using tissue from aborted fetuses, while others use technology or knowledge
acquired from the use of aborted fetuses. We need to consider carefully whether
it is morally permissible to benefit from knowledge or technology obtained from
the intentional destruction of human life. · Using technology that was developed without any intentional destruction of human life or other evil is morally ideal. Most vaccines in use to date fall into this category. · Using technology developed from tissue of an intentionally aborted fetus, but without continuing the cell line from that fetus, may be morally acceptable. · Continued use of a cell line developed from an intentionally aborted fetus poses moral questions and must be decided as a matter of conscience, weighing the clear moral obligation to protect the health of our families and society against the risk of complicity with evil. ·
Using a vaccine that requires the continued destruction of human life is morally
unacceptable. The following information was gleaned from a review of the currently available vaccines as listed in the Physician’s Desk Reference 2004. The table shows the vaccines that are produced using cell cultures derived from aborted tissue. We are not aware of any vaccine whose production requires cell cultures from on-going abortions. In each case, the cell culture that is used was developed 30-40 years ago.
The following vaccines are possible alternatives to the vaccines listed above. They are produced without human embryonic cell cultures. · Mumpsvax (Merck) for Mumps: Note that immunization for measles (rubeola) and German measles (rubella) are not included. · Attenuvax (Merck) for rubeola
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RabAvert (Chiron) for rabies · Anthrax · Diphtheria · DPT (diphtheria, tetanus, pertussis) · Haemophilus B · Hepatitis B · Influenza · Meningococcal Meningitis · Pneumococcal Pneumonia · Tetanus · Typhoid
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Yellow fever · Mumpsvax (Merck) for Mumps: Note that immunization for measles (rubeola) and German measles (rubella) are not included. · Attenuvax (Merck) for rubeola
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RabAvert (Chiron) for rabies · Anthrax · Diphtheria · DPT (diphtheria, tetanus, pertussis) · Haemophilus B · Hepatitis B · Influenza · Meningococcal Meningitis · Pneumococcal Pneumonia · Tetanus · Typhoid · Yellow fever
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