Birth Control
Did you know that there is a guaranteed 100% effective birth control
method and that man has known it since Adam and Eve? This well-known method works at preventing pregnancy with
absolute certainty every time that it is tried. Are you ready? It is
called abstinence!!! Yes indeed,
abstinence works at preventing pregnancy every time that it is practiced.
Now, if you are happily married, then you do not wish to perpetually
abstain. There are basically two types
of birth control methods, natural and chemical. The best natural method is called the symptothermal method. Consult the World Health Organization for
their publications on this and other natural methods. If you choose chemical birth control methods then you are more
than likely killing your offspring through chemically induced micro
abortions.
No, Planned Parenthood along with your liberal teachers and media
talking heads did not tell you that chemical contraceptives cause
abortions. One does not live long in
life before one learns that there is a polemic distinction between the widely
dispensed propaganda of the general public and the real facts of the research
community. We in America have no excuse
for not doing our homework.
Please take note of the date of the following information. Can you trust your information sources to
tell you the truth on this topic? If
not, then promptly abandon them.
The following excerpts are from a book compiled during a
Comprehensive Endocrinology Series edited by Giuseppe Benagiano, M.D. and Egon
Diczfalusy, M.D., entitled, “Endocrine Mechanisms in Fertility Regulation,”
(1983) by Raven Press Books.
Page
7-8: “Implantation: Recent evidence indicates that the following
events associated with implantation are prostaglandin-related: (a) fluid
accumulation by the blastocysts; (b) change in permeability of maternal
capillaries near the blastocysts; (c) decidual reaction and accumulation of
prostacyclin in the myometrium at the site of implantation. Since prostaglandins appear to play a role
in these and other components of the implantation process, prostaglandin
antagonists or inhibitors could be useful contraceptives. Medicated IUDs releasing prostaglandin
inhibitors may be a useful form of contraception. Further, antiprostaglandins suppress uterine motility and
decrease menstrual cramps, suggesting that an improvement in IUD retention
rates with a decrease in IUD-related pelvic pain may result from
antiprostaglandin-medicated IUDs.
A
number of substances which either inhibit implantation or interrupt pregnancy
after implantation have been investigated over the past decade, and a number of
terms have been used to describe these compounds. These include anti-implantation agents, postcoital contraceptives,
morning-after pills, once-a-week pills, interceptive agents, abortifacients,
etc. Estrogens such as
diethylstilbestrol, ethinyl estradiol, and conjugated estrogens prevent
implantation when high does are used for up to 5 days in women starting within
72 hr of coitus. However, intensive
programs have centered around the search for nonestrogenic preimplantative
contragestational agents because of estrogen-related side effects
(14,25,27,34,37).
Since
Corbin and Beattie’s initial report on the abortive effects of administering
large doses of GnRH to pregnant female rats (22), a number of confirmatory
observations have appeared, showing that 100% inhibition of pregnancy
termination occurs in rats treated with as little as 1 mg GnRH per day from
days 1 to 7 of pregnancy. In pregnant
rabbits, higher doses of GnRH appear to cause luteolysis and decreased fetal
survival. Since studies of successful
pregnancy disruption or prevention of implantation have been associated with
decreases in both serum progesterone and estradiol concentrations, it is
tempting to speculate that GnRH-medicated luteolysis may cause pregnancy
termination. Evidence for this
hypothesis is derived from studies where the antinidatory effect of large doses
of GnRH appears to be partially prevented by administration of both
progesterone and estrogens.”
Page
10: “Conclusion: The family of GnRH agonist and antagonist
peptides are now in widespread clinical trials, evaluating a variety of
reproductive processes: (a) follicular maturation; (b) luteolysis; (c)
pituitary gonadotropin secretion; (d) ovulation; (e) implantation; and (f)
abortion.
…if
GnRH can overcome the luteotropic effect of hCG and consequently prevent
implantation or interrupt pregnancy…
…©
disruption of the implanted blastocysts.”
Page
19: “Postcoital Contraception: It is well documented that the administration
of sex hormones immediately postcoitum in an otherwise unprotected intercourse
has a good contraceptive effect. More
recently, there have been studies of estrogen-progestogen combinations, administered
in the form of commercial Oral Contraceptives…rendering the uterine endometrium
unsuitable for implantation.”
Page
36: “Secondary Contraceptive
Mechanisms: Uterine Endometrium: Although suppression of ovulation is the
principal mode of action of all combined Oral Contraceptives, secondary
antifertility actions occur at other sites, reducing the chances of conception
should an escape ovulation occur. One
of the most important of these secondary effects is the development of a
uterine endometrium unsuitable for implantation (103).
The
cyclic pattern of development of the human endometrium is well known.
Many
fixed dose combined Oral Contraceptives completely disrupt the usual cyclic
changes in the endometrium.”
Page
38: “Ovum Transport: A detailed review on ovum transport through
the fallopian tubes to the uterus and its role in fertility and contraception
has been published (68). Fertilization
of an ovum by a spermatozoan occurs in the oviduct, whereas transport of
spermatozoa, unfertilized ova, and fertilized ova through the oviduct depend on
tubal motility and integrity. It is
possible that Oral Contraceptive effects on the fallopian tube may contribute
to secondary contraceptive effects, though for postcoital hormones this may be
a principal effect (177)
Significant
alterations in the human oviducts following use of combined Oral Contraceptives
have been reported by several research groups (8,22,46,53). Changes in zygote transport could be
influenced by alterations in tubal musculature, oviductal fluids, cilial
activity, or a combination of these.
The presence of sex hormone receptors in the human oviduct (130) may
influence any of these physiological aspects.”
Page
40: “Conclusions: Combined Oral
Contraceptives have secondary contraceptive effects, mediated via sex hormone
receptors, on the uterine endometrium, cervical mucus, and oviducts; they may
also interfere with spermatozoan transport and capacitation in the female
tract.”
The following is from the “Symposium on Development Of
Preimplantation Embryos And Their Environment” (1988: Kyoto, Japan) edited
by Koji Yoshinaga and Takahide Mori, Alan R. Liss, Inc. Publisher.
Page
289: “Antiprogestins
And Egg-Implantation: The experimental
work reported here deals with PREVENTION of egg-implantation (Intervention) in
rats by two such compounds, RU 486 (mifepristone) developed by Roussel-Uclaf
and ZK 98734 developed by Schering…”
“We
have recently shown that mifepristone, administered post-coitally in rats,
exerts an antiimplantation effect proportional to the dose administered.”
Page
290: “In the latter studies,
mifepristone, administered to rats on days 1 and 2 or day 2 post coitum, was
found to induce an obvious acceleration of tubal egg transport as well as a
detrimental effect on the prenidatory development of the fertilized egg and its
maintenance in utero.”
Page
292: “Mifepristone as well as ZK 98734
induce a delay in endometrial development, as shown by the “out of phase”
aspect of the luminal surface of the uterine epithelium, when studied under
scanning electron microscopy (Sarantis et al., 1988).”
Page 293: “In conclusion, antiprogestines such as
mifepristone (RU 486) or ZK 98734 given in rats on days 1 and 2 post-coitum,
can reduce the implantation rate to zero.”
Now you know what Planned
Parenthood et al. have known for years.
Chemical contraceptives produce secondary contraceptive effects known as
ABORTIONS!!!!!! Now that you know the
facts, you are no longer innocent but rather GUILTY OF MURDER if you continue your
chemical birth control methods!!!!!!