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Dave (imported) wrote: Sat Jan 04, 2003 10:02 am
Doctors suspect that somehow the human body knows which are viable. On the other hand, if more than one egg is present when implantation takes place, the uterine wall changes chemical properties so that no extra eggs can attach. That's how the morning after pill works. ...
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Generally, the human female only forms one egg cell per menstrual cycle unless she has been on fertility drugs. So, only one fertilization is possible as a rule.
Twins (or multiple pregnancies) can result from...
1. The maturation of more than one ova in a single menstrual cycle.
2. The "splitting" of the zygote before implantation or the cleaving of the embryo after implantation.
Both of the #2 methods produce "identical" twins with identical DNA but the cleaving of the embryo is also responsible for most of the so-called phenomenon of "Siamese twins" of layman terminology.
Spontaneous abortion is a fancy name for miscarriage. It is not a failure of implantation, it is a natural pregnancy termination generally after the major organogenesis phase which is after 6 weeks.
The human body (mother) "knows" if the fetus is viable by way of chemicals, mostly protiens, in the mother's blood that have the ability to cross the placental barrier.
Since fertilization occurs in the fallopian tubes, the "morning after pill" does prevent zygote implantation in the uterine wall, but it also disrupts any implantation that has already occurred, unless the blood supply has become well established.
Because of the interference with the blood supply of the embryo, any use of this medication that does not result in miscarriage necessitates that a surgical abortion be performed to keep the mother from bleeding within the uterus. The fetus, if carried to term, is very likely to have significant birth defects including mental retardation if it is not stillborn. This is a result of the interference with the blood supply.
The zygote becomes an embyo at the time of implantation, and after the first 6 weeks passes the embryo becomes a fetus, with all the body systems and unique DNA (unless there is an indentical twin) and does nothing but grow until birth.
In my previous post I did not mention the fact that the placenta secretes a chemical that causes angiogenesis and that is what establishes the blood supply for the developing embryo. Apparently, in the female-female engineered zygote the mechanism that causes the secretion of the angiogenesis substance is not functioning properly.
Thus, the fetus has no way of parasiticitically establishing itself in the mother's uterus with sufficient blood supply to develop, and so it dies.
In my estimation it is a balance that we deal with here. If too much female influence is present, the fetus develops to a point where it finally "starves" from lack of external nutrient.
If too much male influence is present, however, the placenta develops at the expense of the fetus, hindering fetal development to the point that the fetus loses "viability".
Like I said, we do not understand the chemical processes. We probably never will because of the ethical concerns about human research.
Dave (imported) wrote: Sat Jan 04, 2003 10:02 am
And one last thought - - If I really believed that raging, politically-active lesbians were going to take over the world through cloning, I would change my name to Rush Limbaugh and rant daily about Femi-nazi's on my radio show. Either that, or I would have my cock surgically lenghtened from its normal 2 inches to an average 5 inches.
Dave, I don't think that I would go that far, but I might just make a "cucumber" garden for all of the important females in my life...

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