11/6/17

Cloning--Scientific and Biblical Ramifications [Part II] by Bert Thompson, Ph.D.

http://apologeticspress.org/APContent.aspx?category=7&article=236

Cloning--Scientific and Biblical Ramifications [Part II]
by Bert Thompson, Ph.D.


[EDITOR’S NOTE: Part I of this two-part series appeared in the May issue. Part II follows below and continues, without introductory comments, where the first article ended.]
As a result of the success of recent experiments in genetic engineering, the cloning of humans is on the minds of many, both among the general populace and with in the scientific community. In the past, the cloning of humans was a subject best discussed within the genre of science fiction novels, not scientific journals. When scientists, or science writers, did discuss the possibility of human cloning, their comments usually went something like this:
This is far beyond the reach of today’s science. There is a vast difference between cloning an embryo that is made up of immature, undifferentiated cells and cloning adults cells that have already committed themselves to becoming skin or bone or blood. All cells contain within their DNA the information required to reproduce the entire organism, but in adult cells access to parts of that information has somehow been switched off. Scientists do not yet know how to switch it back on (Elmer-Dewitt, 1993, p. 66).
In this statement, Philip Elmer-Dewitt, a writer for Time magazine, echoed what seemed to be a commonly-shared view among the researchers involved in genetic engineering. No one had been able to clone mammals using adult somatic cells, because for some unknown reason a great portion of the DNA in those cells had been “switched off.” But, as the old saying goes, “That was then; this is now.”

“HELLO, DOLLY!”—
THE STORY OF AN “UDDERLY INCREDIBLE” LAMB

What a difference four years makes in science! In the Table of Contents of the February 27, 1997 issue of Nature (the official organ of the British Association for the Advancement of Science), there appeared what seemed at first glance to be an innocuous article titled “Viable Offspring Derived from Fetal and Adult Mammalian Cells” (Wilmut, et al., 1997). That article, however, announced the results of scientific research so significant that it not only would make history, but change forever the way scientists viewed cloning in both animals and humans.
Researchers from the Roslin Institute near Edinburgh, Scotland had accomplished what almost everyone in the scientific community thought to be impossible. Headed by embryologist Ian Wilmut, Scottish scientists produced a lamb using genetic material from the mammary cell of an adult ewe. The young lamb, named Dolly, did not owe her existence to a procreative act occurring between a ram and a ewe. Instead, Dolly was the result of a laboratory exercise in cloning. When her existence was announced, the entire world gasped—first in disbelief, then in amazement! As Time put it, the Scottish researchers had succeeded in
...scoring an advance in reproductive technology as unsettling as it was startling. Unlike offspring produced in the usual fashion, Dolly does not merely take after her biological mother. She is a carbon copy, a laboratory counterfeit so exact that she is in essence her mother’s identical twin (Nash, 1997, p. 62).
Technique used by Wilmut, et al. to clone a sheep. Their breakthrough involved starving body cells of nutrients, thus interrupting the normal cycle of growth and division. In this quiescent stage, the cell can be “reprogrammed” to function as a newly fertilized egg (after Travis, 1997, 151:215).
Here is what Dr. Wilmut did to make Dolly a reality. As noted earlier, embryonic cells are easier to use in cloning experiments than adult somatic cells because they are, for the most part, undifferentiated. In other words, they have not matured to the point where they have been able to carry out the instructions contained in the DNA within their nucleus that direct them to become skin cells, brain cells, eye cells, etc. In its young, embryonic state, an undifferentiated cell can become any other cell in the body, because it has the capacity to activate any given gene on any given chromosome. Non-embryonic somatic cells, however, already have carried out their DNA instructions, and as a result are differentiated (i.e., in their mature state, they have become hair cells, muscles cells, nerve cells, etc.). As a result, huge portions of the DNAinstructions have been “deactivated,” so that mature cells can carry out their particular function(s). Thus, much of the information coded within the DNA of adult cells no longer is accessible, having been “turned off ” at maturity because it no longer is needed by the cell.
In the past, most scientists involved in the broad area of genetic engineering thought that the differentiation process was irreversible. However, Dr. Wilmut and his coworkers disproved that idea by devising a way to “reactivate” the portions of the DNA molecule that previously had been deactivated, thus making adult somatic cells candidates for cloning.
First, the team of Scottish scientists searched for a mechanism that would allow them to arrest the normal cell cycle (i.e., the process through which all cells go as they mature and prepare to reproduce themselves). They surmised that this might be accomplished by starving cells of the nutrients they normally would need to grow. Some of the cells chosen for the experiment were from the udder of a Finn Dorset ewe. Once deprived of these critical nutrients, the mammary gland cells fell into a sort of “suspended animation” (what, in live animals, would resemble hibernation), a state in which they remained for one week.
Second, using the procedure (discussed previously in this series of articles) known as “nuclear transfer,” Dr. Wilmut took an unfertilized oocyte (i.e., an egg cell) from a Scottish Blackface ewe and carefully removed its nucleus, leaving the remainder of the cell (cytoplasm, cell membrane, etc.) completely intact (see Stewart, 1997). Then, he took the quiescent mammary gland cell, placed it next to the oocyte, and gently applied short bursts of electrical current, which prompted the egg cell to bond with the somatic cell and absorb its nucleus (containing a full complement of chromosomes) as its own. As a result, the egg cell possessed the number of chromosomes it would contain if it had been fertilized by the male’s sperm. The biochemical activity usually associated with a zygote (the cell that results when sperm and egg combine) then began to occur.
Third, after one week of carefully-monitored growth, the laboratory-engineered embryo then was inserted into the uterus of a surrogate ewe, to see if it would implant successfully and grow to term.
All of this may sound quite simple, but it is not. Dr. Wilmut’s success came only after a long string of failures. In fact, he reported in his article in Nature that out of 277 eggs fused with udder cells, he and his team were able to produce only 29 embryos that survived more than six days. Of those 29, all died before birth except Dolly.

CLONING—WHY BOTHER?

To the uninitiated, all of this may seem at best much ado about nothing, or at worst a complete waste of time, effort, and money. Why go to all the trouble and expense to clone an animal, when normal reproductive processes can produce an animal without all the fuss? “Just let nature take its course,” some might say.
There is much more to it than that, however. Cloning has the potential to make animal husbandry more effective and efficient. Imagine (to use just one example) the plight of the dairy farmer searching for a way to breed cattle that produce better milk in greater quantities. If he could isolate one or more cattle that consistently produced more, and better, milk than all the others, he could have them cloned, thus guaranteeing whole herds of the highest quality milk-producing animals.
In addition, cloning has the potential both to reduce human suffering, and to extend human life. Suppose (again, to choose just one hypothetical example) that scientists were able to discover a mechanism by which they could genetically alter chimpanzees so that portions of their immune systems, or products manufactured by those immune systems, were indistinguishable from those found in humans whose own immune systems were diseased or damaged, and thus incapable of fighting off disease to sustain life. These chimpanzees then could be cloned so that as many copies as needed could be produced, thereby ensuring life-saving animal products in an endless supply for use in humans.
Further, cloning has the potential to enlarge our knowledge about how cells differentiate and reproduce. Using the information gleaned from the study of the cell during cloning, scientists believe they could learn more about why cancer cells grow out of control, or why birth defects occur. In short, cloning does hold forth immense potential in many different areas and, used properly, could offer tremendous benefits to mankind (see Scientific American, 1997).
The operative phrase, here, however, is “used properly.” With cloning, as with many of the technologies offered by modern science, there can be serious scientific and biblical ethical implications. Rarely is the technology, in and of itself, morally objectionable; instead, it is the useof the technology that makes it so. Part of the problem is the fact that science itself is not equipped to deal with moral issues. There is nothing within the scientific method, for example, that can dictate whether nuclear energy should be used to destroy cancer cells, or entire cities. That is a judgment far beyond the scope of science to make.
Unfortunately, once the technology is made available, there are those who are prepared to employ it, regardless of any ethical problems that might be associated with it. Since many within the scientific community either do not believe in God, or do so only accommodatively, they neither are interested in, nor restricted by, the guidelines and principles set forth in His Word. As a result, in their eyes the simple fact that the technology is available is reason enough to use it. Within the scientific community, this is referred to as the “technological imperative”—whatever can be done should be done!

WILL WE BE ABLE TO CLONE HUMANS?

In regard to cloning, the most pressing questions on almost everyone’s mind are: (a) why would anyone want to clone a human in the first place; (b) if attempts at cloning humans are successful, would a clone be an exact duplicate of the original; (c) will we eventually be able to clone humans; and (d) most important, would humans produced by cloning possess a soul?
Why would anyone want to clone a human? First, parents might want to clone a child as a “replacement” for one that had died. Second, parents might want to clone a child to provide compatible organ transplants for a diseased relative. [There have been cases of women wanting to become pregnant so they could abort the child to provide fetal brain cells for transplantation into a relative (e.g., a parent suffering from Parkinson’s Disease).] Third, individuals might want to have themselves cloned to guarantee immortality—if not in soul, at least in body. Fourth, some may desire to clone a human simply for the prestige and adulation that inevitably will result from having accomplished what no one else has been able to do. A Nobel Prize can provide a very strong incentive indeed!
If attempts at cloning humans are successful, would a clone be an exact duplicate of the original? A clone would be an exact genetic duplicate of the original—the word “genetic” providing a critical distinction. Merely possessing identical genes does not guarantee identical people. Ask anyone with identical twins. In fact, twins would be more alike than clones for the simple reason that the twins would have shared the same environment, upbringing, etc. People are more than merely a “bag of genes.” Each of us is the end-product of many different external forces that influence us from cradle to grave. Our personalities and attitudes are formed by parents, friends, teachers, daily routines, societal interactions, and many other factors that affect us during our lifetimes.
Will we be able to clone humans eventually? That remains to be seen. No scientist can answer that question, for to do so would be to possess the ability to predict the future—something neither a scientist, nor science, is equipped to do. Furthermore, there are too many unknowns. We do not know if human adult somatic cells will respond the same way adult somatic cells from sheep responded. We do not know if the process used to produce Dolly (nuclear transfer) would work in humans. And so on.
However, if the question were reworded so that it asked, “Will scientists attempt to clone humans?,” I think the answer would be “yes.” An analogy might be helpful. When mountaineers are asked why they ascend a challenging (and often life-threatening) mountain, they routinely respond: “...because it’s there.” Some scientists likely will take the same approach. When asked why current technology should be used to clone humans, they will respond: “...because it’s there.” One writer has suggested:
...it is not a question as to whether we will attempt to clone a human being or not. Many technical hurdles will have to be overcome first before we can attempt to produce cloned humans, so they say. But if the moral and ethical scientists want to wait, or even shrink in fear from such an undertaking, there are many in the world who have the financial means, who do not have any scruples or reservations about cloning humans. What about them? (Sinapiades, 1997, p. 6, emp. in orig.).
I believe it no longer is a matter of if attempts will be made to clone humans using this new technology, but only when. Eventually some scientist, or group of scientists, will yield to the temptation to apply the Scottish scientists’ methodology to the human race.
If (and this is a big “if ”) scientists are successful in cloning humans, the most pressing question then becomes—will the people so produced possess a soul? Much of the debate occurring today (especially in religious circles) centers on this question. For example, three staff writers for U.S. News & World Report posed the question, “Would a cloned person have its own soul?,” and answered it as follows: “Most theologians agree with scientists that a human clone and its DNAdonor would be separate and distinct persons. That means each would have his or her own body, mind, and soul” (Herbert, et al., 1997, p. 63).
In addressing what at the time was the unlikely possibility of the cloning of humans, Gish and Wilson asked: “What do we say, then? Would a clone be truly human? The answer is that, indeed, he would be human, for its life came from human life even though in a manner different than is usually the case” (1981, p. 174). In addition, they noted, the cloned human “is already alive, responsible to God for his actions, needing to preserve his own body against sickness, to see that he is properly fed, and all the rest. Each clone would have its own individual responsibility, its own soul” (p. 172).
I concur with such an assessment. In James 2:26, James made this observation: “The body apart from the spirit is dead.” The point, of course, was that when the spirit departs the body, death results. But there is an obvious, and important, corollary to that statement. If the body is alive, it must be the case that the spirit is present. This is a biblical principle that cannot, and must not, be ignored—especially in light of the present controversy. The simple fact of the matter is that if(again, a very big “if ”) scientists succeed in cloning living humans, those clones would possess a soul.
But only God can instill a soul. It is He Who “giveth to all life, and breath, and all things” (Acts 17:25). It is only “in Him” that “we live, and move, and have our being...” (Acts 17:28). The real issue is not whether man is intelligent enough to clone a human, but whether or not—should that eventually happen—God will choose to instill the lifeless creature in the laboratory with a soul. This is a question no one can answer.

SHOULD WE CLONE HUMANS?

Very often it is the case that with increased knowledge also comes increased power. And with increased power comes the potential for misuse or abuse of that power. The question, “will we be able to clone humans?” is not the same question as “should we clone humans?” The first is a question to be answered by an appeal to science; the second is a question to be answered by an appeal to the Word of God.
Oddly, at times those who do not believe in God or His Word as an objective moral standard seem to understand the ethical/moral issues better than some Christians. For example, long before the technology was available that could lead to human cloning, evolutionist Gunther Stent of the University of Southern California stated: “The idea of cloning humans is morally and aesthetically completely unacceptable” (as quoted in Howard and Rifkin, 1977, pp. 125-126). Compare that with the comment of Christian ethicist Randy Harris of David Lipscomb University: “Although there has been a good deal of rhetoric on the evils that are just ahead, I have yet to hear a cogent ethical argument as to why even the cloning of a human would be wrong” (1997, p. 16).
There are, in fact, several “cogent ethical arguments” that can, and should, be made against the cloning of humans, only two of which I would like to mention here.

Cloning’s “Failures” Represent Dead Human Beings

It is one thing to attempt—and fail—277 times using sheep cells in an attempt at cloning. Sheep are animals that do not possess souls, and that are not made in the “image and likeness of God” (Genesis 1:26-27). But it is quite another thing to try—even once—and fail in an attempt to clone a human. Embryos are living human beings! [On occasion, pro-abortion forces often argue that embryos within the womb are “not living.” If that is the case, then leave them alone. This, of course, is hardly an option, because in nine months the end-result is a human baby—something impossible to explain if the embryo was “not living” to begin with.] A laboratory littered with dead and dying sheep embryos is one thing; a laboratory littered with dead and dying human embryos is quite another!
Ask any knowledgeable ethicist, Christian or otherwise, and he or she will confirm that basic medical ethics requires that in any experiment, the subject must know the risks and give “informed consent.” In the case of cloning, however, the tiny embryo being produced (and that more often than not will die) can do no such thing. With cloning—if the success rate of the Scottish scientists is taken at face value—the failure rate will be staggering.
Basic medical ethics also requires that the experiment be to the subject’s benefit. Laboratory procedures for cloning humans scarcely would be to the benefit of the cloned embryos. Scottish scientist Wilmut and his colleagues saw 277 of the embryos they had produced perish before they saw a single one live. What if the same failure rate held true for the cloning of humans? Or, for the sake of argument, suppose that somehow the failure rate could be cut in half (in other words, out of 277 attempts, “only” 139 human embryos died in the process)? Would that then be ethically and morally acceptable? It would not! Producing human embryos—with the full knowledge that many more of them will die than will live—is indeed (to quote evolutionist Stent) “morally and aesthetically completely unacceptable.” Medical ethicist Paul Ramsey has suggested that we cannot even develop the kinds of reproductive technologies being discussed here “without conducting unethical experiments upon the unborn who must be the mishaps (the dead and retarded ones) through whom we learn how” (as quoted in Restak, 1975, p. 65).
Human life, as a gift from God (Acts 17:25), is sacred. The Proverbs writer observed that “there are six things which Jehovah hateth; yea, seven which are an abomination unto him: haughty eyes, a lying tongue, and hands that shed innocent blood” (6:16-17). Yet there is a tendency to ignore these divine principles, and to view human life as that which may be destroyed capriciously. Should Christians consider laboratories teeming with the dead and dying human embryos that resulted from failed attempts at cloning to be a “cogent ethical argument” against such procedures? Or should they instead, to use Leon Kass’ words, simply “leave it so that discarding laboratory-grown embryos is a matter solely between a doctor and his plumber” (as quoted in Restak, 1975, p. 65)?
Further, in examining the ethical issues surrounding procedures such as these, the implications of the various technologies must be acknowledged. For example, if cloning were possible:
  1. It could be used to provide children for unmarried people.
  2. Parents could pre-select the sex (and many other attributes) of their child(ren).
  3. Women’s liberation would be complete, since no male would be needed. The old Cockney saying, “It takes a man to make a girl,” no longer would be true.
  4. Large batches of human clones could be made for statistical studies.
  5. Clones could be produced in order to harvest “spare parts” for transplants (e.g., bone marrow, organs, etc.).
  6. People enamored of their own importance could ensure that exact genetic replicas of themselves were brought into existence via cloning—by tens or hundreds if they so desired.
If we scrutinize the alleged benefits of human cloning, there is less here than at first meets the eye. Producing people for spare parts, or to use as guinea pigs, is repugnant. David Lygre wrote: “The current risks of abnormality and our reverence for human life should rule these experiments out” (1979, p. 44). Indeed they should.

Cloning Circumvents God’s Plan for Reproduction

In a series of articles authored some years ago, Wayne Jackson remarked that these scientific experiments “strike at the very heart of God’s arrangement for human reproduction within the circle of the family unit and all that this involves” (1979, 15:3; see also Jackson, 1994, pp. 27-36). The use of such things as donor sperm, donor eggs, surrogate mothers, and cloning stand in stark contradistinction to God’s divinely designed plan for the home. While many things, biblically, could be said about God’s design of the home, one thing is clear. It is through the family unit (which includes both a husband and wife in the procreative act) that God intended for children to be brought into this world. According to divine design, marriage is to precede the bearing of children (1 Timothy 5:14). And it is not by accident that Moses recorded: “And the man [Adam—BT] knew Eve, his wife; and she conceived...” (Genesis 4:1; emp. added). Jack Evans correctly observed that God’s
...spiritual law says the oneness of the flesh can be approved only by Him in the marriage of the male and female who are producing another part of their flesh (Hebrews 13:4; I Corinthians 6:16; 7:1-5). Thus, the Bible teaches that the male and female producing the offspring of the one flesh, according to spiritual law, must be married to each other. ...It is obvious that marriage precedes bearing children. Thus, if the female bearing the child is not married to—is not one flesh with—the male in the reproduction process, they violate God’s spiritual law (1987, p. 358).
God’s plan is that children be produced through the husband and wife via their “one flesh” covenant. The world often forgets that childbearing never was intended to be an end within itself, but is part of a much larger plan.
Any action that ignores, or nullifies, God’s plan for the home, and reproduction within the framework of the home, must be avoided and opposed. Cloning does just that. It circumvents the principle of a husband and wife becoming “one flesh,” and through that procedure bringing children into the world. The family unit was planned to provide an atmosphere of love and trust (Proverbs 15:17; 17:1), which would create an ideal environment for spiritual growth. To ignore these truths is to miss the real meaning of the divinely planned family, and the procreative acts that God placed within that family unit.

CONCLUSION

Each day brings exciting new scientific discoveries. Improved techniques block pain and prevent suffering. New medicines cure or prevent diseases. Advancements in knowledge and methodology continually work to mankind’s benefit. As Suzuki and Knudtson concluded:
There is no reason to fear the stunning new conceptions of human hereditary disease now emerging from genetics research. In fact, we can rejoice that this new genetic knowledge is certain to improve the prevention, detection and treatment of many previously untreatable genetic disorders. At the same time, each of us shares responsibility for ensuring that techniques allowing the manipulation of the human genome are never exploited for arbitrary and self-serving ends or in ways that fail to consider the potential long-term consequences of large-scale genetic repair on human populations (1989, pp. 206-207).
Certainly, the faithful child of God may support many scientific advances that cure disease, alleviate suffering, and make life better. But the Word of God is the criterion against which every advance must be measured. The end does not always justify the means.

REFERENCES

Elmer-Dewitt, Philip (1993), “Cloning: Where Do We Draw the Line?,” Time, pp. 65-70, November 8.
Evans, Jack (1987), “Is Surrogate Motherhood Sinful?,” Gospel Advocate, 129:358, June 18.
Gish, Duane T. and Clifford Wilson (1981), Manipulating Life: Where Does It Stop? (San Diego, CA: Master Books)
Harris, Randy (1997), “Will There Ever Be Another You?...Ewe?,” Christian Chronicle, 54[5]:16-17, May. [Harris is one of several scientists, theologians, and philosophers whose positions on cloning are presented in a special two-page spread, edited by Lindy Adams.]
Herbert, Wray, Jeffrey L. Sheler, and Traci Watson (1997), “The World After Cloning,” U.S. News & World Report, 122[9]:59-63, March 10.
Howard, Ted and Jeremy Rifkin (1977), Who Should Play God? (New York: Dell).
Jackson, Wayne (1979), “Ancient Ethics in a Modern World,” Christian Courier, 14:41-47; 15:2-4,6-8, May/June.
Jackson, Wayne (1994), Biblical Ethics & Modern Science (Stockton, CA: Courier Publications).
Lygre, David (1979), Life Manipulation (New York: Walker).
Nash, J. Madeleine (1997), “The Age of Cloning,” Time, 149[10]:62-65, March 10.
Restak, R.M. (1975), Pre-Meditated Man (New York: Viking).
Scientific American, “Special Report: Making Gene Therapy Work,” 276[6]:95-106.
Sinapiades, Mike (1997), “Cloning, Clowning, or What?,” First Century Christian, 19[2& 3]:6, February/March.
Stewart, Colin (1997), “An Udder Way of Making Lambs,” Nature 385:769,771, February 27.
Suzuki, David T. and Peter Knudtson (1989), Genethics (Cambridge, MA: Harvard University Press).
Travis, John (1997), “A Fantastical Experiment,” Science News, 151:214-215, April 5.
Wilmut, Ian, A.E. Schnieke, J. McWhir, A.J. Kind, and K.H.S. Campbell (1997), “Viable Offspring Derived from Fetal and Adult Mammalian Cells,” Nature, 385:810-813, February 27.


Cloning Links
In addition to part one of the current article, other references to cloning are available on our Web site

WWWThe following articles are available off-site. We do not necessarily endorse the material you find at these links. They are provided for information purposes only.
Dolly and Mom
  • Roslin Institute. Information from the Scottish research center that cloned Dolly.
  • Salon. Interview with Ian Wilmut—one of the principal scientists who cloned Dolly.
  • Genomics. Comprehensive links to scientific, legal, and ethical issues. Sponsored by Pharmaceutical Research and Manufacturers of America, and the American Institute of Biological Sciences.
  • Reason Magazine. Favors few restrictions on cloning humans.
  • Yahoo! Cloning Update. Links to news reports and other sites on cloning.
Dolly, the Finn Dorset lamb, and her Scottish Blackface surrogate mother (Roslin Institute)

Cloning--Scientific and Biblical Ramifications [Part I] by Bert Thompson, Ph.D.

http://apologeticspress.org/APContent.aspx?category=7&article=233

Cloning--Scientific and Biblical Ramifications [Part I]

by Bert Thompson, Ph.D.


On April 25, 1953, James Watson and Francis Crick published a scientific paper describing for the first time the intricacies of the DNA molecule. For their attainment, they received the Nobel Prize—and initiated a biological revolution. The elucidation of the molecular biology of the gene clearly ranks among the greatest scientific achievements of all time. Because of this discovery, a new age has dawned—the Genetic Age.
In the opinion of many scientists, the last great revolution in science was the coming of the Nuclear Age. Nuclear technology tends to be viewed as either the most powerful industry for human benefit—or the most dangerous tool for human destruction—ever available for mankind’s use. With the development of genetic engineering, the potential for controversy is even greater because in their experiments scientists no longer are dealing with merely inanimate nature, but instead with human subjects—and the consequences are far-reaching indeed. Some have made comparisons between current advances and those that led, little more than a generation ago, to the dropping of the atomic bombs over Nagasaki and Hiroshima. Science fiction writers have created, in the true tradition of Dr. Frankenstein, modern-day monsters ranging from potentially killer microorganisms to duplicates of Adolf Hitler. Some among us see the immediate demise of the human race; others see, and tremble before, the prospect of a Huxlian Brave New World that promises the complete and utter dehumanization of mankind. What, then, is the truth of the matter?
Today the citizens of most civilized countries are better fed, better clothed, and healthier than they have ever been. Transportation, educational, medical, industrial, and even recreational facilities are vastly improved, compared to those of previous generations. Prospects for the future, then, should be brighter than ever. But are they?
While no one knows exactly what the future will hold, there are growing indications that much of it may not be for good. The fact is that mankind has become more smug as scientific knowledge has increased. Humanity has drifted farther and farther from God, and progressively attempts to cut itself loose from the moral and ethical standards found within God’s Word. It certainly is safe to say that the average person of our day knows far less about the Bible than the common man of a half-century ago. What will happen, then, as science accelerates, while man’s relationship with, and knowledge of, his Creator degenerates? The possibilities are staggering. And the frightening thing is that now we are confronting situations we thought only future generations would have to face.

GENETIC ENGINEERING—AN OVERVIEW

In the past, genetic engineering generally was looked upon as an area of science dealing with the substitution of new (“improved”) genes for old (damaged) ones. But to the man on the street today, it means far more than that—something like conjuring up DNA monsters, or cloning world-renowned figures such as Hitler, Churchill, or Stalin. In this article, the term will be used in its broadest sense to include any form of artificial reproduction or genetic manipulation. Among some of the questions to be considered are these: (a) how extensive is our current reproductive technology; (b) how is it being employed presently; (c) what are the scientific and biblical ramifications; and (d) what should be the Christian’s response to the use of this technology?
The motivation behind much genetic engineering research is commendable. Scientists are anxious to alleviate human suffering by the correction of genetic or behavioral defects, therapeutically control and rehabilitate those who are dangerous to society, and improve the general functioning and future potential of the human race. Few would argue with the goal of helping people function better. Even opponents of human genetic engineering would concede that most scientists are not attempting to be malicious or oligarchical elitists.
We must remember, however, that even scientists are not completely free of the desire for power. Further, some scientists work on underlying assumptions that suggest: (a) we can do better than nature (or as the Christian would say, better than God); (b) we are responsible to no higher Being than ourselves; (c) economic value is the final test in considering what should or should not be done; and (d) the end justifies the means. Clearly, the potential for a very real and very serious problem exists. Should this attitude become dominant, there may be no effective barrier against irresponsible uses of genetic engineering.
As we examine the concepts behind genetic engineering, we must distinguish between various types of genetic research. The first has to do with modification, which involves making minor changes in an existing structure by splicing in new genetic material, or by altering the material already present. Generally, this type of procedure has as its goal the improvement of an organism, or the prevention or cure of disease. Few would oppose such uses of genetic engineering, as long as scientists follow proper guidelines.
A second type of genetic research relating to both animals and humans centers on procreation. Currently, for example, technology that once was available only for use in animals now can be employed in humans, allowing people to reproduce when previously they were unable to do so.
A third, more controversial, type of genetic engineering centers on the creation of new life forms. Some scientists see the day approaching when we shall go beyond small-scale genetic modification to produce more novel living beings. This is a drastic departure from conferring a specific trait on an existing organism, or genetically modifying an organism so as to give it a healthier or longer life. One writer has referred to this as “engineering the engineer,” as opposed to “engineering his engine” (Kass, 1971, p. 779).

A BRIEF HISTORY OF GENETIC ENGINEERING

Historically, experiments intended to alter human life began in 1970 when Stanford Rogers, a physician and biochemist, attempted to introduce into his patients a gene for production of the enzyme arginase. The patients’ systems were incapable of manufacturing the enzyme—a factor that eventually would cause their deaths. Dr. Rogers injected his subjects with a virus that can produce the enzyme, in the hope that the virus would infect their DNA. Subsequently, the host’s immune system would destroy the virus, yet leave behind the gene for arginase production. The experiment failed, resulting in a swift outcry of criticism from the scientific community.
In July of 1980, a more extensive experiment was attempted by Martin Cline, then head of hematology and oncology at the University of California at Los Angeles. Working with him was a team of Israeli medical doctors, headed by Eliezer Rachmilewitz of the Hadassah Hospital in Jerusalem. Patients under the care of Dr. Rachmilewitz had a rare but fatal disease known as beta zero thalassemia. Dr. Cline injected their bone marrow with a new gene, in the hope that it would be able to correct the defect in the patients’ immune systems.
Such was not to be, however. This experiment failed as well, and cost Dr. Cline his job and research grants. Few in the scientific community, at this early stage in the history of genetic experiments, were willing to put their professional careers on the line. With human lives at stake, the risk was too great. Fewer scientists still were willing to forgive those who tried—and failed.
It appeared, then, that whatever benefits might accrue to humanity from biotechnology would come only indirectly. Indeed, early successes in the field of genetic engineering seemed to confirm that fact. By the early 1980s, business ventures had been formed for the specific purpose of advancing and investing in various kinds of genetic research, the offshoots of which certainly would benefit mankind. Compounds such as interferon, and even insulin intended for use in humans, soon were being produced by genetically altered bacteria. Eventually, human growth hormone was added to that list. People were benefiting, indirectly, from genetic engineering.
By the late 1980s and early 1990s, however, the benefits derived from genetic engineering no longer were indirect. Advances in the field were arriving at breakneck speed. Hardly a day passed that scientists from one corner of the globe or another did not announce yet another breakthrough that conferred additional genetic blessings on humanity. For example, an article on “Conquering Inherited Enemies” in Time magazine announced:
Genetic engineers at a handful of U.S. laboratories are getting ready to embark on the first trials of human gene therapy, a revolutionary approach to conquering inherited ailments. Employing the subtlest available techniques of recombinant DNA, the scientists will attempt to inject healthy copies of the affected gene into the bone marrow cells of a victim of a genetic disorder. If all goes well, the good genes will begin producing enough of the missing enzyme to cure the disease. That will be cheering news for the hundreds of thousands of patients who suffer from the 3,000 known genetic disorders (Angier, 1985, p. 59).
Just five years later, another article in Time reported the epochal events surrounding the treatment of a little 4-year-old girl.
Last week, on the 10th floor of the massive Clinical Center of the National Institutes of Health (NIH) in Bethesda, MD, the still unidentified child assumed a historic role. In the first federally approved use of gene therapy, a team of doctors introduced into her bloodstream some 1 billion cells, each containing a copy of a foreign gene. If all goes well, these cells will begin producing ADA, the essential enzyme she requires, and her devastated immune system will slowly begin to recover (Jaroff, 1990, p. 74).
No longer, then, are the potential benefits to humanity from genetic engineering merely indirect in nature. We have moved past the point where people enjoy longer, healthier lives simply because they can take insulin or interferon produced by genetically altered bacteria. Now people themselves are part and parcel of intricate laboratory experiments—experiments that, we are told, will bode well for humanity in both the near and distant future.

THE CURRENT CONTROVERSY OVER CLONING

Genetic engineering (in animals or in humans) potentially can take place: (a) before conception; (b) at conception; (c) prenatally; and (d) postnatally. I have dealt with each of these in an in-depth fashion elsewhere (see Thompson, 1995). For the purposes of this article, however, I would like to restrict the discussion to genetic engineering that occurs at conception.
Discussions of reproductive technologies occurring at conception usually include: (1) cloning; (2) artificial insemination; and (3) in vitro fertilization (IVF). Of these, I will limit my comments here only to cloning.
The English word “clone” derives from the Greek klon, meaning a sprout or twig, and in science refers to an asexual process of reproduction resulting in an exact genetic duplicate of the original. Cloning is quite natural for many of Earth’s life forms. For example, when the amoeba reproduces by splitting into two parts, it is cloning itself. In essence, then, cloning is a way to grow many identical cells or organisms from a single ancestor. However, most plants and animals reproduce sexually—a process that requires a contribution of genes from both the male and female of the species. Therefore, any attempt to clone such organisms, including humans, must involve sophisticated technology. In the science fiction version of cloning, a body cell (also known as a somatic cell) is used to make a copy of an individual. But cloning of relatively complex creatures, such as mammals, for example, usually must begin with an egg, or perhaps even a fertilized egg. Only then can scientists make copies of one unique set of genes.
In one technique known as nuclear transfer, an unfertilized egg is taken from the female, and its nucleus is either destroyed (e.g., by radiation) or removed. The nucleus from a body cell then is placed in the egg, which, when implanted in the uterus, behaves as if it has been fertilized, except that all of its genetic information has been derived from a single individual rather than a pair of parents.
This type of cloning possesses potential benefits. Its greatest value, however, is not as an alternative means of reproduction, but as a powerful laboratory research tool, especially in developmental biology. Cloning can aid in the study of nuclear differentiation by helping scientists to better understand how an embryonic cell becomes a nerve cell, a blood cell, etc. It also can be very helpful in the study of immunology and organ rejection. Additionally, cloning can be used with great benefit in medical research. For example, it can be used in the study of cancer, and also can be used in the study of the aging process.
During the 1950s, F.C. Steward of Cornell University demonstrated how to clone certain plants, and produced carrots by the thousands through such a procedure (see Steward, 1970). In 1952, Robert Briggs and Thomas King of the Institute for Cancer Research in Philadelphia cloned a leopard frog (see Briggs and King, 1952). Since then, carrots, tomatoes, fruit flies, and even frogs have been cloned. The successes (and there were many) were the result of painstaking research carried out using embryonic or neonatal somatic cells (viz., non-adult cells). By the late 1970s, scientists lamented that, in spite of numerous attempts in laboratories around the world, “...no one has yet shown that it is possible to clone a mammal by using a body cell nucleus from an adult” (Lygre, 1979, p. 41). Something—no one quite knew what—seemed to make the somatic cell of the adult an unlikely candidate for cloning procedures. However, investigators did not abandon their efforts, and attempts to clone organisms using adult somatic cells continued at an unprecedented pace.
Clement Markert of Yale University perfected a method that allowed researchers to remove one set of chromosomes—either those from the sperm or those from the egg—just after fertilization. Through biochemical means, the remaining set could be made to double, producing an egg with a double set of the sperm’s (or egg’s) chromosomes. Since the same number of chromosomes as found in a fertilized egg then was present, embryonic development could begin. Peter Hope and Karl Illmensee at the Jackson Laboratory in Bar Harbor, Maine employed this technique in mice, and produced seven offspring, all females. While it is true that none of the seven was a clone of the genetic parents, if the same procedure were repeated on those seven mice (retaining the chromosomes of their eggs), their offspring would be clones.
The first clones of large animals were produced by S.M. Willadsen (1986), who transferred a single cell from an 8-cell sheep embryo to an unfertilized egg whose nucleus had been destroyed. Three of the four reconstituted embryos transferred to ewes’ oviducts developed into lambs that were genetically identical.
But what about attempts at human cloning? Landrum Shettles reported in the American Journal of Obstetrics and Gynecology that he personally had cloned human embryos to the blastocyst stage (the point in early development where the whole embryo has the appearance of a hollow sphere; see Clark, 1979, p. 99). As one writer summarized the experiment:
According to the report, he had removed the genetic material from a human egg cell and replaced it with the nucleus of a human spermatogonium, the precursor of the sperm cell. Because the spermatogonium contains a double set of chromosomes, it is a complete blueprint for the individual. The egg was fertilized, cell division began, and three days later the embryo was at the morula stage, its cluster of cells ready for implantation. If the paper was true, then it meant that the first glimmering of a human being had already been cloned (Kahn, 1988, p. 164, emp. added).
The operative phrase here, of course, is “if the paper was true.” Most scientists working in this field did not believe that it was, and remained skeptical of Dr. Shettles’ experiment. Why? “Shettles never presented evidence that the egg was enucleated, ...nor did he use genetic markers that would have proved that the sole parent of the embryo was indeed the transplanted spermatogonium” (Kahn, 1988, p. 164).
In 1978, science writer David Rorvik authored, and the J.B. Lippincott Company of Philadelphia published, In His Image: The Cloning of a Man. The book reportedly told the story of a 67-year-old eccentric millionaire who had himself cloned successfully, and spawned a serious scientific controversy since it was published as nonfiction. Most scientists dispute claims such as those made by Rorvik and others in regard to the cloning of humans. In its publication, ASM News, the American Society for Microbiology stated:
Four eminent cell biologists have testified before congress that adult cloning of humans has not been and may never be achieved because of biological barriers. They also called David Rorvik’s book, In His Image: The Cloning of a Man, a fictional work replete with scientific errors (1978, p. 334).
One scientist suggested concerning Rorvik’s work: “His book sets new standards for the label ‘nonfiction’ ” (Lygre, 1979, p. 41). In 1981, U.S. District Court judge John Fullam ruled the book to be fiction (Fullam, 1981, p. 2-F) and, several years after its publication, Lippincott publicly acknowledged the book as a hoax.
To some, however, the idea of human clones is not beyond the realm of possibility. Several years ago, Kimball Atwood, professor of microbiology at the University of Illinois, stated that humans could be cloned “within a few years” (as quoted in Rorvik, 1969, p. 9). Nobel laureate James Watson later predicted:
...if the matter proceeds in its current nondirected fashion, a human being born of clonal reproduction most likely will appear on the earth within the next twenty to fifty years, and even sooner, if some nation should actively promote the venture (1971).
To date, there is no credible evidence that humans have been cloned, in the traditional sense of the word.
But who can know what the future may hold in this regard? For example, in October 1993, at a meeting of the American Fertility Society, two Americans, Jerry Hall and Robert Stillman, touched off an unexpected controversy when they presented a research paper on IVF procedures. At the time, Dr. Hall was the director of the in vitro laboratory at George Washington University; Dr. Stillman headed the University’s IVF program. Starting with 17 human embryos ranging from the two-cell to the eight-cell stage, Hall and Stillman used new technology to multiply the embryos from 17 to a total of 48. News magazines and major city newspapers heralded the landmark event with feature articles. The New York Times published a front-page article under a headline that screamed, “Scientist Clones Human Embryos, and Creates an Ethical Challenge.” Newsweek and Time both prepared cover stories on the Hall/Stillman experiments (see Adler, 1993; Elmer-Dewitt, 1993).
The controversy caused by the Hall/Stillman experiment was due, in large part, to the fact that human embryos were involved. However, it is important to note what the experiment did, and did not involve. First, the experiment did not involve the type of cloning of science fiction fame—in which genetic material from a mature individual is nurtured and grown into a replica of the original. Second, the experiment did not involve the cutting and splicing procedures by which DNA strands from cells are mixed and matched. In some instances, to mention just one example, molecular biologists have inserted human genes into the DNA of bacteria to produce insulin in large quantities. But the Hall/Stillman experiment did not involve this kind of genetic engineering.
Hall and Stillman were searching for a way to make IVF more successful. A woman in which only a single embryo is implanted has somewhere between a 10 and 20% chance of becoming pregnant, if all goes well. But if that single embryo could be cloned into three or four, the chances of a pregnancy would increase dramatically. These two researchers were not trying to produce cloned embryos that would be implanted into a potential mother. Instead, they were working with abnormal embryos resulting from fertilization of an egg by multiple sperm cells, and which therefore would not live more than a few days at best.
 Method by which Stillman and Hall produced twin embryos from a single embryo (after Kolberg, 1993)
The experiment involved allowing the single-cell embryos to divide into two cells, and then separating them. To do this, the outer coating around the cells (known as the zona pellucida) that is essential to the embryo’s proper development had to be removed. Once the cells had been separated, an artificial zona pellucida had to be created to take the place of the original one that had been destroyed. Hall and Stillman developed an artificial zona pellucida from a gel derived from seaweed. Once the artificial coating was replaced, the cells began to grow.
The experiment, so far as Hall and Stillman were concerned, had been a success, and was repeated numerous times, producing 48 clones in all. But none of the clones lived more than six days. A detailed description of the process used by Hall and Stillman was published in Science News (see Fackelmann, 1994a). While many praised the novel experiment, criticism from some in the academic and scientific communities was quite strong (see Fackelmann, 1994b). Unfortunately, the headlines in newspapers and magazines were not always representative of the actual facts. Humans had not been cloned. While we cannot condone the manner in which the Hall/Stillman research was carried out (i.e., accepting the inevitable death of living human embryos as the by-product of a scientific experiment), at the same time it is important that we understand exactly what the new technology allowed scientists to do, and that we not overstate the case regarding what was accomplished.

REFERENCES

Adler, Jerry (1993), “Clone Hype,” Newsweek, pp. 60-62, November 8.
Angier, Natalie (1985), “Conquering Inherited Enemies,” Time, pp. 59-60, October 21.
ASM News (1978), (Washington, DC: American Society for Microbiology), p. 334, July.
Briggs, Robert and Thomas J. King (1952), “Transplantation of Living Nuclei from Blastula Cells into Enucleated Frog Eggs,” Proceedings of the National Academy of Sciences, 38:455-463.
Clark, Matt (1979), “Clones Again,” Newsweek, February 12.
Elmer-Dewitt, Philip (1993), “Cloning: Where Do We Draw the Line?,” Time, pp. 65-70, November 8.
Fackelmann, Kathy A. (1994a), “Cloning Human Embryos,” Science News, 145[6]:92-93,95, February 5.
Fackelmann, Kathy A. (1994b), “University Probe Faults ‘Cloning’ Research,” Science News, 146[25]:406, December 17.
Fullam, John (1981), as quoted in “Clone Deemed a Hoax,” Dallas Times Herald, p. F-2, March 22.
Jaroff, Leon (1990), “Giant Step for Gene Therapy,” Time, pp. 74-76, September 24.
Kahn, Carol (1988), “Double Takes,” Omni, 11[1]:58-65,164, October.
Kass, Leon (1971), “The New Biology: What Price Relieving Man’s Estate?,” Science, 174:779-788.
Kolberg, Rebecca (1993), “Human Embryo Cloning Reported,” Science, 262:652-653, October 29.
Lygre, David (1979), Life Manipulation (New York: Walker).
Rorvik, David (1969), “Cloning: Asexual Human Reproduction,” Science Digest, pp. 7-9, November.
Rorvik, David (1978), In His Image: The Cloning of a Man (Philadelphia, PA: Lippincott).
Steward, F.C. (1970), “From Cultured Cells to Whole Plants: The Introduction and Control of Their Growth and Differentiation,” Proceedings of the Royal Society [B], 175:1-30.
Thompson, Bert (1995), The Christian and Medical Ethics (Montgomery, AL: Apologetics Press).
Watson, James (1971), “Moving Toward the Clonal Man: Is This What We Want?,” Atlantic, 227:50-53.
Willadsen, S.M. (1986), “Nuclear Transplantation in Sheep Embryos,” Nature, 320:63-65.

When Did Jesus Go to Egypt? by Eric Lyons, M.Min.

http://apologeticspress.org/AllegedDiscrepancies.aspx?article=4132&b=Matthew

When Did Jesus Go to Egypt?

by Eric Lyons, M.Min.

Most people familiar with the few details given in Scripture about the early life of Jesus are aware of the fact that following the visit from the wise men, Matthew indicates that Joseph and Mary took Jesus and fled to Egypt at the command of God (Matthew 2:13-14). Later, after Herod’s death, Jesus’ family departed Egypt for Nazareth where they made their home (Matthew 2:19-23). According to some, however, Luke’s account of the early life of Jesus contradicts Matthew’s (Wells, 2011; cf. Ehrman, 2005, p. 10). Luke indicates that after Jesus’ birth, and once Mary’s days of “purification according to the law of Moses were completed” (2:22), which would have been about six weeks after Jesus was born (Leviticus 12:3-4), Joseph and Mary took Jesus to the temple in Jerusalem (Luke 2:22-38). The inspired physician then writes: “So when they had performed all things according to the law of the Lord, they returned to Galilee, to their own city, Nazareth” (Luke 2:39, emp. added). Since Luke mentions nothing about Egypt, and Matthew says nothing about a trip to Nazareth soon after Jesus’ birth, allegedly either Matthew or Luke is mistaken.
The allegation that Matthew and Luke’s accounts are contradictory is actually based on an assumption: the skeptic assumesthat Matthew and Luke each included all of the whereabouts of Jesus’ family during His early life. The fact is, however, such a conjecture cannot logically be upheld unless both of the inspired writers claimed to write exhaustive, chronological accounts of everything Jesus did. Neither writer made such a declaration (cf. John 21:25).
Could it be that Joseph, Mary, and Jesus “returned to Galilee, to their own city, Nazareth” (Luke 2:39) before going to Egypt, and then after traveling to and from Egypt they returned to Nazareth again (Matthew 2:23)? The Holy Spirit certainly could have inspired Matthew to write his truthful account of some of the life of Christ without mentioning a brief “return” to Galilee. However, it is also very possible, and perhaps more likely, that Luke simply omitted Joseph, Mary, and Jesus’ trip to Egypt, which sequentially could be placed between Luke 2:38 and 2:39. Bible writers frequently moved from one subject to the next without intending to give every action that took place during a particular time or the exact order in which something was done or taught (cf. Luke 4:1-3; Matthew 4:1-11). Later, for example, in chapter 24, Luke omitted the post-resurrection appearances of Jesus in Galilee, which both Matthew and John mentioned. The events that Luke recorded in the first 43 verses of chapter 24 all took place on the very day of Jesus’ resurrection. The final four verses of Luke 24 (vss. 50-53), however, took place more than five weeks later (see Acts 1:1-12). Yet Luke simply recorded the various events in chapter 24 (vss. 1-43,44-49,50-53) and connected them with the Greek conjunction de (“but” or “and”), which has no specific chronological implications. The same is true with the Greek conjunction kai, which Luke used in 2:39.
Consider also an example from Luke’s account of some of the acts of some of theapostles (in the book we call Acts). In chapter 9, Luke mentions that Paul went to Jerusalem after becoming a Christian (Acts 9:26). But, according to Galatians 1:17-18, Paul actually went to Arabia, back to Damascus, and then after three years he went up to Jerusalem. Once again, Luke, by inspiration of the Holy Spirit (cf. 1 Timothy 5:18), omitted a part of someone’s life. But such an omission is in no way proof of dishonesty—anymore than if, at the funeral of a 90-year-old man, someone gives a synopsis of his life, and omits the two years he spent in Warner, Oklahoma in junior college.
Keep in mind that the Bible is a book that covers approximately 4,000 years—from Creation to the end of the first century A.D. God’s purpose in giving us His Word was not to tell us about everything that every person ever did up to that point in time. In fact, even the one Person, Who is the main theme of Scripture—Jesus—has relatively little recorded about Him in comparison to every place He ever went and everything He ever did or said. As the apostle John proclaimed, “Jesus did many other signs in the presence of His disciples, which are not written in this book, but these are written that you may believe that Jesus is the Christ, the Son of God, and that believing you may have life in His name” (20:30-31, emp. added). In truth, “there are also many other things that Jesus did, which if they were written one by one, I suppose that even the world itself could not contain the books that would be written” (21:25, emp. added).
Simply because Matthew or Luke or any other Bible writer does not mention everything that every other Bible writer mentions about the same general time or event, does not mean that someone has erred. Rather, just as we oftentimes tell stories today and include certain details that others omit, so did the inspired writers of Scripture. Honest truth-seekers (Proverbs 8:17) will come to the logical conclusion that the Bible writers supplemented (not contradicted) each others’ accounts of biblical events.

REFERENCES

Ehrman, Bart (2005), Misquoting Jesus: The Story Behind Who Changed the Bible and Why (San Francisco, CA: Harper).
Wells, Steve (2011), Skeptic’s Annotated Bible, http://www.skepticsannotatedbible.com/contra/egypt.html.

“The love of Christ compels us” 2 Corinthians 5:14 by Roy Davison

http://www.oldpaths.com/Archive/Davison/Roy/Allen/1940/049-compelledbylove.html

“The love of Christ compels us”
2 Corinthians 5:14
What does it mean to be compelled by the love of Christ?
A Christian serves God with heart and soul, moved by the love of Christ.
In this context, the word translated ‘compels’ [συνέχω] means to powerfully urge along a line of conduct. Force is not involved, but some impulse is so great that it evokes a strong intellectual and emotional inclination to respond appropriately. In this case, the impulse is the love of Christ, which is so immense that it demands a response as complete and radical as His love for us.
Paul is explaining the compelling force in his own life. His aim is to please God and to persuade others (verses 9-11). The motivating force is the love of Christ: “For the love of Christ compels us, because we judge thus: that if One died for all, then all died; and He died for all, that those who live should live no longer for themselves, but for Him who died for them and rose again” (2 Corinthians 5:14, 15).
What if someone gave his life to save your life? Would you be thankful? Without his help, you would be dead.
What if He saved your life so you could live for ever? Jesus saved our life. In gratitude, we live for Him. We are compelled by the love of Christ.

How can we know the love of Christ?
We must know about the love of Christ before it can be a compelling force in our lives.
Paul prayed that his fellow Christians might truly know the love of Christ: “For this reason I bow my knees to the Father of our Lord Jesus Christ, from whom the whole family in heaven and earth is named, that He would grant you, according to the riches of His glory, to be strengthened with might through His Spirit in the inner man, that Christ may dwell in your hearts through faith; that you, being rooted and grounded in love, may be able to comprehend with all the saints what is the width and length and depth and height - to know the love of Christ which surpasses knowledge; that you may be filled with all the fullness of God” (Ephesians 3:14-19).
As small children, many of us sang, “Jesus loves me! This I know, for the Bible tells me so.” This song was written by Anna Warner in 1860 for a novel by her sister, Susan Warner. In the book, a Sunday school teacher sings ‘Jesus loves me’ to a dying child. The melody and refrain were added by William Bradbury two years later.
Yes, we learn about the love of Christ through the Scriptures.
How do we know someone loves us? By what he gives us and does for us. What has Jesus given us and done for us?

Because He loves us, Jesus gave Himself for us.
“And walk in love, as Christ also has loved us and given Himself for us, an offering and a sacrifice to God for a sweet-smelling aroma” (Ephesians 5:2); “who Himself bore our sins in His own body on the tree, that we, having died to sins, might live for righteousness” (1 Peter 2:24); “who gave Himself for us, that He might redeem us from every lawless deed and purify for Himself His own special people, zealous for good works” (Titus 2:10).
The vicarious, substitutional sacrifice of Christ was the driving force in the life of Paul. “I have been crucified with Christ; it is no longer I who live, but Christ lives in me; and the life which I now live in the flesh I live by faith in the Son of God, who loved me and gave Himself for me” (Galatians 2:20).

Because He loves us, Jesus died for us.
“But God demonstrates His own love toward us, in that while we were still sinners, Christ died for us” (Romans 5:8). “For God did not appoint us to wrath, but to obtain salvation through our Lord Jesus Christ, who died for us, that whether we wake or sleep, we should live together with Him” (1 Thessalonians 5:9, 10). “By this we know love, because He laid down His life for us” (1 John 3:16).

Because He loves us, Jesus gave us the word of God.
When praying for His followers, Jesus said, “I have given them Your word” (John 17:14). “For I have given to them the words which You have given Me; and they have received them, and have known surely that I came forth from You; and they have believed that You sent Me” (John 17:8). “Sanctify them by Your truth. Your word is truth” (John 17:17).

Because He loves us, Jesus gave us the right to become sons of God.
“But as many as received Him, to them He gave the right to become children of God, to those who believe in His name: who were born, not of blood, nor of the will of the flesh, nor of the will of man, but of God” (John 1:12, 13).
To become a child of God, one “must be born again” (John 3:7), “born of water and the Spirit” (John 3:5).
This is not a physical birth. It cannot be achieved by man’s will in his own way.
It is a spiritual birth, accomplished only by the will of God in His way through His word. “Of His own will He brought us forth by the word of truth” (James 1:18), “having been born again, not of corruptible seed but incorruptible, through the word of God” (1 Peter 1:23).
Because He loves us, Jesus gave us the word of God through which we can become children of God if we believe. “So then faith comes by hearing, and hearing by the word of God” (Romans 10:17).
Notice that a believer is not automatically a child of God, but is given the right to become a child of God.
Many never perfect their faith by appropriate obedience. See James 2:22 where it says that Abraham’s faith was made perfect by works. “Nevertheless even among the rulers many believed in Him, but because of the Pharisees they did not confess Him, lest they should be put out of the synagogue” (John 12:42). “Faith only” is dead faith (James 2:14-26).
To become a child of God, a believer must obey the gospel (Romans 10:16; 2 Thessalonians 1:8; 1 Peter 4:17) which includes publicly confessing Christ (Matthew 10:32; Romans 10:10), repentance (Luke 13:3; Acts 3:19) and baptism for the forgiveness of sins (Acts 2:38) to be saved (Mark 16:16; 1 Peter 3:21).
“But when the kindness and the love of God our Savior toward man appeared, not by works of righteousness which we have done, but according to His mercy He saved us, through the washing of regeneration and renewing of the Holy Spirit, whom He poured out on us abundantly through Jesus Christ our Savior” (Titus 3:4-6).
Because He loves us, Jesus gave us the right to become sons of God by being born again, “born of water and the Spirit” (John 3:5). “Behold what manner of love the Father has bestowed on us, that we should be called children of God!” (1 John 3:1).

Because He loves us, Jesus intercedes for us.
“We have an Advocate with the Father, Jesus Christ the righteous. And He Himself is the propitiation for our sins” (1 John 2:1, 2).
“Who shall bring any charge against God’s elect? It is God who justifies. Who is to condemn? Christ Jesus is the one who died - more than that, who was raised - who is at the right hand of God, who indeed is interceding for us” (Romans 8:33, 34 ESV).
“He who did not spare his own Son but gave him up for us all, how will he not also with him graciously give us all things?” (Romans 8:32 ESV).
What love can be greater than this? Jesus paid the penalty for our sins and now He intercedes with the Father on our behalf!
“Who shall separate us from the love of Christ? Shall tribulation, or distress, or persecution, or famine, or nakedness, or danger, or sword? As it is written, ‘For your sake we are being killed all the day long; we are regarded as sheep to be slaughtered.’ No, in all these things we are more than conquerors through him who loved us” (Romans 8:35-37 ESV).
Christians experience the hardships of life like everyone else. In addition, they are opposed and persecuted by the enemies of God in heaven and on earth.
Yet, we are never separated from the love of Christ: “For I am sure that neither death nor life, nor angels nor rulers, nor things present nor things to come, nor powers, nor height nor depth, nor anything else in all creation, will be able to separate us from the love of God in Christ Jesus our Lord” (Romans 8:38, 39 ESV).

Because He loves us, Jesus wants us to be with Him.
“And the glory which You gave Me I have given them, that they may be one just as We are one: I in them, and You in Me; that they may be made perfect in one, and that the world may know that You have sent Me, and have loved them as You have loved Me. Father, I desire that they also whom You gave Me may be with Me where I am, that they may behold My glory which You have given Me; for You loved Me before the foundation of the world” (John 17:22-24).

The whole Bible helps us understand the love of Christ.
These passages about the love of Christ show only the tip of the iceberg. Read the Gospels, and study the New Testament to learn more about His love.

How are we affected by the love of Christ?
We no longer live for ourselves, but we live for Him who died for us. We walk in love, live for righteousness, and are zealous for good works. We accept the words of God. We are more than conquerors through Him who loved us. Nothing can separate us from His love, and we will be with Him for ever.

Is the love of Christ the mainspring of our life?
May our motives and priorities enable us to say with Paul: “The love of Christ compels us!” Amen.
Roy Davison
The Scripture quotations in this article are from
The New King James Version. ©1979,1980,1982, Thomas Nelson Inc., Publishers, unless indicated otherwise.
Permission for reference use has been granted.
Published in The Old Paths Archive
(http://www.oldpaths.com)

Restoring the "happy train" by Gary Rose

"The happy Train"? Not for this little girl! I marvel at the look on her face! What could have caused it? Was she punished for misbehavior? My guess is that she did something wrong and doesn't like her fate.

Nobody likes to be punished, but there is value in it.

Consider...

Job, Chapter 5 (WEB)

 17 “Behold, happy is the man whom God corrects. 
Therefore do not despise the chastening of the Almighty. 

And..


2 Corinthians, Chapter 2 (WEB)
4 For out of much affliction and anguish of heart I wrote to you with many tears, not that you should be made to grieve, but that you might know the love that I have so abundantly for you. 5 But if any has caused sorrow, he has caused sorrow, not to me, but in part (that I not press too heavily) to you all.  6 This punishment which was inflicted by the many is sufficient for such a one;  7 so that on the contrary you should rather forgive him and comfort him, lest by any means such a one should be swallowed up with his excessive sorrow.  8 Therefore I beg you to confirm your love toward him.


Job spoke correctly and Paul (in the 2 Corinthians passage, above) urges that the congregation forgive, comfort and show love toward the one who sinned. 

After awhile, there will be happiness again. And the happy train will take on its true meaning once again.