Why are humans so full of genetic diseases today?

 As a scientist, having studied most of the major causes of human suffering from diseases, this idea of not having sex during menses is proven today by modern medical to be all about preserving life and not getting sick from infections.

I discussed this before but here is what is why it is bad to have sex during a woman’s period. And why it is bad to have sex with anyone but a monogamous marriage free from infections.  

1. The flora inside of a woman is there to protect the area of conception from pathogens. It produces H2O2, hydrogen peroxide to keep the area clean of infections.
2. The pH (potenz hydrogen is the measure of acid or base levels in terms of H+ ions) of the healthy vagina is between 2.7 and 4.7 in order for this flora to live and flourish.
3. The pH of blood is about 7000 to 10000 times base H+ ions than the flora at pH of 7.4 . It is a logarithmic scale.
4. The pH of sperm is on average 8.0 and is over 10,000 times more base than the area of the healthy woman’s vagina.
5. When one stops the flow of blood from the menses you are risking raising the pH to unsafe levels. This is why there was a massive number of women using “dirty” tampons dying from “toxic shock” syndrome (horrible bacterial infections) in the 1970’s. Tampons were not sterilized. I still recommend never using tampons to block the flow.
6. When you have blood and sperm and are living in the “wild” with limited bathing this drastically increased BV bacterial vaginosis, and in the wild with no medical 3000 years ago or in modern places where medical is not available and people have limited bathing today BV is common.
7. 3000 plus years ago this would kill a woman and cause the spread of diseases to the Jewish tribe living in the wild.
8. Today with medical, antibiotics are used and then a cultured flora is added to the vagina with a sort of large syringe.
9. Having BV and then having sex is one of the primary ways to spread STD’s and having multiple sex partners also destroys the flora in the vagina. Just too much pH of 8.0 in a place where disturbing the pH is not a good idea.
10. A study done by the head of the CDC’s women’s sexually transmitted diseases states that women who have sex with uncircumcised men in places with limited bathing have 140% more BV.
11. The WHO sends out “circumcision vans” in Africa; offering free circumcisions to men. This is to curtail the HIV / AIDs epidemic there.
12. Obtaining from sex during menses and waiting to see if a woman is infected was the procedure given to the Jews in the wilderness.
13. It was all about keeping women alive and healthy. It was not some sort of patriacial nonsense that people seem to think. When one is a scientist we look at the conditions, the parameters and causes under any circumstance. Living in the wilderness for 40 years and having no antibiotics, no drugs, no vaccines, no surgery, no testing and modern medical treatments, one would rely on God’s instructions to be healthy.
14. The Jews lived on average 70 to 80 years and some to 120 living this way. Whereas the “nations” were all dying very young from many infections and diseases, they spread in ignorance.
15. The fact is today modern humans are experiencing the most rapid genetic degradation ever seen on earth.   The evidence is overwhelming that humans cannot follow the simplest rules for healthy reproduction and are infecting their own offspring with mutagenic pathogens like rabid animals.  
16. At the current rate in the rise of genetic diseases, and MD's not being able to even come close to dealing with this genetic succeed, we have less than 100 years before extinction, or at least the only humans living would be out in the wilderness with no contact with STD's nor other humans. 
17. Humans are losing intelligence faster than ever.  A resent study of human DNA from 2000 to 6000 years ago by a prestigious, Stanford, university professor and his team of genetic researchers shows we are dumber than ever, and that also shows we are way more mentally ill and compulsively emotional compared to our ancestors.  They would be way more intelligent and be the most stable people on earth if one were to appear today. 
18. With this rapid rise in genetic diseases caused by sexually transmitted diseases infecting and mutating babies we went from 1 in 625 born dead (still births) to 1 in 200 in less than 10 years.  There is no way for humanity to survive with that rapidly rising statistic.   And all the other statistics showing clearly we are rapidly heading for extinction. Think about that next time you have random sex, and think it was a good idea.
19.  The CDC has issued the following warning about this hyper pandemic of sexually transmitted diseases:  "The most reliable ways to avoid transmission of sexually transmitted diseases (STDs), including human immunodeficiency virus (HIV), are to abstain from sexual activity or to be in a long-term mutually monogamous relationship with an uninfected partner. However, many infected persons may be unaware of their infections because STDs are often asymptomatic or unrecognized." 
20. Even though the CDC has posted this STD's keep rising and most young people of reproduction age are infected, so there is no hope for human kind to exist in the future.  
21. The fastest rising mortality (rate of death) is in children in the USA even with all the medical ages 1 to 4 years old is the fastest rising death rate.  And the average age to death in the USA is under 48 years now.  That is easy for anyone to research.   As an example, 1 in 3 adults ages 15 to 64 are dead from just one disease, invasive cancer and cancer rates are rising like never before, from INFECTED sex mutating babies like never before. 
22. Even in the 1950's doctors were aware of how bad "venereal diseases" are for having kids.  And you could not get married without a test for "VD".  Most every state had a law that you cannot get married if you are infected.  What happened?   This is to protect the children from being mutated and having new and horrible diseases.
23. Now we have 18,000 genetic disease these "fertility doctors" test for with DNA studies of these "invitro fertilizations". This way the parents can choose what diseases their children will have and try to not have some horrible diseases.  But no child is born without a horrible genetic diseases today as we are dying so young now.  
24. 1 in 9 babies are born with a horrible beyond belief genetic disease, and this is the reason for the rapid rise in babies born dead also, as well as the teen suicides and extreme rise in childhood cancer.  

Jehovah God knows what He is talking about because He is the creator of humans and knows every molecule of our being. It is, still to this day, a good idea to not have sex during menses and that uncircumcised men wash that thing every day, because under the foreskin is a breeding ground for all sorts of bacteria, fungus and viruses to flourish.

And one should follow the CDC which issued Bible like warnings on "safe sex".  No sex outside of a clean not infected marriage between a man and a woman and NEVER go outside that for sex, even kissing spreads STD's now. 

God’s way is the healthy way. It has always been that way, and the Bible is 100% correct on how to live, how to have sex and with whom, and how to raise kids who grow up healthy and well balanced. Divorce is like taking a huge emotional sledgehammer to your children. They never get over it.

Deuteronomy also states to “not eat bats, and don’t touch their carcasses”.

God did not say: “Listen we know from virology that this bat corona virus has the keys to your receptor cells and when it enters your cells it replicates very rapidly and destroys your cells causing you to die of suffocation, from your own fluids in your lungs.”

He said to the Jews (paraphrased); “Don’t do these things because I love you and want you to live and it is for your benefit.”

Isaiah 48:

17 This is what Jehovah says, your Repurchaser, the Holy One of Israel:d

“I, Jehovah, am your God,

The One teaching you to benefit yourself,

The One guiding you in the way you should walk.

18 If only you would pay attention to my commandments!

Then your peace would become just like a river

And your righteousness like the waves of the sea.

“Righteousness, means living healthy and not harming life on earth including yourself. In other words doing what God told us to do from his “owner's manual of life” : the Bible.

The Main Reason there is NO EVIDENCE FOR EVOLUTION

 

The main argument is there is NO evidence for “evolution”.

That by some magical process and mystical causes not found in scientific evidence, creatures can ever gain in new cells, and those new cells having a new purpose.

It is ridiculous to believe such nonsense, because all we REAL scientists see is genetic degradation in every speciation event and eventual extinction. It is the LAW of GENETIC DEGRADATION LEADING TO EXTINCTION FOR ALL MULTICELLULAR CREATURES.

All of the modern evidence from molecular biology and from medical history of humans only shows a process of gene losses, and more and more genetic diseases and then extinction. We already see several examples of this in the real world with all of our “cousins” going extinct from being unable to survive even with human help.

There is no evolution found in any physical evidence. It is just a faith based idea. And most people who believe in this magical stuff, have never just looked at the evidence.

There is only genetic degradation found in the 30,000,000 DNA studies so far.

And humans are extremely degraded and sickly compared to our ancestors. Proven by recent studies in comparison of modern human DNA to our ancestors of 2000 to 6000 years ago.

You probably don’t understand what HOX genes are and what the immune system is supposed to do with incorrectly coded cells? You really don’t understand this? It is how it is from molecular biology and the study of the human genome. This is common knowledge in biology.

This is something that ever MD knows about, every molecular biologist knows about. The HOX genes are a huge number of base pairs that do not produce genes but rather they direct where these cells that are created by the DNA/RNA replication process are placed in the Body. They direct the zygote’s cells into the correct location. It is the map of the human body and how it is constructed.

When a cell is first made, in the womb for heart, lung, eyes, etc the HOX system of genes directs the “tissue placement”. It is an amazingly complex DESIGNED system.

Any mutation MUST integrate with that original design in the HOX system of genes. If not it causes diseases.

This is why the evolutionists idea of a “duplication” mutation as the “engine of evolution” is completely debunked. Every duplication of a protein is found in some horrible diseases and has NO place in the genome where it can even function. So it makes for horrible diseases that can kill, maim cause people to not be able to breath correctly. It is found in Autism also. I looked up every duplication mutation I could stand to look at, because after a while it starts to affect my brain with all that suffering caused by the “engine of evolution”.

And when a cell is not made correctly to the original programmed design of that cell, it is to be fixed by an enzyme process or it is to be destroyed by the immune system for being defective. This is by DESIGN so that we have good cells. But because of some 247,000 really bad mutations found in humans our immune system attacks our badly made cells.

This is why there is so many autoimmune diseases today. The cells are not made correctly and so the immune system attacks them, even if they are the only cells you have. People suffer immensely from this. Our bodies were never designed to be this sick, and our cells were not designed to be mutated so badly. We were never designed to even grow old and die. Our cell replication was to just keep on going.

Now the fact that we know from evidence that we are vastly degraded from the Human Genome Project and other DNA studies, and we know that the HOX system is the ORIGINAL design of the human body, and the IMMUNE SYSTEM is looking for that original correct coding so it can correct and keep us healthy, but instead it attacks most of our cells in our bodies, then WE KNOW WE WERE EXTREMELY BETTER MADE to a level of perfection and this is OBVIOUS from the evidence.

Can you show me any evidence at all in your comments? Please! If you believe in something and you have never studied the evidence then that does not make one into a scientist.

When I took classes and asked many believers in this evolution religion for evidence, all they had was religious slogans about some “natural selection” and then I asked them to show me even one experiment where they can prove it exists that has ever been performed by any scientist? Guess what?

***There NEVER has been even one study one experiment to show that positive natural selection is even plausible. It is only “believed to have happened.” ***And all attempts have been failures to show this. The creature wound up as a mutant or it degraded into extinction (Lenski experiment).It is just a belief system handed to students who are eager to “believe” in this concept.

So they absorb the aphorisms (religious slogans) and believe because they think their teachers are telling the truth. And these teachers were taught the same way with aphorisms and no evidence of “natural positive selection”. Do you know this?

In every Jerry Coyne lecture, he only shows genetic degradation as “evidence” for evolution. It is obvious to anyone with intelligence and just looks at the evidence.

In the 41,000 studies, peer journals, and papers on human development; studied for evidence showing what is really going on: genetics, and cell replication from peer evidence. All we see is extreme degradation in humans and no indication whatsoever of any increased health, increased fitness, increased new genes with new functions. We have lost over 40% of our once coding genes. And we have some (USA statistics) 18,000 known genetic diseases. Now, 1 in 9 babies are born with serious genetic diseases.

Evolution: The idea that any creature has gained in genetic feature, better health, more complexity is utter nonsense. There is no evidence for it. It has been debunked for over 40 years.

The only reason it still is around is because humans are weak and emotional and sexually compulsive: cannot deal with reality. Myths are “far better” for us in our degraded condition.

Syllogistic fallacies; Also called circular logic. Where one assumes one thing to be true that others believe, and one builds other assumptions on top of assumptions.

Sometimes this goes to four or five assumptions on top of assumptions .

On of the most common is the radiometric dating system used to date “old things”.

1/ The assumption is that radiometric isotopes decay at a constant rate “forever” and that the rate of decay never changes. That has never been shown to be true or not. Since everything in the universe is changing, why is that not changing?.

2/ That somehow this method is accurate, when there is no way to prove it’s accuracy. It is assumed to be an accurate way to measure ‘old things’. There is no way to test it by going back in a time machine and see it is correct. We can’t do that.

3/ When dating fossils they date the dirt the animal died in. And that is supposed to be the “time of death”. The earth could be millions (and is millions of years since the radiometric materials ‘reset”) of years older than the actual animal. And as is the policy with this “science” of fossil dating if the measured date doesn’t “look right” or fit with the belief then they go and find dirt near by that fits better with the belief system.

4/ Then by this same idea they make the strata of the earths layers are dated this way also, and so they use the strata which was falsely assumed to be correct by the other three assumptions above. So, they use the strata or “in situ” in the layers (that were dated by the same assumptions) to “verify” (yea right?) the radiometric dating of the dirt. They think one verifies the other. You can’t be more illogical in this fallacious way of dating “old things”.

There is no tissue in replacement fossils or imprint fossils, no carbon dating can be done, and no guess by condition. There is nothing to date in these fossils because the original organic matter is completely replaced with the minerals around the dead creature. So they use this assumption, on top of assumption, on top of assumption, on top of assumption to date fossils, which are now just rocks.

This list is pretty accurate;

https://en.wikipedia.org/wiki/List_of_fallaciesThe only thing we can actually trust is modern evidence we find now in genetics and DNA on this subject, and some fossils just by appearance, and not by some extremely inaccurate dating method.***Einstein said, 'If the facts don't fit the theory, change the facts.***

I have asked many hundreds of believers in "evolution"; this idea that fish evolved into humans, to show me even ONE beneficial mutation that could show this is possible. Without a (genetics) molecular bases for evolution then it is fraud.

So far out of all the ones believed to be beneficial they are part of a disease or are purely speculative and cannot be proven where they came from. This gene for lactase is obviously a pre-existing gene that was defective in some people and working in others. The Evotards all think that the non working version was prior to the working version, but how can that possibly be, because it is only 2 base pair difference out of 49,335 base pairs.

The most ridiculous of this is the lactose tolerance mutation. First of all making lactase enzyme is made in a gene that is 49,335 base pairs for just one of the THREE lactase genes. This is the most common of the defective one found in lactose intolerance. Which is just another type of disease which makes people sick if they drink milk or have milk products.

This is the most common gene found in lactose intolerance.

This is from the United States "genes" library.

**Where is the LCT gene located?**

Cytogenetic Location: 2q21

Molecular Location on chromosome 2: base pairs 135,787,844 to 135,837,179

Base pairs are numbered by location. The math is simple:

From 135,837,179 minus 135,787,844 is a total of 49,335 base pairs in this gene.

Your average gene has about 26,000 base pairs.

According to the article claiming that this was some great event creating this new gene. It turns out that it is only 2 base pairs were changed to cause this gene to function. Where did the other totally designed 49332 BP come from that were aligned perfectly and just needed two base pairs to change to make the lactose enzyme?

Do you see how ridiculous this religion is that has gotten into the classroom?

It was a pre-existing gene from ancient ancestors prior to this finding and they found a group where it was turned off, LATER, and then a group where they drank milk where it was functioning. The two base pairs were not mutated from disease in the functioning gene and in the malfunctioning gene it was and is a disease.

Your entire argument {this was an answer to and Evolutionist} is that there is a "theory of evolution". The real findings in ALL the verifiable physical evidence leads a real scientist to ***"The Theory Of Genetic Degradation Leading To Extinction"***. Or "Theory of Genetic Atrophy" Because that is ONLY what is found.

There have been found in the fossil record some 1.5 million species extinct and we now have 47000 on the list to go extinct. This includes our genetic cousins, the great apes, who are degraded to the point of 15 years max life in the wild and 25000 diseases. Humans can't go near then without giving them serious viral infections that kill them because they are so degraded. Chimp tourism is not allowed when a cold or flu in humans is taking place for this reason.

1/Any mutation MUST integrate with that original design in the HOX system of genes. If not it causes diseases.

This is why the evolutionists idea of a “duplication” mutation as the “engine of evolution” is completely debunked. Every duplication of a protein is found in some horrible diseases and has NO place in the genome where it can even function. So it makes for horrible diseases that can kill, maim cause people to not be able to breath correctly. It is found in Autism also. I looked up every duplication mutation I could stand to look at, because after a while it starts to affect my brain with all that suffering caused by the “engine of evolution”.

2/And when a cell is not made correctly to the original programmed design of that cell, it is to be fixed by an enzyme process or it is to be destroyed by the immune system for being defective.

3/ It is impossible, not only by the facts on how our DNA functions to make cells, but that there is NO possible way for an immune system to develop on earth, when the bacteria that eats and digests human tissue proliferated the entire earth and the ocean some 40,000,000 years before the first evidence of humans.

Today we get a scratch, and because our immune system is so weak, we get a horrible flesh eating bacteria infection and must take some form of poison to kill this bacteria, called antibiotics.

Our immune system was much stronger in the past at defending us from pathogens, because we survived for thousands of years without them. It was this path of genetic degradation that created the medical industry.

https://evolutionsciencenow.blogspot.com/2013/04/are-humans-getting-better-what-is.html

More Clear Health Instructions from the Bible: Author; James Arjuna

OK let us start with the medical reasons why women who were menstruating were kept away from sexual contact and for 7 days after.

Many people who are not MD's or nurses cannot deal with this information because it is not taught to the public unless you go to med school or take courses in female diseases.

It is well known that any infections at conception destroy healthy coding in the babies. This is the molecular basis for not having diseased sex.  This is also why women have two forms of protection against infections.  But if one is completely destroyed from bad choices in life, the baby has no chance to develop without a new form of disease.

Here is the zika virus that is an extreme of this effect. If you have any viral infections at conception the baby will have deleterious mutations from the way that viruses infect and change DNA in cells. ANY viral infection that looks for a "host" cell in your reproductive cells, sperm, egg, or first cell so of the zygote, can cause genetic mutations.  It is the nature of viruses to infect and to impose changes to the host cell's DNA.  Never in all of science has even ONE beneficial mutation ever been found.

http://media.npr.org/assets/img/2016/01/19/img_4086-2a3a5f0f573a8760561ef08e1d5b466b49acfe5d-s900-c85.jpeg

It is well know that if a woman has sex during menses she can easily contract a disease because the pH of the Blood at a pH of 7.4 vs the pH of the vagina of  2.7 to 4.0 cannot stand to have the pH raised for any length of time.  It kills the bacteria flora in the vagina that stops infections. That bacteria produces hydrogen peroxide.  This is why tampons that were not clean caused many women to die in the 1960's and 1970 from "toxic shock" in their bodies.

When the blood is contained by a tampon, the pH of the vagina is raised and so it must really be allowed to bleed naturally and flow out to do what was intended. Blocking the flow of this natural process is very bad.
Now if you raise the pH it will eventually destroy the flora.  If a woman were to  have sex and using tampons the odds are very high of contracting a bacterial infection.  Sperm has a pH of 8.0 about 14,000 to 16,000 times more base than the flora and natural pH of a woman.
pH has a logarithmic scale base 10. That means each number is 10 times more or 10 times less acid from the prior number.
A pH of 7.4 is approximately 10,000 times more base than normal vagina pH.

Starting with the vagina pH of 3 average going to 4 is 10 times more base. Going to 5 is 100 times more base, Going to 6 is 1000 times more base, going to 7 is 10,000 times more H+ ions changes from pH of 2.  So we are about 10,700 times more base with just the blood.

So you can see how dangerous this time of menses can be for a woman living in a tent in the wild with no medical at all.  This was how it was for the Jews wandering in the wilderness.

Now if you add Sperm of 8.0 pH you are in the danger zone of serious problems. The extra amount of fluid at extremely "high pH" compared to the vagina added to the blood of 7.4 pH is a very bad thing to do.  Now you  are adding a volume of extra fluid at 100,000 times more H+ ions base than pH of 3.

And if a woman were to have sex during this time any bacteria on the penis or on the outside of the area,  would take root immanently and she would get sick and die.  This is why they checked the women for bad smells after one week and then they were allowed to have sex with their husband.

If women did this today the GYN's would be less than 1/2 the number they are today.

Today the treatment for bacterial vaginosis is to flush with vinegar (lower the pH), infuse cultured flora and give antibiotics to kill the infection; apply an antibacterial cream or whatever the doctor likes to do.

If she were to live and were to get pregnant with no protective flora at the time of conception the zygote stands a HUGE chance of being mutated. The way viruses destroy fetal development is clear and obvious as found in medical journals on this subject.

Here We Are At the End......: Author, James Arjuna

There has been the most rapid and accelerated degradation of the human species in the last 100 years. We now have diseases in children that are so bad and yet people, because of mental degradation and magical thinking believe this is "normal". The new normal is rapid extinction. If you are born into a world of disease, suffering and death and your parents tell you this is normal, then you will think that having babies born with horrible diseases is "normal".

Revelation 12:9
9  So down the great dragon was hurled, the original serpent, the one called Devil and Satan, who is misleading the entire inhabited earth; he was hurled down to the earth, and his angels were hurled down with him.

Whereas in the 1800's Childhood cancer was not even recognized as a statistic for childhood death. Today it is the number one disease killer of Children. That is the claim to fame of ignorant humans living in the darkness of delusions, degradation, sexual compulsions and drugs mixed with alcohol.

In just 39 years unborn babies with spinal and brain cancerous tumors is up 200%. It was already a horrible statistic to begin with in the 1970's. Childhood cancer has risen faster than all the cancers. This is becasue we are now so degraded that it wasn't bad enough that adults die from it we had to insure that our children die from it also.

Romans 5:12
12  That is why, just as through one man sin entered into the world and death through sin, and so death spread to all men because they had all sinned—.

Adult cancer is up well over 60 times the incidents or 6000% since 1900. Cancer now kills 1 in 3 ages 15 to 64. The statistics on childhood cancer rising is beyond numbers because it did not exist in the 1800's to do a chart on it in percentage. but it is well over 30,000% rise from obscure to common now. There were no child hospitals needed because there were no pandemic childhood genetic diseases.

Romans 6:23
23  For the wages sin pays is death, but the gift God gives is everlasting life by Christ Jesus our Lord.

Diabetes is up 400% in less than 40 years. At the present rate of rise of this disease, 1 in 3 will have it by 2050 according to the American Diabetes Association.

1 in 9 children (if they get past birth) are born with severe genetic diseases now that need life long treatments.

Along with physical degradation comes mental retardation and mental illnesses.

50% of adults and about 14% of children are on drugs for mental problems. That is by definition a pandemic.

2 Timothy:
3  But know this, that in the last days+ critical times hard to deal with will be here. 2  For men will be lovers of themselves, lovers of money, boastful, haughty, blasphemers, disobedient to parents, unthankful, disloyal, 3  having no natural affection, not open to any agreement, slanderers, without self-control, fierce, without love of goodness, 4  betrayers, headstrong, puffed up with pride, lovers of pleasures rather than lovers of God, 5  having an appearance of godliness but proving false to its power;+ and from these turn away. 6  From among these arise men who slyly work their way into households and captivate weak women loaded down with sins, led by various desires, 7  always learning and yet never able to come to an accurate knowledge of truth.

Autism in the USA is now 1 in 36 Boys, as it is more male than female. It is up from 1 in 80 in the 2011-2013 surveys to 1 in 45 in the 2014 survey. From 1975 up 800% now.

Autism Stats now 3 years old.

Then comes mental retardation and poor training of Medical Doctors. They think their "difficult" education somehow reflects intelligence. It does not. What reflects intelligence and competence is the extreme rise in death by doctor and malpractice lawsuits.

The "official government" report is 400,000 people die each year from misdiagnoses and death caused by the "treatment" or lack of proper treatment. It is up from 160,000 reported in the prior year 2013. 250% increase in death by doctor. With all the technology they cannot keep track of what a disease looks like or how to test for it, or how to treat it.  That is evidence of human degradation.  12,000,000 cases of harm done to patients by incompetence in one year.
The non-official reports are over 750,000 people die each year from medical incompetence.

Now here is the conclusion. Because we only survive by artificial means from vaccines, antibiotics, drugs, surgery from all the genetic diseases we have, as soon as the medical industry has lost all intelligence (by calculation based on current rise of retardation statistics), we have less than 100 years before extinction from pandemic diseases that wipes out the entire species.  (Hint: it does not take intelligence to be saved by Jehovah God.  It takes a loving kind heart that Jehovah will call you to Him.)

Joel 2:32
32  And everyone who calls on the name of Jehovah will be saved; For on Mount Zion and in Jerusalem there will be those who escape, just as Jehovah has said, The survivors whom Jehovah calls.”

The reason for this rapid and accelerating degradation is from infected reproduction. We now have some 40 STD's recorded and most of them are viral infections.

In case you do not understand how a virus enters the host cells of your zygotes, and fetuses to permanently mutate our children, you need to take a course in virology to understand. When it disrupts the normal cell replication, the cells are changed permanently by mutations and only for the worse.

We now have over 120,000,000 cases of infected sex recorded and that number has risen by 20,000,000 each year for over 11 years in the USA. The result is sick babies with increased genetic deformity and diseases. Lower intelligence and rapid rise of insanity. If you just go on any message forum you will see the crazies all over the place.

Moral degradation has always proceeded the destruction of "empires". The problem now is there is anything left in the "gene pool" to correct for this and humans have created huge numbers of pathogens that spread by sexual contact. It was only a few diseases like this in history 200 years ago.


The more tribal and animal people become, the more they make up reasons to hate one another. We can see that division, hate, war, disease, suffering and death is the outcome of human ignorance. It has no other cause.

2 Timothy:
3  But know this, that in the last days+ critical times hard to deal with will be here. 2  For men will be lovers of themselves, lovers of money, boastful, haughty, blasphemers, disobedient to parents, unthankful, disloyal, 3  having no natural affection, not open to any agreement, slanderers, without self-control, fierce, without love of goodness, 4  betrayers, headstrong, puffed up with pride, lovers of pleasures rather than lovers of God, 5  having an appearance of godliness but proving false to its power;+ and from these turn away. 6  From among these arise men who slyly work their way into households and captivate weak women loaded down with sins, led by various desires, 7  always learning and yet never able to come to an accurate knowledge of truth.

This time in history is clearly spoken of in the Bible. Life so full of fear, anxiety, and mental/physical suffering. It is called the "harvest time" or the time of full fruition of the evil weeds vs the good crop of people.

Luke 10:2
2  Then he said to them: “Yes, the harvest is great, but the workers are few. Therefore, beg the Master of the harvest to send out workers into his harvest.

Matthew 9:38
38  Therefore, beg the Master of the harvest to send out workers into his harvest.”

Matthew 13:24-30
24  He presented another illustration to them, saying: “The Kingdom of the heavens may be likened to a man who sowed fine seed in his field. 25  While men were sleeping, his enemy came and oversowed weeds in among the wheat and left. 26  When the stalk sprouted and produced fruit, then the weeds also appeared. 27  So the slaves of the master of the house came and said to him, ‘Master, did you not sow fine seed in your field? How, then, does it have weeds?’ 28  He said to them, ‘An enemy, a man, did this.’ The slaves said to him, ‘Do you want us, then, to go out and collect them?’ 29  He said, ‘No, for fear that while collecting the weeds, you uproot the wheat with them. 30  Let both grow together until the harvest, and in the harvest season, I will tell the reapers: First collect the weeds and bind them in bundles to burn them up; then gather the wheat into my storehouse.’”

The weeds will be destroyed off the earth and only the "Meek will inherit the earth."Matthew 5:5

God promises to heal everyone who can come to Jehovah and ask for salvation. Only the mild and meek people who are haters of seeing children dying (love seeing children happy and healthy), hate war (do not go to war for any politician of any part of this world that belongs to Satan) , hate diseases (Love health and happiness), hate suffering and hate death (Only those who love life enough to stop sinning) will live in a new Kingdom about to come on the earth. This "Kingdom" is talked about in many ancient scrolls. But the Bible has the way out for those who love life enough to seek it.



Only the true lovers of life are the ones whom Jehovah God grants life to. If you love life and seeing healthy kind and loving people as the only type of people who will be allowed to live, then you need to seek the Truth and stop living in the darkness of suffering. It is the only way to life.

Revelation 21:1
21  And I saw a new heaven and a new earth; for the former heaven and the former earth had passed away, and the sea is no more.

(The "sea" is often referred to by God's Word as the sea of human emotional garbage that is the root cause of suffering.)

2 Peter 3:13
13  But there are new heavens and a new earth that we are awaiting according to his promise, and in these righteousness is to dwell.

Isaiah 65:17
17  For look! I am creating new heavens and a new earth; And the former things will not be called to mind, Nor will they come up into the heart.

And Jesus Christ, himself, will be made King of the earth and the Heavens and to rule forever.  No longer will man rule man.  That mistake is over.

Revelation 11:15
15  The seventh angel blew his trumpet. And there were loud voices in heaven, saying: “The kingdom of the world has become the Kingdom of our Lord and of his Christ, and he will rule as king forever and ever.”




Revelation 21:4

And he will wipe out every tear from their eyes, and death will be no more, neither will mourning nor outcry nor pain be anymore. The former things have passed away.”

More Absolutely Irrefutable Evidence of Humanity's Condition: Author, James Arjuna

All of the evidence from the historical records of the rapid rise of diseases,

The historical records of massive new huge hospitals treating diseases that did not exist before the 1700's
The medical industry did not exist prior to the 1600's.  So from nearly ZERO costs to $4,200,000,000,000 (2015 figures) per year in the USA is an indication of the complete failure of humanity to curb their genetic suicide.  That is over $13,000  spent per citizen per year on medical and still there are no cures.  If you spent 43,000 years counting one dollar at a time, you would get to 4.2 TRILLION, just to give you some perspective.

Greed, lust, anger, division, hate, race, are all disgusting human characteristics.    Greed is a disease and it causes human diseases and suffering.  Lust is a disease and we can see how that works.   300% rise in Childhood cancer in 45 years!

Diseased (STD"s) parents have diseased babies.  It is not magical.  You cannot have rampant STD's and the highest rate of STD's in a country (USA) and not have diseased babies.   How can we continue to destroy all life on earth for greed?

It is not even stoppable by humans, because humans are the problem.  No morals, no science, and the medical industry is a total failure.

12,000,000 causes of medical misdiagnoses causing harm to patients.

http://www.livescience.com/44888-misdiagnosis-doctors-visits.html

The third leading cause of death is death by doctor.


*Deaths by medical mistakes hit records*
400,000 people die each year from medical mistakes.
http://www.healthcareitnews.com/news/deaths-by-medical-mistakes-hit-records

Number one cause of death  Heart disease.   A proven genetic disease in which the arteries are etched by the immune system and that normally slick artery becomes like a gravel road and it collects lipids.

Number 2 cause of Death is Cancer, proven by over 500,000 peer DNA studies to be a genetic disease of the immune system.  Cancer cells are a normal occurrence in humans.  The healthy immune system will destroy those defective cells. The weak and defective immune system cannot even recognize them as defective anymore.

Number 3 cause of death,  Medical incompetence.  The MD's today have all sorts of technology and still they cannot diagnoses and treat diseases correctly because they are retarded from mutations causing an overall retardation of humans.  Memory loss is the most common disease.

If the medical industry was a success there would be a reduction in diseases leading to no disease at all.  Why do people think that having more and more doctors, medical centers, and diseases is a good thing? 

http://evolutionsciencenow.blogspot.com/2013/06/the-medical-industry-and-what-it-tells.html

We cannot even build a simple jet airplane because it is continually grounded for safety issues. Now, the DC 3 aircraft made in the 1930's is still a functional airplane after 80 years.  http://www.cnn.com/2014/06/04/travel/aviation-douglas-dc-3/

https://en.wikipedia.org/wiki/Douglas_DC-3

We cannot make a rocket that will not explode, because of mental degradation in the engineers.

http://www.space.com/27583-antares-rocket-explosion-captured-by-journalist-video.html

In 1969 we put a man on the moon with a rudimentary mechanical calculator, and slide rules to make calculations on engineering.  I know because I was there.  The difference is the much higher intelligence of that generation.

In less that 4 generations, 1914, we went from less than 2% of high school students who were "special" (we called them retarded because that is a medical term for low intelligence).  Less than 2% of seniors in high school could not pass an English, Math, History, Science test in order to graduate.   (Now, that test would be useless, because less than 20% could pass it today.)

Now 40% of high school senior students are incapable of reading in English, writing in English nor can they do simple math.  They cannot even pass any college entrance exams and the universities have drastically lowered their academic standards, because if they did not do that there would be no "students".

http://nces.ed.gov/nationsreportcard/pubs/main2005/2007468.asp

Only 23% of students tested above BASIC standards. That would mean that 23% got a "D" or above.  In my day if you got a D you were considered "retarded", "lazy", and not wanting to learn.

We are watching a human tragedy take place with mental retardation as the normal human.   There are very few people who can concentrate long enough to even read my postings.   If you can read and understand this, you are in the top 10% of intelligence on the planet.

Humanity is degrading faster than ever.  Over ten times the diseases, over 20 times the mental retardation.

For over 200,000 years (by some unproven dating methods) humans did not write things down, because they had a nearly perfect memory.
Like all technology. The invention of writing is evidence of human degradation.

For over 200,000 years humans (by some unproven dating methods) lived with no medical, because disease was not prevalent.
Like all technology. The invention of medical treatments came from genetic degradation.

Now even with all the electronic memories we cannot keep from killing 400,000 humans a year from medical incompetence.

No wonder there are so many "believers" in the evolution fraud.

http://evolutionsciencenow.blogspot.com/2013/06/the-medical-industry-and-what-it-tells.html

CCR5 Delta 32 Deletion more diseases caused by this mutation.

1. Akcay A, Nguyen Q, Edelstein CL (2009) Mediators of inflammation in acute kidney injury. Mediat Inflamm 2009:137072. doi:10.​1155/​2009/​137072 View Article
2. Albelda SM, Smith CW, Ward PA (1994) Adhesion molecules and inflammatory injury. FASEB J 8(8):504–512PubMed
3. Anders HJ, Vielhauer V, Frink M et al (2002) A chemokine receptor CCR-1 antagonist reduces renal fibrosis after unilateral ureter ligation. J Clin Invest 109(2):251–259. doi:10.​1172/​JCI14040 PubMed CentralPubMedView Article
4. Barcellos LF, Schito AM, Rimmler JB et al (2000) CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis. Multiple sclerosis genetics group. Immunogenetics 51(4–5):281–288PubMedView Article
5. Broide DH, Humber D, Sullivan S, Sriramarao P (1998) Inhibition of eosinophil rolling and recruitment in P-selectin- and intracellular adhesion molecule-1-deficient mice. Blood 91(8):2847–2856PubMed
6. Coenen M, Nattermann J (2010) The role of CCR5 in HCV infection. Eur J Med Res 15(3):97–101PubMed CentralPubMedView Article
7. Cunningham PN, Dyanov HM, Park P, Wang J, Newell KA, Quigg RJ (2002) Acute renal failure in endotoxemia is caused by TNF acting directly on TNF receptor-1 in kidney. J Immunol 168(11):5817–5823PubMedView Article
8. Cunningham PN, Wang Y, Guo R, He G, Quigg RJ (2004) Role of Toll-like receptor 4 in endotoxin-induced acute renal failure. J Immunol 172(4):2629–2635PubMedView Article
9. Dawson TC, Beck MA, Kuziel WA, Henderson F, Maeda N (2000) Contrasting effects of CCR5 and CCR2 deficiency in the pulmonary inflammatory response to influenza A virus. Am J Pathol 156(6):1951–1959. doi:10.​1016/​S0002-9440(10)65068-7 PubMed CentralPubMedView Article
10. Day YJ, Huang L, Ye H, Linden J, Okusa MD (2005) Renal ischemia-reperfusion injury and adenosine 2A receptor-mediated tissue protection: role of macrophages. Am J Physiol Renal Physiol 288(4):F722–F731. doi:10.​1152/​ajprenal.​00378.​2004 PubMedView Article
11. Dong Z, Atherton SS (2007) Tumor necrosis factor-alpha in cisplatin nephrotoxicity: a homebred foe? Kidney Int 72(1):5–7. doi:10.​1038/​sj.​ki.​5002320 PubMedView Article
12. Fadel SA, Bromley SK, Medoff BD, Luster AD (2008) CXCR3-deficiency protects influenza-infected CCR5-deficient mice from mortality. Eur J Immunol 38(12):3376–3387. doi:10.​1002/​eji.​200838628 PubMed CentralPubMedView Article
13. Fantuzzi G, Zheng H, Faggioni R et al (1996) Effect of endotoxin in IL-1 beta-deficient mice. J Immunol 157(1):291–296PubMed
14. Fattori E, Della Rocca C, Costa P et al (1994) Development of progressive kidney damage and myeloma kidney in interleukin-6 transgenic mice. Blood 83(9):2570–2579PubMed
15. Faubel S, Ljubanovic D, Reznikov L, Somerset H, Dinarello CA, Edelstein CL (2004) Caspase-1-deficient mice are protected against cisplatin-induced apoptosis and acute tubular necrosis. Kidney Int 66(6):2202–2213. doi:10.​1111/​j.​1523-1755.​2004.​66010.​x PubMedView Article
16. Furuichi K, Wada T, Iwata Y et al (2003) CCR2 signaling contributes to ischemia-reperfusion injury in kidney. J Am Soc Nephrol 14(10):2503–2515PubMedView Article
17. Furuichi K, Gao JL, Horuk R, Wada T, Kaneko S, Murphy PM (2008) Chemokine receptor CCR1 regulates inflammatory cell infiltration after renal ischemia-reperfusion injury. J Immunol 181(12):8670–8676PubMed CentralPubMedView Article
18. Gadient RA, Patterson PH (1999) Leukemia inhibitory factor, Interleukin 6, and other cytokines using the GP130 transducing receptor: roles in inflammation and injury. Stem Cells 17(3):127–137. doi:10.​1002/​stem.​170127PubMedView Article
19. Homsi E, Ribeiro-Alves MA, Lopes de Faria JB, Dias EP (2002) Interleukin-6 stimulates tubular regeneration in rats with glycerol-induced acute renal failure. Nephron 92(1):192–199PubMedView Article
20. Jo SK, Cho WY, Sung SA, Kim HK, Won NH (2005) MEK inhibitor, U0126, attenuates cisplatin-induced renal injury by decreasing inflammation and apoptosis. Kidney Int 67(2):458–466. doi:10.​1111/​j.​1523-1755.​2005.​67102.​x PubMedView Article
21. Kayama F, Yoshida T, Elwell MR, Luster MI (1995) Cadmium-induced renal damage and proinflammatory cytokines: possible role of IL-6 in tubular epithelial cell regeneration. Toxicol Appl Pharmacol 134(1):26–34. doi:10.​1006/​taap.​1995.​1165 PubMedView Article
22. Kelly KJ, Williams WW Jr, Colvin RB, Bonventre JV (1994) Antibody to intercellular adhesion molecule 1 protects the kidney against ischemic injury. Proc Natl Acad Sci U S A 91(2):812–816PubMed CentralPubMedView Article
23. Knotek M, Rogachev B, Wang W et al (2001) Endotoxemic renal failure in mice: role of tumor necrosis factor independent of inducible nitric oxide synthase. Kidney Int 59(6):2243–2249. doi:10.​1046/​j.​1523-1755.​2001.​00740.​xPubMedView Article
24. Lee YK, Kwak DH, Oh KW et al (2009) CCR5 deficiency induces astrocyte activation, Abeta deposit and impaired memory function. Neurobiol Learn Mem 92(3):356–363. doi:10.​1016/​j.​nlm.​2009.​04.​003 PubMedView Article
25. Li L, Huang L, Sung SS et al (2007) NKT cell activation mediates neutrophil IFN-gamma production and renal ischemia-reperfusion injury. J Immunol 178(9):5899–5911PubMedView Article
26. Linas SL, Shanley PF, Whittenburg D, Berger E, Repine JE (1988) Neutrophils accentuate ischemia-reperfusion injury in isolated perfused rat kidneys. Am J Physiol 255(4 Pt 2):F728–F735PubMed
27. Mehta RL, Kellum JA, Shah SV et al (2007) Acute kidney injury network: report of an initiative to improve outcomes in acute kidney injury. Crit Care 11(2):R31. doi:10.​1186/​cc5713 PubMed CentralPubMedView Article
28. Meldrum KK, Meldrum DR, Hile KL et al (2001) p38 MAPK mediates renal tubular cell TNF-alpha production and TNF-alpha-dependent apoptosis during simulated ischemia. Am J Physiol Cell Physiol 281(2):C563–C570PubMed
29. Messmer UK, Briner VA, Pfeilschifter J (1999) Tumor necrosis factor-alpha and lipopolysaccharide induce apoptotic cell death in bovine glomerular endothelial cells. Kidney Int 55(6):2322–2337. doi:10.​1046/​j.​1523-1755.​1999.​00473.​xPubMedView Article
30. Mishima K, Baba A, Matsuo M, Itoh Y, Oishi R (2006) Protective effect of cyclic AMP against cisplatin-induced nephrotoxicity. Free Radic Biol Med 40(9):1564–1577. doi:10.​1016/​j.​freeradbiomed.​2005.​12.​025 PubMedView Article
31. Moreno C, Gustot T, Nicaise C et al (2005) CCR5 deficiency exacerbates T-cell-mediated hepatitis in mice. Hepatology 42(4):854–862. doi:10.​1002/​hep.​20865 PubMedView Article
32. Patel NS, Chatterjee PK, Di Paola R et al (2005) Endogenous interleukin-6 enhances the renal injury, dysfunction, and inflammation caused by ischemia/reperfusion. J Pharmacol Exp Ther 312(3):1170–1178. doi:10.​1124/​jpet.​104.​078659PubMedView Article
33. Perez de Lema G, Maier H, Franz TJ et al (2005) Chemokine receptor Ccr2 deficiency reduces renal disease and prolongs survival in MRL/lpr lupus-prone mice. J Am Soc Nephrol 16(12):3592–3601. doi:10.​1681/​ASN.​2005040426PubMedView Article
34. Ramesh G, Reeves WB (2002) TNF-alpha mediates chemokine and cytokine expression and renal injury in cisplatin nephrotoxicity. J Clin Invest 110(6):835–842. doi:10.​1172/​JCI15606 PubMed CentralPubMedView Article
35. Ramesh G, Reeves WB (2003) TNFR2-mediated apoptosis and necrosis in cisplatin-induced acute renal failure. Am J Physiol Renal Physiol 285(4):F610–F618. doi:10.​1152/​ajprenal.​00101.​2003 PubMedView Article
36. Ramesh G, Reeves WB (2005) p38 MAP kinase inhibition ameliorates cisplatin nephrotoxicity in mice. Am J Physiol Renal Physiol 289(1):F166–F174. doi:10.​1152/​ajprenal.​00401.​2004 PubMedView Article
37. Ramesh G, Kimball SR, Jefferson LS, Reeves WB (2007) Endotoxin and cisplatin synergistically stimulate TNF-alpha production by renal epithelial cells. Am J Physiol Renal Physiol 292(2):F812–F819. doi:10.​1152/​ajprenal.​00277.​2006PubMedView Article
38. Remick DG, Newcomb DE, Bolgos GL, Call DR (2000) Comparison of the mortality and inflammatory response of two models of sepsis: lipopolysaccharide vs. cecal ligation and puncture. Shock 13(2):110–116PubMedView Article
39. Russell JA, Singer J, Bernard GR et al (2000) Changing pattern of organ dysfunction in early human sepsis is related to mortality. Crit Care Med 28(10):3405–3411PubMedView Article
40. Rybak SL, Murphy RF (1998) Primary cell cultures from murine kidney and heart differ in endosomal pH. J Cell Physiol 176(1):216–222. doi:10.​1002/​(SICI)1097-4652(199807)176:​1<216:​AID-JCP23>3.​0.​CO PubMedView Article
41. Samson M, Labbe O, Mollereau C, Vassart G, Parmentier M (1996) Molecular cloning and functional expression of a new human CC-chemokine receptor gene. Biochemistry 35(11):3362–3367. doi:10.​1021/​bi952950g PubMedView Article
42. Schrier RW, Wang W (2004) Acute renal failure and sepsis. N Engl J Med 351(2):159–169. doi:10.​1056/​NEJMra032401351/​2/​159 PubMedView Article
43. Segerer S, Nelson PJ, Schlondorff D (2000) Chemokines, chemokine receptors, and renal disease: from basic science to pathophysiologic and therapeutic studies. J Am Soc Nephrol 11(1):152–176PubMed
44. Segerer S, Banas B, Wornle M et al (2004) CXCR3 is involved in tubulointerstitial injury in human glomerulonephritis. Am J Pathol 164(2):635–649. doi:10.​1016/​S0002-9440(10)63152-5 PubMed CentralPubMedView Article
45. Sorce S, Bonnefont J, Julien S et al (2010) Increased brain damage after ischaemic stroke in mice lacking the chemokine receptor CCR5. Br J Pharmacol 160(2):311–321. doi:10.​1111/​j.​1476-5381.​2010.​00697.​x PubMed CentralPubMedView Article
46. Turner JE, Paust HJ, Steinmetz OM et al (2008) CCR5 deficiency aggravates crescentic glomerulonephritis in mice. J Immunol 181(9):6546–6556PubMedView Article
47. Turner JE, Paust HJ, Bennstein SB et al (2012) Protective role for CCR5 in murine lupus nephritis. Am J Physiol Renal Physiol 302(11):F1503–F1515. doi:10.​1152/​ajprenal.​00382.​2011 PubMedView Article
48. Wang W, Faubel S, Ljubanovic D et al (2005) Endotoxemic acute renal failure is attenuated in caspase-1-deficient mice. Am J Physiol Renal Physiol 288(5):F997–F1004. doi:10.​1152/​ajprenal.​00130.​2004 PubMedView Article
49. Xu C, Chang A, Hack BK, Eadon MT, Alper SL, Cunningham PN (2014) TNF-mediated damage to glomerular endothelium is an important determinant of acute kidney injury in sepsis. Kidney Int 85(1):72–81. doi:10.​1038/​ki.​2013.​286 PubMedView Article
50. Yanaba K, Mukaida N, Matsushima K, Murphy PM, Takehara K, Sato S (2004) Role of C-C chemokine receptors 1 and 5 and CCL3/macrophage inflammatory protein-1alpha in the cutaneous Arthus reaction: possible attenuation of their inhibitory effects by compensatory chemokine production. Eur J Immunol 34(12):3553–3561. doi:10.​1002/​eji.​200425426 PubMedView Article
51. Zhang D, Li Y, Liu Y, Xiang X, Dong Z (2013) Paclitaxel ameliorates lipopolysaccharide-induced kidney injury by binding myeloid differentiation protein-2 to block Toll-like receptor 4-mediated nuclear factor-kappaB activation and cytokine production. J Pharmacol Exp Ther 345(1):69–75. doi:10.​1124/​jpet.​112.​202481 PubMed CentralPubMedView Article