Comments by "Flook D" (@flookd5516) on "Response to Globebusters - The Earth Still Isn't Flat" video.
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@imjustanant Key points of any science experiment is falsifiability and reproducibility. You make a prediction according to your hypothesis then perform tests that would not work if your hypothesis is incorrect. Your prediction is that Chicago would be visible from a certain location only if your hypothesis of a FE is correct. A shot from a mile down the coast would demonstrate nothing; if can be accounted for by the existing model then you haven't demonstrated that your model is more accurate. The conditions during repeated tests need to be as close as possible to identical.
How far you should be able to see is dependent on curvature, elevation and atmospheric refraction; all three have to be accounted for, not just one (the usual FE screw-up) and correctly accounted for (the other usual FE screw-up; 8"/mile^2 is not the correct formula). (If you want to test a battery-powered torch (flashlight) then you need a battery that is charged, inserted and correctly oriented; all three criteria have to be met for you to be testing the torch and a 9V is not interchangeable with a D). If you want to shoot from the top of a 6ft dune with a 4ft tripod that extra 10ft has to be included in the calculations (plus however far up the beach the dune is). The atmospheric fraction has to be as close as possible to constant; the simplest would be to go with an approximate average for Xft above water.
In terms of distance you need a location that will test your hypothesis. With all criteria accounted for it needs to be impossible (for real) on a globe but possible with a FE.
In terms of reproducibility, conditions have to be near identical on multiple occasions. The pictures need to be taken with the same camera, using the same lens and same tripod height from exactly the same location (top of a specific dune) in near as identical weather/atmospheric conditions. A mirage is not a typical condition and would render that test useless unless your hypothesis is specifically about what is visible during a mirage. Taking several shots in the course of 1hr tests nothing; if there is something unusual occurring at the time (known or unknown, e.g., mirage) then that could explain your results rather than any veracity of your hypothesis. The least you need to do is being there every day at a similar time for a week in similar weather conditions. In making any reports you need to specify what the conditions were and what you did to meet all the necessary criteria.
The results you obtain will be evidence, not proof. If you find evidence of a FE then, even correctly done, there is a still an element of the unknown involved. It needs to be reproduced by other people, not simply there but in other places to account for anything unusual that may exist at Lake Michigan at that time (e.g., deviation from a perfect sphere, unusually high humidity). If, and only if, the same can be readily reproduced in all or nearly all locations do you have a case. If you can't find evidence of a FE then it won't disprove the hypothesis but will indicate you're barking up the wrong tree.
There's nothing fussy about this; it's just basic science.
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@EdenCultures As I understand it there are just two vaccines that make use of fetal cells in generating antigens. Neither is the HepB vaccine.
Your argument is that the serial purification processes fails to filter out all the DNA from ruptured cells, that the DNA is injected into the bloodstream, manages to make it out of the bloodstream, manages to disperse through the body, reaching the stem cells that give rise to ova & sperm, manages to penetrate the cell, manages embed itself in the genome without initiating self-destruct, coincidentally be able express a viable mRNA (that would create a human protein that you already possess) and this somehow produces a point mutation in a gene that would then be heritable by offspring who would possess it in all their cells. Or have I misunderstood and you're arguing that contaminating DNA manages to transfect stem cells throughout your body and inducing a common point mutation in all?
I'm sorry to hear that you are hypersensitive to vaccinations. However, simply because you are is not a case for vaccines not being used on anybody; few people have such hypersensitivity. Assuming there was fetal DNA contamination in the vaccine shot you received, it would not lead to you or your kids having a point mutation in one or all body cells.
"they are free of chronic illness, have fully functioning immune systems"
One would hope they would be healthy since that applies to the great majority of people. How does that tie into not having been vaccinated?
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@EdenCultures The excipient list covers all possible content in a vaccine, not just routine ingredients. They do clearly state "Others are residual trace amounts of materials that were used during the manufacturing process and removed"; this covers all the cell culture materials that may have made it through purification, e.g., cells, protein, DNA.
I want to see evidence of Deisher's claims of a whole genome found, DNA outweighing antigen content and antigen being absent.
Lack of liability exists in the US; the US is not the only country manufacturing vaccines.
I commented on which stem cells would be affected because it wasn't clear how you thought all your cells became mutated. Either you think DNA has penetrated every stem cell in your body and had exactly the same affect or you think one of your parent had mutated sperm or ova.
There is a huge difference between a mutagen and DNA contamination. The former can penetrate the cell without getting digested by the cell; it would be small enough to penetrate the nucleus and can either inflict damage on the DNA or affect the repair mechanisms; the damage would be limited to small changes in the coding. You're suggesting fragments of DNA are making it into the cell, through to the nucleus and inserting themselves like a virus DNA into a chromosome. That would produce an insertion mutation, not a point mutation. There would not be the change to a single codon that you have but whole inserted sequence.
Stem cell therapy means isolating stem cells, "swapping out" genes and reintroducing them into the body.
Viruses inject their DNA/RNA by a specific mechanism, binding to the cell membrane and injecting the DNA/RNA into the cell. The presence of a viral antigen, or even a whole virus, is not going to replicate that effect. Viruses can only be used as a carrier if the target gene sequence has been inserted in their DNA/RNA i.e., we are using a modified virus.
If a single cell starts expressing a non-self protein then the immune system destroys it; that happens routinely in the body with no symptoms apparent to the human. Despite the high efficiency of DNA repair nothing is perfect in replication and mutations do occur. They usually result the cell's self-destruction and few are going to be competent long enough to expression a non-self protein. Only if the cells can also expression an "all clear" signal for the immune system will it survive.
"The similarity of the genes from the human DNA make it MORE likely to insert into whichever cell."
To be accurate it makes sequence swapping easier, not sequence insertion. DNA is DNA; there is no difference between different sources other than the actual coding within it. The source makes no difference on penetrating the cell.
The numbers vary due to the way numbers are collated, which vaccines are being looked at and by what criteria a reaction is categorised. Very few people have a severe reaction; more have mild fever & headache. Norm covers the average effects, not a specific genome.
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