Earlier quoted context omitted.
Hmm...except that cryopreservation is still, as of this point, a complete crock of shit. Trying to find a necromancer would be more productive. As an ex-biologist, I can assure you that horrible cellular damage is being committed to these "preserved" people. I used to flash-freeze all sorts of cells, ranging from bacteria (e. coli) to animal (IMCD3 and MDCK kidney) to human (Human Embryonic Kidney, Primary cortical a…
You don't seem to be all that up to date on present practice and theory in cryonics. Take some time to read up on the publications, such as by groups like 21st Century Medicine: http://www.21cmpublications.com/ Or for a simpler starting point, the FAQs for scientists at Alcor: http://alcor.org/sciencefaq.htm You might also look at ongoing results from the Brain Preservation Technology Prize: http://www.fightaging.org…
Like I said, the current state of "businses cryonics" is basically astrology and wishful thinking. I also don't doubt that in ten, twenty, fifty years, scientists will have figured out how to do it (much better).
But right now? I'm saying nope.
(Addendum: most of those publications listed at 21cm are about thin slices, which isn't exactly relevant. The even better ones are oocytes, which are practically tanks of the cellular world. Drosophila oocytes are so large you can see them with your naked eye and can withstand enormous punishment before dieing. Using them as case studies of vitrification is not really being honest.
This brings me back to my original point: the science is solid...at an academic level. Once you move past 50 micron tissue slices, it all goes to hell.)