Dec 17, 2012
There are a lot of steps that all need to go correctly for cryonics to work. People who had gone through the potential problems, assigning probabilities, had come up with odds of success between 1:4 and 1:435. About a year ago I went through and collected estimates, finding other people's and making my own. I've been maintaining these in a googledoc.
Yesterday, on the bus back from the NYC mega-meetup with a group of people from the Cambridge LessWrong meetup, I got more people to give estimates for these probabilities. We started with my potential problems, I explained the model and how independence works in it . For each question everyone decided on their own answer and then we went around and shared our answers (to reduce anchoring). Because there's still going to be some people adjusting to others based on their answers I tried to randomize the order in which I asked people their estimates. My notes are here. 
The questions were:
To see people's detailed responses have a look at the googledoc, but bottom line numbers were:
|person||chance of failure||odds of success|
(These are all rounded, but one of the two should have enough resolution for each person.)
The most significant way my estimate differs from others turned out to be for "the current cryonics process is insufficient to preserve everything". On that question alone we have:
|person||chance of failure|
My estimate for this used to be more positive, but it was significantly brought down by reading this lesswrong comment:
Let me give you a fuller view: I am a neuroscientist, and I specialize in the biochemistry/biophysics of the synapse (and interactions with ER and mitochondria there). I also work on membranes and the effect on lipid composition in the opposing leaflets for all the organelles involved.
Looking at what happens during cryonics, I do not see any physically possible way this damage could ever be repaired. Reading the structure and "downloading it" is impossible, since many aspects of synaptic strength and connectivity are irretrievably lost as soon as the synaptic membrane gets distorted. You can't simply replace unfolded proteins, since their relative position and concentration (and modification, and current status in several different signalling pathways) determines what happens to the signals that go through that synapse; you would have to replace them manually, which is a) impossible to do without destroying surrounding membrane, and b) would take thousands of years at best, even if you assume maximally efficient robots doing it (during which period molecular drift would undo the previous work).
Etc, etc. I can't even begin to cover complications I see as soon as I look at what's happening here. I'm all for life extension, I just don't think cryonics is a viable way to accomplish it.
In the responses to their comment they go into more detail.
Should I be giving this information this much weight? "many aspects of synaptic strength and connectivity are irretrievably lost as soon as the synaptic membrane gets distorted" seems critical.
Other questions on which I was substantially more pessimistic than others were "all cryonics companies go out of business", "the technology is never developed to extract the information", "no one is interested in your brain's information", and "it is too expensive to extract your brain's information".
I also posted this on my blog
 Specifically, each question is asking you "the chance that X happens and this keeps you from being revived, assuming that all of the previous steps all succeeded". So if both A and B would keep you from being successfully revived, and I ask them in that order, but you think they're basically the same question, then A basically only A gets a probability while B gets 0 or close to it (because B is technically "B given not-A")./p>
 For some reason I was writing ".000000001" when people said "impossible". For the purposes of this model '0' is fine, and that's what I put on the googledoc.