I'm looking for alternative funding strategies for cryonics.

You might get better responses at New Cryonet or r/cryonics. The cryonics community doesn't seem to be very active here.

It's a tricky question and depends a lot on your circumstances.

First, there are often cheaper options available. For example, CI is cheaper than Alcor. See

If you have a terminal illness and don't have enough money for even cheaper options like CI, you can try to get in touch with the Venturists, who might be able to vouch for your situation and coordinate a fundraiser (they have done this in the past). Their website seems to be down but I think they are still active:

Best of luck. I'm really sorry for your situation. It's a shame that cryonics is ridiculed and stigmatized and as a result the costs are much higher and this kind of situation is so hard to coordinate.

Why I think worse than death outcomes are not a good reason for most people to avoid cryonics

Upvoted -- I agree that the probability is higher if you do cryonics.

However, a lot of the framing of this discussion is that "if you choose cryonics, you are opening up Pandora's box because of the possibility of worse-than-death outcomes." This triggers all sort of catastrophic cognitions and causes people to have even more of an ugh field around cryonics. So I wanted to point out that worse than death outcomes are certainly still possible even if you don't do cryonics.

Can we decrease the risk of worse-than-death outcomes following brain preservation?

Well, this is certainly a reasonable response. But if there is a mechanism to decrease the probability that a worse-than-death outcome would occur so that people who had expressed these concerns are more likely to want to do brain preservation and more people could be a part of the future, that seems like an easy win. I don't think people are particularly fungible.

Can we decrease the risk of worse-than-death outcomes following brain preservation?

I think I did not explain my proposal clearly enough. What I'm claiming is if that you could see intermediate steps suggesting that a worst-type future is imminent, or merely crosses your probability threshold as "too likely", then you could enumerate those and request to be removed from biostasis then. Before those who are resuscitating you would have a chance to do so.

You Only Live Twice

it is very likely that my ticket out will be Alzheimer's or another neurodegenerative disease. In that case, cryopreservation will only make sense if I commit suicide at the very onset of the disease and am frozen right away which may not be possible. If I get Alzheimer's I may as well donate all my money to SIAI or Africa.

Consider two possibilities:

1) Alzheimers breaks long-distance communication more than it does actual information such as memories. Cf moments of lucidity. It's not clear how true this is, though.

2) It may in fact be possible to undergo controlled legal death at the onset of death in some number of years. See the Oregon laws, which are likely to start to be passed elsewhere. See also

I want you to live too :)

You Only Live Twice

Can you describe the reasons are that make you think it is not likely enough to work? Totally understandable if you can't articulate such reasons, but I'm just curious about what the benchmarks are that you might find useful in informing your probability estimate.

That is to say, it's unlikely that actual reversible cryopreservation would be possible; if it were, the technique probably wouldn't be called cryonics anymore. So, other more intermediate steps that'd you'd find informative might be good to know about.

More Cryonics Probability Estimates

"Brain degradation after death" is the key point in this list that I'd be interested in learning about. I'm not sure if it's proper to ask this in a comment now or should I be studying diligently around the issue, but I think it's also an interesting subject so excuse me.

Yes, good intuition. This is what Mike Darwin considers the largest problem in cryonics:

More Cryonics Probability Estimates

simply long-term structural changes in the brain to seeing memories as the products of "continuous enzymatic activity"

Long-term structural maintenance requires continuous enzymatic activity. For example, the average AMPA receptor lasts only around one day: The actin cytoskeleton, made up of molecules which largely specify the structure of synapses, also requires continuous remodeling. If a structure is visibly the same after vitrification (not trivial), that means the molecules specifying it are likely to not have changed much.

More Cryonics Probability Estimates

but another large part of it is mediated by hormones going to and from the rest of your body

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