The diagnosis of a legendary women's basketball coach at my school, Pat Summit, with early onset dementia, Alzheimer's type, got me thinking about Cryonics and Alzheimer's. For the purposes of this thought experiment, we will ignore the legal implications of the fact that you can't be frozen until you are legally dead. Let us further assume (which given my knowledge of Alzheimer's, is pretty reasonable) that the damage done by Alzheimer's is complete, and that future technology will be unable to reconstruct the destroyed components.
If you were diagnosed with Alzheimer's, or really any neurodegenerative disorder, at what point in the degradation would you want to be frozen? This would fairly easily prevent further degradation, but might further damage you/all of the other risks associated with cryonics that everyone knows. Obviously, you wouldn't have the agency of mind (or perhaps you still would, depending on when you made the decision) to do it yourself, but suppose you were caring for a loved one, or writing a living will. Assume you operate healthily at the onset of your diagnosis.
Things to consider:
How would your loved ones react to your being frozen versus coping with you having Alzheimer's? Should this matter in your decision? If it does, what implications does that have for a duty to die?
How much degradation of the mind is acceptable (and the added damage potentially done by cryonics) before one should freeze onesself?
Would you avoid the risk of being frozen all together because you believe we will or may have a cure for Alzheimer's soon, and waiting for it would do less damage than cryonics?
23andMe recently showed that people of my genotype are more than twice as likely to develop Alzheimer's as others in my ethnic group. I have a 15% chance of getting Alzheimer's before I'm 80, up from 7%. See Patri's post about this.
An initial Googling has generated things like 'eat paleo', 'get caffeine', 'exercise', and 'use your brain'. I'm planning to do further research about decreasing Alzheimer's risk.
I really recommend that everyone do 23andMe for this precise reason.
I wonder, how much does that single bit of information (doubling the chance) matter to those decisions? Should you have been doing those things anyway, for the Alzheimer's prevention and the other benefits? Is it the motivational factor of the formal personal certification that is important or the actual information?