Alzheimer's: The News Is Not Getting Better
pipeline.corante.com
pipeline.corante.com
This is absolutely how I feel. I may not take this kind of treatment in the early stages of the disease, but as soon as feel that I might be losing myself, I'd roll the dice without blinking.
Now, if those numbers would show something like 50% chance, that would be much better.
Different diseases / treatments cause different pain levels and suffering in those that have them and the ones close to them. Spending 3 months next to your loved ones or 6 months in a hospital bed is a heart-breaking decision to make. The ability to manipulate the probabilities regarding how one's diseases progresses is the most basic human right that an ill person can have. I really hope you're not advocating taking that liberty away from them.
It's hard to describe unless you've watched a loved one go through it.
It sounds like we could be on the verge of understanding something fundamental about alzheimers. I'd say that's fantastic news in the long-term.
Not trying to be hopeless here: just remember to thank your local Alzheimer's researcher, the job has not been that rewarding to date.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2898565/
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"Neuroprotective and disease-modifying effects of the ketogenic diet"
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2367001/
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" Study of the ketogenic agent AC-1202 in mild to moderate Alzheimer's disease: a randomized, double-blind, placebo-controlled, multicenter trial"
http://www.biomedcentral.com/content/pdf/1743-7075-6-31.pdf
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http://scholar.google.com/scholar?q=alzheimers+ketogenic+die...
Anyway, is it a stretch to think that some mad cow cases are being mis-diagnosed as Alzheimer's desease? It seems like it is at least a possibility.
BTW, I don't think that the Obama administration has lifted the ban on testing. One lacky president is as good as another.
A friend of my parents in California died several years ago from mad cow desease (v/CJD) and it took many years.
Anyway, this is outside my area of expertise - my wife however spent a lot of time looking into this and she very much believes that mis-diagnosis is common.
For "regular" CJD it's closer to half that.
Long term progressions are known to happen but are rare even given the rareness of CJD, so your friend was quite the outlier.
That said, there is zero chance of an epidemic of CJD being misdiagnosed as alzheimers.
Put the tinfoil hat away, citation needed, man.
Ratchet up the level of discourse, okay?