(Sent to US president and PM Modi ji)
Anti-aging is brand-new with unimaginable number of potential users. After 5000 years of recorded human existence, for once there is scientific possibility of it (means bio-age can be measured and decremented. None of what follows may make sense to medical doctors but will to Geneticists.
FDA is the US agency responsible for drugs. They exist to shield USA citizens from corrupt makers and inspector fraud and injurious advertisement to prohibit corrupt producers/middlemen. They have developed a four stage process for testing drugs. Furthermore, they achieve graded safety and efficacy. They have saved USA (unlike Britain and Europe) from Thalidomide-babies because of their slowness from thoroughness. FDA certified medicine are known over the world as properly certified despite every nation having own FDA in some name.
FTD is my own nomenclature. It is when the maker is self and family user, forbidden from acting as an amount specifier and commercially pushing a product. I claim that in circumstances where such a person can legitimately deny any conflict of interest, then the result could be faster. Then this FTD is superior! It is not first occasion of FDA slowness. Stevia was legalized in Japan in 1970. USA's slowness (courts and FDA) pushed US acceptance well after 2010 with 40 year gap and unknown number of victims in diabetic class forced to eat cancerous sweeteners!
This is the case of Dr. Sinclair and anti-aging. I have no need for FDA testing and protection because I independently corroborate safety, RDS claim of efficacy, and I can not afford to wait for FDA to protect me. The sane way is to beef up FDA with FTD equivalent and develop an FDA (supplement) for safety only and statistical data on claimed benefit. Lacking both, I will move our PM to establish for FSSAI expansion and supplement and fast FTD certification. This will be welcomed by ethical supplement makers and self-apply scientists.
Why is NMN/NR safe?
It is a form of vitamin B3.
Why is NMN/NR efficacious?
Dr. Sinclair FTD claim. No criminal will ingest own drug, convince family to do so, and open results for scientific RDS. Such subhuman will achieve some 2 steps but not all 3. I want results for human and refuse to wait for FDA. I am open to futile experimentation. Unlike the USA, I don't have to submit to FDA. India can become source of self-sufficient in NMN and open NOIDA/Ghaziabad to medical tourism. Risk but so what? My own aging is super-important!
Why is plasma exchange safe?
It is no different from blood transfusion.
Why is plasma exchange efficacious?
Salk data for mice. UCB for mice. Human efficacy if not known but very likely with intermittent 3 Yamanaka factors. I want results for human and refuse to wait for FDA. I am open to futile experimentation. Unlike the USA, I don't have to submit to FDA. India can become source of self-sufficient in plasma replacement and open NOIDA/Ghaziabad to medical tourism. Risk but so what? My own aging is super-important! I see no reason to wait for Yamanaka factor improvement, a third and repeatable method.
Why it is at least as old as Jan 28, 2021 and Feb 5, 2021?
Day saw links on general Horvath and on mice plasma benefit. Must be before GOOGLE BACKUP OF FEB 5, 2021.
No comments:
Post a Comment