Genetics as it relates to the fluoroquinolone toxicity sufferer
Based on many years of anecdotal evidence by citizen scientists, and the results of some recent research findings, this paper proposes a theory that, if proven true, would suggest a novel mechanism behind FQAD in an otherwise healthy population in the absence of genetic predispositions.
The fluoroquinolone antibiotics have the ability to reach yet to be discovered pathogenic genetic variants before we have had a chance to research their ability to cause potential harm.
Dr. Bennett at the University of South Carolina School of Medicine is conducting a study into Fluoroquinolone (FQ) genetic predispositions.
Could hydrogen sulfide (H2S) be driving some of your chronic floxing symptoms? Evidently it is in a subset of individuals who are chronically floxed.
In this article I refute the smoking gun scenario, discuss why some people seemingly do not have adverse events, reveal why Cipro damages the brain, why they are still on the market, and, again, reiterate just how horribly damaging the FQ’s are to mitochondria.
A follow-up to my muscle biopsy from February 7th, 2017 and subsequent mitochondrial DNA sequencing.
Drug’s that can mutate DNA and create a disease process are downright scary. They start the ball rolling on a pathology that often appears later on..
After so many unremarkable tests, and so many years, some of the bigger pieces of the puzzle, for me, are starting to fall into place.
This plan features a unique perspective of science and natural methods, to offer, in my opinion, one of the best plans to place our bodies on the path to healing and a healthier lifestyle post Fluoroquinolones.
Although this mutation is fairly uncommon, however if you do have this mutation it can significantly impact many areas of your health.
I have found that there is a great misconception by many, including doctors, about the concept of senescence. Most believe it is just simply ‘old age’, but its far more....
Since our physiology is not static and things such as enzyme levels and trace mineral are in a constant state of flux, not to mention genetic variances, all which affect metabolization, combined with the fact that the FQ molecule is very complex, there is no way of determining if the same decomposed and identifiable compound will form an adduct in each person.
In this knee jerk reaction the FDA ruling makes the assumption that "We the People" are not responsible enough or smart enough to own or understand our own genetic information.
Just learning if adductions exist or not is not the end, just the opposite, it would open up a vast array of questions, resulting in the need for far more research. If you are looking with an unbiased filter you will see a highly heterogeneous mix of results.There may end up being one cause, but there definitely is not one destination.
The rate of one MTHFR mutation in the standard population is a whopping 50%.
