Biden doesn't need a misinformation governance board. He's already got one in charge of spreading misinformation. It's called the CDC.

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The cleverness of the fox is often overestimated, because the stupidity of the chickens is also credited to him.

-Hans Kasper-

TESTING ORGANIC ACIDS IN YOUR URINE (OAT)
(Urine is your filtered blood. This test looks for markers of gut bacteria and fungi in your urine, as well as indications of vitamin levels and compounds like oxalates and glutathione). The OAT is a snapshot, taken from one morning’s urine.). You will want to look at your test results alongside other information like your enzymes (DNA), salivary and urine pH, hair (or big toenail) mineral test, and other data.
ALWAYS ASK ‘WHY’? For example, you may have a high level of 4-cresol, a marker for the bacteria called Clostrdium dificil (C dif for short). Elevated C. dif can cause elevated levels of dopamine. Why do you have elevated levels of C. dif? In some postings above, on mercury, you will read that mercury can elevate levels of C. dif? Do you have high levels of mercury? If so, why?
(note that the presentation is based on ‘germ theory’ and references ‘killing viruses” which is impossible since they are not alive, and the ones he mentions have never been isolated/purified or met Koch’s Postulates. I am looking around for interpretation of OAT from terrain theory ...)
https://youtu.be/k8nnBFdk32o

EXCESS DOPAMINE THEN CREATES OXIDATIVE STRESS (SUPEROXIDE, HYDROGEN PEROXIDE) WHICH DEPLETE GLUTATHIONE
And now because you are short on glutathione, you can’t clear toxic compounds and drugs and that in turn can cause toxicity and neurological damage. If you have variants in the enzymes involved in clearing oxidative stress (like SOD, CAT, GSH) then there is even more potential for toxicity.

YOU SAY TOXIN, I SAY TOXICANT
I have been using the words incorrectly all along!
https://discardstudies.com/2017/09/11/toxins-or-toxicants-why-the-difference-matters/

TRYPTOPHAN & QUINOLYTIC ACID & NEURO INFLAMMATION.
Here 👇👇👇👇Brandon Vermeire walks through the biochem of quinolytic acid which is assessed in an organic acids test. You can take an amino acid like tryptophan with all good expectations that it will turn into serotonin and melatonin ... but things can go awry, and you might be making quinolytic acid instead. Which would really stink since it contributes to brain (neuro) damage, as Brandon describes. I have posted previously a list of Brandon's brain inflammation markers and how to test for them.

Quinolytic acid revs up glutamate and glycine which are (ahem) two amino acids comprising glutathione (the third is cysteine, aka NAC)
Obviously you can do your own search on glutamate and NMDA but here is a quick rundown of neurodegerative illnesses linked to NMDA
Alzheimer's disease
Amyotrophic lateral sclerosis (ALS)
Huntington's disease
Parkinson's disease
Epilepsy

Other central nervous system conditions with suspected NMDA receptor involvement include:
Fibromyalgia
Chronic fatigue syndrome
Migraine aura
Some types of headache
Anxiety
Depression
Schizophrenia
Post-traumatic stress disorder
Obsessive-compulsive disorder

Never let a good virus scare go to waste. The next 'virus' will be called The Ukraine Flu, mark my words!

I was making a juice last night and came across a decomposing lemon in my fruit bowl. None of the other pieces of fruit or vegetables had become "infected". This is a great visual example of why I question the theory of "contagion".

If the mould caused this lemon to rot, why didn't it cause the others to rot as well? Mould and bacteria and fungi are mother nature's waste disposal unit. They are there to clean up the mess, not cause disease. More experiments on this to come in the near future.

Don't forget to sign up to my upcoming webinar on the microbiome.

www.humanley.com/microbiome

Early bird discount for my next webinar The Microbiome.

The human microbiome is one of the most widely researched, yet misunderstood parts of the human body. The current understanding of the microbiome is that there are “good bacteria” which are conducive to good health and “bad bacteria” which cause dysbiosis and disease. But what if there weren’t “good” or “bad” bacteria? What if parasitic, fungal and bacterial infections weren’t actually the cause of disease but the answer to it? What if everything we thought we know about the microbiome was completely misguided? This webinar will challenge everything you thought you knew about the microbiome and might change the way you view the body, health and disease, forever.

This webinar will discuss the following topics;

- The microbiome and its function in health and disease
- Terrain theory and the microbiome
- The false dichotomy of “good” and “bad” bacteria
- Dysbiosis, parasitic and fungal infections are a healing response rather than the cause of disease
- New perspectives around pro-biotic, anti-bacterial, anti-fungal and anti-parasitic treatments
- Practical considerations and interventions to promote gut health and wellbeing

Join me on Wednesday the 25th of May at 6 pm AEST for a 90 minute webinar on the microbiome.

Use the code "Microbiome22" when signing up to receive a 25% early bird discount.

https://www.humanley.com/microbiome

Not to mention the faulty germ theory, incorrect cell theory, they have no idea what cancer is, they ritualistically abuse children, and more…

ORGANIZED MEDICINE IS MOVING TO TAKE OVER ‘NUTRICEUTICALS’ using natural compounds (like NAC, glutathione, NAD, B vitamins, hormones like Vit D) as they use pharma drugs, treating symptoms, ignoring cause (toxins, malnutrition).
If you have a pain in your ass from sitting on a tack, no amount of nutriceuticals will truly help you. You need to take the tack out of your ass. (Removing the source of the illness, the tack, is the first step in the ‘therapeutic order’ — see below.)