So far I’ve been compiling and compiling various articles from journals. If you want the list pm me.
I’m learning an awful lot and it is fair to say things are extremely complicated. The more I read the more I think Awor is correct. I, for a long time took issue with his idea on the grounds of the presence of prostate issues but the more I read the more it made sense.
Overall it seems there are 4 issues:
- AR hypersensitivity - due to acetylation, methylation?
ncbi.nlm.nih.gov/pubmed/10084600 - methylation?
ncbi.nlm.nih.gov/pubmed/19855091 - acetylation?
The reasoning is that when we take finasteride we reduce androgens greatly as DHT is far more potent than testosterone. So when we stop, we crash as the surge of DHT takes our bodies by surprise leading to the next step… I know my story fits in with this.
- Downregulated and altered AR signal - due to methylation??? - locating which part or parts here is crucial. There are many co-regulators of the AR. ARA 70 is one and is the one thyroxine helps regulate. Some are involved in the previous step too.
ncbi.nlm.nih.gov/pubmed/17364555
It also should be noted that it is unlikely every tissue in the body has reacted the same way. The places where finasteride affected most will be most affected.
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An altered estrogen/testosterone ratio either due to the initial drop in DHT or the tissue specific insensitivity to androgens- inducing a form of prostatitis (in some of us). This has immune and neurogenic elements. Some people have been diagnosed with a pudendal neuropathy. Estrogen induced prostatitis is not immediately “fixed” by reducing estrogen.
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This inflammatory state can perpetuate the AR hypersensitivity and therefore potentially the downregulated signal and the altered ratio. I know some people have taken contention with this statement. So here is article about how TNF alpha (an inflammatory cytokine) affects AR sensitivity and one about how IL 6 (interleukin 6) affects AR activity:
ncbi.nlm.nih.gov/pubmed/11241555
ncbi.nlm.nih.gov/pubmed/12431817
Now i don’t think we all have 3) and 4) as some people don’t have prostate issues and don’t display an inflammatory element.
The brain fog elements can be explained by the effect on neurosteroids. But the improvements some people have had with anti-inflammatories and antibiotics give some credence to this.
Now let us assume for a moment what i have said is true. A problem arises. Which part is the most important to treat? Are we still hypersensitive? Or just suffering from the persistent down regulated signal? I suppose this can be answered by your own experience with testosterone supplementation. Do you get worse with androgen supplementation from an androgen perspective? Some people with only minor epigenetic changes (so receptor is no longer hypersensitive) might in fact benefit from androgen supplementation as it will drive their system. One simple test is to see how you respond to creatinine.
Assuming this is true (and it is possible it is not) how would we treat this? All these elements are modifiable.
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Reduce inflammation - this i don’t think this is a cure but might provide an environment that might sort itself out. Fasting, a good diet etc…
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Find out where the silenced or altered co-regulators are. This is hopefully what research will tell us.
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Treat methylation or acetylation accordingly. It might be we all have silenced the signal in slightly different ways. T3 might help due to its effects on a different co-regulator (but becoming hyperthyroid will not be beneficial). Xyrem is a HDAC inhibitor and can explain ithappens success on it:
ncbi.nlm.nih.gov/pubmed/19427877
Awor when he tried procaine - a demethylating agent improved at first in every domain. It didn’t stick however but it pointed in this direction. There is a problem in being unspecific with the treatment as you might awaken one aspect but silence another.
Research is the key.
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Below is a list of recoveries so far:
mrmoskowitz – time – 4.5 years
ithappens – ghb dhea cream
Scaredin MD - Complete ED, no libido, brain fog, anxiety attacks - Hdrol and reboot with Blue Up and estrogen blocker
Searchfhealth – 7 yrs – recovered – just happened
Japanther – brainfog - rawfood diet
Mitch – brain fog, sexual symptoms, - 9yrs later - He did try but not at the time of recovery - Armour thyroid, exercise, liver detox, no soy or sugar, no caffeine, adrenal support (isocort) – did try TRT for short period but did not help
Oneday - Sustain Alpha, paravol
Cytochorme – recovered once and then re took drug - Dexamethasone, Herbs – mucuna pruriens, stacker T, Creatine Monohydrate
Dury – low energy, sexual symptoms, visual issues, dry skin, klonopin and Oxycodone (5mg) then synthyroid
Big Softie – time + dermacrine sustain, sleep well, no caffeine, alcohol, small meals - no perineal problems – low Testosteorne – boosted + creatinine with test (diesel 2040)
Hopingformore – high dose tribulus 5 days.
Time – 3.5yrs recovered
tryingnottoworry - recovered on dolichol via spinach ingestion - back to normal