Hello all, i want to continue to update my experiment on SARMS and ADT.
Currently on darolutamide and Orgovyx + Osterine 10mg/day. I stopped Carderine for now to see if my next lipid profile goes from good to bad. Just wanted to see if carderine was responsible for my improvements from previous numbers.
I have my E2 tested every other quarter to keep an eye on bone and mental health, and heart health. Surprisingly my E2 has not decreased on ADT after 9 months.
I have done quarterly updates so here is the next quarter.
PSA 0.09
T =16, SHBG=53, Albumin=4.4, Free T=7, E2 estrodiol=32, LDH=146, CBCwDiff=all in normal range, CMP-ALT, and ALP=normal.
the only number out of normal is bilirubin high.
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KocoPr
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I certainly will post on next quarter results with a lipid profile.
The E2 is very interesting. I need to go back to my 23andme from 2013 just around the time i got my PCa diagnosis. I know i had very bad ratio’s of good to bad estrogens and it was due to certain CYP450 genetic mutations according to Genova diagnostics tests (“complete Male Hormone” and “Detox Genomics” Tests i had done in 2013). I’ll look it up.
interesting. What androgen it benefits are you perceiving from the SARM while T is castrate from ADT? Improved muscle strength, mass and response to strength training? Any libido improvement? Cognitive or mood improvement? Thanx
Also taking 5mg RAD 140 + 1 mg Cardarine per day. I have found that my strength training has improved, I am able to do 20-30% more lifts per set. purely anecdotal but I feel stronger
Libido and mood have been been good for entire period since diagnosis.
i have improved joint and pain reduction, no labido change, i have muscle strength improvements, working on endurance with new puppy with walks several times a day and just started training her on hikes except she ate one of my boots today so off i go to store for another pair.
i think I will go on 1mg Carderine instead of no cardarine. I feel it is better for glucose/carb metabolism to put on less weight and give me a little energy boost. When I do my hikes I’ll probably boost with a 5 mg.
Thats a good question. I would also ask then why am i taking Orgovyx if darolutamide blocks the androgen receptor.
I “think” Osterine bring synthetic and designed for muscle health and agonistic to aromatase and 5a-DHT and the reason i take it is to counteract those ADT side effects.
I keep researching this but there are no studies done with safe doses of gtx-024 (Osterine) other than a large super physiological doses like with BAT and SPT with a lutamide.
Cardarine is also a PPAR alpha and delta agonist and a slight PPAR gamma antagonist. All good things.
The whister rats they used with the large cardarine dose are also highly susceptible to tumor growth equivalent to human 40mg/day. We take much smaller doses and has been used by body builders at 20mg doses. Granted they take it in cycles.
if you had cancer you would throw everything thing you could at it starting with SOC, Osterine has no affinity to aromatase and 5a-DHT enzymes. Even though daro is a strong AR inhibitor it is not 100% and Osterine is designed specifically as strong binder to muscle AR receptors.
If darolutamide is a100% block you you insinuate then why even take an ADT drug like lupron or Orgovyx?
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