You are just digging yourself a deeper hole.
Think about how the HPTA works, GNRH stimulates production of LH, which leads to testosterone production, right? What feeds back and controls GNRH production? Estradiol. Now where does ALL estradiol come from? Aromatization of testosterone.
Ok now look at your first labs, testosterone is only double digits, but E2 is somehow 40! There is only one way this is possible: hyperactive aromatase.
Everything you are doing is just causing aromatase to be MORE hyperactive. All the "positive" results on your future labs are meaningless, you are just artificially stimulating testosterone production. You are SO hyperactive that even with the aromasin and natty test you are STILL pushing 40 E2. This is because of your hyperactive asromatase AND testicular aromatase is going crazy under those megadoses of HCG.
The idea of "PCT" is to minimize the impact of the TRANSITION from exo test to endo test. There isn't a way to "jumpstart" your HPTA once you are off. HCG helps you from become sterile during AAS or TRT use, but it just further shuts you down by stimulating testicular aromatase if used in PCT or later. You gotta go back 20 years before most people believed the dogma of megadosing HCG after a cycle.
The only thing I think you may have some success with is the triptorelin, if you don't destroy it's positive effects with further suppression by AIs and SERMS.
Sorry to be harsh and not very optimistic, but I wouldn't want others to get fooled by this...