PCT after 10 months ON

Jin23

Well-known Member
I was playing around with the idea of a trt+ regime for the past 10 months. Dosages were ranging anywhere from 75 to 300 mg's of a total androgen load and I was using HCG all the time. I'm a slow metabolizer of androgens and thus, my TT levels are app a factor of 12. So 100mg's equals around 1200 ng/dl for me. This, I presume, is due to my Gilberts syndrome and it also effects the metabolization of other androgens. So a 300mg dose of androgens probably ends up in higher blood plasma levels then yours, meaning, I don't need huge dosages to see effects ...

In any case, I used test, bold C and primo, hcg, with some GH. Nothing else. I ended up quitting, because the loss of intelligence, emotional blunting and anxiety problems, were not something I could live with long term and honestly, I couldn't stand it anymore. I'm very happy to be getting back to my old self again. And from now on, will be advocating shorter cycle's and not the trt+ approach that is gaining in popularity lately.

For the last month and a half I was on:
125mg test E, 100mg bold C, 100IU HCG ed and 2iu's GH.

I waited 20 days from last Test E pin (60mg) and 25 days from last Bold C pin (50mg).
I used hcg up until the start of Enclomiphene, which is at 12.5 x 2 (AM/PM).

I did bloods to check TT levels 5 days before the use of enclom and it was at 250 ngdl. So presumably, I started the serm at app 100 ngdl test and an equally small amount of bold c still being present.

After two weeks of 25mg Enclom my levels are:

TT: 600 ngdl
LH: 2.2
FSH: 1.8
AST is slightly above the range, ALT slightly belove the range, so enclom definitely has a small burden on my liver.

My natty TT before this "cycle" was 700 - 850 ngdl and LH usually sits at 3 - 3.5. So clearly, my lower TT levels are a reflection of a still low LH, not totally recovered pituitary function. But the results are very good for 2 weeks of PCT - after being suppressed for 10 months. I should also add that the bloods were drawn rather late, at 12am and I didn't have a good night's sleep in a weeks time.

I must say, this is the first time I'm using enclomiphene and GH on cycle (2iu's). It's absolutely the best pct I've ever gone through. My dick is functional, have been having night time boners and morning wood throughout the whole pct. This is also due to the high dosages of oral ALCAR that I am taking. Which is around 3 to 10g's a day (taking it primarily as a nootropic, found out about it's effect on testosterone and night boners later on). I also have zero depression, zero estrogenic sides; mental and physical, my dick isn't shriveled, etc. My libido isn't really up yet, but I can have sex and am "stimulated" if I see a fine ass, so I'd say I'm 50% less horny then I normally am as a natty. I remember doing PCT's with tamox, or clomid, just the thought of sex would make me nauseous ... So needles to say, I'm starting to feel some love towards enclomiphene.

I'll update the thread with next bloods in two weeks time.

So, what did I learn from all of this? Well, first, long term cycles aren't such a problem, at least for me, if you use actual, lab tested hcg, and don't use 19nor's. I would advise to use hcg right up until the serms. Secondly, enclomiphen is awesome, no perceivable sides. I would also advise to check ALCAR and it's effect on testosterone production. It's also a very good nootropic to keep up dopamine and LTP while recovering from a chronically elevated dopamine state due to aas. I would also advise to use something for cortisol. I'm using phosphatidylserine.

I'll be using enclom until my LH hits normal levels or above. I would like to quit tamox at the 4 weeks mark, honestly. Later on I'll be using low dose proviron (5mg's eod, or something in those lines) to keep shbg in check and GH will be lowered to 1.5 iu shortly after pct, because it's giving me huge problems with post prandial brain fog, ie. blood glucose problems ...

Writing this in a bit of a hurry, so it's a bit of a messy post, congratulations for coming all this way. Anyway, any comments and opinions welcomed.
 
Seems to working for you. Many guys have PCT overkill that isn't necessary IMO. I used 25mg of Clomid EOD for 3 weeks after quitting 2 years of TRT and my levels were back to their albeit shitty natural levels within a month and my wife was pregnant 4 months later.
 
Seems to working for you. Many guys have PCT overkill that isn't necessary IMO. I used 25mg of Clomid EOD for 3 weeks after quitting 2 years of TRT and my levels were back to their albeit shitty natural levels within a month and my wife was pregnant 4 months later.

Oh, that's a small dose indeed. Glad it worked out for ya!
 
I was playing around with the idea of a trt+ regime for the past 10 months. Dosages were ranging anywhere from 75 to 300 mg's of a total androgen load and I was using HCG all the time. I'm a slow metabolizer of androgens and thus, my TT levels are app a factor of 12. So 100mg's equals around 1200 ng/dl for me. This, I presume, is due to my Gilberts syndrome and it also effects the metabolization of other androgens. So a 300mg dose of androgens probably ends up in higher blood plasma levels then yours, meaning, I don't need huge dosages to see effects ...

In any case, I used test, bold C and primo, hcg, with some GH. Nothing else. I ended up quitting, because the loss of intelligence, emotional blunting and anxiety problems, were not something I could live with long term and honestly, I couldn't stand it anymore. I'm very happy to be getting back to my old self again. And from now on, will be advocating shorter cycle's and not the trt+ approach that is gaining in popularity lately.

For the last month and a half I was on:
125mg test E, 100mg bold C, 100IU HCG ed and 2iu's GH.

I waited 20 days from last Test E pin (60mg) and 25 days from last Bold C pin (50mg).
I used hcg up until the start of Enclomiphene, which is at 12.5 x 2 (AM/PM).

I did bloods to check TT levels 5 days before the use of enclom and it was at 250 ngdl. So presumably, I started the serm at app 100 ngdl test and an equally small amount of bold c still being present.

After two weeks of 25mg Enclom my levels are:

TT: 600 ngdl
LH: 2.2
FSH: 1.8
AST is slightly above the range, ALT slightly belove the range, so enclom definitely has a small burden on my liver.

My natty TT before this "cycle" was 700 - 850 ngdl and LH usually sits at 3 - 3.5. So clearly, my lower TT levels are a reflection of a still low LH, not totally recovered pituitary function. But the results are very good for 2 weeks of PCT - after being suppressed for 10 months. I should also add that the bloods were drawn rather late, at 12am and I didn't have a good night's sleep in a weeks time.

I must say, this is the first time I'm using enclomiphene and GH on cycle (2iu's). It's absolutely the best pct I've ever gone through. My dick is functional, have been having night time boners and morning wood throughout the whole pct. This is also due to the high dosages of oral ALCAR that I am taking. Which is around 3 to 10g's a day (taking it primarily as a nootropic, found out about it's effect on testosterone and night boners later on). I also have zero depression, zero estrogenic sides; mental and physical, my dick isn't shriveled, etc. My libido isn't really up yet, but I can have sex and am "stimulated" if I see a fine ass, so I'd say I'm 50% less horny then I normally am as a natty. I remember doing PCT's with tamox, or clomid, just the thought of sex would make me nauseous ... So needles to say, I'm starting to feel some love towards enclomiphene.

I'll update the thread with next bloods in two weeks time.

So, what did I learn from all of this? Well, first, long term cycles aren't such a problem, at least for me, if you use actual, lab tested hcg, and don't use 19nor's. I would advise to use hcg right up until the serms. Secondly, enclomiphen is awesome, no perceivable sides. I would also advise to check ALCAR and it's effect on testosterone production. It's also a very good nootropic to keep up dopamine and LTP while recovering from a chronically elevated dopamine state due to aas. I would also advise to use something for cortisol. I'm using phosphatidylserine.

I'll be using enclom until my LH hits normal levels or above. I would like to quit tamox at the 4 weeks mark, honestly. Later on I'll be using low dose proviron (5mg's eod, or something in those lines) to keep shbg in check and GH will be lowered to 1.5 iu shortly after pct, because it's giving me huge problems with post prandial brain fog, ie. blood glucose problems ...

Writing this in a bit of a hurry, so it's a bit of a messy post, congratulations for coming all this way. Anyway, any comments and opinions welcomed.

Just sow that I wrote quiting tamox after 4 weeks, obviously wanted to write enclom there. And I also wanted to say problems with brain glucose not blood ... But obviously they are connected ...
 
Interesting, not gonna comment on your personal choice. Please update after some time, as most people who succeed or fail are gone. It will be very valuable information. Good luck.
 
So, it hasn't actually been going as great as I've eluded to in the op.

My sleep went to total shit. My cognition is way down, which is in part due to bad sleep, but also in part to enclom by it self. I'm totally foggy.

I started getting really bad ibs symptoms and now I've even got active hemorrhoids, first time in my life. I also feel totally toxic, like I've been downing some small dose of SD. That toxic feeling you get from orals ...

While the sexual sides weren't as apparent in the first two weeks, they are pretty obvious now. Sex is a total no go. Dick is functional, don't get me wrong, but I'm totally a sexual.

Oh, and I just shed a tear watching Cobra kai season 5. So ... yes, definitely emotional and more fearful. I'm also more angry, which is weird, but yes, emotional af. Still nowhere near clomid or tamox though.

I've dropped the enclom dosage to 12.5mg since yesterday.

I'm going to do another set of bloods on friday, and if I'm in my normal range (or above) I'm quitting the serm.

* Just noting, again, that I have a bad liver (Gilbert's) and am especially susceptible to serm toxicity because of problems with glucoronidation, second pass detoxification.
 
So, it hasn't actually been going as great as I've eluded to in the op.

My sleep went to total shit. My cognition is way down, which is in part due to bad sleep, but also in part to enclom by it self. I'm totally foggy.

I started getting really bad ibs symptoms and now I've even got active hemorrhoids, first time in my life. I also feel totally toxic, like I've been downing some small dose of SD. That toxic feeling you get from orals ...

While the sexual sides weren't as apparent in the first two weeks, they are pretty obvious now. Sex is a total no go. Dick is functional, don't get me wrong, but I'm totally a sexual.

Oh, and I just shed a tear watching Cobra kai season 5. So ... yes, definitely emotional and more fearful. I'm also more angry, which is weird, but yes, emotional af. Still nowhere near clomid or tamox though.

I've dropped the enclom dosage to 12.5mg since yesterday.

I'm going to do another set of bloods on friday, and if I'm in my normal range (or above) I'm quitting the serm.

* Just noting, again, that I have a bad liver (Gilbert's) and am especially susceptible to serm toxicity because of problems with glucoronidation, second pass detoxification.
Bro, it's because hCG is what was stimulating LH & T from the testes (what you need, in part; given AAS-induced transient secondary hypogonadism). Dropping that in lieu of SERMs, that merely artificially stimulate LH & T secretion (that negatively feedback on T synthesis & secretion in the Leydig cell), rather than stimulating testes steroidogenesis, was a mistake.

I think enclom is so similar to clomid that it's likely to have the very same side effect profile. I'd speculate that in combination with Gilbert's syndrome, it could be a particularly intolerable drug. I'd be steering clear of SERMs if that were an option for me in your shoes (and it is).

@PeterBond gave away the crown jewels for HPG axis recovery in Anabolic Steroids and Fertility - MESO-Rx
 
Bro, it's because hCG is what was stimulating LH & T from the testes (what you need, in part; given AAS-induced transient secondary hypogonadism). Dropping that in lieu of SERMs, that merely artificially stimulate LH & T secretion (that negatively feedback on T synthesis & secretion in the Leydig cell), rather than stimulating testes steroidogenesis, was a mistake.

I think enclom is so similar to clomid that it's likely to have the very same side effect profile. I'd speculate that in combination with Gilbert's syndrome, it could be a particularly intolerable drug. I'd be steering clear of SERMs if that were an option for me in your shoes (and it is).

@PeterBond gave away the crown jewels for HPG axis recovery in Anabolic Steroids and Fertility - MESO-Rx

Hm, I'm a bit confused, ... are you implying, I should have continued to use hcg and not use a serm at all? I am not trying to make a baby, rather, just restart my HPTA and hence forth; be natty. Without a serm, and with keeping the hcg, my recovery would have been impaired. I need the serm in order to speed up the pituitary releasing the LH. And besides, hcg is suppressive in all by it self, so, it really shouldn't be used much in pct. Did you misread something?
 
Hm, I'm a bit confused, ... are you implying, I should have continued to use hcg and not use a serm at all? I am not trying to make a baby, rather, just restart my HPTA and hence forth; be natty. Without a serm, and with keeping the hcg, my recovery would have been impaired. I need the serm in order to speed up the pituitary releasing the LH. And besides, hcg is suppressive in all by it self, so, it really shouldn't be used much in pct. Did you misread something?
Try to help, get this shit. You'll figure out what you're looking for at some point hopefully.
 
Interesting, not gonna comment on your personal choice. Please update after some time, as most people who succeed or fail are gone. It will be very valuable information. Good luck.

I've always been cycling. App 6 years I think. My natural production always came back without much problems and always to the same level as per before the cycle. This is the first time that I've tried doing a long cycle though, so was a bit worried, but (knock on wood) it seem it's also not such a problem as a lot of folks seem to make the duration of suppression ...

My natural test production was always in the 750 range, so I would be amiss to shut that down for ever, for some contractile fibers. I mean, it's cool, all this experimenting, but in the end, imo and experience, aas are a moronic drug category, being a low iq gym rat is not something I inspire to be. And aas do turn me into a tunnel visioned idiot.
 
Are you under the impression I was condescending? I genuinely don't understand mate, no pun intended.
I think your judgment is probably affected by your T being in the hypogonadal range, not condescending, more like cranky/moody. I think that you should view fertility and T secretion as a bit more connected than you seem to be. Basically, in recovering from secondary hypogonadism, fertility (spermatogenesis) & T secretion (steroidogenesis) are one in the same, this originates in a functional Leydig cell (these are the cells that are not working for you right now). Get one (fertility), get the other (T secretion).
 
I think that you should view fertility and T secretion as a bit more connected than you seem to be. Basically, in recovering from secondary hypogonadism, fertility (spermatogenesis) & T secretion (steroidogenesis) are one in the same, this originates in a functional Leydig cell (these are the cells that are not working for you right now). Get one (fertility), get the other (T secretion).

Hm, I understand what you mean now. I dismissed this idea, because idk if you've read; in the op, that I've been using hcg through the whole 10 months off being on aas. So my leydig cells, my nuts, have been working this whole time. Thus, what would have been the point of me continuing pct just with hcg? I could have continued a bit longer just with hcg, albeit with higher dosages, but I was borderline high estrogen with the dosages I've been using as is, so going higher was not something I wanted to do.

The response of my nuts, TT being at 600, to the low endogenous LH secretion of 2.2, kinda corroborates the above, don't you think so? It's a good response to a low pituitary output. Idk however, if enclom has any direct action on testosterone production, that is, agonism of leydig cells. If this is true, then the favorable response to LH is a bit construed, but still, not bad ...

I think your judgment is probably affected by your T being in the hypogonadal range, not condescending, more like cranky/moody.

Sometimes when I'm writing in a hurry, I may come across harsh ... My adhd is also acting up, due to loss of quality sleep, so it's hard being composed and not impulsive. Heh, I'm definitely moody, and granted, I'm not to sharp atm ... but still, I'm not an idiot; your semiotics are still very revealing ,) But I'm leaving it at that.

Either way, I appreciate your input.

Do you have any thoughts on calcium d glucarate to help with the 2. pass detox of the serm?
 
Hm, I understand what you mean now. I dismissed this idea, because idk if you've read; in the op, that I've been using hcg through the whole 10 months off being on aas. So my leydig cells, my nuts, have been working this whole time. Thus, what would have been the point of me continuing pct just with hcg?
Not just with hCG. HCG & hMG.
I could have continued a bit longer just with hcg,
You probably would want to continue some time longer (see the Peter Bond article for an actual protocol) on hCG & hMG.
albeit with higher dosages, but I was borderline high estrogen with the dosages I've been using as is, so going higher was not something I wanted to do.
What does borderline high mean? Normal? I'm skeptical that both A) exogenous T has cleared your system and B) hCG is stimulating aromatization beyond normal levels are concurrently true.
The response of my nuts, TT being at 600, to the low endogenous LH secretion of 2.2, kinda corroborates the above, don't you think so?
LH value of 2.2 in what units? (important)
It's a good response to a low pituitary output. Idk however, if enclom has any direct action on testosterone production, that is, agonism of leydig cells. If this is true, then the favorable response to LH is a bit construed, but still, not bad ...
Enclom, as a SERM, exerts antagonist action at the ER in the hypothalamus & pituitary, to stimulate LH & FSH. However, post-cessation (if in fact T has cleared your system), estrogens are already low (because E2 is formed by aromatase action on T). Effectively, SERMs can acutely stimulate some T, make you feel better, but do not go to the root of the problem of transient AAS-induced secondary hypogonadism.
Sometimes when I'm writing in a hurry, I may come across harsh ... My adhd is also acting up, due to loss of quality sleep, so it's hard being composed and not impulsive. Heh, I'm definitely moody, and granted, I'm not to sharp atm ... but still, I'm not an idiot; your semiotics are still very revealing ,) But I'm leaving it at that.

Either way, I appreciate your input.

Do you have any thoughts on calcium d glucarate to help with the 2. pass detox of the serm?
No, I have not looked into this topic.
 
@Jin23 how is it going man?

Supp bro, I'm holding it together, tnx.

I switched from 12.5mg's to 6.25mg's on sunday. And today was the last time I took enclom.

Physically I have a few symptoms:

- orthostatic hypotension, and low bp in general
- my RHR is lower, sitting around 56, normally it's around 61
- I'm experiencing cold and almost feeling like I have the flue middle of the night. This has now happened two nights in a row. I'll try and dress more warm tonight. But my HR is very low when I sleep; goes down to 45 - 48 bps.
- Libido is at it's lowest point and getting really hard is a problem.
- Feeling like a 10yo boy. Missing the high androgen assertiveness and aggression. But I know it'll get better in time.
- IBS and hemorrhoids are much better.

Mentally I'm much better. My brain is definitely healing from the aas abuse. I'm feeling a bit more anxious. I've taken 2 x 50mg of etifoxine today and it did wonders for the anxiety. But it's a reported hepatoxic drug, so I'm hesitant to celebrate just yet.

I'll be doing bloods on friday but need to get off of the serm as I have a gastroenterologist app next week and we'll be doing tests on my liver and functional bowel tests. If it would not have been for this, I would have continued with 12.5mg enclom till the end of this week. I hope the lower enclom dosages didn't hinder the pct too much.
 
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