I've taken it before in the past. I'm not sure if any of my threads are left on here regarding it. It did nothing for my sexual dysfunction. All it did was raise my testosterone levels from 200s to 600s. The number went up. My function stayed the same.

I am evidence that windows really do happen and improvements can stick and for longer periods of time. Each time I get a window I get a new aspect or feeling of how my function used to be. Each week or weeks of improvement are usually ended with brain zaps.

Sylv, it is hard to pinpoint and next time I have one I will pay attention and take note of where it is located. And yes, I was able to trigger some by looking left to right quicjly back and forth.

Sad Keanu, it actually marks the end of an improvement (when I lose it).

I wanted to keep all of you updated on my progress. I have 2-3 weeks of off and on improvements that showcase some new aspect of my function that was not there before. I want to bring something to your attention that may be useful in our research: *They almost always end with the presence of brain &...

Yes, I was very hypersexual and I've actually thought of it as a cause for this before too. I think we're on to something as you can see that most replies to this thread point to a similar quality we all had.

I've been reading through your recent posts on the progesterone theory and ella. I'm in. Count on a prgesterone test + ella trial from me in the near future. I'm back on cdp choline right now due to worsening pssd (and it's working a little like it did last time), but I want to get in on the hype wi...

I have that too.

Ghost, Thanks for the heads up on the possible heavy metals concern. I have actually been thinking about how to increase SERT as well lately as this is the "logical" solution to our problem. I mean, the SSRI's main mechanism of action is blocking SERT. But I do worry about it's ability to ...

Citalopram was the drug I was on. I was on 60mg for 8-9 months. I know the struggle this drug can cause during and after use.

I have been looking into this for a while as it would explain a lot of my symptoms. My doctors refused to give me a pudendal nerve conduction study because "very few doctors do it" and "it wouldn't be able to pick up anything accurately." There is definitely a dysfunction of the ...