Recent content by Ghost

@cnb30 What is the condition that you are on the Abilify for?

This is great. Just goes to show that people seem to find the weirdest ways out of PSSD and PFS. That dude had it for 11 YEARS and basically overnight recovered. Incredible. I wonder how old that posting is. Edit: Appears to be about 2 years old, so 2015-2016 era.

I also feel that I've maybe been worse since my randro run. I can't really tell, but I've waited for a snap-back and haven't felt one. I had a HUGE window for 2 days in early Jan, and that's been about it. Started andro mid-jan, and ran it for 5 weeks until about a week over a week ago. I'm on...

I've tried to find this article but haven't. Do you know where it might exist? I've heard that androgens protect them, but haven't seen an article saying that. Something in the sacral nerves could be to blame. Especially s2-4 which innervate the pudenal nerve. There was a day when I was on...

Yes come off it. Do it slowly.

FIFA is my shit. Love that game. I've always been on xbox though, and haven't paid for online for a few years now, but my friends and l spend entire nights on that game.

I've been blending 3 beets a day into my smoothies - while waiting for HCl to arrive. Every time I go to the bathroom urine is red. Noticed little else so far.

In response to the earlier question, accutane raised 5ht1a in the 5ht projection areas. I don't think they talked about the RN. You can't really tell from that study if they were presynaptic or postsynaptic receptors. I'd assume postsynaptic. It also increases SERT in some regions, which excited...

The sleep thing is common with PSSD people. I get it when I'm cramming for exams and stuff.

"End of december 2017 - I've read on peaktestosterone.com about naltrexone, that it helps with "idiopathic erectile dysfunction". There was also a link to medical articles about naltrexone and ED stating that naltrexone in normal doses (25 - 50 mg, not LDN) restores morning erections. Since I...

Here are some more PSSD ones Success Stories

@Flynn 1) Yea most people do. It's a spectrum though. I have some degree of it, but there are others who have it really bad. I can still feel all the emotions, but maybe they are a bit dulled. It's hard to tell these days because it's been 3.5 years. But yes, I'd say over 1/2 of people have it...

I've always gotten canker sores my whole life. This fall I was eating tons of spinach each day (a whole bag), and I think it aggravated it a LOT. I had one sore that was huge and lasted an entire month. I think it caused some sort of nerve damage/scarring because it still feels weird and tingles...

The people who recover from this say that you need to hit the trigger points, treat anxiety (or more just learn about how HF isn't a big deal - it's just a muscle being stuck in a tense state), and then stretches. I got the best trigger point book in the world on inter-college library loan. It's...

I am of the opinion that many of the physical changes in PSSD/PFS are due to pelvic floor problems of some sort. This could be soft glans, hard flaccid, how your balls hang, some forms of pain and numbness too.