The map can be used for this purpose: zeemaps.com/map?group=976852
Have there been any updates on what the Italian doctors are saying about PFS? They seem to be informing their patients on what is going on. Anyone here talk to any of the Italian patients?
Although I don’t know whether PFS is auto-immune, here is an interesting article on curing auto-immune conditions:
healthline.com/health-news/o … ses-090514
It’ll be interesting to hear what the Italian scientists say.
Its interesting though that the people that recovered cleaned up their diets/fasted. Dr. Mark Hyman has interesting articles on beating auto-immune conditions and is actually similar to what Chi and CDnuts followed to recover.
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Any way we could try injecting 5 ar enzyme at escalating doses as discussed the paper I just posted? It suggests that (provided we do have 5 ar auto-immunity) starting at very low doses and increasing the amount injected, we may be able to train our immune system to stop attacking 5 ar.
So what happens after these studies are released? I know we are all patiently waiting to see what they discover. Any other studies in the works or we will be years out after these three are published?
The foundation is financing ongoing and future studies. The studies will stop as soon as we stop donating. Without financial support the foundation cant fund new studies.
It would be good to be given an indication of when these current studies, in particular the one in Milan will be published, for awareness but also to help give hope.
Haha no money for foundation. One million of my dollars goes to the families of anyone who knocks off the Merck CEO or former FDA chief who approved this poison 
. Yes I know the studies are looking for route causes. So far the Italians have noted certain metabolites and neuro steroid levels that are off. It would be awesome to get updates from these researchers. This entire thread gave me hope, especially Newbie 86 comments, but I’m sure they wouldnt want to give false hope if they really have no results.
Anyone here know if the Italian doctors are seeing patients with PFS? Dr Khera at Baylor I believe finds HCG and an AI as his current weapon of choice. Wonder what they would use currrently. Thought Id throw it out there. Anyone go to to the study and ask or receive treatment?
Becareful about that sort of talk publicly, that sort of talk about Merck, is something the federal government doesn’t take kindly to. (Since they serve the corporations) Of course that is why they came after me.
Maybe instead of taking this approach… We should ask the question… What if we were your son? How would you feel? But most of us live with people that hardly believe us so…
I just have seen from personal experience that there is very little compassion in this world. People in the US have more compassion for their pets than other human beings. The scum at Merck and in the FDA only care about themselves and their money, it changes of course when it happens to someone they know.
Although I am certain that they wouldn’t let their own families near any of the products they so vociferously defend and push on others. It would be interesting if a son of a Merck employee was going bald, how they would broach the subject with them regarding one of their products. I’m sure that the families of Merck employees must know to some extent that the lifestyle they live is paid for through immoral acts. I suspect however that these same families are church goers who see no conflict in how they live the American dream.
Frazier himself is bald.
Does anyone know if there has been any progress made with any of these clinical studies?
Dr. Malcagni and I are lovers. I think I accidentally gave him PFS
Just kidding yall. Hopefully put a rare smile on your faces. I don’t think much is going to come out of that camp until they publish the study. I emailed the guy a month or so ago. Probably shouldn’t be bugging them, but I’m thinking it could be at least another year till his study is released.
And if you are curious what he said, nothing important enough to post here. Just said they are working on it and that these things take time
I have Peyronie’s, diagnosed last year by Dr. Goldstein. I think it’s important to note that he (and Dr. Jacobs here in NYC for that matter) have both told me that studies show that in guys with Peyronie’s that is the result of androgen deprivation, the tissue damage can probably be reversed by T replacement. We don’t respond to T right now, but if there were a cure for PFS we would start responding to it again – and it might undo a lot of the damage that’s been done.
viewtopic.php?t=346
Also, I experienced one real recovery during my PFS ordeal. It didn’t last long, but I can tell you: It completely restored my sexual function. In the two-week window of my recovery, I was getting hard at the slightest erotic/romantic thought, lusting over everything, and jerking off 4-5 times per day. I had sex one night after jerking off several times during the day and I was still rock hard and totally into it. That’s what the old days were like.
So my point is: Even with physical damage to our dicks, I think we can be fine if we just start responding to androgens again.
What I would like to know is all of the guys who have peyronies, how many have low free T. That would be an interesting poll
I think once 5ar enzymes are corrected, we’ll start responding to therapies.
I think this is a topic for a different thread. …