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Hi guys, Im new on this forum and I have been suffering from the propecia permanent sides for like 8 months now. I am still trying to figure out what is my specific problem and I was considering giving HCG a try, but I don't know if im a potencial candidate. Could anyone help me?
My labs test show the following results:
SHBG 28,20 (7 - 59)
TESTOSTERONE 6,27 (1,9 - 15,8)
PROLACTINE 12,19 (2,5 - 16,3)
FSH 1,3 (1,0 - 42,5)
LH 2,5 (1,7 - 11,2)
ESTRADIOL 64,1 (<25 - 75)
I also tested DHT but I don't know if it is really accurate, the result was: 115 (250 - 750) .. very low.
I appreciate the help in advance and I hope everyone get well soon.
Yup, you look like a perfect candidate for a PCT cycle, low levels of test and LH,...Hi guys, Im new on this forum and I have been suffering from the propecia permanent sides for like 8 months now. I am still trying to figure out what is my specific problem and I was considering giving HCG a try, but I don't know if im a potencial candidate. Could anyone help me?
My labs test show the following results:
SHBG 28,20 (7 - 59)
TESTOSTERONE 6,27 (1,9 - 15,8)
PROLACTINE 12,19 (2,5 - 16,3)
FSH 1,3 (1,0 - 42,5)
LH 2,5 (1,7 - 11,2)
ESTRADIOL 64,1 (<25 - 75)
I also tested DHT but I don't know if it is really accurate, the result was: 115 (250 - 750) .. very low.
I appreciate the help in advance and I hope everyone get well soon.
Yup, in the same boat as you. I trusted the advice of "just wait" on propeciahelp but that was a big mistake.only you can really make that decision. For 4 years I have tried waiting, diets and lots of different expensive supplements.
I have recovered a good bit but I still have PFS and Looking back I wish I have tried this protocol and not wasted all that time.
Yup, in the same boat as you. I trusted the advice of "just wait" on propeciahelp but that was a big mistake.
If you don't recover from PFS after 6 months, it's time to take action.
Meanwhile I also wasted 5 years doing nothing besides gym, eating healthy and trying a couple of supplements. Time to get serious and begin PCT, etc.
Hi everyone,
planning on speaking with my doctor this Monday. Any pointers in convincing your doctor to prescribe HCG? I haven’t done a hormonal panel yet and he’s just waiting for the medication to get flushed out after 1 week
Post-Finasteride Syndrome (PFS): A Surmountable Challenge for Clinicians and a Newfound Hope for Patients
That’s doctor Gordon. I know he’s a fan of hcg for pfs but if you want to go the route of a doctor, I think he has a way to remotely help.
I really believe propeciahelp and pfsfoundation do more harm than good most of the time with guidance and making people worry even more. This is one of only a few threads with practical minded and logical people.
@Migotyou yea I posted his info because we had two videos of him referencing his treatment of pfs and I was thinking if someone wanted to go that route, at least (hopefully) they wouldn’t feel alone. I still tried to help as many as possible learn the steps , etc.
@Jayvee @Mister i still can’t get over how a few ppl reacted to my experience and posting. Fortunately the results are great and the thread is definitely much cleaner and level headed. Mister is posting tons of quality research so that’s awesome and very helpful for those following.
I will add to my personal recovery that I continue to see erection strength and ejac strength improve. I know the area I’m referring to is tissue and muscle with very unique qualities that lend itself to healing and repair. I believe 4 years of weakened tissue and lowered instance of use, to the last 8 or so months of strengthening and increased use lends itself to heal and recover like a muscle after surgery , to find an analogy. At least that’s what it feels like to me.
Good luck to all
Completely agree, the PFS forum is full of (unnecessary) despair and badly managed. It should be the Mecca for everyone with PFS but it's completely ruined by the bad moderators, I remember when it got so bad a different forum was made, solvepfs. Many people also get banned for the most petty reasons, people who dare to disagree with mods or have a different view than them on how to fight PFS. It's very sad, they're also deluded into thinking a new study will come up with a cure, they obviously do not know how the medical/pharma world works... Also no transparency, where does all the money go that people donated?
And I'm sure new PFS studies will come to the same solutions as people have talked about in this thread. I'm on a supplement regimen now but when I end this I will start PCT asap.