Pentox two years+ later too late?

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leftleaningpeen

Hey guys I have a question. Is two years plus since the first onset of symptoms considered too late to start taking pentox? Has anyone had a positive experience with pentox after this period of time when combined with VED treatment? I apologise if this has been covered elsewhere (I'm sure it probably has), I did a search but couldn't find what I was looking for.

Cheers :)

RoyHobbs

I went back on Pentox in Dec, about 18 months after the onset of Peyronies, as prescribed by Dr. Lue. At about the six month mark I noticed increased girth and combined with VED a reduction in curvature. Dr. Lue also believes it can reduce calcification and plaque size. I have some calcified plaques. It can take up to 9 months to show results from Pentox (per Dr Lue). So even after two years I believe it may help you.

I should add that I take 2400 mg a day vs the normal dosage of 1200mg.

leftleaningpeen

Thanks for the reply, glad to see it's benefitted you - this is exactly the reply I was hoping for. I guess I will bring the recommended studies with me to my uro next visit and try and get a prescription :)

james1947

Myself had many benefits with Pentox even I started 36 months after the onset of Peyronies.
Combined with VED, gained girth and length, better erections and reduced calcified plaques.

James
Age 71, Peyronies from Jan 2009 following penis fracture during sex. Severe ED.
Lost 2" length and a lot of girth. Late start, still VED, Cialis & Pentox helped. Prostate surgery 2014.
Got amazing support on the forum

George999

I started taking Pentox more than two years after the onset of Peyronie's and its benefits were significant.  Immediate relief from pain and moderation of the progression of deformity.  I am off of it for over a year now with no regression.  In my case what helped me even more was a combination of Pentox and Ubiquinol.  Both of them are of huge potential benefit even after two years from onset.  I could not recommend them more highly.  Pentox is DEFINITELY worth the money and Ubiquinol was for me.  Ubiquinol is significantly more expensive than Pentox, but if you can't afford Ubiquinol, I would recommend you try plain old CoQ10 since many seem to have found it helpful as well.  But DON'T believe the lie that oral treatments are of no use after a certain amount of time.  Its just not true.  - George

leftleaningpeen

Thanks for the replies guys. It fills me with hope to see such a positive reaction. I am glad you've all found improvement. I think with Peyronies Disease, any kind of improvement no matter how small is welcome and can be seen as a major morale booster. I have an appointment with my GP tomorrow and will be taking along the pentox studies to help my case.

Really appreciate the replies.

Leftie