I have heard that vitamin E is the only known treatment. Is that correct? If so, can it be taken by injection for more effectiveness? Is there stem cell research going on for Peyronie’s disease, and is it possible to get involved with it?

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Vitamin E is one of the first oral agents used for the treatment of PD. However, there is no convincing evidence that alone or in combination with other agents it is of any significant benefit. Its use advocated by generations of urologists without any real understanding of the medical literature. Recently, in older men and men with heart disease, vitamin E has been shown to worsened cardiac health. It is likely that vitamin E is a placebo and has not real benefit.

Stem cell research is a hot topic at the moment and it is only a matter of time before it will be used for PD. There are no studies ongoing at this time.

Previous I have had Peyronie’s disease for 1 year and 10 months and just went through Intron A injections every 2 weeks for 3 months. I have not seen any change. The Peyronie’s specialist wants to do a second wave of injections. If this did not work at all, do you think it is wise to go through a second injection battery?
Next I have Peyronie’s disease now for 12 years. All the ED pills will give an erection, but I quickly lose it. Is there anything I can do or take so the blood stays trapped? A cock ring does not work.
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