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Topical Verapamil for Peyronies Disease, experience anyone -gt; chem pe

Topical Verapamil for Peyronies Disease, experience anyone -gt; chem pe


I just read about the verapamil transdermal treatment for Peyronies disease, I found that study:


Do you know anyone which PD, who tried this treatment method and with what results if any? Could this also be useful for the chem pe priapism method? I have a slight bend in my penis to the left and I plan to provoke priapism to get an enlargment for my small member (5.5”.) I am just afraid, that it could make the peyronies disease worse.
Any experience on that aswell is very welcome


By the way, I have no diagnosis of Peyronies from the urologist I go to. I told him about the curvate, and he told me to get a photo of it without checking any further

You need to take an ultrasound if I’m not mistaken. Anyway chemical priapism induced should be no longer than 4 hours I guess.

Starting stats: 6.4" / 5.6" Current Stats: 7.4" / 5.8" Short term goal: 7" / 6" Long term goal: 8" / 6.5"

From what I have read on a number of boards, this product does not work, or works very occasionally. A study was done on men undergoing penile surgery. They were asked to apply topical verapamil beforehand. The surgeons took a sample from inside the placque and found that no verapamil had absorbed through. This suggests that the chemical is absorbed into the blood streem and does not penetrate into the penile placque.

Personally I am looking to acquire some injectable verapamil to aurgment my chemical pe routine. I want to use it pre-emptively to guard against the possible risk of fibrosis.

I dont have PD. Would a urologist prescribe this without examining you?

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