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Author Topic: Verteporfin - another fibrotic inhibitor of specific to Peyronies Disease. Study says it works.  (Read 892 times)

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Dipstick

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Check this out guys,

Looks relatively new. https://www.researchgate.net/publication/327961732_Verteporfin_as_a_Medical_Treatment_in_Peyronie's_Disease

Another fibrosis inhibitor. I’m pretty sure long term use with these types of creams will eventually reduce the fibrosis surely.
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melting

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Great find!
verteporfin molecular weight:
718.794 g/mol

Maybe possible for transdermal(for example + DMSO) delivery.
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Daily Transdermals and Traction/VED solved my Peyronies Disease https://www.peyroniesforum.net/index.php/topic,12587.0.html (DMSO+X)

samsung

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Can you buy it at the local Walmart? :)
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45 y.o. Single. Onset of symptoms (pain-stinging like a wasp) @ 6/2018. No sudden injury. Curve developed slowly. 40 deg. dorsal. Hourglassing. Torsion to left flaccid. 4 rounds xiaflex. Restorex, DMSO+, heat, arginine, cialis, lipoic acid, vit. K2

projectpd

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available from a uk site for the bargain price of £1,190.00 for 15mg  :o
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Bud luck

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If it works, why the "uros" do not prescribe them? The same with heat therapy, nobody talks about it, but in one study showed great benefits. I feel like nobody cares about finding solutions, just us, this is devastating
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My first symptoms started 18 months ago
I tried Traction device, Pentofixiline, Q10, TRT, L-Argenine, cialis
I have narrowing/dent/hinge on the left side of my shaft
My Erectile Dysfunction is getting worse
I have a girlfriend

pey ron

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I tried bringing this study up with an uro ~2 years ago. He didn't want to hear about it. If you can find a doctor with an open mind please let us know.
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