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JM

I was diagnosed with peyronies early this year.  I took 6 month of vitamin E and now I have started using Transdermal Verapamil 15% gel.  Any ideas on how successful it is?  Am i wasting my time?  What else should a person do?  I don't feel pain during an erection but I have lost length and stiffness.  Its very discouraging but luckily I went to the doctor as soon as I seen something and now am trying to follow my urologist advice and medication.  I'll be reading this site over the next few days to try and educate myself further.  but again, and advice or encouragement would be appreciated.  

Hawk

Welcome to the forum JM,

The reported results on this forum for transdermal verapamilhave have not been good.  The results have not even been very good for Iontophoresis.  It also tends to be an expensive treatment.

The best reported results on this forum are from the PAV cocktail, along with traction or the VED.

Before you ask for Pentox, make sure you educate yourself because most urologists do not prescribe it for Peyronies Disease and you may have to encourage, educate, introduce, or sell the concept.

Prostatectomy 2004, radiation 2009, currently 70 yrs old
After pills, injections, VED - Dr Eid, Titan 22cm implant 8/7/18
Hawk - Updated 10/27/18 - Peyronies Society Forums

JM

Thanks, That's what it looks like.  I paid 200 bucks for this gel and they are telling me 3 month for any progress and 9-12 months for good results.  I hate to waste all that money.  I'll talk to the urologist about the PAV.  Where do you buy VED at?  I'm sure they are all over the internet but don't want to buy a cheap one.  Thanks again for the advice.  I'll check back in later this evening.

james1947

JM

My daily treatment is:
2*400mg Pentox – morning/evening (if you can tolerate 3*400mg daily better)
4mg Cialis (cutting the 20mg in 5pcs) – evening
2*500mg Acetyl L-Carnitine – morning/evening
2*1000mg L-Arginine – evening
2*100mg Ubiquinol – morning/evening (if younger than 40 may use 3*100mg CoQ10, much cheaper)
VED, 20 minutes

You can find on our forum the reason to take  each.
I would like to say follow Hawk advice, not just regarding Pentox:
QuoteBefore you ask for Pentox, make sure you educate yourself because most urologists do not prescribe it for Peyronies Disease and you may have to encourage, educate, introduce, or sell the concept.

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