WWW.CUREPEYRONIES.NET
email:curepeyronies@yahoo.com

Comments = Hi, Just a short comment. I am 65 and about a month or six weeks ago I
woke up 'bent'! No other symptoms. No pain, not welts, nothing. Three or four weeks
ago I started feeling an elongated lump at the point of the bend. This morning I
experienced my first "pain". I have an appt with a urologist this coming week. I'm
really glad I ran across your web site this evening. I will do what I can to add any
information. Neither I nor my wife is ready to give up on this. We will be supporters
and do what we can.  

Comments = Hi, I developed peyronies after taking beta-blockers for about 6 months.
Seems to be a trend from what I am reading. I have had it for about 18 months now
and it is not getting better with any of the OTC vitamins and concoctions I have read
about over the internet. The penis pump has been the only thing that seems to make
any positive difference although it has not reduced the scar at all.

Comments = I have recently met a man who has been diagnosed with Peyronie's. This
is the first time I have encountered any disease of this type. I am willing to help in
any way but need information as the male has had limited advise and is not aware of
were to go but willing to try. I am a female with some sexual experience but nothing
that gives me a clue how to deal with this except positive regard, no demands and a
willingness to support


Comments = Hi thank you for allowing me read your site I was diagnosed with
patronizes in November 2007 its just terrible I am going out of my mind I don’t know
where to turn I live in Dublin Ireland I am 53 and my life just seems empty, if you hear
of any medication I can take or get would you please inform me as I am desperate.
Cheers

Comments = If there is supposed to be one, your "Your email address" box is not
showing up on this page. Count on me for a donation of $100 on or before 1 April.
Just tell me when and where to send it.

comments = I am 53 and have had peyroines for 3 plus years! I too tried 3 urologist
before settling on Verapamil injections. Started with 6...then 12...then 16 total at a
noted Boston clinic. I'm still searching for help since surgury is not a viable option
because an still function...well sort of??? I've been reading on human cell break-
thru's and am convinced that in the near future injections of this type will cure us! My
sex life with my wife of 15 yrs has been greatly affected although we find ways to
satisfy each other. I take ED meds for added confidence but sometimes they are
more of a hassle and actually make the condition worse? I have my good days and
bad but not a day goes by that I don't think about it!If there's a cure anywhere I would
go no matter how far or how much! If you know of any new break-thru treatments
please post them or e-mail

comments = Great site for people like me... It makes me feel normal. A
man who just happens to have a non life threatening problem.
I developed Peyronies around 6 months ago, (I'm 46) and I can tell you
that it came as a complete shock.  I like to think of myself as
reasonably intelligent but when this happened I did not have a clue about the
condition and began to become withdrawn and depressed.  I did not think
that something like this could have such psychological side effects.
My marriage suffered as I could not confront my wife with what was
happening to me.  She began the assumption that I didn't love her anymore
and all of the other emotions that go along with this.
The greatest hurdle for me was diagnosing myself, sharing the
information with her and then gaining her full support.  When I did this my life
turned around.  I checked out as many websites as possible(I didn't
realise there were so many).  I went to see my Doctor, something I
couldn't have done 6 months ago (Guy thing), and I'm currently awaiting an
appointment with a speacialist.
I do not want surgery under any circumstances.
I am thinking of attempting the traction type device.  The webs I've
read so far seem to show this as reasonably acceptable.
I'll keep on reading.

comments = Thank you for the site. I am just now looking at what's been
said & done to cure peyronies, trying to filter & catagorize them. It
may be of benifit to start a page on this site with nothing more than
bullet points about each of the past, present & future cures. You have
that [somewhat] on your home page, but not very beginner friendly. On
each of those bullet-point links have a comment/testimony section with
reader feedback from those familiar (or experienced) with the treatment.
The good, the bad & the ugly (so to speak). If any of us have a true
story to tell about that treatment (success or not) it would be good to
see this feedback under one topic (rather than a spot hit seen on most
blogs). I am trying to find an option for a cure and have yet to get a
concise story about where to start.