I would like to start a 501(c)(3) foundation for Peyronies. Is there an attorney who would like to
volunteer his time?
Why a pledge instead of a donation? This is new web site and I am not sure it will be
successful. I don't want to be in a position to collect money and have no useful way to spend it.
Therefore, if you want to pledge and I have to discontinue the site, there is nothing for me to
I read a number of Men's magazines and have never seen an article about Peyronies. Is
anyone willing to contact them and suggest they write an article about our condition?
As you can see, this is a very basic web site. Is there anyone who wants to be a Webmaster?
I would like to raise money an hire a lobbyist to assist us in obtaining Federal research funding
for this impairment.
I sure readers has better ideas. Feel free to submit them.
Our condition is not going to heal itself. Take action to help yourself.