except our forum i didn’t find anything in other language on pfs
nothing in french nor in german, what a pity.
Also in spanish or in portuguese …
ok maybe there are other site in languages that i don’t know …
or simply i didn’t found 
in italian i found 2 site, one underconstruction, another small blog
postfinasteridesyndrome.blogspot.com/2011/08/la-sindrome-post-finasteride.html
anyone known others ?
I am starting one in portuguese in four months. I need to adjust some things about my work life and i will have enough time then to dedicate to this cause. I have it all planned and the website name registered already. I want to do something big, and advertise the website in Universities and other places that are not too expensive to do so. I also plan to do some work with doctors but have not decided how yet.
It would be great if you could start one in french… there s lots of people that don t speak english and take this poison. I am constantly checking on sites like Yahoo answers for people asking in portuguese about Finasteride. This is a way of helping too, some people are stubborn and and will take it anyways. Other people follow your advice and thank you a lot. It is a great feeling to know you have helped someone not to fall into this hell.
Man, you gave me a good idea seeing the italian blog you posted the link. So while i don t build the big site with studies, stories and all, i just did a blog. It is very easy, and fast, it takes 10 min if so to create it. We should all do it in our languages. I posted and translated the video from CBS philadelphia in the first post.
very good!
Post link of ur blog all over the uro-andrology forums, we need spreading awarness expecially in that area
we start now the PFS warning alliance
LOL! 
.
Good job guys. Don’t underestimate the power of a simple blog to attract attention and show up on search engines.
If even one man is saved, your efforts will have been worthwhile.
we need some eastern language speaking members
thare is a big amount of people that could be advised
chinese, arabic, russian speaking member r needed asap
Do you guys know how to increase the odds of google showing my blog as a result of a search? I ve added the blog yesterday to google, but untill now, even if i search for the exact address riscosdofinasterida.blogspot.com it does not show up as a result. Any suggestions?
be patient, at least one week for be finded on google 
hmm ok. Thanks prop!
Hi guys,
I would like to ask you for a little help for my blog. The number of visits is growing faster than what i expected, which makes me glad. I have posted links on brazilian hairloss foruns and orkut. I am going to start sending emails to dermatologists and health related reporters in Brazil, with recent studies and a link to the blog. Although the blog is in portuguese and is intended to create awareness about Finasteride risks to brazilians who don’t speak english, many doctors and some of the visitors do speak english. So i would like to ask you to please post your summarized story, as a comment, on the first post there (there is an indication in english). It can be brief, it will take you 2 min. You may think it would not make a difference, but you wouldn’t believe how much misinformation there is here about this. From the feedback i am getting, it is worse than what i thought. If a doctor visits the blog and sees many stories posted spontaneously from visitors, it makes the blog more credible. Most brazilians don’t google about Finasteride in english so Propeciahelp is not so popular here unfortunately (There is a link to it on the blog). The macho culture makes it harder for men to admit to a friend or to the doctor he is having sexual problems. And to make matters worse, Finasteride is sold over the counter in this country and is pretty afordable in generic form. So Finasteride is still the “perfect drug” here. Please help. Thank you very much.
riscosdofinasterida.blogspot.com/
well done correio,
i’ll put links to your blog in every baldingforum that i know
Thanks man! Thats really nice of you.
no prob your work deserve attention,is useful to make more and more reliable the
PFS sufferers
you know man here ther’s one thing that we really need,
doctors that hangs around this forum
we r too much left to our speculations without some competent supervision
Hi Prop,
Yeah, i agree man. I guess we need to find doctors with a taste for investigation. Because other doctors are not interested.
There are some doctors who like to research new diseases and problems. Like Dr. Alan Jacobs for example. We need now specific studies with people like us, PFS sufferers. But i think there is a going trend in that direction.