For those who’ve donated, you should’ve received this newsletter with a summary of all the great work the foundation has done so far.
Exactly one year later, I see that the PFS Foundation is once again touting its accomplishments:
pfsfoundation.org/news/2014- … l-address/
And rightfully so.
On behalf of the tens of thousands of men the word over whose lives – in Dr. Santmann’s words – have been needlessly decimated by finasteride, let me thank the foundation for all it has done these past 12 months.
Yes, hopefully everyone on this forum got this. Its very exciting to hear that more research projects should is planned and should be announced later this year. PFS is clearly so complicated that we’re not going to fix it without rigorous scientific research, so I’d urge everyone to give what they can to the Foundation to support this.
I’ve got huge respect for those on Foundation, and the people who set it up. Look forward to buying them a beer once we’ve sorted out the problem.
I also want to add my thanks! Because we suffer so much it’s easy to take for granted all of the the work that the foundation, the mods and other active members of the community do (Adam, Paul, Ben for instance), but without them we’d have no hope whatsoever.
I’m encouraged that there are two more studies in the works. Hopefully that suggests the research so far is leading to some findings and hypotheses worth testing.
Well done everyone. Let’s stay positive.
Big thanks to the PFS foundation for all the good work they have done.
I can’t wait for the research to be published so I can show it to all the “doctors” who dismissed me as crazy.
Exactly – the end is finally in sight: 2015 will be the year that the naysayers say, well, nothing.
Because it’s hard to argue with Harvard Medical School.
Huge congratulations to Mew, Awor, and everyone at the PFS Foundation.
These are such huge accomplishments. There are numerous things in the newsletter which didn’t seem to be open-knowledge on this board until now. E.g. two new studies are in the works, and the PFS Foundation has opened communications channels with doctors around the world.
This is hugely encouraging.
Wonderful e-mail to wake up to. It is important to remember that Rome wasn’t built overnight. But here we see that Rome is being built. Encouraging, hang in there everyone 
THANKS TO FOUNDATION!
Just noticed that Lawyers and Settlements did a story on the PFS Foundation:
lawyersandsettlements.com/ar … ChyFhYUWSp
Nice.
Why the hell they still think pfs=sexual dysfunction? Enough is enough.
This is all promising to hear and thank you to the foundation, it is being studied more, all the doctors who discharged people from their practices, banned them, sent them for psychiatric treatment, should be sued too (once the disorder is defined).