Hey @cooper !
The PFS Foundation is the official non profit of the post finasteride syndrome.
Read above to see what their goals, plans, and board of directors are. I made this fundraising drive to raise money for the Foundation so that they may use our money for marketing, research, website maintenance, and whatever else we need. It takes money to make money, so I’m trying to help out as much as I can.
Phil Roberts of the Foundation told me to keep on raising money and making noise for the Foundation. It’s 2019 and more and more people know about PFS thanks to the internet and all of our efforts and the Foundation’s efforts. The studies coming out are getting less and less ignorable. I’m doing this to keep the hype alive in hopes that my libido, fatigue, and all my other symptoms get addressed and fixed one day.
The goal is to raise $2000 between members this summer, and so far, we are one tenth of the way there!