Now is the time to rise up. The PFS Network has announced a board of molecular biologists, geneticists and clinicians involved in designing research projects: https://www.pfsnetwork.org/about
We have a golden opportunity to support leading scientists from a wide range of disciplines to get to the bottom of this issue: https://www.pfsnetwork.org/blog/pfs-network-hosts-groups-first-research-conference-into-post-finasteride-syndrome
We need to be constantly moving towards official recognition of this disease. No more lurking in the shadows as ignored sufferers labelled as hypochondriacs.
We need to humanize this issue. 1500 men on a forum can be ignored, but real, genuine faces telling their story are a lot harder to ignore. Even if it’s difficult, you have nothing to be ashamed of. Tell your story. If you’d like to speak on Moral Medicine, PM me. You can also share your story on Medium.
Join our fundraising group. We have a group of 125+ people donating monthly. We have many mothers of sufferers and our fallen brethren with us supporting with monthly donations. If you’d like to join this group, PM me. Every dollars helps; even if you can’t give substantial sums of money.
We are not going to get an opportunity like this again. It is down to us. We can live and die as forgotten castrated eunuchs hiding in the dark or we can rise up, raise resources, make ourselves heard and get the hell out of this nightmare and justice for those murdered by this poison.
Let’s go.