I lurked for about a year and 9 months. I recon the lurkers outnumber the registered members by untold amounts. I regret not reaching out sooner. The red carpet is rolled out for you. Don’t be shy! I welcome you!
Yes I agree
I was afraid to register because I thought than everybody recognize me and all my friends know about my ED and that I’m a victim of this horrible disease.
I registered last year. Someone who know that I have PFS maybe could find me here. But with time I can count my friends on one hand.
They all study your Facebook, Instagram and other accounts, where you present yourself as a good looking guy living a funny lifestyle.
Going sick, they all go on with their lives without you. Only your loving family, your parents stay with you.
So if you share your story you can share your suffering you’ll get real sympathy and love from the other victims. And the power of the community increases.
Looking for a co fighter you’ll find a fighter, who tries every protocol to feel better.
Sharing painful thoughts, no one will laugh about you and you’ll find others living in pain.
Looking for recovery, you’ll find recovered members.
So please join the community, you never wanted to join, but you made the same mistake of your life, as we all did and now you are here.
You need us and we need you! It’s my personal view. I’m not a staff member.
you are guys who can say what I want to say.
Neither of the two people I’ve provided the full PFS story to have enough practical interest to come digging here. However I’m going to amend my…notes…to direct the reader to this site and my posts and to avenge me.
Lurkers: Whether you are a patient, a friend or relative of a patient, a doctor, scientist, researcher, or whatever, please say hi at least and consider telling us about yourself.
If you are thinking about taking a risky substance for cosmetic reasons, think again. If you are already taking, I hope you have no adverse reactions.