I frequently post about my horrible feeling with this condition and how it destroyes my life and my body more day after day. I never force anyone to read my posts. But after all many members here don’t feel like very much. So some only want to vent, to share their pain. Hoping to get some loving answers.
But more and more people here and in other forums only want to here success stories.
On the one hand it gives some hope on the other hand for all the media, pharma and medical mainstream lurkers it seems the truth that PFS isn’t anymore than a kind of depression in the head of some oversensible young guys.
That’s not true. PFS is an horrible, life changing and for many deadly disease. And them who suffer so much have the right to write about their suffering and how bad they feel this day.