Seeing as almost everyone with PFS was once prescribed the drug from a doctor or dermatologist: wouldn’t it make sense to ask a (small) donation to the PFS Foundation from those who got us into this mess by precribing the drug? Or is it naive to think some would be willing to donate, as that would mean they admit there’s something (terribly) with the drug they prescribed? I would like to hear people’s thoughts on this idea.
I do not think is a good idea
I would but mine died two days before I went asking him explanations of what he did to me…your’s the thought.