A Nephrogenic Systemic Fibrosis anonymous support group with information on diagnosis, treatment, symptoms, along with personal stories and experiences with Nephrogenic Systemic Fibrosis. You're not alone.
I've been telling docs about sx, they say they don't know, no extensive workups, nothing, no exams, minimal tests if at all. they all know they poisoned me and others. today, md discharged me from clinic, my comments to him, so what. had 2 scans with dye 3 mo apart, vadenver 2010...