About Me:
Lynn Anderson who had two children (now deceased) who were born with epidermolysis bullosa
"Two of Lynn Anderson’s natural born children carried a rare genetic disease — epidermolysis bullosa (EB) — which prevents a child’s skin from growing with their body. After thirty years of nursing her children and grieving their deaths, Lynn founded an organization that raised money for EB research at Stanford University. Lynn now rejoices in a newly-approved treatment that will save the lives of many EB children."