By Rare2Aware
In Advocacy & Awareness, Angiokeratomas, Changes in the eye, Community, Fabry Disease, Hearing problems, Impaired ability to sweat, Patient Stories, Pedigree Analysis, Stomach problems
Posted Gina’s Story: The long walk to a diagnosis
Meet Gina, a 56-year old mother to E (Fabry patient), based in Ontario, Canada. After five years of jumping through hurdles she finally received a diagnosis of Fabry disease for her then [...]
