Learn languages naturally with fresh, real content!

Popular Topics
Explore By Region
Ireland’s EB patients lack consistent care, supplies, and support, prompting calls for better funding and coordination.
A new report reveals significant gaps in care for Ireland’s approximately 300 people with epidermolysis bullosa (EB), a rare, painful skin condition causing severe blistering from minor friction.
Patients face inconsistent access to essential wound care supplies, no national bandage scheme forcing out-of-pocket costs, and inadequate psychological and dental support.
Home nursing services are strained by staff shortages and poor training.
Financial and welfare systems are complex and difficult to navigate, leaving many, including severe cases like Amanda Nugent and Liz Collins’ daughter, feeling invisible and unsupported.
The EB Butterfly Review, commissioned by charity Debra, recommends improved home nursing, simplified benefits access, and affordable medical supplies.
Debra’s CEO noted progress in securing dedicated annual funding for integrated care and mental health services at St James’s Hospital, with patients and caregivers urging coordinated support to reduce the emotional and financial burden.
Los pacientes de EB en Irlanda carecen de atención, suministros y apoyo constantes, lo que ha provocado que se soliciten mejores fondos y coordinación.