The” Fundación Debra de Costa Rica” is a not-for-profit organization, formed to provide patient support services and to promote research into treatment and cures for those living with EB ( Epidermolysis Bullosa). At Debra we work to raise awareness of EB and also raise funds to help these families.
The organization is recognized by the National Council of Rehabilitation and Special Education ( Consejo Nacional de Rehabilitación y Educación Especial) and by the Children’s Hospital ( Hospital Nacional de Niños), and also is authorized by the Tax Administration of Heredia ( Tributación Directa) to receive tax deductible donations.
Debra de Costa Rica is associated with the International Dystrophic Epidermolysis Bullosa Research Association .
With your help we can continue to offer our EB children medical, moral and economic support.