Debra Lafave Book Florida Teacher
Debra of america is a non-profit organization providing free programs & eb support services to those living with epidermolysis bullosa. Its mission is to help patients, families, and doctors in countries where there is no debra structure to support them and to assist new groups to form and develop. Get to know the dedicated team behind debra of america, working tirelessly to support individuals and families affected by epidermolysis bullosa (eb).
Explore our mentorship programs, eb nurse educator program, new family advocate program, debra care conference & additional support services. Founded in 1980, debra of america is dedicated to improving the quality of life of all people impacted by epidermolysis bullosa (eb) in the u.s. Learn about epidermolysis bullosa (eb), a rare genetic disorder, its symptoms, treatments, and personal stories from the eb community at debra of america.
When there seems to be no way out, there's debra of america, a lifeline for thousands of families living with “the worst disease you’ve never heard of,” epidermolysis bullosa (eb). Whether it’s finding answers to everyday challenges, accessing free wound care supplies, or connecting with others who understand— debra is here, every step of the way. Debra of america offers free programs, personalized support, and trusted online resources to help individuals and families navigate life with eb.
La pagina de internet de debra provee pacientes, cuidadores y profesionales de salud con la información mas reciente sobre eb, mientras ofrece un lugar donde la comunidad de eb puede.
