DEBRA Australia
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Description
DEBRA Australia is a not for profit volunteer based organisation which aims to educate and support families living with EB, investigate and implement programs to help EB sufferers to improve their care and quality of life, offer financial and emotional support and also networking opportunities to families, educate health professionals and the general public about EB, and to raise funds for research to find a cure for EB.
Type
Online or Phone Service
Alternative Names:
Dystrophic Epidermolysis Bullosa Research Association (DEBRA) Australia
Areas Served:
National
Last review date:
4/5/22 0:00
- Epidermolysis Bullosa
- Support Groups
- People with a Disability
- Phone or Web Information Services
- Health Education
- Other Volunteering(Fundraising)
- Children and Families
- Community Education
- Cotton Wool Babies
- EBD
- Epidermolysis Bullosa - YR
- Dystrophic Epidermolysis Bullosa
- Hallopeau-Siemens
- Herlitz Junctional Epidermolysis Dystrophica
- Mutual Support
- Peer Support
- Support Groups
- Self Help
- Self Help Groups
- Support Group
- People with Disability
- Disabled
- People with Disabilities
- Disability
- handicapped
- People with Disability
- People with disability
- Disability Support
- Telephone Information Services
- Information Hotlines
- Phone or Web Help Services
- Health Promotion
- Patient Education
- Mental Health Education
- Children
- Primary Children
- Preschool Children
- teenagers
- Infants
- Preschool Children (3-5)
- Infants (0-2)
- Children (0-18)
- Junior
- Kids
- Childhood
- Preschoolers
- Babies
- Toddlers
- infants(0-2)
- Preschool Children (2-5)
- Families
- Public Awareness
- Awareness Training
- Pittsworth, QLD 4356
- 07 4693 7003, 0427 9
-
admin@debra.org.au
- https://www.debra.org.au