Spina Bifida Foundation Victoria
The most frequently occurring, permanently disabling birth defect, spina bifida is broadly described as the incomplete formation of the spine and spinal cord.
Spina Bifida Foundation Victoria (SBFV) provides members and the community with a wide range of resources for living with, managing, and preventing spina bifida. We were founded in the mid-1990s by a group of parents, physiotherapists and doctors to improve services and life chances for Victorians with spina bifida.
SBFV does not receive any government funding and relies solely on the generosity of community members.
For more information, please refer to our website.
Help to send a child or adult with spina bifida on a fun activity in a supported environment, increasing their social interaction, self-esteem and independence.
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