What we offer:
Emotional support for everyone affected by Spina Bifida, including meetings at numerous local cluster support groups throughout the state.
The Evergreen newsletter, which details local SBAWS activities, provides news on medical, therapeutic, rehabilitative advances, recreational and legislative issues.
Social events for children, teens and adults to gather, have fun and share their life experiences.
New Parents Packets to help parents learn about Spina Bifida and to help manage their child’s health care needs.
Educational scholarships may be awarded for educational purposes.
Access to national’s Insights magazine and to other current information on Spina Bifida.
A limited equipment fund to assist people with mobility devices, medical supplies and other necessary items not covered by insurance, as well as computer purchases.
I am the mother to 4 beautiful children, Tristram, Ariel, Balin and Kelahna. Kelahna is our youngest and she was born with spina bifida, hydrocephalus, and Arnold Chiari Malformation. Kelahna […]Read More
My wife and I have 5 wonderful children. Tristram, Ariel, Balin, Kelahna, and Percival. Kelahana was born with Spina Bifida, Hydrocephalus, and Arnold Chiari Malformation. Kelahna is an amazing little […]Read More