Helping children and adults born with spina bifida to reach their God given potential by fighting complications, advocating for whatever is needed to improve current function or abilities and preparing for future Possibilities...
This 501c3 nonprofit foundation was created in 2011 by a small group of moms whose children were born with spina bifida. We are dedicated to finding alternative treatments and therapies for adults and children as well as spreading awareness about the birth defect. WFBSB FOUNDATION is the first of its kind created for spina bifida supporting families in many ways over a wide range of categories. We ARE the spina bifida advocates! While we support the U.S. in finding a cure, we are here to make a difference in lives now. Our children, especially, need so much attention to their bodies in order to keep them growing and well proportioned in preparation for a cure. It is important that we find any and all safe and non-invasive methods to do so. We have faith in God alone, who has supplied all of our needs and has answered so many prayers and we desire to spread our hope and faith to anyone in need. WFBSB FOUNDATION was not only created to inform others on what therapies and treatments are helping, but also to provide grants or financial assistance and support to families who are in need of medical treatments, therapies, medical stay, equipment or anything related to this condition that is not covered by insurance. We have seen so many miracles in the lives of many and we want this to happen for everyone! Please stay updated on the progress of children who are pursuing a range of therapies by joining our group and page on Facebook.
A BIG THANK YOU TO: 
FOR YOUR AMAZING WORK IN GRANTING WISHES FOR
CHILDREN ALL OVER THE WORLD INCLUDING SOME OF OUR VERY OWN WARRIOR FAMILIES KIDS! ALSO A BIG THANK YOU TO UNCLE SI ROBERTSON AND FAMILY!
I was born with spina bifida. The doctors said I wouldn't live past the age of five. I have beaten the odds. I believe its due to the fact that God has blessed me with an amazing mother. She never gave up hope and taught me never to give up. She made sure I never missed an appointment and even stayed at the hospital with me. Alot of people criticized her for the way she was taking care of me. Whether it was school officials saying she babied me or family members accusing her of abuse because she cathed me, she never backed down. When faced with criticism, she would say, "until you have a disabled child, don't tell me how to take care of mine. She must have done something right. I continue to celebrate birthdays..
- Grants and financial assistance for medical treatments, therapies, equipment, medical stay or anything related to the condition that is not covered by insurance
- Donated therapy equipment / bracing from willing families within the social network
- Fundraising assistance / Help A Child Program
- Experience and updates regarding amazing new therapies or equipment which shows any improvement in spina bifida as well as advice on other forms of assistance.
www.facebook.com/spinabifidawarriors Co Founder recently nominated for the Women of Distinction Award and article in the
-Article to be printed late fall 2015___________________________________
1.000.00 Community Grant awarded from
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1,000.00 Grant and Brian T. Wagner Award from
and winner of the award, Jessica McCulloch, Co Founder of WFBSB FOUNDATION.
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THANK YOU SO MUCH TO THE FOLKS AT:
FOR YOUR GENEROSITY IN GRANTING WISHES AND FUN FILLED TRIPS FOR FAMILIES ON MEDICAL TRIPS!