


About SBF
The Spina Bifida Foundation (SBF), a not-for-profit organization was formed by Medical Professionals and parents of Spina Bifida Children. Since 1997, we – a group of doctors, parents and well wishers have been consistently working for Rehabilitation, Care and Prevention of Spina Bifida thereby improving the lives of Spina Bifida (SB) patients.
Upcoming Events
Tabassum Wakil was born with a birth defect of the Spinal cord called Spina bifida and has a serious problem with the control of her urine and stool(incontinence). She had a bad odour because of a Urinary tract infection, so other children started avoiding her.
Her younger brother was also born with Spina bifida.
Her father is a daily wage worker who cannot afford her treatment.
She needs to undergo a super major operation (Augmentation Cystoplasty) on her Urinary tract and bowels.
The estimate expenses for this operation is about Rs. 300,000/- (all inclusive in concessional class)
This operation will make her incontinence more manageable and for her social rehabilitation.
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Support Tabbasum

Description : Thank you all the donors for your generous gift. We are thrilled to have your support.
Through your donation we have been able to raise more than ₹ 200,000 to accomplish our goal of buying active wheelchair for Ms. Khushi Ganatra. You truly make the difference for us, and we are extremely grateful.
Today your donation is going towards Khushi’s wheelchair.
A Warm note to say THANK YOU
Glimpses Of Events
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Member Achievement
Posts & Articles
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Health Checkup Program
December 3, 2020 -
World Birth Defect Day Event
August 18, 2020