
Keeping Collins Moving
Donation protected
Money raised will go toward any of Collins' medical bills and equipment to keep her moving through her journey with Spina Bifida, as well as travel costs for appointments. Currently, any new funds raised will be applied toward a wheelchair and daily use equipment.
Our story: We found out at 20 weeks prenatal gestation that Collins has SB, a birth defect in which her spine is not closed and required surgery. She was born on 9/7/20 and within her first 3 days of life, had surgery to close her defect on her back and another surgery to place a shunt in her head to reduce fluid buildup. We do not know at this time how much this will impact our life or hers, but we are all in this journey together and want to make sure our baby girl can have everything she needs to keep moving!
Our story: We found out at 20 weeks prenatal gestation that Collins has SB, a birth defect in which her spine is not closed and required surgery. She was born on 9/7/20 and within her first 3 days of life, had surgery to close her defect on her back and another surgery to place a shunt in her head to reduce fluid buildup. We do not know at this time how much this will impact our life or hers, but we are all in this journey together and want to make sure our baby girl can have everything she needs to keep moving!
Organizer
Lenae Mitchell
Organizer
Nevada, IA