About Us
MI SB FAM is dedicated to serving individuals with spina bifida as well as their family members and supporters by providing networking opportunities and creating awareness, as well as through resources, education, community outreach, advocacy, and special assistance grants. MI SB FAM believes in means to improve and promote good health and well being along with empowering each other through our struggles and our strengths. We hope you will support us as our purpose is to support you and we are very excited about this!
Meet the Team
Lisa
Dedicated mother to an amazing daughter with Spina Bifida
Passionate about serving the SB community
Stacy
Stacy
Stacy
Adoring mother to a charismatic son with Spina Bifida. Passionate about advocating and educating. Changing the world through inclusion, knowledge, and awareness.
Owen
Stacy
Stacy
Dedicated disability advocate who believes strongly that accessibility is a matter of civil rights and basic principles of equality.
Dave
Stacy
Dave
Overjoyed father to an intelligent daughter with Spina Bifida. Changing the narrative that SB means a low quality of life.
Sherrie
Sherrie
Sherrie
Energetic adult with spina bifida and helps provide information and resources to the SB adults in our community.
Will
Sherrie
Sherrie
Proud father to a beautiful daughter. Here to support and educate expecting families as well as assist others who may already have children with Spina Bifida and just need someone to talk to. Main goal is to help others in this community; acting as a counterbalance to any negativity and misinformation out there.
Sarah
Sherrie
Sarah
Devoted mom to an athletic son with Spina Bifida who is changing the world, one sport at a time.