If you are an expectant parent who has been told that your pregnancy is affected by Spina Bifida, we can help you find resources or connect you to people who can share their experience and expertise.
Or if you are a parent of a young child or an adult who has just been diagnosed with Spina Bifida, we have information and resources available for you also.
We know that you are searching for information to help you understand more about your unanticipated diagnosis, and we want you to start in the right place.
Iowa and the MidwestIf you live in Iowa, we are here as an affiliated chapter of the Spina Bifida Association to serve you. If you live in a surrounding state, there might be a chapter closer to you that we can help you locate. Please contact us about referrals to local providers. We can also connect you to families in Iowa who have shared your experience. We are here to help and invite you to contact us by either filling out our form or by emailing us at firstname.lastname@example.org.
The Spina Bifida Association provides information on what Spina Bifida is, what we know about its causes, and suggested do’s and don’ts during the first days and weeks after the diagnosis.
You can access that information here.
What To Do:
The Spina Bifida Association has compiled this list that may be helpful to you at this time of your diagnosis.
Don’t feverishly search for “Spina Bifida” online or on social media. Although many organizations offer valuable resources, there are even more who have out-of-date or inaccurate information.
Do make sure that the information you gather is from a trusted, experienced source, and that you follow the advice of health and medical professionals who are knowledgeable about Spina Bifida. Search our list of clinics and providers, and contact our National Resource Center for more information, including how to connect with parents and caregivers who have been in your shoes.
Don’t exhaust yourself trying to determine exactly what the future holds. A diagnosis of Spina Bifida is a lot to take in. While you can’t help but wonder what having a child with Spina Bifida will be like, it’s important to take one step at a time.
Do speak with other parents and caregivers who have experienced what you are going through. Contact our National Resource Center, visit our many Facebook groups, or ask your local Chapter to direct you to their network of parents.