About Nikki
Nikki is a writer, speaker, and fierce advocate. She is passionate about birth, prenatal diagnosis research + awareness, education, supporting other families who have a child with a diagnosis and celebrating rare.
After receiving a prenatal diagnosis at her 20-week-anatomy scan with her fourth child, Nikki soon learned she didn’t live in the world she thought she did.
Along with being a local support group leader for the OI Foundation, Nikki is a resource for other OI families, the medical community interested in rare conditions and improving the patient experience for a pregnant woman who receives a diagnosis, as well as early intervention services education. This includes sharing tools and tips she has learned from her incredible physical, occupational and speech therapists.
Disclaimer- this is not medical advice, i am not a medical professional – this is for educational purposes and is not intended to diagnose, treat, cure or prevent disease or condition.
Diagnosis during pregnancy 