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.
Contact her here or connect with her on social media!