Christine, Erin, and Jenna are young, ambitious women living with a rare neurological disorder, NMO (Neuromyelitis Optica). By sharing their stories, they hope to inspire others with medical challenges to live life to the fullest.
We, the authors of this blog are sharing individual personal accounts. Other than our experiences, we have no medical or other expertise on the subject matter referenced. It is not intended for medical advice. Please consult your physician before making any decisions.