Mighty Member since April 2022
Kassondra Lambert is a work-from-home mom with a three year-old son and five year-old golden retriever. She left her career in child welfare social work in 2018 to be a full-time mom, not knowing anything about disability or rare diseases. Her son was diagnosed with a rare genetic illness (KIF1A Associated Neurological Disorder or KAND) in 2021 that launched her into a mission to share her story and bring awareness to the world of rare disease. She lives in Michigan and enjoys writing, hiking, and all things social media.