03/05/2026
✨ Aplastic Anemia Awareness Week – March 1 - 7 ✨
This week, we honor warriors like Livy — and all those affected by Aplastic Anemia — who remind us to cherish every moment, dream big, and stay brave. 💛
At just 7 years old, Olivia was diagnosed with Severe Aplastic Anemia, a rare and life-threatening blood disorder. Her family had never even heard of it before — but suddenly, everything changed. Olivia’s bone marrow had stopped producing the blood cells her body needed to survive, and she required frequent transfusions while her dedicated Pediatric Stem Cell Transplant team at Maria Fareri Children’s Hospital quickly moved into action.
When no suitable donor match was found in the national registry, Olivia qualified for an innovative clinical trial at the hospital. She underwent a haploidentical bone marrow transplant and spent five months in the hospital bravely pushing through every challenge that came her way.
With unwavering trust in her extraordinary transplant team, Livy persevered — and today, she is 4 years posttransplant and thriving.
Now a vibrant survivor, Livy loves school, treasures her close friendships, and has returned to all the things that bring her joy. She absolutely lights up on stage and dreams of one day performing on Broadway. She loves trips into the city to see musicals, exploring new places, and embracing every “adventure” with her incredible zest for life.
Most beautifully, Livy has taken everything she learned during her illness and transformed it into a way of living — never taking a single second for granted, always dreaming big, and choosing a life that truly makes her happy.
Her journey is a powerful reminder of the resilience of children facing rare diseases and the importance of awareness, research, and compassionate care.
Thank you to Livy and her family for sharing their story during Aplastic Anemia Awareness Week (March 1–7). 💛