Jacquie was diagnosed with sickle cell anemia during routine testing shortly after she was born, a lifelong blood disorder that affects red blood cells, causing them to become sickle-shaped instead of round. These abnormal cells can block blood flow, leading to severe pain, illness and serious health complications. For her family, the diagnosis brought fear, uncertainty and countless questions about what the future might hold.
Those fears began to ease when they arrived at Phoenix Children’s.



At one of their very first appointments, Jacquie’s doctor spent more than an hour sitting with her family, patiently answering questions and helping them process an overwhelming diagnosis. There was no rush, only reassurance. In that moment, her family knew they had found not only experts to care for Jacquie, but people who would walk beside them through every step of her journey.
Since then, Phoenix Children’s has become a constant source of support. Jacquie regularly returns for blood draws and checkups so her care team can monitor her condition. While she has been fortunate to avoid frequent hospitalizations, the times she has needed inpatient care have been especially difficult. Because children with sickle cell disease are more vulnerable to infection, many of Jacquie’s hospital stays have required isolation precautions, an often very lonely experience for a child.
That’s where the Child Life team makes all the difference.


From bringing toys and iPads to distract her during IV placements to creating moments of normalcy during long hospital days, Child Life specialists, donor-supported positions, helped turn fear into comfort and anxiety into smiles. One of Jacquie’s favorite places is The Child Life Zone, where she can play video games, connect with others and forget about her medical challenges for a while.
Today, Jacquie is a vibrant 9-year-old who doesn’t let sickle cell anemia define her. “Having sickle cell anemia hasn’t slowed down Jacquie at all. She’s usually found twirling or dancing her way through life with the most infectious smile on her face. She is joy personified!” Danielle, Jacquie’s mom says.
Her joyful personality and resilience inspire those who know her, and she approaches life with remarkable enthusiasm despite the challenges she faces.
All About Jacquie
Favorite subjects: Math and science
Favorite TV show: Pokémon
Hobbies: Drawing, dancing and video games
When I grow up, I want to be a: Scientist
- “Having sickle cell anemia hasn’t slowed down Jacquie at all. She’s usually found twirling or dancing her way through life with the most infectious smile on her face. She is joy personified!”DanielleJacquie’s mom
Phoenix Children’s Patient Ambassadors are a valiant bunch—they’ve shown immense strength amidst great setbacks. They’re also athletes, intellectuals, artists and the best siblings.
Even though their lives are full of medical appointments, they want to help other patients. Each ambassador has created a fundraising page to support Phoenix Children’s. Support kids like Jacquie.



