Meet Kendalyn
Treated for a Pseudo-obstruction
Born six weeks early, Kendalyn faced severe feeding struggles until doctors at Intermountain Primary Children’s Hospital, supported by Children’s Miracle Network, diagnosed her with Chronic Intestinal Pseudo-Obstruction.
Kendalyn relies on IV nutrition, has undergone multiple surgeries and spends months each year in the hospital. Still, she fills every room with joy through dance parties, art projects and her bright spirit.
Thanks to donations, Kendalyn has access to life-saving medications, child life, music therapy and art therapy. Now 11, she loves ballet, robotics club, her service dog Reggie and helping others understand her medical journey with confidence.
Meet Barbie
Treated for Leukemia
Just before her second birthday, Barbie was diagnosed with acute lymphoblastic leukemia. After two years of chemotherapy and months in isolation, she was declared in remission, but three years later, her cancer returned.
During the pandemic, Barbie’s family relocated to Miami so she could receive advanced care at Nicklaus Children’s, supported by Children’s Miracle Network. There, she found comfort through child life, music therapy, pet therapy, volunteers and social workers.
After nearly three more years of treatment, Barbie rang the bell to mark the end of chemotherapy. Today, she is in remission, loves to dance and spend time with her sister, and continues to receive checkups at Nicklaus Children’s.
Meet Lanna
Treated for Achondroplasia
During pregnancy, Lanna’s parents learned she wasn’t growing as expected. At one month old, she was referred to Arkansas Children’s Hospital, supported by Children’s Miracle Network, where genetic testing revealed achondroplasia, the most common form of short-limbed dwarfism.
Her family found answers, support and a care team that has guided every step, from orthopedic evaluations to growth monitoring and genetic consultations.
Today, 12-year-old Lanna is part of a clinical trial designed to support bone growth for children with achondroplasia. With weekly injections and ongoing care, she continues to show what expert care, research and community support can make possible.
Meet Merveilles
Treated for Cleft Lip/Palate Repair
Before Merveille was born, her parents learned she would have a cleft lip and palate. After arriving early at 32 weeks by emergency cesarean section, she was life-flighted to Sacred Heart Children’s Hospital, supported by Children’s Miracle Network, where she spent 11 weeks in the NICU.
Through the hospital’s Maxillofacial Program, Merveille’s family received specialized support with feeding, surgery and ongoing care close to home. Children’s Miracle Network funding helps support the nurses, speech therapists and feeding resources that make this care possible.
Now a bright, curious kindergartener, Merveille is thriving with the support of expert care and a community committed to helping kids grow up strong.