Lurie Children's Blog Search Results
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Aerodigestive Program Helps Madison Breathe Easier
Born with her vocal cords fused together and subglottic stenosis, Madison underwent laryngeotracheal reconstruction, enlarging her narrow airway.
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Keeping Hope for Hendrix
When Hendrix Mascara, 2, was born four-weeks early, his parents knew immediately something was more concerning than his premature arrival.
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One in One Million – Opsoclonus Myoclonus Syndrome
In February 2017, Kate became one in a million. She was diagnosed with Opsoclonus Myoclonus Syndrome (OMS), a very rare neurological disorder.
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Then and Now: A Look Back on Move Day, June 9, 2012 with Jodi
Jodi has been a patient of Lurie Children’s since she was 6 months old when she underwent her first brain surgery for hydrocephalus.
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Then and Now: A Look Back on Move Day, June 9, 2012 with Emiliano
Emiliano “Emi” was the first patient we moved on June 9, 2012 from Lincoln Park to Streeterville.
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Multidisciplinary Care Helps Darcie Thrive with Rare Congenital Muscular Dystrophy
Darcie was diagnosed with merosin deficient muscular dystrophy- a very rare form of congenital muscular dystrophy.
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Father Battling Aggressive Cancer Sees Son Receive Life-Saving Kidney Transplant from High School Classmate
Just one week after learning Ashley was pregnant with Miles, the Wagners received devastating news.
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Jonah’s Story – Raising Awareness for Infantile Spasms
Jonah’s 6-month EEG soon showed that he was at high risk for developing a devastating form of childhood epilepsy known as Infantile Spasms.
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Eleven Years After an Intestinal Transplant, Nicolas is Still Going Strong
At Mindy's 29-week ultrasound, her obstetrician noticed a problem believed to be easily fixed but turned out to be a life-threatening condition for her son.
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ECMO Survivors: Samantha's Story
Samantha was born via a C-section 12 days after her original due date. Soon after birth, doctors discovered that she had a diaphragmatic hernia.
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Children at Heaven's Door - ECMO Survivors: Tyler's Story
In 1992, Tyler was born and immediately diagnosed with 100% meconium aspiration syndrome. His case was serious enough to need a form of life support called ECMO.
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ECMO Survivors: Baby Eleanor's Story
Baby Eleanor was born with a diaphragmatic hernia that required surgery as one-week old. ECMO helped her survive and recover from her operation.
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ECMO Survivors - Jessica's Story
After Jessica was born with a severe case of meconium aspiration syndrome, she needed to be transferred to Lurie Children's to be put on ECMO.
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ECMO Survivors - Madeline's Story
Read about Madeline's journey with ECMO as a newborn.
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ECMO Survivors - Chelsea's Story
Chelsea was on ECMO for 30 days, which is the longest amount of time anyone is allowed to be on the machine.
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ECMO Survivors - Drew's Story
When Drew was two months old, he was admitted to Lurie Children’s with respiratory distress and bilateral pleural effusions. ECMO was Drew’s only shot at survival.