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Stories

Kennedy Krieger Magazine

Story about grant to renovate patient recreation space

Kennedy Krieger to Transform the Inpatient Recreation Room into Vibrant and Inclusive Space for All Individuals

Kennedy Krieger Institute is renovating its 30-year-old inpatient Recreation Room, creating a vibrant, inclusive and developmentally appropriate space for patients and their families.
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Story about Emmy

Meet Emmy

After years of uncertainty, Emmy was diagnosed with Coffin-Siris Syndrome at age 5. Now a thriving teenager, she communicates through sign language and inspires everyone around her.
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What is SYNGAP1? podcast episode.

What is SYNGAP1? Learn About This Rare Disease and How Our Brains Work

Listen in as our host, Dr. Brad Schlaggar, president and CEO of Kennedy Krieger, talks with neurologist Dr. Connie Smith-Hicks, an expert on SYNGAP1-related disorder.
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Stella Cotton article.

A New Branch of Love: Stella Cotton’s Journey Meeting and Adopting Her Son, Jasper, through Kennedy Krieger’s Therapeutic Foster Care Program

When Stella Cotton accepted a role at Kennedy Krieger Institute over a decade ago, she wasn’t just choosing a job. Though she didn’t know it then, she was taking the first steps on a path that would lead her to her son.
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Tomorrow's discoveries webinar summary and video.

Watch: Tomorrow's Discoveries: Innovation in Rare Neurodevelopmental Disease Treatment at Kennedy Krieger

In this special webinar, join Dr. Brad Schlaggar as he convenes a distinguished panel of Kennedy Krieger neurologists, both pediatric and adult, with expertise in clinical care and research on rare diseases of the developing nervous system, who will discuss recent advances, and innovations on the horizon, in this very dynamic and promising area.
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Partnering to Solve Complex Pediatric Cancer Challenges article

Kennedy Krieger Is Partnering to Solve Complex Pediatric Cancer Challenges

With a recent $5.5 million philanthropic investment, our researchers are launching a pioneering three-year neurorehabilitation program aimed at proactively safeguarding and improving brain health in children with brain tumors—from diagnosis through long-term survivorship.
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Kabuki Syndrome podcast episode.

Kabuki Syndrome: Why Studying Rare Diseases Is So Important to All of Us

Join Dr. Brad Schlaggar, president and CEO of Kennedy Krieger, as he discusses research around rare disease with Dr. Jacqueline Harris, a pediatric neurologist and an international leader in the study of Kabuki syndrome.
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Investigating the Mysteries of Rare Diseases article

Kennedy Krieger is Investigating the Mysteries of Rare Diseases

Kennedy Krieger Institute has long been a leader in understanding and treating complex neurodevelopmental and genetic conditions, serving children and families affected by disorders that most clinical specialists may encounter only once, if ever, in their careers.
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Article and video about Ayden

Meet Ayden

Diagnosed with a rare terminal disease, Ayden defied expectations thanks to breakthrough treatment and donor support. Today, he’s a joyful Pokémon expert who lights up every room.
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