33^rd Annual Miracle Tournament and Celebration Dinner

Treated at John R. Oishei Children's Hospital in Buffalo, NY.

Born in India, Vignesh was adopted by his family at five years old. Vignesh was diagnosed with spina bifida, as well as hydrocephalus, a condition in which the body is not able to rid of excess fluid in the brain. He also experienced hearing loss and needed a cochlear implant surgery while in India. At Oishei Children’s Hospital, Vignesh underwent four surgeries, one of which was to replace his current shunt with a new one. At the age of nine, Vignesh received a new cochlear implant and is doing amazing. His family is grateful for the tremendous support and care at Oishei Children’s Hospital.

Donations to Children’s Miracle Network Hospitals help patients like Vignesh receive exceptional care and specialized occupational therapy.

Treated at Maria Fareri Children's Hospital in Hudson Valley, NY.

Camryn was diagnosed with Sickle Cell disease three weeks after birth. For most of her life, her disease had been managed. Four years ago, Camryn was diagnosed with Moyamoya disease (a narrowing of blood vessels in the brain). Her sickled blood cells would only complicate this condition. Camryn was in need of a stem cell transplant and her oldest sister, Skylar, was selected as her donor. Camryn was admitted to Maria Fareri Children’s Hospital and Skylar’s stem cells were harvested and transplanted into Camryn. It was inspiring for her family to witness this life-saving exchange among sisters! Camryn was hospitalized for 88 days and she found solace in the extraordinary care, and encouragement she received before, during and after her transplant. Today Camryn is feeling great and is an incredible advocate for the care she received at Maria Fareri Children’s Hospital.

Thanks to donations to Children’s Miracle Network Hospitals, Camryn received care and support as she underwent a stem cell transplant at Maria Fareri Children’s Hospital.

Treated at Children's Specialized Hospital in Mountainside, New Jersey.

Thirteen-year-old Gabriella (Gabby) was running at track practice when suddenly she felt her left arm drop on her last lap. After she lost feeling in her arm, she quickly lost sensation in her left leg and fell to the ground. Gabby was rushed to the pediatric unit of a local trauma center. The hospital immediately took her for a CAT scan, which revealed a brain bleed. After several tests, the doctors diagnosed Gabby with a rare brain arteriovenous malformation (AVM) rupture in her right frontal lobe.

She had to wait 10 days for a craniotomy to remove the AVM because they needed the blood to settle in her brain. A few days after surgery, Gabby was transferred to Children’s Specialized Hospital (CSH) for inpatient therapy. AVMs cause stroke-like symptoms, in Gabby’s case, paralysis of the left side of her body and facial weakness. For 19 days in a pediatric intensive care unit, Gabby couldn’t move or sit up. During the five weeks she spent at CSH, Gabby received physical, occupational, speech, and recreational therapies, including aquatic therapy and targeted ways to help her walk again and smile symmetrically. Gabby arrived wheelchair-bound and successfully walked out of CSH on her own. Since then, started practicing soccer and lacrosse again.

Donations to Children’s Miracle Network Hospitals helped Gabby benefit from various forms of therapies that supported her road to recovery.