Jarel Santiago: A Cardiac and ENT Success Story


Read Previous Read Next

Related News

Patient of the Month: Juan Diego

After a completely normal pregnancy in Nicaragua, Juan Diego was born with blue skin and shortness of breath. He was immediately diagnosed with a congenital heart disease and given a 50% chance of life if mom and dad didn’t seek treatment. Check out how far Juan Diego has come with the help of the Nicklaus Children’s Hospital Heart Program!

Cardiac Catheterization Procedure Helps Jackson's Start to Life

Baby Jackson, born after only 24 weeks of gestation, was very fragile and required oxygen around the clock. His parents were referred to Nicklaus Children's Hospital to repair his patent ductus arteriosus (PDA) a congenital heart defect that occurs commonly in premature infants.

Speak Now for Kids Family Advocacy: Tad's Story

Over the last two years, Theodore “Tad” Hartrick has spent months at a time at Nicklaus Children’s Hospital. Like Tad, there are many children in the state and in the nation who rely on access to pediatric care and Medicaid funding. Here is a message from the Hartrick family in support of this year’s Speak Now For Kids Family Advocacy Week campaign.

The Heart Program at Nicklaus Children's Acquires FDA-Approved Amplatzer Piccolo™ Occluder to Perform Non-Surgical Closures of Patent Ductus Arteriosus (PDA) in Premature Infants in its Cardiac Catheterization Laboratory

The Heart Program now offers the recently FDA-approved Amplatzer Piccolo™ Occluder to close PDAs in very premature babies in the Cath Lab. This self-expanding, wire mesh device is designed specifically to fit within the PDA of very low weight preemies with little risk of interference with adjacent structures.