by Luca John Foundation | Jun 19, 2015 | blog, press release
It has been nearly ten years since Nickie and I founded the Luca John Foundation. It has been an absolute privilege to serve the hundreds of families throughout the country, who have come to us for financial and emotional support during their time of grief. It has...
by Luca John Foundation | May 22, 2015 | blog, Newsroom
Kevin Baranowski and his wife, Nickie, were excited for the ultrasound appointment so they could learn if their baby was going to be a little boy or girl. They never could have anticipated what the ultrasound also revealed. Their baby had a fatal form of skeletal...
by Luca John Foundation | Aug 15, 2008 | blog, Newsroom
Inspiring New Hope [su_row][su_column size=”1/2″]When Kevin and Nickie Baranowski’s unborn son was diagnosed with a lethal form of Skeletal Dysplasia, they searched for information in a cure. Unfortunately, research on the condition had yet to yield a...
by Luca John Foundation | Aug 8, 2007 | blog, Newsroom
Jersey’sHelpingHands [su_row][su_column size=”1/2″]Who: Kevin and Nickie Baranowski of Ewing. What: Co-founders of the Luca John Foundation, named in memory of their son, who dies shortly after his birth from a form of skeletal dysplasia. Mission:...