by Luca John Foundation | Aug 15, 2008 | blog, Newsroom
Inspiring New Hope 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 treatment, and Luca John Baranowski died 90...
by Luca John Foundation | Nov 10, 2007 | blog, Newsroom
Tabernacle, NJ Declares November 10, National Day of Mourning for Deceased Children Whereas, on November 10th 2006, Kevin and Nickie Baranowski lost baby boy Luca after his birth as a result of complications from an extremely rare form of skeletal dysplasia. Upon...
by Luca John Foundation | Nov 10, 2007 | blog, Newsroom
I appreciate your work to help children afflicted with skeletal dysplasia and their families. These terrible disorders affect too many individuals, and I commend everyone at your foundation for working hard to fund medical research and support the families who must...
by Luca John Foundation | Oct 1, 2007 | blog, Newsroom
SKELETAL DYSPLASIAThe Luca John Foundation Established to raise money for skeletal dysplasia research, the Luca John Foundation also provides financial assistance for funeral expenses to families who have lost a child 12 months or younger to the disease. ...
by Luca John Foundation | Sep 17, 2007 | blog, Newsroom
Dear Mr. and Mrs. Baranowski, The Holy Father has received your letter and he has asked me to thank you. He appreciates the concern which prompted you to write him. His Holiness extends his condolences for the loss of Luca, and he willingly joins you in praying for...
by Luca John Foundation | Aug 8, 2007 | blog, Newsroom
Jersey’s Helping Hands 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: There are two missions, according to the...
