Our Mission
Our foundation focuses on the importance of educating healthcare providers & parents on the proper treatment options for premature infants & infants with Bronchopulmonary Dysplasia that have been released from the NICU care. It is our goal and passion to bring the proper educational lectures and tools so that healthcare providers & parents can properly learn how to treat and understand these precious individuals.
Furthermore, we will be supporting NICU’s, Pediatric Units, PICU’s, Family Rooms and Child Life organizations – bags full of hats, blankets, preemie clothing and supplies for NICU babies and families. Bags full of coloring books, toys, games etc will be donated directly to the pediatric patients of all ages. We will have catered dinners for the families that are supporting those patients, and the Ronald McDonald family rooms/houses that help to give a place for the parents to eat, drink, shower and do laundry.
Our Vision
Our goal is to give back to the people that touched us directly and helped our daughter AMARA MIA ZEB when she was in the NICU for 134, and then re-admitted to the hospital on Sept 12, 2016 and passed away exactly 30 days later on October 12, 2016. She had a short life but was able to touch so many lives & hearts. In doing so, she has allowed us to continue her journey with this foundation. We will continue to touch & support everyone that has played an important part in her short life and those who supported us through the most devastating days of our lives. Amara’s Butterflies will fly and watch over as many families, children and babies for as long as we can. She would have wanted this way.
October 12th will forever be our most treasured day.