Ladies and gentlemen, we would like to introduce you to Brandon! This sweet little dude had a rocky start to life, and he worried his mama later in November of last year when he had his complete repair for Atrioventricular septal defect (AVSD). Despite Brandon’s trials, his mom still found the time to become a champion for breastfeeding while inpatient. She also contributes to the local heart community on a regular basis with her kind and caring input. We so enjoy this little family!
Meet Emiliana, the very first of many special young warriors we can’t wait to introduce to you! New Year, New Projects Announcing the launch of our newest program, Heart Kid of the Month! As our organization continues to see the Southern Arizona community support our CHD Warriors, we felt it would be supercool to introduce…
CHD Families of Tucson has been working for the past year to stretch beyond “Tucson” and support CHD kiddos from Southern Arizona in general. We love to connect Heart parents with one another, and watch as little communities pop up across the lower half of the Grand Canyon State. We find ourselves particularly heart-warmed by…
Addison may very well be the face of CHD in Tucson, and yet, at five years old, her light is such a shining force that her defect in no way defines her. Whether its organizing an energized team for the local Heart and Stroke Walk, or encouraging the community to “Open Their Hearts” and support…
Esme’s parents want other military families to know that “the EFMP program (exceptional family members) may be helpful to ensure you can be stationed in places that have civilian or military care to meet your child’s needs. Moving with a medically fragile child and changing their care team can be very stressful, however, Tricare can…
As we wrap up our Heart Kid of the Month program for 2018, and prepare to re-launch it in 2019, we wanted to close with a special family. Adelina, along with her parents and her sisters Charlize and Melani, were featured in last year’s community report. Her mama shared a heartfelt letter with our base…
Gabriel and his family have been with our group since it’s early days. Since Gabriel is more of a young man than a “kid”, his mom has seen many things that are still new for parents of younger CHD kids, and she is quick to share her experiences or offer helpful input. She has also…