Parker Joy is a bright and loving 15-month-old who was recently diagnosed with Noonan Syndrome, a rare genetic disorder. PJ as she is known by family and friends is facing Pulmonary Stenosis. Her parents, Michelle and David, live in Rawlins, Wyoming, where specialized medical care is generally not available. This diagnosis has brought many challenges and uncertainties for their family, especially since Parker’s father, David, had open heart surgery at age 3.

To get Parker the care she needs, the family must travel 367 miles one way to Denver, Colorado, for specialized treatment. The costs of travel, a week-long hotel stay, and food quickly add up, putting a significant financial strain on Michelle and David. With this latest diagnosis, there may be future treatments and surgeries ahead for this sweet little girl, making ongoing support even more important.

Your generosity can help ease the burden on Parker’s family and ensure she receives the best possible care. Any support you can give—whether through donations or by sharing this fundraiser—means the world to Michelle, David, and especially Parker. Thank you for being part of their journey and for helping this young family during such a difficult time.