About Our Journey

CamO’s Story

After being a born a happy & healthy boy, at 2 months old Cameron was losing weight & breathing unusually. This lead to an extensive workup during a week long inpatient hospital stay. Cam was discharged from the hospital with a rare diagnosis of Neuroendocrine Cell Hyperplasia of Infancy (NEHI), which is a subtype of Childhood Interstitial Lung Disease (chILD).

With this chronic lung disease and the effects on his body, Cam has many increased needs. Cam requires 24/7 oxygen use, a heart rate/oxygen level monitor, multiple types of breathing therapy devices, and nutritional support with a surgically implanted feeding tube. With his lung disease, a simple cold can lead him to need additional oxygen support and hospitalization. He has spent many nights hanging out with his family and getting to know the nurses at M Health Fairview Masonic Children’s Hospital. He has received incredible care at Masonic and with the many different specialties that he interacts with there.

Despite his medical needs, Cameron is a rambunctious toddler boy. His parents have strived to promote normalcy in his life, sending him to daycare, playing with friends, attending community events, and engaging in sports. Although it remains unclear when he may outgrow his need for these additional supports, they have navigated the logistics of his medical needs to allow him to have this normalcy whenever possible.

Meet the Olson Family

Cameron’s medical journey has been one that has been full of support & love from family, friends, and the community. His parents, Dexter & Kelsey, and big sister, Kennedy, have relied on their support system each day as they navigate the frequent changes, ups, and downs. Throughout this journey, they quickly noticed the lack of resources, awareness, and support available to families impacted by rare diagnoses, such as chILD.

With the support of Team CamO, they took on the mission of tackling this resource and support discrepancy to improve the lives of kiddos like Cam & families like their own. In 2024, they formally launched the CamO Fund! They continue to manage Cameron’s medical needs and work their full time jobs, but they are now raising their two energetic kiddos to help others & give back!

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