My Moving Encounter With the McCalls
When it comes to helping others deal with chronic diseases, few families offer as much of themselves as the McCall family. Daughter Morgan was born with cystic fibrosis, a genetic disease that can appear when both parents carry the trait, but that is almost always a surprise when it appears in their child. Over the years, the McCalls have transitioned from the initial shock and learning how to cope to becoming a model for other families. Today they use Morgan’s disease as a springboard for their tireless hours of volunteering to teach and fundraise for other families who must cope with a child’s cystic fibrosis.
At age 11, Morgan is a remarkable young lady, and a great deal of the credit for that goes to her parents. They have never put limits on her, have never suggested that she couldn’t or shouldn’t do something she wanted to try. As a result, Morgan is fearless in her approach to life. She is an A student and accomplished at both gymnastics and dance.
Of course, Morgan doesn’t remember being diagnosed, nor does she make decisions about her treatment. But she is most definitely a participatory and proactive patient, handling much of her treatment herself and reporting to her doctor.
Morgan McCall, age 11, living well with cystic fibrosis
Read her story of empowerment and strength in her own words
Meet Brandt McCall, Morgan’s brother, protector, and passionate fundraiser
Read his story of gaining acceptance of his sister’s disease
Paula and Steve McCall, Morgan’s parents, and outspoken ambassadors for parents of children with illnesses
Read their story of embracing caregiving in their own words