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Lisa and her husband welcomed their beautiful, healthy baby girl, Olivia, and so began their parenting journey. When Olivia was 10 months old, Lisa began to notice that instead of progressing and meeting the typical milestones, Olivia seemed to be regressing, and slowly losing her ability to function. After numerous tests, doctors’ appointments, and visits with specialists, Olivia was eventually diagnosed with Alexander Disease- an extremely rare, degenerative brain disease. As Lisa listened to the doctor relay Olivia’s diagnosis over the phone, telling her to find a support group and do what she could to make her daughter comfortable, all of her hopes and dreams about what her future with her daughter would look like were shattered. Over the course of the next 8 years of Olivia's life, Lisa and her family were thrust into the strange, and often scary, world of hospitals, in-home care, medications, insurance nightmares, and watching their daughter lose brain function and her ability to move.
Truthfully? She didn’t know. She was sad. She was depressed. And she felt so incredibly empty. She had neglected her own physical and mental health. She had lost sight of what her gifts, talents, and interests were. And on top of all of that, she had to try and keep her marriage intact, while also now raising a healthy, vibrant little boy, who was born in the midst of immense family trauma.
To learn more about The Olivia Kay Foundation, all that they do for patients in pediatric units at hospitals all over the U.S. and into Canada, and how YOU can support them, click here.
Photographer: Megan Hansen Photography
Location: Shades of Teal
Apparel: Self Love Beauty
Hair: Reckless Hair
Make-up: Adrienne Stratton