Stone Soup Group Board Member, Matt Findley, explains how his son reached the lifetime cap imposed by his employer-based healthcare plan in less than two years. Hear one way Alaskans like his son who are living with a disability would be impacted by potential changes to healthcare. Thank you Matt for sharing your story!
Having a child with a rare genetic disease or a lifelong disability opens your eyes up to a whole new understanding of how medical care, prescriptions, and insurance work. Before my kids, I thought I understood… You had insurance, you had a co-pay and a deductible, and you got the treatment and medication you needed Learn More