My book is now available! It is a guide for those who want to support caregivers in meaningful ways, and is based on my personal experiences over the past six years.
Has your friend or relative received a diagnosis for their child, and you want to know how to help?
Are you a parent feeling overwhelmed and at times isolated by your own child’s needs?
Right now there is such a gap between parents of disabled kids and the “villages” we look to for support.
In 2018, I started this website as a way to process my thoughts and emotions after my young son JB was diagnosed with a genetic syndrome.
By sharing my experience, I want to bridge that divide through honest conversation about friendship, parenting, disability, and inclusion.