Blog
Announcing The Glory Days Foundation
Through The Glory Days Foundation, a 501(c)3 nonprofit, we can all work together to create a huge, positive impact in the lives of families. We are offering the support families need to feel equipped in their role as a special needs parent. Connecting them to resource guides, support organizations and handing them a planner to help navigate the coming months and years at the time if diagnosis and beyond.
How to Make the Most of The Glory Days Launch!
The Glory Days Daily Planner Launch Day is in TWO days! We are so THRILLED that we have the opportunity to share The Glory Days Daily Planner with all of you in a few short days. Some upcoming fun for launch week is on it’s way to you along with launch day tips.
Get To Know Us!
The Glory Days Daily Planner was designed to meet the unique needs of a parent or caregiver raising a child who is differently abled. This planner was created by a mom living the everyday life of a special needs parent. Each page was thoughtfully designed with you in mind.
The Bigger Picture
A Weekend with Community
Nine families gathered with their children to film a Down Syndrome Awareness video for Down Syndrome Awareness month. We’ve been connected via The DSDN and Instagram for a little over a year now. We have processed our diagnosis, our fears, and joys together.
A day in her shoes- Loving a little one with Trisomy 18
How to Support a Friend or Family Member Whose Child Has Received a Special Needs Diagnosis
September Simplicity
Five Tips to Share a Special Needs Diagnosis with Friends and Family
Sharing the news with friends and family that our daughter was born with Down Syndrome was a task that filled me with anxiety. In the beginning, I just wasn’t ready to talk about it. I needed time to get my mind right and understand our new reality.
If you’re currently navigating how to share your child’s special needs diagnosis with friends and family, here are a few things to consider before you begin sharing the news.