In Loving Memory of Hazel Grace

10/03/2026

https://www.facebook.com/share/p/1F6yrACKpq/

10/03/2026

We love and miss you like crazy Hazel Grace Bradshaw!! 💔😭

10/02/2026

https://www.facebook.com/share/p/19sEHgfdSa/

Every year the month of October is recognized as Child Death Awareness Month. Please remember all our children and their families who lost a child. We would love to show our love and remember your child with you…

09/25/2026

https://www.facebook.com/share/p/19aRMmQk1D/

Still here 🦋🤍

09/20/2026

💚 Mitochondrial Disease Awareness Week 💚

This week, we are shining a little extra green for the children and families living with mitochondrial disease.

Mitochondria are often called the “powerhouses” of our cells because they help create the energy our bodies need. When they don’t work the way they should, it can affect many different parts of the body. Mitochondrial disease can also look very different from one person to another, which can sometimes make the road to answers a long one.

For families living this journey, awareness is about so much more than wearing green. It is about helping others understand the appointments, therapies, hospital stays, uncertainty, celebrations, milestones, and victories that are part of their everyday lives.

It is also about hope. Hope for more research. Hope for better treatments. Hope for earlier answers. Hope for a future where families feel seen, supported, and understood. 💚

Throughout Mitochondrial Disease Awareness Week, we stand with every child and family affected by mitochondrial disease, including the families within our own Born Abel community.

We see your children. We celebrate their stories. We are cheering them on every step of the way.

09/20/2026

09/20/2026

💛🎗️💛

09/20/2026

💚 Mito Awareness Week — Day 7
Your voice can make a difference. By sharing, learning, advocating, and participating in research, we can build a brighter future for everyone living with Leigh syndrome. 💚

09/19/2026

💚 Mito Awareness Week — Day 6
Our data can drive research. More than 470 individuals are part of the Leigh Syndrome Global Patient Registry. Every participant helps us learn more.

09/19/2026

A genetic counselor can be the first person to actually explain a mitochondrial disease diagnosis to a family. Urge Congress to pass the Access to Genetic Counselor Services Act so that guidance isn't limited by geography or insurance. Take action via the Mitochondrial Disease Advocacy Coalition: https://mitoadvocacy.org/wmdw/