RARE MAMAS RISING- EPISODE 39

Blazing Trails to Cure and Care with The Charlotte and Gwenyth Gray Foundation to Cure Batten Disease Founder Kristen Gray

Kristen Gray is an extraordinary mom of four incredible children: Charlotte, Gwenyth, Callan, and Gavin. From the moment her eldest two, Charlotte and Gwenyth, were diagnosed with Batten Disease, she embarked on a courageous journey blazing trails in rare disease advocacy. She founded The Charlotte & Gwenyth Gray Foundation to Cure Batten Disease and established The Gray Academy, a beacon of hope and education for children facing complex neurological disorders. Her unwavering dedication and pioneering spirit have been a driving force behind groundbreaking initiatives to find treatments and support families in similar situations. Join us as we delve into her inspiring story of resilience, hope, and relentless determination to change the future for her children and others.

EPISODE HIGHLIGHTS

• The discovery of Charlotte and Gwenyth’s Batten Disease diagnoses
• Founding The Charlotte & Gwenyth Gray Foundation to Cure Batten Disease
• Development of The Gray Academy and their approach to education
• Balancing advocacy and motherhood
• Kristen’s vision for the future of children and families affected by neurological disorders
• Kristen’s best learnings for other rare mamas

LINKS

The Charlotte & Gwenyth Gray Foundation to Cure Batten Disease

Website: www.curebatten.org 

Instagram: @curebatten
Facebook: @curebatten

The Gray Academy

Website: www.thegrayacademy.org

Instagram: @thegrayacademy

Facebook: @thegrayacademy

CONNECT WITH NIKKI

Website

https://raremamas.com/

Instagram

https://www.instagram.com/Rare_Mamas/

Email

info@raremamas.com