"Inclusivity. Our Strength. our power."

Our vital mission which serves as our guiding light to reach our destination; is to raise awareness for Amniotic Band Syndrome, by helping educate the public, support affected families, and encourage research for this rare condition.

This initiative and the accompanying book exist to shine a light on Amniotic Band Syndrome, inspired by our incredible, one-of-a-kind boy, Kairo Lexington Lowe. Kairo’s journey reminds us of the strength and resilience that can emerge in the face of challenges.

Through sharing Kairo's story and that of many other beautiful people, we aim to raise awareness, educate others, and create a supportive community for families navigating similar experiences. Together, we can turn Kairo's journey into a source of hope and inspiration for many, fostering understanding and compassion for all those affected by ABS.

"Son - I will always champion your uniqueness and ensure it empowers you victoriously - love mommy!"

Our vision is our destination!  Our vision is to first educate everyone about what ABS is. We hope to do this by utilizing Social Media, Websites, and Community Events to disseminate knowledge. 

We also wish to support all affected families impacted by ABS, by creating a safe space that will offer resources, support groups and allow for sharing of experiences and advice. Visibility and representation is vital and therefore highlighting stories of individuals affected by ABS and help us humanize this rare condition will further help us foster understanding and empathize within the community. 

Events such as awareness days, and a yearly ABS Walk, is our commitment to engage the communities and raise funds for support services and research. 

Lastly - by bringing awareness to ABS, this may increase the need for funding and research into this rare condition to better understand its causes, improve diagnosis, and enhance treatment options pre and post birth. The hope is also for possible medical professional collaborations, which will allow for health care providers to share the latest information and resources to support our families dealing with ABS.