Kinslee’s Story: The Heart Behind Our Mission
On August 30, 2016, the Curtis family welcomed a bright, bubbly, beautiful little girl into the world — Kinslee Elizabeth Curtis. From the very beginning, Kinslee was full of life. She loved cheerleading, pageants, painting, swimming, shopping, dressing up, and doing everything that makes childhood magical. She quickly became the girl who could light up any room with her presence and her smile.
For the first eight years of her life, Kinslee lived a healthy and joyful life. There were no major health concerns, just everyday moments filled with laughter, family, and community. The Curtis family has always been known for being deeply rooted in their community — constantly helping others, supporting local events, and lifting up those in need without ever expecting anything in return.
But everything changed on March 3, 2025.
Kinslee began experiencing sudden symptoms: nausea, dizziness, and intense chest pains. After a series of tests and specialist evaluations, the Curtis family received news that no parent is ever prepared to hear — Kinslee had been diagnosed with a Coarctation of the Aorta, a life-threatening congenital heart defect (CHD). Her case was considered critical, requiring immediate open-heart surgery to correct the narrowing of her aorta and restore proper blood flow.
Due to Kinslee’s age and stage of development, less invasive options like a stent were not viable — her growing body meant that surgery was the only path forward. Though doctors were optimistic about the outcome, the procedure would mark the beginning of a lifelong journey of monitoring, care, and heart health management.
Through fear and uncertainty, Kinslee remained brave, her spirit unshaken. Her resilience became a beacon of hope not only for her family but for an entire community that rallied behind her. Out of this powerful movement of support, love, and strength, the Kinslee Strong nonprofit was born.
💖 Why We Exist
Kinslee Strong was created in honor of Kinslee’s courage and to carry forward her light — a light that now shines in support of other children and families battling congenital heart defects.
Our mission is to:
Support families navigating the emotional and financial hardships of CHD
Fund critical pediatric cardiac research that can improve survival rates and quality of life
Advocate for awareness, education, and early detection
Build a community of connection and hope
🌈 The Journey Continues
On March 10, 2025, Kinslee underwent open-heart surgery. It was a success, but it was just the beginning. Her journey through recovery, strength, and lifelong care inspired thousands, and her story is now a symbol of resilience for so many others.
We know that Kinslee’s fight is not over—but neither is our commitment. Through every step, Kinslee continues to inspire others to stand strong, love deeply, and fight with everything they have.
Kinslee Strong isn’t just a name — it’s a movement. A community. A promise.
To Kinslee. To every child born with a CHD. To every family walking this path.
🙏 Thank you for being part of this journey.
Learn how you can support our mission at www.KinsleeStrong.com
#KinsleeStrong #KinsleesJourney #CurtisFamilyStrong #HeartWarrior #CHDAwareness #EveryHeartbeatMatters
News(sub page to blogs and news)
Links to news announcements
Example
Media outlets
Local news journals etc
Share Your Story (sub page to blogs and news)
At Kinslee Strong, we believe that every story has the power to inspire, heal, and connect. Whether you're a parent, patient, sibling, caregiver, or friend—your journey matters. By sharing your story, you help raise awareness, offer hope to families facing similar challenges, and remind others that they are not alone. Your voice can light the way for someone else navigating the path of congenital heart defects. We invite you to share your heart, your strength, and your experience with our community. Together, our stories become a source of courage and change. 💙