Scott Center for Observation Treatment and Transition

The Scott Center for Observation, Treatment, and Transition (S.C.O.T.T.)

The Scott Center for Observation, Treatment, and Transition is a nonprofit organization dedicated to improving the lives of individuals and families impacted by sickle cell disease (SCD) and sickle cell trait. As the first nonprofit in the state of Ohio to focus specifically on the transition from pediatric to adult care, the Scott Center bridges a critical gap in healthcare by ensuring that young people with SCD are not lost in the system during one of the most vulnerable points in their health journey.

Who We Serve

We serve:

Children, adolescents, and adults living with sickle cell disease

Individuals who carry the sickle cell trait

Families and caregivers in need of education, advocacy, and community support

Healthcare providers, educators, and policymakers seeking resources and training to better support patients

Our service area includes all 11 counties of Northwest Ohio, with growing outreach in Michigan and beyond. Since our founding, we have touched the lives of over 1,000 families, walking alongside them with compassion, knowledge, and advocacy.

Services Provided

The Scott Center provides a holistic suite of programs and services designed to address not just the medical, but also the educational, emotional, and social aspects of sickle cell care:

Patient & Family Support

Case management, education, and navigation of healthcare and social service systems

Support groups for patients and families to build community and reduce isolation

Crisis prevention resources to reduce hospitalizations and improve outcomes

Education & Awareness

Community workshops on sickle cell disease, trait, genetic counseling, and family planning

School-based education for teachers, administrators, and peers to foster understanding and reduce stigma

Professional trainings for healthcare providers to strengthen competency in SCD care

Advocacy & Policy

Legislative and policy advocacy to ensure sickle cell families have equitable access to care

Collaboration with local, state, and national representatives to expand resources and support for the SCD community

Transition Care Programs

Guidance for adolescents moving from pediatric to adult healthcare systems

Coaching for families to navigate insurance, medical appointments, and treatment changes

Development of individualized transition plans to ensure continuity of care

Community Engagement & Events

Annual Heal Together Race for Sickle Cell 5K, bringing awareness and unity to the community

Public health campaigns to dispel myths, reduce stigma, and amplify the voices of warriors and families

Partnerships with schools, libraries, healthcare providers, and civic organizations to expand impact

Why We Exist

Sickle cell disease is one of the most common genetic blood disorders in the U.S., yet it remains widely misunderstood, underfunded, and stigmatized. In Northwest Ohio, families historically lacked dedicated resources and advocacy. The Scott Center was created out of lived experience and deep commitment—founded by Dr. La’Shardae Scott, a mother of two sons thriving with sickle cell disease—who recognized firsthand the urgent need for a trusted, community-centered hub of support.

We exist because patients deserve competent, compassionate, and continuous care—and families deserve hope, education, and empowerment. Our work ensures that warriors are not defined by their diagnosis but are supported to live healthy, fulfilling, and resilient lives.