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About SCD/SCT

Patient education

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About Sickle Cell Disease & Trait

SCD is the world's most common genetic blood disorder. Understanding it changes everything.

Why SCMA exists

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Three commitments that guide every call.

 

Our Mission

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Our Vision

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Our Objective

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Sickle Cell Medical Advocacy Inc. empowers patients, caregivers, and community advocates with comprehensive education and advocacy training to improve healthcare outcomes for individuals with sickle cell disease.

 

Through education on national sickle cell management guidelines and one-on-one advocacy training, participants gain the skills to navigate timely medical intervention, leading to faster recovery and reduced hospital stays

Our vision is to optimize medical management, decreasing the incidence of end-organ damage
and increasing the quality of life and lifespan in sickle cell patients.

Our objective is to dismantle the barriers that obstruct effective ER and hospital treatments for those with sickle cell disease through a comprehensive virtual healthcare  navigation center. We offer services such as medical advocacy, mental health support, community outreach, and educational courses for sickle cell patients.

Our commitment is to empower sickle cell patients with improved healthcare access and enhance their treatment outcomes in hospital settings.

DISEASE

An inherited blood disorder where red blood cells form a rigid sickle shape, blocking blood flow and causing pain crises, organ damage, and increased infection risk. About 100,000 people in the US live with SCD; 1 in 365 African American babies are born with it.

TRAIT

Research increasingly shows the trait can be symptomatic — causing patients to need medical care. SCMA extends its services to cover those with the trait who may need medical intervention.

U.S. STATISTICS 

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Who is affected

100,000

People with SCD in the US

1 in 13

African American babies born with sickle trait

1 in 365

African American babies born with SCD

1 in 16,300

Latino babies born with SCD

GLOBAL REACH

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SCD affects millions worldwide

SCD affects millions with ancestral ties to sub-Saharan Africa, Central and South America, and the Caribbean. People living with SCD are also found in Saudi Arabia, India, and Mediterranean countries.

Sub-Saharan Africa

Central & South America

Caribbean

Saudi Arabia

India

Mediterranean

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Courses & training

Sickle Cell Healthcare Navigator Certification
(10 weeks)

Empowered Patient Training

Contact Us: 

Patients Seeking SCD Navigator

Caregiver needing a SCD Navigator

Questions?

TRANSFORMATIVE and QUALITY healthcare for Sickle Cell patients.

 

©SCMA2021

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