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Welcome to SCDAA CT

We are a registered 501(C)(3) nonprofit organization.

Give Today

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WALK  RUN  BIKE

     September 26th 2026

Edgewood Park Coogan Pavilion

7 am - 1 pm

Our Mission

At Sickle Cell Disease Association of America, Connecticut (Michelle's House), we embrace prevention strategies to enhance the quality of life and well-being of the community affected by Sickle Cell Disease (SCD), Sickle Cell Trait, and related conditions and provide individuals and families with critical education and access to support services through
partnerships and advocacy.

Modern Office
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Boost Your Career!
Job Readiness Training Program.

Walk Run Bike
September 26, 2026

Warrior Trips

Join SCD Members on exciting trips to NASA, the Smithsonian, national conferences, and more! Experience unforgettable adventures and connect with fellow members while exploring amazing destinations. Don’t miss out on these incredible opportunities to learn and grow together!

Our Vision

To enhance all aspects of the quality of life of the Sickle Cell Community inclusive of finding a cure!

Recent state data shows
a
17% increase in the number
of babies born with the Sickle Cell Trait (SCT).

National annual percentage of students that repeat a grade: 4.5% without SCD, up to 40% with SCD.

In Connecticut, nearly 40,000 residents carry the Sickle Cell Trait (SCT).

EVERY DOLLAR MAKES A DIFFERENCE

Help create hope within the Sickle Cell Disease Community.

Contact Us

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SCDAA CT is the first Sickle Cell Disease Community Center in Connecticut. We're here to help you and your family navigate the challenges associated with SCD and/or SCT. Please reach out to one of our staff members for more information.
 

Main Office:  203-859-5355

Our Services

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Teen Ambassador

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Sickle Cell Tutorial Program

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Public Awareness Program

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Hours ​

 

 

Monday        9:00am - 5:00pm

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Tuesday        9:00am - 5:00pm

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Wednesday  9:00am -5:00pm

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Thursday       9:00am - 5:00pm

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Friday            9:00am - 5:00pm

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©2026 by SCDAA-CT. Proudly created with Wix.com. Designed by Monica Vinston.

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