American Sickle Cell Anemia Association

52 Years Est. 1971

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Getting to Know Our Non-Profit Organization

The American Sickle Cell Anemia Association (ASCAA) is a Cleveland-based 501(C)(3) organization operating in the state of Ohio. Founded in 1971, the ASCAA is the world’s oldest sickle cell and hemoglobinopathy service organization. We are also the largest repository of statistical and case information beneficial to the worldwide patient network and the medical establishment.
In addition, our overall focus is to provide a wide range of medical-social-work-oriented services to individuals and families diagnosed with either the sickle cell trait or variants of the disease itself. Since its inception, the agency has served more than 400,000 families.

Key Agency Services Include:

  • Ongoing follow-up diagnostic testing
  • Counseling and tracking services for parents with infants who screen positive by the State of Ohio Laboratory
  • Family counseling and support services for the program’s clientele
  • Teacher education to facilitate program participant school adjustment
  • Community education and screening upwards of 75 health fairs annually
  • Outreach to the region’s African American, Hispanic, Asian, Arab, and Mediterranean communities for the purposes of education and identifying the incidence of sickle cell disease and the trait

Staff and Board of Trustees

ASCAA’s governance is provided by a 15-member board of trustees and an executive committee. Day-to-day operations are managed by Executive Director Ira Bragg-Grant and a staffing team.
Our staff serves across the domains of:
  • Social Work
  • Genetic Counseling
  • Health Promotions
  • Accounting
  • Clerical Support

Key Agency Services Include:

  • Ongoing follow-up diagnostic testing
  • Counseling and tracking services for parents with infants who screen positive by the State of Ohio Laboratory
  • Family counseling and support services for the program’s clientele
  • Teacher education to facilitate program participant school adjustment
  • Community education and screening upwards of 75 health fairs annually
  • Outreach to the region’s African American, Hispanic, Asian, Arab, and Mediterranean communities for the purposes of education and identifying the incidence of sickle cell disease and the trait

Staff and Board of Trustees

ASCAA’s governance is provided by a 15-member board of trustees and an executive committee. Day-to-day operations are managed by Executive Director Ira Bragg-Grant and a staffing team.
Our staff serves across the domains of:
  • Social Work
  • Genetic Counseling
  • Health Promotions
  • Accounting
  • Clerical Support

Staff List

Ira Bragg-Grant

Executive Director

Gilberto Peña

Bilingual Health Educator / Coordinator

TBA

Newborn Screening Coordinator

Jacqulene A. Riley, Clerical

Medical Records/Clerical

Larry Osayamwen, CPA

Accounting

Board of Trustees List

Officers

Pamela Bradford

Board Chairman

Dr. Duncan Shepherd

 Vice Chairman

Wanda Blount

Secretary

Dr. Mark Worford

 Treasurer

Dr. Grace Onimoe

Medical Director

Board

D'Wana Davis

Gary Williams, Attorney

Earsler Lesure

Dr. Duncan Shepherd

Leah Williams, Attorney

Amonte Littlejohn

Deborah Friedman, M.D.

Jagina McIntyre

Artis Gaines

Board Member Emeritus

Dr. Andrew Fishleder

Dr. Harold Ford

Dr. George Hoffman

Dr. Edgar Jackson

Dr. George Jackson

Mr. Lewis Frauenthal (Posthumous)

Dr. Anthony Stallion

Mr. Herman Leggon

Dr. Lewis Wright

Dr. John Lewis (Posthumous)

Mrs. Anita Polk (Posthumous)

Dr. Clifton Turner (Posthumous)
Ms. LeJoyce Naylor
American Sickle Cell Anemia Association
Service Area
Our organization helps people with SCD nationwide.
Hours of Operation

Monday to Friday:
8:00 AM – 4:30 PM

Phone

(216) 229-8600

Fax

(216) 229-4500

Email

irabragg@ascaa.org

Disclaimer

Please read this disclaimer carefully before using the ASCAA website or asking for advice or assistance.
All information is merely for educational and informational purposes for sickle cell anemia. It is not intended as a substitute for professional advice. Please seek an appropriately qualified and licensed physician for medical advice. Should you decide to act upon any information given, you do so at your own risk.
While the information has been verified to the best of our abilities, we cannot guarantee that there are no mistakes or errors.
We reserve the right to change this policy at any given time, which will be promptly updated. If you want to make sure that you are up to date with the latest changes, we advise you to frequently visit this page.

© 2021 American Sickle Cell Anemia Association. All rights reserved. Website by web.com.

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