STATEWIDE STEERING COMMITTEE ON SERVICES FOR ADULTS WITH SICKLE CELL DISEASE


[photo, Herbert R. O'Conor State Office Building, 201 West Preston St., Baltimore, Maryland] c/o Office for Genetics & People with Special Health Care Needs
Maryland Department of Health
Herbert R. O'Conor State Office Building, 201 West Preston St., Baltimore, MD 21201 - 2399
(410) 767-6737
e-mail: monika.piccardi@maryland.gov
web: https://phpa.health.maryland.gov/genetics/Pages/SCD_Commitee_Meetings.aspx


Herbert R. O'Conor State Office Building, 201 West Preston St., Baltimore, Maryland, December 2000 (on right is 301 West Preston St.). Photo by Diane F. Evartt.


Appointed by Secretary of Health:
Sophie Lanzkron, M.D., Co-Chair (chosen by Committee to 2-year term), 2022
Derek Robertson, Co-Chair (chosen by Committee to 2-year term), 2022
Francine Baker; Camille Butler; Charles Callahan, M.D.; Andrew Campbell, M.D.; Jason Fixler, M.D.; Shanita Fitzgerald; Beverley Francis-Gibson; Virginia Brown Gray, R.N.; Jennie Law, M.D.; Abbie Martin: Ijeoma Nnake; Lydia Pecker, M.D.; Crystal Riley, Pharm.D.; Dyshekia Strawberry, R.N.; James Taylor, M.D.; Paul Williams, Jr.; Rudolph Williams. Terms expire 2022.

Staff: Monika Piccardi, R.N.

In October 2007, the Statewide Steering Committee on Services for Adults with Sickle Cell Disease was formed (Chapter 435, Acts of 2007).

The Committee is charged with educating those with sickle cell disease, health care providers, and the public about State care and treatment. For that purpose, the Committee establishes partnerships with institutions and communities, as well as a statewide network of service providers for adults with sickle cell disease. Moreover, to implement or support its recommendations for action studies, policy, regulations, or laws, the Committee identifies funding sources, both private and from State, federal or local governments.

In consultation with the Committee, the Maryland Department of Health may provide some services relating to sickle cell disease. These include educational programs; social services support; testing; genetic counseling; assistance with reimbursement for medical expenses; education and counseling services for parents of newborns with the sickle cell trait; and any other services that decrease the use of acute care services by persons with sickle cell disease (Chapter 452, Acts of 2019).

From May 2009 to July 2019, the Committee did not meet. It was reactivated by legislation in 2019 (Chapter 452, Acts of 2019).

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