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Social Work Excellence Fellowships

2009-20010 Recipient

Jacqueline Lefkowitz, LCSW, MA, MSW
New York Presbyterian Hospital – NY Weill Cornell Medical Center
New York, New York

Women with Severe and Moderate Hemophilia A and B and Other Bleeding Disorders: A Grounded Theory Study

This study will collect data from interviews with women who have moderate or severe hemophilia or another congenital bleeding disorder. Participants will be asked to express the impact that a congenital bleeding disorder has on the development and maintenance of identity and social relationships. It will provide women a chance to share how they feel about the impact that living with a bleeding disorder has on their lives. The results of this study will be of benefit to treatment providers and the entire community as we come to better understand the unique experiences of this segment of the bleeding disorders population.

Click Here to Learn About Previously Funded Recipients


All grant and fellowship applications are subjected to a rigorous peer review process. Applications are critiqued on scientific merit and relevance to NHF research priorities. Applications are reviewed and scored in terms of significance, approach, innovation, investigator, and environment. A panel selected by the Research Working Group, a volunteer group of scientific and lay leaders, reviews applications received. The NHF Medical and Scientific Advisory Council (MASAC) and the NHF Board of Directors grant final funding approval.

To be eligible for the fellowship the applicant must: be an MSW from an accredited school of social work or be a student in a DSW program or have a master's degree in a social work related field, be licensed by the state to practice as a master's level clinical social worker and work in a bleeding disorders program. Professional experience in a hemophilia treatment center is desirable but not required. The proposed project, however, must have relevance to current practice in bleeding disorders care and may incorporate casework, group work, organizational and public health, education and research perspectives.

It is expected that the project will: (1) promote the integration of psychosocial care with biomedical components of comprehensive care; (2) promote the delivery of quality services to patients and families; (3) contribute to the literature on the psychosocial aspects of bleeding disorders; (4) demonstrate social work outcomes of the research or clinical project.

Areas of research interest might include some of the following topics: impact of social work practice on coping with chronic illness and/or disability; impact of case management on patient care; improved clinical practice; research skills and goals for psychosocial providers; mental health issues of those affected with bleeding disorders or bleeding disorders/HIV; development and use of media projects and/or learning tools for professional or patient evaluation. A focus on cultural diversity is welcomed.

NHF awards one new research fellowship per year of $10,000.


A letter of intent should be submitted to NHF. This should be a brief letter identifying the applying researcher and organization and the intended area of research.

Multidisciplinary applications are welcomed. If a multidisciplinary project is sought, you are encouraged to indicate in the letter of intent and in the application how the project would proceed if only one Fellowship is awarded.

For inquiries regarding applications, policy and procedures and programmatic information, contact:

Morgan Johnson, CAE, Manager of Healthcare Provider Programs
National Hemophilia Foundation
116 West 32nd Street, 11th Floor
New York, NY 10001
(800) 424-2634 ext. 3745 or (212) 328-3745
Fax: (212) 328-3799

Direct inquiries regarding fiscal matters to:

Department of Finance and Administration
National Hemophilia Foundation
116 West 32nd Street, 11th Floor
New York, NY 10001
(800) 424-2634 ext. 3726 or (212) 328-3726
Fax 212-328-3766